Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.43063955_43071241del | CA10575957 | BRCA1 | c.4674_5072del c.4677_5075del c.4551_4949del c.4671_5069del c.4599_4997del c.1365_1763del c.1227_1625del c.3789_4187del c.4554_4952del c.4743_5141del c.4536_4934del c.1239_1637del c.4740_5138del c.1064_1462del c.1251_1649del c.*4460_*4858del c.990_1388del c.5-7286_5del c.150_548del c.-98-21047_-98-13761del (n.-98-21047_-98-13761del) n.4813_5211del n.4854_5252del | |
17 | g.43066661_43072815del | CA913190336 | BRCA1 | c.4672+1532_5071+963del c.4675+1532_5074+963del c.4549+1532_4948+963del c.4669+1532_5068+963del c.4597+1532_4996+963del c.1363+1532_1762+963del c.1225+1532_1624+963del c.3787+1532_4186+963del c.4552+1532_4951+963del c.4741+1532_5140+963del c.4534+1532_4933+963del c.1237+1532_1636+963del c.4738+1532_5137+963del c.1062+1532_1461+963del c.1249+1532_1648+963del c.*4458+1532_*4857+963del c.988+1532_1387+963del c.5-8848_5-2694del (n.5-8848_5-2694del) c.148+1532_547+963del c.-98-22609_-98-16455del (n.-98-22609_-98-16455del) n.4811+1532_5210+963del n.4852+1532_5251+963del | ClinVar |
17 | g.43067611_43071241del | CA2581463406 | BRCA1 | c.4673_5071del c.4676_5074del c.4550_4948del c.4670_5068del c.4598_4996del c.1364_1762del c.1226_1624del c.3788_4186del c.4553_4951del c.4742_5140del c.4535_4933del c.1238_1636del c.4739_5137del c.1063_1461del c.1250_1648del c.*4459_*4857del c.989_1387del c.5-7287_5-3657del (n.5-7287_5-3657del) c.149_547del c.-98-21048_-98-17418del (n.-98-21048_-98-17418del) n.4812_5210del n.4853_5251del | |
17 | g.43070037_43072667del | CA10602585 | BRCA1 | c.4673-1420_4983+900del c.4676-1420_4986+900del c.4550-1420_4860+900del c.4670-1420_4980+900del c.4598-1420_4908+900del c.1364-1420_1674+900del c.1226-1420_1536+900del c.3788-1420_4098+900del c.4553-1420_4863+900del c.4742-1420_5052+900del c.4535-1420_4845+900del c.1238-1420_1548+900del c.4739-1420_5049+900del c.1063-1420_1373+900del c.1250-1420_1560+900del c.*4459-1420_*4769+900del c.989-1420_1299+900del c.5-8707_5-6077del (n.5-8707_5-6077del) c.149-1420_459+900del c.-98-22468_-98-19838del (n.-98-22468_-98-19838del) n.4812-1420_5122+900del n.4853-1420_5163+900del | ClinVar |
17 | g.43070145_43072775del | CA2697559917 | BRCA1 | c.4673-1528_4983+792del c.4676-1528_4986+792del c.4550-1528_4860+792del c.4670-1528_4980+792del c.4598-1528_4908+792del c.1364-1528_1674+792del c.1226-1528_1536+792del c.3788-1528_4098+792del c.4553-1528_4863+792del c.4742-1528_5052+792del c.4535-1528_4845+792del c.1238-1528_1548+792del c.4739-1528_5049+792del c.1063-1528_1373+792del c.1250-1528_1560+792del c.*4459-1528_*4769+792del c.989-1528_1299+792del c.5-8815_5-6185del (n.5-8815_5-6185del) c.149-1528_459+792del c.-98-22576_-98-19946del (n.-98-22576_-98-19946del) n.4812-1528_5122+792del n.4853-1528_5163+792del | ClinVar |
17 | g.43070208_43078359dup | CA16043350 | BRCA1 | c.4358-1732_4983+736dup c.4358-1729_4986+736dup c.4232-1729_4860+736dup c.4352-1729_4980+736dup c.4280-1729_4908+736dup c.1046-1729_1674+736dup c.908-1729_1536+736dup c.3470-1729_4098+736dup c.4235-1729_4863+736dup c.4423+991_5052+736dup c.4217-1729_4845+736dup c.923-1732_1548+736dup c.4423+991_5049+736dup c.744+991_1373+736dup c.932-1729_1560+736dup c.*4141-1729_*4769+736dup c.1049-1732_1674+736dup c.671-1729_1299+736dup c.5-14392_5-6241dup (n.5-14392_5-6241dup) c.-43-3822_459+736dup c.-98-28153_-98-20002dup (n.-98-28153_-98-20002dup) n.4494-1729_5122+736dup n.4535-1729_5163+736dup | |
17 | g.43070192_43078360dup | CA2580612611 | BRCA1 | c.4358-1749_4983+736dup c.4358-1746_4986+736dup c.4232-1746_4860+736dup c.4352-1746_4980+736dup c.4280-1746_4908+736dup c.1046-1746_1674+736dup c.908-1746_1536+736dup c.3470-1746_4098+736dup c.4235-1746_4863+736dup c.4423+974_5052+736dup c.4217-1746_4845+736dup c.923-1749_1548+736dup c.4423+974_5049+736dup c.744+974_1373+736dup c.932-1746_1560+736dup c.*4141-1746_*4769+736dup c.1049-1749_1674+736dup c.671-1746_1299+736dup c.5-14409_5-6241dup (n.5-14409_5-6241dup) c.-43-3839_459+736dup c.-98-28170_-98-20002dup (n.-98-28170_-98-20002dup) n.4494-1746_5122+736dup n.4535-1746_5163+736dup | |
17 | g.43071092_43071107delinsCAACTTTCAATTGGGG | CA2260772908 | BRCA1 | c.4804_4819delinsCCCCAATTGAAAGTTG (p.Pro1602=) c.4807_4822delinsCCCCAATTGAAAGTTG (p.Pro1603=) c.4681_4696delinsCCCCAATTGAAAGTTG (p.Pro1561=) c.4801_4816delinsCCCCAATTGAAAGTTG (p.Pro1601=) c.4729_4744delinsCCCCAATTGAAAGTTG (p.Pro1577=) c.1495_1510delinsCCCCAATTGAAAGTTG (p.Pro499=) c.1357_1372delinsCCCCAATTGAAAGTTG (p.Pro453=) c.3919_3934delinsCCCCAATTGAAAGTTG (p.Pro1307=) c.4684_4699delinsCCCCAATTGAAAGTTG (p.Pro1562=) c.4873_4888delinsCCCCAATTGAAAGTTG (p.Pro1625=) c.4666_4681delinsCCCCAATTGAAAGTTG (p.Pro1556=) c.1369_1384delinsCCCCAATTGAAAGTTG (p.Pro457=) c.1414_1429delinsCCCCAATTGAAAGTTG (p.Pro472=) c.4870_4885delinsCCCCAATTGAAAGTTG (p.Pro1624=) c.1194_1209delinsCCCCAATTGAAAGTTG c.1381_1396delinsCCCCAATTGAAAGTTG (p.Pro461=) c.*4590_*4605delinsCCCCAATTGAAAGTTG (n.*4590_*4605delinsCCCCAATTGAAAGTTG) c.1120_1135delinsCCCCAATTGAAAGTTG (p.Pro374=) c.5-7156_5-7141delinsCCCCAATTGAAAGTTG (n.5-7156_5-7141delinsCCCCAATTGAAAGTTG) c.280_295delinsCCCCAATTGAAAGTTG (p.Pro94=) c.-98-20917_-98-20902delinsCCCCAATTGAAAGTTG (n.-98-20917_-98-20902delinsCCCCAATTGAAAGTTG) n.4943_4958delinsCCCCAATTGAAAGTTG n.4984_4999delinsCCCCAATTGAAAGTTG | |
17 | g.43071103_43071117del | CA003026 | BRCA1 | c.4804_4818del (p.Pro1602_Val1606del) c.4807_4821del (p.Pro1603_Val1607del) c.4681_4695del (p.Pro1561_Val1565del) c.4801_4815del (p.Pro1601_Val1605del) c.4729_4743del (p.Pro1577_Val1581del) c.1495_1509del (p.Pro499_Val503del) c.1357_1371del (p.Pro453_Val457del) c.3919_3933del (p.Pro1307_Val1311del) c.4684_4698del (p.Pro1562_Val1566del) c.4873_4887del (p.Pro1625_Val1629del) c.4666_4680del (p.Pro1556_Val1560del) c.1369_1383del (p.Pro457_Val461del) c.1414_1428del (p.Pro472_Val476del) c.4870_4884del (p.Pro1624_Val1628del) c.1194_1208del c.1381_1395del (p.Pro461_Val465del) c.*4590_*4604del (n.*4590_*4604del) c.1120_1134del (p.Pro374_Val378del) c.5-7156_5-7142del (n.5-7156_5-7142del) c.280_294del (p.Pro94_Val98del) c.-98-20917_-98-20903del (n.-98-20917_-98-20903del) n.4943_4957del n.4984_4998del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071102_43071127del | CA2695225907 | BRCA1 | c.4784_4809del (p.Ser1595PhefsTer17) c.4787_4812del (p.Ser1596PhefsTer17) c.4661_4686del (p.Ser1554PhefsTer17) c.4781_4806del (p.Ser1594PhefsTer17) c.4709_4734del (p.Ser1570PhefsTer17) c.1475_1500del (p.Ser492PhefsTer17) c.1337_1362del (p.Ser446PhefsTer17) c.3899_3924del (p.Ser1300PhefsTer17) c.4664_4689del (p.Ser1555PhefsTer17) c.4853_4878del (p.Ser1618PhefsTer17) c.4646_4671del (p.Ser1549PhefsTer17) c.1349_1374del (p.Ser450PhefsTer17) c.1394_1419del (p.Ser465PhefsTer17) c.4850_4875del (p.Ser1617PhefsTer17) c.1174_1199del c.1361_1386del (p.Ser454PhefsTer17) c.*4570_*4595del (n.*4570_*4595del) c.1100_1125del (p.Ser367PhefsTer17) c.5-7176_5-7151del (n.5-7176_5-7151del) c.260_285del (p.Ser87PhefsTer17) c.-98-20937_-98-20912del (n.-98-20937_-98-20912del) n.4923_4948del n.4964_4989del | |
17 | g.43071107del | CA658825007 | BRCA1 | c.4807del (p.Gln1603AsnfsTer2) c.4810del (p.Gln1604AsnfsTer2) c.4684del (p.Gln1562AsnfsTer2) c.4804del (p.Gln1602AsnfsTer2) c.4732del (p.Gln1578AsnfsTer2) c.1498del (p.Gln500AsnfsTer2) c.1360del (p.Gln454AsnfsTer2) c.3922del (p.Gln1308AsnfsTer2) c.4687del (p.Gln1563AsnfsTer2) c.4876del (p.Gln1626AsnfsTer2) c.4669del (p.Gln1557AsnfsTer2) c.1372del (p.Gln458AsnfsTer2) c.1417del (p.Gln473AsnfsTer2) c.4873del (p.Gln1625AsnfsTer2) c.1197del c.1384del (p.Gln462AsnfsTer2) c.*4593del (n.*4593del) c.1123del (p.Gln375AsnfsTer2) c.5-7153del (n.5-7153del) c.283del (p.Gln95AsnfsTer2) c.-98-20914del (n.-98-20914del) n.4946del n.4987del | ClinVar dbSNP |
17 | g.43071105G>A | CA500231824 | BRCA1 | c.4806C>T (p.Pro1602=) c.4809C>T (p.Pro1603=) c.4683C>T (p.Pro1561=) c.4803C>T (p.Pro1601=) c.4731C>T (p.Pro1577=) c.1497C>T (p.Pro499=) c.1359C>T (p.Pro453=) c.3921C>T (p.Pro1307=) c.4686C>T (p.Pro1562=) c.4875C>T (p.Pro1625=) c.4668C>T (p.Pro1556=) c.1371C>T (p.Pro457=) c.1416C>T (p.Pro472=) c.4872C>T (p.Pro1624=) c.1196C>T c.1383C>T (p.Pro461=) c.*4592C>T (n.*4592C>T) c.1122C>T (p.Pro374=) c.5-7154C>T (n.5-7154C>T) c.282C>T (p.Pro94=) c.-98-20915C>T (n.-98-20915C>T) n.4945C>T n.4986C>T | ClinVar dbSNP |
17 | g.43071105G>C | CA500231822 | BRCA1 | c.4806C>G (p.Pro1602=) c.4809C>G (p.Pro1603=) c.4683C>G (p.Pro1561=) c.4803C>G (p.Pro1601=) c.4731C>G (p.Pro1577=) c.1497C>G (p.Pro499=) c.1359C>G (p.Pro453=) c.3921C>G (p.Pro1307=) c.4686C>G (p.Pro1562=) c.4875C>G (p.Pro1625=) c.4668C>G (p.Pro1556=) c.1371C>G (p.Pro457=) c.1416C>G (p.Pro472=) c.4872C>G (p.Pro1624=) c.1196C>G c.1383C>G (p.Pro461=) c.*4592C>G (n.*4592C>G) c.1122C>G (p.Pro374=) c.5-7154C>G (n.5-7154C>G) c.282C>G (p.Pro94=) c.-98-20915C>G (n.-98-20915C>G) n.4945C>G n.4986C>G | dbSNP |
17 | g.43071105G>T | CA500231823 | BRCA1 | c.4806C>A (p.Pro1602=) c.4809C>A (p.Pro1603=) c.4683C>A (p.Pro1561=) c.4803C>A (p.Pro1601=) c.4731C>A (p.Pro1577=) c.1497C>A (p.Pro499=) c.1359C>A (p.Pro453=) c.3921C>A (p.Pro1307=) c.4686C>A (p.Pro1562=) c.4875C>A (p.Pro1625=) c.4668C>A (p.Pro1556=) c.1371C>A (p.Pro457=) c.1416C>A (p.Pro472=) c.4872C>A (p.Pro1624=) c.1196C>A c.1383C>A (p.Pro461=) c.*4592C>A (n.*4592C>A) c.1122C>A (p.Pro374=) c.5-7154C>A (n.5-7154C>A) c.282C>A (p.Pro94=) c.-98-20915C>A (n.-98-20915C>A) n.4945C>A n.4986C>A | dbSNP |
17 | g.43071106G>A | CA10591902 | BRCA1 | c.4805C>T (p.Pro1602Leu) c.4808C>T (p.Pro1603Leu) c.4682C>T (p.Pro1561Leu) c.4802C>T (p.Pro1601Leu) c.4730C>T (p.Pro1577Leu) c.1496C>T (p.Pro499Leu) c.1358C>T (p.Pro453Leu) c.3920C>T (p.Pro1307Leu) c.4685C>T (p.Pro1562Leu) c.4874C>T (p.Pro1625Leu) c.4667C>T (p.Pro1556Leu) c.1370C>T (p.Pro457Leu) c.1415C>T (p.Pro472Leu) c.4871C>T (p.Pro1624Leu) c.1195C>T c.1382C>T (p.Pro461Leu) c.*4591C>T (n.*4591C>T) c.1121C>T (p.Pro374Leu) c.5-7155C>T (n.5-7155C>T) c.281C>T (p.Pro94Leu) c.-98-20916C>T (n.-98-20916C>T) n.4944C>T n.4985C>T | ClinVar dbSNP |
17 | g.43071106G>C | CA10591903 | BRCA1 | c.4805C>G (p.Pro1602Arg) c.4808C>G (p.Pro1603Arg) c.4682C>G (p.Pro1561Arg) c.4802C>G (p.Pro1601Arg) c.4730C>G (p.Pro1577Arg) c.1496C>G (p.Pro499Arg) c.1358C>G (p.Pro453Arg) c.3920C>G (p.Pro1307Arg) c.4685C>G (p.Pro1562Arg) c.4874C>G (p.Pro1625Arg) c.4667C>G (p.Pro1556Arg) c.1370C>G (p.Pro457Arg) c.1415C>G (p.Pro472Arg) c.4871C>G (p.Pro1624Arg) c.1195C>G c.1382C>G (p.Pro461Arg) c.*4591C>G (n.*4591C>G) c.1121C>G (p.Pro374Arg) c.5-7155C>G (n.5-7155C>G) c.281C>G (p.Pro94Arg) c.-98-20916C>G (n.-98-20916C>G) n.4944C>G n.4985C>G | dbSNP gnomAD v4 |
17 | g.43071106G= | CA2260772921 | BRCA1 | c.4805C= (p.Pro1602=) c.4808C= (p.Pro1603=) c.4682C= (p.Pro1561=) c.4802C= (p.Pro1601=) c.4730C= (p.Pro1577=) c.1496C= (p.Pro499=) c.1358C= (p.Pro453=) c.3920C= (p.Pro1307=) c.4685C= (p.Pro1562=) c.4874C= (p.Pro1625=) c.4667C= (p.Pro1556=) c.1370C= (p.Pro457=) c.1415C= (p.Pro472=) c.4871C= (p.Pro1624=) c.1195C= c.1382C= (p.Pro461=) c.*4591C= (n.*4591C=) c.1121C= (p.Pro374=) c.5-7155C= (n.5-7155C=) c.281C= (p.Pro94=) c.-98-20916C= (n.-98-20916C=) n.4944C= n.4985C= | |
17 | g.43071106G>T | CA10591904 | BRCA1 | c.4805C>A (p.Pro1602His) c.4808C>A (p.Pro1603His) c.4682C>A (p.Pro1561His) c.4802C>A (p.Pro1601His) c.4730C>A (p.Pro1577His) c.1496C>A (p.Pro499His) c.1358C>A (p.Pro453His) c.3920C>A (p.Pro1307His) c.4685C>A (p.Pro1562His) c.4874C>A (p.Pro1625His) c.4667C>A (p.Pro1556His) c.1370C>A (p.Pro457His) c.1415C>A (p.Pro472His) c.4871C>A (p.Pro1624His) c.1195C>A c.1382C>A (p.Pro461His) c.*4591C>A (n.*4591C>A) c.1121C>A (p.Pro374His) c.5-7155C>A (n.5-7155C>A) c.281C>A (p.Pro94His) c.-98-20916C>A (n.-98-20916C>A) n.4944C>A n.4985C>A | dbSNP |
17 | g.43071107G>A | CA10591905 | BRCA1 | c.4804C>T (p.Pro1602Ser) c.4807C>T (p.Pro1603Ser) c.4681C>T (p.Pro1561Ser) c.4801C>T (p.Pro1601Ser) c.4729C>T (p.Pro1577Ser) c.1495C>T (p.Pro499Ser) c.1357C>T (p.Pro453Ser) c.3919C>T (p.Pro1307Ser) c.4684C>T (p.Pro1562Ser) c.4873C>T (p.Pro1625Ser) c.4666C>T (p.Pro1556Ser) c.1369C>T (p.Pro457Ser) c.1414C>T (p.Pro472Ser) c.4870C>T (p.Pro1624Ser) c.1194C>T c.1381C>T (p.Pro461Ser) c.*4590C>T (n.*4590C>T) c.1120C>T (p.Pro374Ser) c.5-7156C>T (n.5-7156C>T) c.280C>T (p.Pro94Ser) c.-98-20917C>T (n.-98-20917C>T) n.4943C>T n.4984C>T | dbSNP |
17 | g.43071107G>C | CA10591906 | BRCA1 | c.4804C>G (p.Pro1602Ala) c.4807C>G (p.Pro1603Ala) c.4681C>G (p.Pro1561Ala) c.4801C>G (p.Pro1601Ala) c.4729C>G (p.Pro1577Ala) c.1495C>G (p.Pro499Ala) c.1357C>G (p.Pro453Ala) c.3919C>G (p.Pro1307Ala) c.4684C>G (p.Pro1562Ala) c.4873C>G (p.Pro1625Ala) c.4666C>G (p.Pro1556Ala) c.1369C>G (p.Pro457Ala) c.1414C>G (p.Pro472Ala) c.4870C>G (p.Pro1624Ala) c.1194C>G c.1381C>G (p.Pro461Ala) c.*4590C>G (n.*4590C>G) c.1120C>G (p.Pro374Ala) c.5-7156C>G (n.5-7156C>G) c.280C>G (p.Pro94Ala) c.-98-20917C>G (n.-98-20917C>G) n.4943C>G n.4984C>G | dbSNP |
17 | g.43071107G>T | CA10591907 | BRCA1 | c.4804C>A (p.Pro1602Thr) c.4807C>A (p.Pro1603Thr) c.4681C>A (p.Pro1561Thr) c.4801C>A (p.Pro1601Thr) c.4729C>A (p.Pro1577Thr) c.1495C>A (p.Pro499Thr) c.1357C>A (p.Pro453Thr) c.3919C>A (p.Pro1307Thr) c.4684C>A (p.Pro1562Thr) c.4873C>A (p.Pro1625Thr) c.4666C>A (p.Pro1556Thr) c.1369C>A (p.Pro457Thr) c.1414C>A (p.Pro472Thr) c.4870C>A (p.Pro1624Thr) c.1194C>A c.1381C>A (p.Pro461Thr) c.*4590C>A (n.*4590C>A) c.1120C>A (p.Pro374Thr) c.5-7156C>A (n.5-7156C>A) c.280C>A (p.Pro94Thr) c.-98-20917C>A (n.-98-20917C>A) n.4943C>A n.4984C>A | dbSNP COSMIC COSMIC |
17 | g.43071107_43071108delinsGA | CA2260772922 | BRCA1 | c.4803_4804delinsTC (p.Val1601=) c.4806_4807delinsTC (p.Val1602=) c.4680_4681delinsTC (p.Val1560=) c.4800_4801delinsTC (p.Val1600=) c.4728_4729delinsTC (p.Val1576=) c.1494_1495delinsTC (p.Val498=) c.1356_1357delinsTC (p.Val452=) c.3918_3919delinsTC (p.Val1306=) c.4683_4684delinsTC (p.Val1561=) c.4872_4873delinsTC (p.Val1624=) c.4665_4666delinsTC (p.Val1555=) c.1368_1369delinsTC (p.Val456=) c.1413_1414delinsTC (p.Val471=) c.4869_4870delinsTC (p.Val1623=) c.1193_1194delinsTC c.1380_1381delinsTC (p.Val460=) c.*4589_*4590delinsTC (n.*4589_*4590delinsTC) c.1119_1120delinsTC (p.Val373=) c.5-7157_5-7156delinsTC (n.5-7157_5-7156delinsTC) c.279_280delinsTC (p.Val93=) c.-98-20918_-98-20917delinsTC (n.-98-20918_-98-20917delinsTC) n.4942_4943delinsTC n.4983_4984delinsTC | |
17 | g.43071108A>C | CA500231825 | BRCA1 | c.4803T>G (p.Val1601=) c.4806T>G (p.Val1602=) c.4680T>G (p.Val1560=) c.4800T>G (p.Val1600=) c.4728T>G (p.Val1576=) c.1494T>G (p.Val498=) c.1356T>G (p.Val452=) c.3918T>G (p.Val1306=) c.4683T>G (p.Val1561=) c.4872T>G (p.Val1624=) c.4665T>G (p.Val1555=) c.1368T>G (p.Val456=) c.1413T>G (p.Val471=) c.4869T>G (p.Val1623=) c.1193T>G c.1380T>G (p.Val460=) c.*4589T>G (n.*4589T>G) c.1119T>G (p.Val373=) c.5-7157T>G (n.5-7157T>G) c.279T>G (p.Val93=) c.-98-20918T>G (n.-98-20918T>G) n.4942T>G n.4983T>G | ClinVar dbSNP |
17 | g.43071108A>G | CA500231826 | BRCA1 | c.4803T>C (p.Val1601=) c.4806T>C (p.Val1602=) c.4680T>C (p.Val1560=) c.4800T>C (p.Val1600=) c.4728T>C (p.Val1576=) c.1494T>C (p.Val498=) c.1356T>C (p.Val452=) c.3918T>C (p.Val1306=) c.4683T>C (p.Val1561=) c.4872T>C (p.Val1624=) c.4665T>C (p.Val1555=) c.1368T>C (p.Val456=) c.1413T>C (p.Val471=) c.4869T>C (p.Val1623=) c.1193T>C c.1380T>C (p.Val460=) c.*4589T>C (n.*4589T>C) c.1119T>C (p.Val373=) c.5-7157T>C (n.5-7157T>C) c.279T>C (p.Val93=) c.-98-20918T>C (n.-98-20918T>C) n.4942T>C n.4983T>C | |
17 | g.43071108A>T | CA500231827 | BRCA1 | c.4803T>A (p.Val1601=) c.4806T>A (p.Val1602=) c.4680T>A (p.Val1560=) c.4800T>A (p.Val1600=) c.4728T>A (p.Val1576=) c.1494T>A (p.Val498=) c.1356T>A (p.Val452=) c.3918T>A (p.Val1306=) c.4683T>A (p.Val1561=) c.4872T>A (p.Val1624=) c.4665T>A (p.Val1555=) c.1368T>A (p.Val456=) c.1413T>A (p.Val471=) c.4869T>A (p.Val1623=) c.1193T>A c.1380T>A (p.Val460=) c.*4589T>A (n.*4589T>A) c.1119T>A (p.Val373=) c.5-7157T>A (n.5-7157T>A) c.279T>A (p.Val93=) c.-98-20918T>A (n.-98-20918T>A) n.4942T>A n.4983T>A | dbSNP |
17 | g.43071109del | CA10586607 | BRCA1 | c.4803del (p.Gln1603AsnfsTer2) c.4806del (p.Gln1604AsnfsTer2) c.4680del (p.Gln1562AsnfsTer2) c.4800del (p.Gln1602AsnfsTer2) c.4728del (p.Gln1578AsnfsTer2) c.1494del (p.Gln500AsnfsTer2) c.1356del (p.Gln454AsnfsTer2) c.3918del (p.Gln1308AsnfsTer2) c.4683del (p.Gln1563AsnfsTer2) c.4872del (p.Gln1626AsnfsTer2) c.4665del (p.Gln1557AsnfsTer2) c.1368del (p.Gln458AsnfsTer2) c.1413del (p.Gln473AsnfsTer2) c.4869del (p.Gln1625AsnfsTer2) c.1193del c.1380del (p.Gln462AsnfsTer2) c.*4589del (n.*4589del) c.1119del (p.Gln375AsnfsTer2) c.5-7157del (n.5-7157del) c.279del (p.Gln95AsnfsTer2) c.-98-20918del (n.-98-20918del) n.4942del n.4983del | ClinVar dbSNP gnomAD v4 |
17 | g.43071109A>C | CA10591908 | BRCA1 | c.4802T>G (p.Val1601Gly) c.4805T>G (p.Val1602Gly) c.4679T>G (p.Val1560Gly) c.4799T>G (p.Val1600Gly) c.4727T>G (p.Val1576Gly) c.1493T>G (p.Val498Gly) c.1355T>G (p.Val452Gly) c.3917T>G (p.Val1306Gly) c.4682T>G (p.Val1561Gly) c.4871T>G (p.Val1624Gly) c.4664T>G (p.Val1555Gly) c.1367T>G (p.Val456Gly) c.1412T>G (p.Val471Gly) c.4868T>G (p.Val1623Gly) c.1192T>G c.1379T>G (p.Val460Gly) c.*4588T>G (n.*4588T>G) c.1118T>G (p.Val373Gly) c.5-7158T>G (n.5-7158T>G) c.278T>G (p.Val93Gly) c.-98-20919T>G (n.-98-20919T>G) n.4941T>G n.4982T>G | dbSNP |
17 | g.43071109A>G | CA10591909 | BRCA1 | c.4802T>C (p.Val1601Ala) c.4805T>C (p.Val1602Ala) c.4679T>C (p.Val1560Ala) c.4799T>C (p.Val1600Ala) c.4727T>C (p.Val1576Ala) c.1493T>C (p.Val498Ala) c.1355T>C (p.Val452Ala) c.3917T>C (p.Val1306Ala) c.4682T>C (p.Val1561Ala) c.4871T>C (p.Val1624Ala) c.4664T>C (p.Val1555Ala) c.1367T>C (p.Val456Ala) c.1412T>C (p.Val471Ala) c.4868T>C (p.Val1623Ala) c.1192T>C c.1379T>C (p.Val460Ala) c.*4588T>C (n.*4588T>C) c.1118T>C (p.Val373Ala) c.5-7158T>C (n.5-7158T>C) c.278T>C (p.Val93Ala) c.-98-20919T>C (n.-98-20919T>C) n.4941T>C n.4982T>C | dbSNP |
17 | g.43071109A>T | CA10591910 | BRCA1 | c.4802T>A (p.Val1601Asp) c.4805T>A (p.Val1602Asp) c.4679T>A (p.Val1560Asp) c.4799T>A (p.Val1600Asp) c.4727T>A (p.Val1576Asp) c.1493T>A (p.Val498Asp) c.1355T>A (p.Val452Asp) c.3917T>A (p.Val1306Asp) c.4682T>A (p.Val1561Asp) c.4871T>A (p.Val1624Asp) c.4664T>A (p.Val1555Asp) c.1367T>A (p.Val456Asp) c.1412T>A (p.Val471Asp) c.4868T>A (p.Val1623Asp) c.1192T>A c.1379T>A (p.Val460Asp) c.*4588T>A (n.*4588T>A) c.1118T>A (p.Val373Asp) c.5-7158T>A (n.5-7158T>A) c.278T>A (p.Val93Asp) c.-98-20919T>A (n.-98-20919T>A) n.4941T>A n.4982T>A | dbSNP |
17 | g.43071110C>A | CA10591911 | BRCA1 | c.4801G>T (p.Val1601Phe) c.4804G>T (p.Val1602Phe) c.4678G>T (p.Val1560Phe) c.4798G>T (p.Val1600Phe) c.4726G>T (p.Val1576Phe) c.1492G>T (p.Val498Phe) c.1354G>T (p.Val452Phe) c.3916G>T (p.Val1306Phe) c.4681G>T (p.Val1561Phe) c.4870G>T (p.Val1624Phe) c.4663G>T (p.Val1555Phe) c.1366G>T (p.Val456Phe) c.1411G>T (p.Val471Phe) c.4867G>T (p.Val1623Phe) c.1191G>T c.1378G>T (p.Val460Phe) c.*4587G>T (n.*4587G>T) c.1117G>T (p.Val373Phe) c.5-7159G>T (n.5-7159G>T) c.277G>T (p.Val93Phe) c.-98-20920G>T (n.-98-20920G>T) n.4940G>T n.4981G>T | ClinVar dbSNP |
17 | g.43071110C= | CA2260772924 | BRCA1 | c.4801G= (p.Val1601=) c.4804G= (p.Val1602=) c.4678G= (p.Val1560=) c.4798G= (p.Val1600=) c.4726G= (p.Val1576=) c.1492G= (p.Val498=) c.1354G= (p.Val452=) c.3916G= (p.Val1306=) c.4681G= (p.Val1561=) c.4870G= (p.Val1624=) c.4663G= (p.Val1555=) c.1366G= (p.Val456=) c.1411G= (p.Val471=) c.4867G= (p.Val1623=) c.1191G= c.1378G= (p.Val460=) c.*4587G= (n.*4587G=) c.1117G= (p.Val373=) c.5-7159G= (n.5-7159G=) c.277G= (p.Val93=) c.-98-20920G= (n.-98-20920G=) n.4940G= n.4981G= | |
17 | g.43071110C>G | CA10591912 | BRCA1 | c.4801G>C (p.Val1601Leu) c.4804G>C (p.Val1602Leu) c.4678G>C (p.Val1560Leu) c.4798G>C (p.Val1600Leu) c.4726G>C (p.Val1576Leu) c.1492G>C (p.Val498Leu) c.1354G>C (p.Val452Leu) c.3916G>C (p.Val1306Leu) c.4681G>C (p.Val1561Leu) c.4870G>C (p.Val1624Leu) c.4663G>C (p.Val1555Leu) c.1366G>C (p.Val456Leu) c.1411G>C (p.Val471Leu) c.4867G>C (p.Val1623Leu) c.1191G>C c.1378G>C (p.Val460Leu) c.*4587G>C (n.*4587G>C) c.1117G>C (p.Val373Leu) c.5-7159G>C (n.5-7159G>C) c.277G>C (p.Val93Leu) c.-98-20920G>C (n.-98-20920G>C) n.4940G>C n.4981G>C | dbSNP |
17 | g.43071110C>T | CA10591913 | BRCA1 | c.4801G>A (p.Val1601Ile) c.4804G>A (p.Val1602Ile) c.4678G>A (p.Val1560Ile) c.4798G>A (p.Val1600Ile) c.4726G>A (p.Val1576Ile) c.1492G>A (p.Val498Ile) c.1354G>A (p.Val452Ile) c.3916G>A (p.Val1306Ile) c.4681G>A (p.Val1561Ile) c.4870G>A (p.Val1624Ile) c.4663G>A (p.Val1555Ile) c.1366G>A (p.Val456Ile) c.1411G>A (p.Val471Ile) c.4867G>A (p.Val1623Ile) c.1191G>A c.1378G>A (p.Val460Ile) c.*4587G>A (n.*4587G>A) c.1117G>A (p.Val373Ile) c.5-7159G>A (n.5-7159G>A) c.277G>A (p.Val93Ile) c.-98-20920G>A (n.-98-20920G>A) n.4940G>A n.4981G>A | dbSNP |
17 | g.43071110_43071111delinsCT | CA2260772923 | BRCA1 | c.4800_4801delinsAG (p.Lys1600=) c.4803_4804delinsAG (p.Lys1601=) c.4677_4678delinsAG (p.Lys1559=) c.4797_4798delinsAG (p.Lys1599=) c.4725_4726delinsAG (p.Lys1575=) c.1491_1492delinsAG (p.Lys497=) c.1353_1354delinsAG (p.Lys451=) c.3915_3916delinsAG (p.Lys1305=) c.4680_4681delinsAG (p.Lys1560=) c.4869_4870delinsAG (p.Lys1623=) c.4662_4663delinsAG (p.Lys1554=) c.1365_1366delinsAG (p.Lys455=) c.1410_1411delinsAG (p.Lys470=) c.4866_4867delinsAG (p.Lys1622=) c.1190_1191delinsAG c.1377_1378delinsAG (p.Lys459=) c.*4586_*4587delinsAG (n.*4586_*4587delinsAG) c.1116_1117delinsAG (p.Lys372=) c.5-7160_5-7159delinsAG (n.5-7160_5-7159delinsAG) c.276_277delinsAG (p.Lys92=) c.-98-20921_-98-20920delinsAG (n.-98-20921_-98-20920delinsAG) n.4939_4940delinsAG n.4980_4981delinsAG | |
17 | g.43071111T>A | CA10591914 | BRCA1 | c.4800A>T (p.Lys1600Asn) c.4803A>T (p.Lys1601Asn) c.4677A>T (p.Lys1559Asn) c.4797A>T (p.Lys1599Asn) c.4725A>T (p.Lys1575Asn) c.1491A>T (p.Lys497Asn) c.1353A>T (p.Lys451Asn) c.3915A>T (p.Lys1305Asn) c.4680A>T (p.Lys1560Asn) c.4869A>T (p.Lys1623Asn) c.4662A>T (p.Lys1554Asn) c.1365A>T (p.Lys455Asn) c.1410A>T (p.Lys470Asn) c.4866A>T (p.Lys1622Asn) c.1190A>T c.1377A>T (p.Lys459Asn) c.*4586A>T (n.*4586A>T) c.1116A>T (p.Lys372Asn) c.5-7160A>T (n.5-7160A>T) c.276A>T (p.Lys92Asn) c.-98-20921A>T (n.-98-20921A>T) n.4939A>T n.4980A>T | dbSNP |
17 | g.43071111T>C | CA10575939 | BRCA1 | c.4800A>G (p.Lys1600=) c.4803A>G (p.Lys1601=) c.4677A>G (p.Lys1559=) c.4797A>G (p.Lys1599=) c.4725A>G (p.Lys1575=) c.1491A>G (p.Lys497=) c.1353A>G (p.Lys451=) c.3915A>G (p.Lys1305=) c.4680A>G (p.Lys1560=) c.4869A>G (p.Lys1623=) c.4662A>G (p.Lys1554=) c.1365A>G (p.Lys455=) c.1410A>G (p.Lys470=) c.4866A>G (p.Lys1622=) c.1190A>G c.1377A>G (p.Lys459=) c.*4586A>G (n.*4586A>G) c.1116A>G (p.Lys372=) c.5-7160A>G (n.5-7160A>G) c.276A>G (p.Lys92=) c.-98-20921A>G (n.-98-20921A>G) n.4939A>G n.4980A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.43071111T>G | CA10591915 | BRCA1 | c.4800A>C (p.Lys1600Asn) c.4803A>C (p.Lys1601Asn) c.4677A>C (p.Lys1559Asn) c.4797A>C (p.Lys1599Asn) c.4725A>C (p.Lys1575Asn) c.1491A>C (p.Lys497Asn) c.1353A>C (p.Lys451Asn) c.3915A>C (p.Lys1305Asn) c.4680A>C (p.Lys1560Asn) c.4869A>C (p.Lys1623Asn) c.4662A>C (p.Lys1554Asn) c.1365A>C (p.Lys455Asn) c.1410A>C (p.Lys470Asn) c.4866A>C (p.Lys1622Asn) c.1190A>C c.1377A>C (p.Lys459Asn) c.*4586A>C (n.*4586A>C) c.1116A>C (p.Lys372Asn) c.5-7160A>C (n.5-7160A>C) c.276A>C (p.Lys92Asn) c.-98-20921A>C (n.-98-20921A>C) n.4939A>C n.4980A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071111T= | CA2260772925 | BRCA1 | c.4800A= (p.Lys1600=) c.4803A= (p.Lys1601=) c.4677A= (p.Lys1559=) c.4797A= (p.Lys1599=) c.4725A= (p.Lys1575=) c.1491A= (p.Lys497=) c.1353A= (p.Lys451=) c.3915A= (p.Lys1305=) c.4680A= (p.Lys1560=) c.4869A= (p.Lys1623=) c.4662A= (p.Lys1554=) c.1365A= (p.Lys455=) c.1410A= (p.Lys470=) c.4866A= (p.Lys1622=) c.1190A= c.1377A= (p.Lys459=) c.*4586A= (n.*4586A=) c.1116A= (p.Lys372=) c.5-7160A= (n.5-7160A=) c.276A= (p.Lys92=) c.-98-20921A= (n.-98-20921A=) n.4939A= n.4980A= | |
17 | g.43071113del | CA658656622 | BRCA1 | c.4800del (p.Val1601PhefsTer4) c.4803del (p.Val1602PhefsTer4) c.4677del (p.Val1560PhefsTer4) c.4797del (p.Val1600PhefsTer4) c.4725del (p.Val1576PhefsTer4) c.1491del (p.Val498PhefsTer4) c.1353del (p.Val452PhefsTer4) c.3915del (p.Val1306PhefsTer4) c.4680del (p.Val1561PhefsTer4) c.4869del (p.Val1624PhefsTer4) c.4662del (p.Val1555PhefsTer4) c.1365del (p.Val456PhefsTer4) c.1410del (p.Val471PhefsTer4) c.4866del (p.Val1623PhefsTer4) c.1190del c.1377del (p.Val460PhefsTer4) c.*4586del (n.*4586del) c.1116del (p.Val373PhefsTer4) c.5-7160del (n.5-7160del) c.276del (p.Val93PhefsTer4) c.-98-20921del (n.-98-20921del) n.4939del n.4980del | ClinVar dbSNP |
17 | g.43071112T>A | CA10591916 | BRCA1 | c.4799A>T (p.Lys1600Ile) c.4802A>T (p.Lys1601Ile) c.4676A>T (p.Lys1559Ile) c.4796A>T (p.Lys1599Ile) c.4724A>T (p.Lys1575Ile) c.1490A>T (p.Lys497Ile) c.1352A>T (p.Lys451Ile) c.3914A>T (p.Lys1305Ile) c.4679A>T (p.Lys1560Ile) c.4868A>T (p.Lys1623Ile) c.4661A>T (p.Lys1554Ile) c.1364A>T (p.Lys455Ile) c.1409A>T (p.Lys470Ile) c.4865A>T (p.Lys1622Ile) c.1189A>T c.1376A>T (p.Lys459Ile) c.*4585A>T (n.*4585A>T) c.1115A>T (p.Lys372Ile) c.5-7161A>T (n.5-7161A>T) c.275A>T (p.Lys92Ile) c.-98-20922A>T (n.-98-20922A>T) n.4938A>T n.4979A>T | dbSNP |
17 | g.43071112T>C | CA10591917 | BRCA1 | c.4799A>G (p.Lys1600Arg) c.4802A>G (p.Lys1601Arg) c.4676A>G (p.Lys1559Arg) c.4796A>G (p.Lys1599Arg) c.4724A>G (p.Lys1575Arg) c.1490A>G (p.Lys497Arg) c.1352A>G (p.Lys451Arg) c.3914A>G (p.Lys1305Arg) c.4679A>G (p.Lys1560Arg) c.4868A>G (p.Lys1623Arg) c.4661A>G (p.Lys1554Arg) c.1364A>G (p.Lys455Arg) c.1409A>G (p.Lys470Arg) c.4865A>G (p.Lys1622Arg) c.1189A>G c.1376A>G (p.Lys459Arg) c.*4585A>G (n.*4585A>G) c.1115A>G (p.Lys372Arg) c.5-7161A>G (n.5-7161A>G) c.275A>G (p.Lys92Arg) c.-98-20922A>G (n.-98-20922A>G) n.4938A>G n.4979A>G | ClinVar |
17 | g.43071112T>G | CA10591918 | BRCA1 | c.4799A>C (p.Lys1600Thr) c.4802A>C (p.Lys1601Thr) c.4676A>C (p.Lys1559Thr) c.4796A>C (p.Lys1599Thr) c.4724A>C (p.Lys1575Thr) c.1490A>C (p.Lys497Thr) c.1352A>C (p.Lys451Thr) c.3914A>C (p.Lys1305Thr) c.4679A>C (p.Lys1560Thr) c.4868A>C (p.Lys1623Thr) c.4661A>C (p.Lys1554Thr) c.1364A>C (p.Lys455Thr) c.1409A>C (p.Lys470Thr) c.4865A>C (p.Lys1622Thr) c.1189A>C c.1376A>C (p.Lys459Thr) c.*4585A>C (n.*4585A>C) c.1115A>C (p.Lys372Thr) c.5-7161A>C (n.5-7161A>C) c.275A>C (p.Lys92Thr) c.-98-20922A>C (n.-98-20922A>C) n.4938A>C n.4979A>C | |
17 | g.43071113T>A | CA003028 | BRCA1 | c.4798A>T (p.Lys1600Ter) c.4801A>T (p.Lys1601Ter) c.4675A>T (p.Lys1559Ter) c.4795A>T (p.Lys1599Ter) c.4723A>T (p.Lys1575Ter) c.1489A>T (p.Lys497Ter) c.1351A>T (p.Lys451Ter) c.3913A>T (p.Lys1305Ter) c.4678A>T (p.Lys1560Ter) c.4867A>T (p.Lys1623Ter) c.4660A>T (p.Lys1554Ter) c.1363A>T (p.Lys455Ter) c.1408A>T (p.Lys470Ter) c.4864A>T (p.Lys1622Ter) c.1188A>T c.1375A>T (p.Lys459Ter) c.*4584A>T (n.*4584A>T) c.1114A>T (p.Lys372Ter) c.5-7162A>T (n.5-7162A>T) c.274A>T (p.Lys92Ter) c.-98-20923A>T (n.-98-20923A>T) n.4937A>T n.4978A>T | ClinVar dbSNP |
17 | g.43071113T>C | CA10591919 | BRCA1 | c.4798A>G (p.Lys1600Glu) c.4801A>G (p.Lys1601Glu) c.4675A>G (p.Lys1559Glu) c.4795A>G (p.Lys1599Glu) c.4723A>G (p.Lys1575Glu) c.1489A>G (p.Lys497Glu) c.1351A>G (p.Lys451Glu) c.3913A>G (p.Lys1305Glu) c.4678A>G (p.Lys1560Glu) c.4867A>G (p.Lys1623Glu) c.4660A>G (p.Lys1554Glu) c.1363A>G (p.Lys455Glu) c.1408A>G (p.Lys470Glu) c.4864A>G (p.Lys1622Glu) c.1188A>G c.1375A>G (p.Lys459Glu) c.*4584A>G (n.*4584A>G) c.1114A>G (p.Lys372Glu) c.5-7162A>G (n.5-7162A>G) c.274A>G (p.Lys92Glu) c.-98-20923A>G (n.-98-20923A>G) n.4937A>G n.4978A>G | |
17 | g.43071113T>G | CA053263 | BRCA1 | c.4798A>C (p.Lys1600Gln) c.4801A>C (p.Lys1601Gln) c.4675A>C (p.Lys1559Gln) c.4795A>C (p.Lys1599Gln) c.4723A>C (p.Lys1575Gln) c.1489A>C (p.Lys497Gln) c.1351A>C (p.Lys451Gln) c.3913A>C (p.Lys1305Gln) c.4678A>C (p.Lys1560Gln) c.4867A>C (p.Lys1623Gln) c.4660A>C (p.Lys1554Gln) c.1363A>C (p.Lys455Gln) c.1408A>C (p.Lys470Gln) c.4864A>C (p.Lys1622Gln) c.1188A>C c.1375A>C (p.Lys459Gln) c.*4584A>C (n.*4584A>C) c.1114A>C (p.Lys372Gln) c.5-7162A>C (n.5-7162A>C) c.274A>C (p.Lys92Gln) c.-98-20923A>C (n.-98-20923A>C) n.4937A>C n.4978A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071113T= | CA2260772926 | BRCA1 | c.4798A= (p.Lys1600=) c.4801A= (p.Lys1601=) c.4675A= (p.Lys1559=) c.4795A= (p.Lys1599=) c.4723A= (p.Lys1575=) c.1489A= (p.Lys497=) c.1351A= (p.Lys451=) c.3913A= (p.Lys1305=) c.4678A= (p.Lys1560=) c.4867A= (p.Lys1623=) c.4660A= (p.Lys1554=) c.1363A= (p.Lys455=) c.1408A= (p.Lys470=) c.4864A= (p.Lys1622=) c.1188A= c.1375A= (p.Lys459=) c.*4584A= (n.*4584A=) c.1114A= (p.Lys372=) c.5-7162A= (n.5-7162A=) c.274A= (p.Lys92=) c.-98-20923A= (n.-98-20923A=) n.4937A= n.4978A= | |
17 | g.43071113_43071114delinsTC | CA2260772927 | BRCA1 | c.4797_4798delinsGA (p.Leu1599=) c.4800_4801delinsGA (p.Leu1600=) c.4674_4675delinsGA (p.Leu1558=) c.4794_4795delinsGA (p.Leu1598=) c.4722_4723delinsGA (p.Leu1574=) c.1488_1489delinsGA (p.Leu496=) c.1350_1351delinsGA (p.Leu450=) c.3912_3913delinsGA (p.Leu1304=) c.4677_4678delinsGA (p.Leu1559=) c.4866_4867delinsGA (p.Leu1622=) c.4659_4660delinsGA (p.Leu1553=) c.1362_1363delinsGA (p.Leu454=) c.1407_1408delinsGA (p.Leu469=) c.4863_4864delinsGA (p.Leu1621=) c.1187_1188delinsGA c.1374_1375delinsGA (p.Leu458=) c.*4583_*4584delinsGA (n.*4583_*4584delinsGA) c.1113_1114delinsGA (p.Leu371=) c.5-7163_5-7162delinsGA (n.5-7163_5-7162delinsGA) c.273_274delinsGA (p.Leu91=) c.-98-20924_-98-20923delinsGA (n.-98-20924_-98-20923delinsGA) n.4936_4937delinsGA n.4977_4978delinsGA | |
17 | g.43071114del | CA919844205 | BRCA1 | c.4797del (p.Val1601PhefsTer4) c.4800del (p.Val1602PhefsTer4) c.4674del (p.Val1560PhefsTer4) c.4794del (p.Val1600PhefsTer4) c.4722del (p.Val1576PhefsTer4) c.1488del (p.Val498PhefsTer4) c.1350del (p.Val452PhefsTer4) c.3912del (p.Val1306PhefsTer4) c.4677del (p.Val1561PhefsTer4) c.4866del (p.Val1624PhefsTer4) c.4659del (p.Val1555PhefsTer4) c.1362del (p.Val456PhefsTer4) c.1407del (p.Val471PhefsTer4) c.4863del (p.Val1623PhefsTer4) c.1187del c.1374del (p.Val460PhefsTer4) c.*4583del (n.*4583del) c.1113del (p.Val373PhefsTer4) c.5-7163del (n.5-7163del) c.273del (p.Val93PhefsTer4) c.-98-20924del (n.-98-20924del) n.4936del n.4977del | dbSNP |
17 | g.43071114C>A | CA10591920 | BRCA1 | c.4797G>T (p.Leu1599Phe) c.4800G>T (p.Leu1600Phe) c.4674G>T (p.Leu1558Phe) c.4794G>T (p.Leu1598Phe) c.4722G>T (p.Leu1574Phe) c.1488G>T (p.Leu496Phe) c.1350G>T (p.Leu450Phe) c.3912G>T (p.Leu1304Phe) c.4677G>T (p.Leu1559Phe) c.4866G>T (p.Leu1622Phe) c.4659G>T (p.Leu1553Phe) c.1362G>T (p.Leu454Phe) c.1407G>T (p.Leu469Phe) c.4863G>T (p.Leu1621Phe) c.1187G>T c.1374G>T (p.Leu458Phe) c.*4583G>T (n.*4583G>T) c.1113G>T (p.Leu371Phe) c.5-7163G>T (n.5-7163G>T) c.273G>T (p.Leu91Phe) c.-98-20924G>T (n.-98-20924G>T) n.4936G>T n.4977G>T | dbSNP |
17 | g.43071114C= | CA2260772928 | BRCA1 | c.4797G= (p.Leu1599=) c.4800G= (p.Leu1600=) c.4674G= (p.Leu1558=) c.4794G= (p.Leu1598=) c.4722G= (p.Leu1574=) c.1488G= (p.Leu496=) c.1350G= (p.Leu450=) c.3912G= (p.Leu1304=) c.4677G= (p.Leu1559=) c.4866G= (p.Leu1622=) c.4659G= (p.Leu1553=) c.1362G= (p.Leu454=) c.1407G= (p.Leu469=) c.4863G= (p.Leu1621=) c.1187G= c.1374G= (p.Leu458=) c.*4583G= (n.*4583G=) c.1113G= (p.Leu371=) c.5-7163G= (n.5-7163G=) c.273G= (p.Leu91=) c.-98-20924G= (n.-98-20924G=) n.4936G= n.4977G= | |
17 | g.43071114C>G | CA10591921 | BRCA1 | c.4797G>C (p.Leu1599Phe) c.4800G>C (p.Leu1600Phe) c.4674G>C (p.Leu1558Phe) c.4794G>C (p.Leu1598Phe) c.4722G>C (p.Leu1574Phe) c.1488G>C (p.Leu496Phe) c.1350G>C (p.Leu450Phe) c.3912G>C (p.Leu1304Phe) c.4677G>C (p.Leu1559Phe) c.4866G>C (p.Leu1622Phe) c.4659G>C (p.Leu1553Phe) c.1362G>C (p.Leu454Phe) c.1407G>C (p.Leu469Phe) c.4863G>C (p.Leu1621Phe) c.1187G>C c.1374G>C (p.Leu458Phe) c.*4583G>C (n.*4583G>C) c.1113G>C (p.Leu371Phe) c.5-7163G>C (n.5-7163G>C) c.273G>C (p.Leu91Phe) c.-98-20924G>C (n.-98-20924G>C) n.4936G>C n.4977G>C | dbSNP |
17 | g.43071114C>T | CA500231828 | BRCA1 | c.4797G>A (p.Leu1599=) c.4800G>A (p.Leu1600=) c.4674G>A (p.Leu1558=) c.4794G>A (p.Leu1598=) c.4722G>A (p.Leu1574=) c.1488G>A (p.Leu496=) c.1350G>A (p.Leu450=) c.3912G>A (p.Leu1304=) c.4677G>A (p.Leu1559=) c.4866G>A (p.Leu1622=) c.4659G>A (p.Leu1553=) c.1362G>A (p.Leu454=) c.1407G>A (p.Leu469=) c.4863G>A (p.Leu1621=) c.1187G>A c.1374G>A (p.Leu458=) c.*4583G>A (n.*4583G>A) c.1113G>A (p.Leu371=) c.5-7163G>A (n.5-7163G>A) c.273G>A (p.Leu91=) c.-98-20924G>A (n.-98-20924G>A) n.4936G>A n.4977G>A | ClinVar dbSNP COSMIC COSMIC |
17 | g.43071115A>C | CA10591922 | BRCA1 | c.4796T>G (p.Leu1599Trp) c.4799T>G (p.Leu1600Trp) c.4673T>G (p.Leu1558Trp) c.4793T>G (p.Leu1598Trp) c.4721T>G (p.Leu1574Trp) c.1487T>G (p.Leu496Trp) c.1349T>G (p.Leu450Trp) c.3911T>G (p.Leu1304Trp) c.4676T>G (p.Leu1559Trp) c.4865T>G (p.Leu1622Trp) c.4658T>G (p.Leu1553Trp) c.1361T>G (p.Leu454Trp) c.1406T>G (p.Leu469Trp) c.4862T>G (p.Leu1621Trp) c.1186T>G c.1373T>G (p.Leu458Trp) c.*4582T>G (n.*4582T>G) c.1112T>G (p.Leu371Trp) c.5-7164T>G (n.5-7164T>G) c.272T>G (p.Leu91Trp) c.-98-20925T>G (n.-98-20925T>G) n.4935T>G n.4976T>G | dbSNP |
17 | g.43071115A>G | CA10591923 | BRCA1 | c.4796T>C (p.Leu1599Ser) c.4799T>C (p.Leu1600Ser) c.4673T>C (p.Leu1558Ser) c.4793T>C (p.Leu1598Ser) c.4721T>C (p.Leu1574Ser) c.1487T>C (p.Leu496Ser) c.1349T>C (p.Leu450Ser) c.3911T>C (p.Leu1304Ser) c.4676T>C (p.Leu1559Ser) c.4865T>C (p.Leu1622Ser) c.4658T>C (p.Leu1553Ser) c.1361T>C (p.Leu454Ser) c.1406T>C (p.Leu469Ser) c.4862T>C (p.Leu1621Ser) c.1186T>C c.1373T>C (p.Leu458Ser) c.*4582T>C (n.*4582T>C) c.1112T>C (p.Leu371Ser) c.5-7164T>C (n.5-7164T>C) c.272T>C (p.Leu91Ser) c.-98-20925T>C (n.-98-20925T>C) n.4935T>C n.4976T>C | dbSNP |
17 | g.43071115A>T | CA10591924 | BRCA1 | c.4796T>A (p.Leu1599Ter) c.4799T>A (p.Leu1600Ter) c.4673T>A (p.Leu1558Ter) c.4793T>A (p.Leu1598Ter) c.4721T>A (p.Leu1574Ter) c.1487T>A (p.Leu496Ter) c.1349T>A (p.Leu450Ter) c.3911T>A (p.Leu1304Ter) c.4676T>A (p.Leu1559Ter) c.4865T>A (p.Leu1622Ter) c.4658T>A (p.Leu1553Ter) c.1361T>A (p.Leu454Ter) c.1406T>A (p.Leu469Ter) c.4862T>A (p.Leu1621Ter) c.1186T>A c.1373T>A (p.Leu458Ter) c.*4582T>A (n.*4582T>A) c.1112T>A (p.Leu371Ter) c.5-7164T>A (n.5-7164T>A) c.272T>A (p.Leu91Ter) c.-98-20925T>A (n.-98-20925T>A) n.4935T>A n.4976T>A | dbSNP |
17 | g.43071116dup | CA003027 | BRCA1 | c.4796dup (p.Leu1599PhefsTer22) c.4799dup (p.Leu1600PhefsTer22) c.4673dup (p.Leu1558PhefsTer22) c.4793dup (p.Leu1598PhefsTer22) c.4721dup (p.Leu1574PhefsTer22) c.1487dup (p.Leu496PhefsTer22) c.1349dup (p.Leu450PhefsTer22) c.3911dup (p.Leu1304PhefsTer22) c.4676dup (p.Leu1559PhefsTer22) c.4865dup (p.Leu1622PhefsTer22) c.4658dup (p.Leu1553PhefsTer22) c.1361dup (p.Leu454PhefsTer22) c.1406dup (p.Leu469PhefsTer22) c.4862dup (p.Leu1621PhefsTer22) c.1186dup c.1373dup (p.Leu458PhefsTer22) c.*4582dup (n.*4582dup) c.1112dup (p.Leu371PhefsTer22) c.5-7164dup (n.5-7164dup) c.272dup (p.Leu91PhefsTer22) c.-98-20925dup (n.-98-20925dup) n.4935dup n.4976dup | ClinVar dbSNP |
17 | g.43071116del | CA2499224396 | BRCA1 | c.4796del (p.Leu1599Ter) c.4799del (p.Leu1600Ter) c.4673del (p.Leu1558Ter) c.4793del (p.Leu1598Ter) c.4721del (p.Leu1574Ter) c.1487del (p.Leu496Ter) c.1349del (p.Leu450Ter) c.3911del (p.Leu1304Ter) c.4676del (p.Leu1559Ter) c.4865del (p.Leu1622Ter) c.4658del (p.Leu1553Ter) c.1361del (p.Leu454Ter) c.1406del (p.Leu469Ter) c.4862del (p.Leu1621Ter) c.1186del c.1373del (p.Leu458Ter) c.*4582del (n.*4582del) c.1112del (p.Leu371Ter) c.5-7164del (n.5-7164del) c.272del (p.Leu91Ter) c.-98-20925del (n.-98-20925del) n.4935del n.4976del | ClinVar dbSNP |
17 | g.43071116A= | CA2260772929 | BRCA1 | c.4795T= (p.Leu1599=) c.4798T= (p.Leu1600=) c.4672T= (p.Leu1558=) c.4792T= (p.Leu1598=) c.4720T= (p.Leu1574=) c.1486T= (p.Leu496=) c.1348T= (p.Leu450=) c.3910T= (p.Leu1304=) c.4675T= (p.Leu1559=) c.4864T= (p.Leu1622=) c.4657T= (p.Leu1553=) c.1360T= (p.Leu454=) c.1405T= (p.Leu469=) c.4861T= (p.Leu1621=) c.1185T= c.1372T= (p.Leu458=) c.*4581T= (n.*4581T=) c.1111T= (p.Leu371=) c.5-7165T= (n.5-7165T=) c.271T= (p.Leu91=) c.-98-20926T= (n.-98-20926T=) n.4934T= n.4975T= | |
17 | g.43071116A>C | CA10591925 | BRCA1 | c.4795T>G (p.Leu1599Val) c.4798T>G (p.Leu1600Val) c.4672T>G (p.Leu1558Val) c.4792T>G (p.Leu1598Val) c.4720T>G (p.Leu1574Val) c.1486T>G (p.Leu496Val) c.1348T>G (p.Leu450Val) c.3910T>G (p.Leu1304Val) c.4675T>G (p.Leu1559Val) c.4864T>G (p.Leu1622Val) c.4657T>G (p.Leu1553Val) c.1360T>G (p.Leu454Val) c.1405T>G (p.Leu469Val) c.4861T>G (p.Leu1621Val) c.1185T>G c.1372T>G (p.Leu458Val) c.*4581T>G (n.*4581T>G) c.1111T>G (p.Leu371Val) c.5-7165T>G (n.5-7165T>G) c.271T>G (p.Leu91Val) c.-98-20926T>G (n.-98-20926T>G) n.4934T>G n.4975T>G | |
17 | g.43071116A>G | CA053253 | BRCA1 | c.4795T>C (p.Leu1599=) c.4798T>C (p.Leu1600=) c.4672T>C (p.Leu1558=) c.4792T>C (p.Leu1598=) c.4720T>C (p.Leu1574=) c.1486T>C (p.Leu496=) c.1348T>C (p.Leu450=) c.3910T>C (p.Leu1304=) c.4675T>C (p.Leu1559=) c.4864T>C (p.Leu1622=) c.4657T>C (p.Leu1553=) c.1360T>C (p.Leu454=) c.1405T>C (p.Leu469=) c.4861T>C (p.Leu1621=) c.1185T>C c.1372T>C (p.Leu458=) c.*4581T>C (n.*4581T>C) c.1111T>C (p.Leu371=) c.5-7165T>C (n.5-7165T>C) c.271T>C (p.Leu91=) c.-98-20926T>C (n.-98-20926T>C) n.4934T>C n.4975T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071116A>T | CA10591926 | BRCA1 | c.4795T>A (p.Leu1599Met) c.4798T>A (p.Leu1600Met) c.4672T>A (p.Leu1558Met) c.4792T>A (p.Leu1598Met) c.4720T>A (p.Leu1574Met) c.1486T>A (p.Leu496Met) c.1348T>A (p.Leu450Met) c.3910T>A (p.Leu1304Met) c.4675T>A (p.Leu1559Met) c.4864T>A (p.Leu1622Met) c.4657T>A (p.Leu1553Met) c.1360T>A (p.Leu454Met) c.1405T>A (p.Leu469Met) c.4861T>A (p.Leu1621Met) c.1185T>A c.1372T>A (p.Leu458Met) c.*4581T>A (n.*4581T>A) c.1111T>A (p.Leu371Met) c.5-7165T>A (n.5-7165T>A) c.271T>A (p.Leu91Met) c.-98-20926T>A (n.-98-20926T>A) n.4934T>A n.4975T>A | dbSNP |
17 | g.43071117T>A | CA500231829 | BRCA1 | c.4794A>T (p.Ala1598=) c.4797A>T (p.Ala1599=) c.4671A>T (p.Ala1557=) c.4791A>T (p.Ala1597=) c.4719A>T (p.Ala1573=) c.1485A>T (p.Ala495=) c.1347A>T (p.Ala449=) c.3909A>T (p.Ala1303=) c.4674A>T (p.Ala1558=) c.4863A>T (p.Ala1621=) c.4656A>T (p.Ala1552=) c.1359A>T (p.Ala453=) c.1404A>T (p.Ala468=) c.4860A>T (p.Ala1620=) c.1184A>T c.1371A>T (p.Ala457=) c.*4580A>T (n.*4580A>T) c.1110A>T (p.Ala370=) c.5-7166A>T (n.5-7166A>T) c.270A>T (p.Ala90=) c.-98-20927A>T (n.-98-20927A>T) n.4933A>T n.4974A>T | dbSNP |
17 | g.43071117T>C | CA290831752 | BRCA1 | c.4794A>G (p.Ala1598=) c.4797A>G (p.Ala1599=) c.4671A>G (p.Ala1557=) c.4791A>G (p.Ala1597=) c.4719A>G (p.Ala1573=) c.1485A>G (p.Ala495=) c.1347A>G (p.Ala449=) c.3909A>G (p.Ala1303=) c.4674A>G (p.Ala1558=) c.4863A>G (p.Ala1621=) c.4656A>G (p.Ala1552=) c.1359A>G (p.Ala453=) c.1404A>G (p.Ala468=) c.4860A>G (p.Ala1620=) c.1184A>G c.1371A>G (p.Ala457=) c.*4580A>G (n.*4580A>G) c.1110A>G (p.Ala370=) c.5-7166A>G (n.5-7166A>G) c.270A>G (p.Ala90=) c.-98-20927A>G (n.-98-20927A>G) n.4933A>G n.4974A>G | ClinVar dbSNP gnomAD v4 |
17 | g.43071117T>G | CA500231830 | BRCA1 | c.4794A>C (p.Ala1598=) c.4797A>C (p.Ala1599=) c.4671A>C (p.Ala1557=) c.4791A>C (p.Ala1597=) c.4719A>C (p.Ala1573=) c.1485A>C (p.Ala495=) c.1347A>C (p.Ala449=) c.3909A>C (p.Ala1303=) c.4674A>C (p.Ala1558=) c.4863A>C (p.Ala1621=) c.4656A>C (p.Ala1552=) c.1359A>C (p.Ala453=) c.1404A>C (p.Ala468=) c.4860A>C (p.Ala1620=) c.1184A>C c.1371A>C (p.Ala457=) c.*4580A>C (n.*4580A>C) c.1110A>C (p.Ala370=) c.5-7166A>C (n.5-7166A>C) c.270A>C (p.Ala90=) c.-98-20927A>C (n.-98-20927A>C) n.4933A>C n.4974A>C | ClinVar |
17 | g.43071117T= | CA2260772930 | BRCA1 | c.4794A= (p.Ala1598=) c.4797A= (p.Ala1599=) c.4671A= (p.Ala1557=) c.4791A= (p.Ala1597=) c.4719A= (p.Ala1573=) c.1485A= (p.Ala495=) c.1347A= (p.Ala449=) c.3909A= (p.Ala1303=) c.4674A= (p.Ala1558=) c.4863A= (p.Ala1621=) c.4656A= (p.Ala1552=) c.1359A= (p.Ala453=) c.1404A= (p.Ala468=) c.4860A= (p.Ala1620=) c.1184A= c.1371A= (p.Ala457=) c.*4580A= (n.*4580A=) c.1110A= (p.Ala370=) c.5-7166A= (n.5-7166A=) c.270A= (p.Ala90=) c.-98-20927A= (n.-98-20927A=) n.4933A= n.4974A= | |
17 | g.43071118G>A | CA053237 | BRCA1 | c.4793C>T (p.Ala1598Val) c.4796C>T (p.Ala1599Val) c.4670C>T (p.Ala1557Val) c.4790C>T (p.Ala1597Val) c.4718C>T (p.Ala1573Val) c.1484C>T (p.Ala495Val) c.1346C>T (p.Ala449Val) c.3908C>T (p.Ala1303Val) c.4673C>T (p.Ala1558Val) c.4862C>T (p.Ala1621Val) c.4655C>T (p.Ala1552Val) c.1358C>T (p.Ala453Val) c.1403C>T (p.Ala468Val) c.4859C>T (p.Ala1620Val) c.1183C>T c.1370C>T (p.Ala457Val) c.*4579C>T (n.*4579C>T) c.1109C>T (p.Ala370Val) c.5-7167C>T (n.5-7167C>T) c.269C>T (p.Ala90Val) c.-98-20928C>T (n.-98-20928C>T) n.4932C>T n.4973C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071118G>C | CA10591927 | BRCA1 | c.4793C>G (p.Ala1598Gly) c.4796C>G (p.Ala1599Gly) c.4670C>G (p.Ala1557Gly) c.4790C>G (p.Ala1597Gly) c.4718C>G (p.Ala1573Gly) c.1484C>G (p.Ala495Gly) c.1346C>G (p.Ala449Gly) c.3908C>G (p.Ala1303Gly) c.4673C>G (p.Ala1558Gly) c.4862C>G (p.Ala1621Gly) c.4655C>G (p.Ala1552Gly) c.1358C>G (p.Ala453Gly) c.1403C>G (p.Ala468Gly) c.4859C>G (p.Ala1620Gly) c.1183C>G c.1370C>G (p.Ala457Gly) c.*4579C>G (n.*4579C>G) c.1109C>G (p.Ala370Gly) c.5-7167C>G (n.5-7167C>G) c.269C>G (p.Ala90Gly) c.-98-20928C>G (n.-98-20928C>G) n.4932C>G n.4973C>G | dbSNP |
17 | g.43071118G= | CA2260772931 | BRCA1 | c.4793C= (p.Ala1598=) c.4796C= (p.Ala1599=) c.4670C= (p.Ala1557=) c.4790C= (p.Ala1597=) c.4718C= (p.Ala1573=) c.1484C= (p.Ala495=) c.1346C= (p.Ala449=) c.3908C= (p.Ala1303=) c.4673C= (p.Ala1558=) c.4862C= (p.Ala1621=) c.4655C= (p.Ala1552=) c.1358C= (p.Ala453=) c.1403C= (p.Ala468=) c.4859C= (p.Ala1620=) c.1183C= c.1370C= (p.Ala457=) c.*4579C= (n.*4579C=) c.1109C= (p.Ala370=) c.5-7167C= (n.5-7167C=) c.269C= (p.Ala90=) c.-98-20928C= (n.-98-20928C=) n.4932C= n.4973C= | |
17 | g.43071118G>T | CA10591928 | BRCA1 | c.4793C>A (p.Ala1598Glu) c.4796C>A (p.Ala1599Glu) c.4670C>A (p.Ala1557Glu) c.4790C>A (p.Ala1597Glu) c.4718C>A (p.Ala1573Glu) c.1484C>A (p.Ala495Glu) c.1346C>A (p.Ala449Glu) c.3908C>A (p.Ala1303Glu) c.4673C>A (p.Ala1558Glu) c.4862C>A (p.Ala1621Glu) c.4655C>A (p.Ala1552Glu) c.1358C>A (p.Ala453Glu) c.1403C>A (p.Ala468Glu) c.4859C>A (p.Ala1620Glu) c.1183C>A c.1370C>A (p.Ala457Glu) c.*4579C>A (n.*4579C>A) c.1109C>A (p.Ala370Glu) c.5-7167C>A (n.5-7167C>A) c.269C>A (p.Ala90Glu) c.-98-20928C>A (n.-98-20928C>A) n.4932C>A n.4973C>A | |
17 | g.43071119C>A | CA10591929 | BRCA1 | c.4792G>T (p.Ala1598Ser) c.4795G>T (p.Ala1599Ser) c.4669G>T (p.Ala1557Ser) c.4789G>T (p.Ala1597Ser) c.4717G>T (p.Ala1573Ser) c.1483G>T (p.Ala495Ser) c.1345G>T (p.Ala449Ser) c.3907G>T (p.Ala1303Ser) c.4672G>T (p.Ala1558Ser) c.4861G>T (p.Ala1621Ser) c.4654G>T (p.Ala1552Ser) c.1357G>T (p.Ala453Ser) c.1402G>T (p.Ala468Ser) c.4858G>T (p.Ala1620Ser) c.1182G>T c.1369G>T (p.Ala457Ser) c.*4578G>T (n.*4578G>T) c.1108G>T (p.Ala370Ser) c.5-7168G>T (n.5-7168G>T) c.268G>T (p.Ala90Ser) c.-98-20929G>T (n.-98-20929G>T) n.4931G>T n.4972G>T | dbSNP |
17 | g.43071119C= | CA2260772932 | BRCA1 | c.4792G= (p.Ala1598=) c.4795G= (p.Ala1599=) c.4669G= (p.Ala1557=) c.4789G= (p.Ala1597=) c.4717G= (p.Ala1573=) c.1483G= (p.Ala495=) c.1345G= (p.Ala449=) c.3907G= (p.Ala1303=) c.4672G= (p.Ala1558=) c.4861G= (p.Ala1621=) c.4654G= (p.Ala1552=) c.1357G= (p.Ala453=) c.1402G= (p.Ala468=) c.4858G= (p.Ala1620=) c.1182G= c.1369G= (p.Ala457=) c.*4578G= (n.*4578G=) c.1108G= (p.Ala370=) c.5-7168G= (n.5-7168G=) c.268G= (p.Ala90=) c.-98-20929G= (n.-98-20929G=) n.4931G= n.4972G= | |
17 | g.43071119C>G | CA10591930 | BRCA1 | c.4792G>C (p.Ala1598Pro) c.4795G>C (p.Ala1599Pro) c.4669G>C (p.Ala1557Pro) c.4789G>C (p.Ala1597Pro) c.4717G>C (p.Ala1573Pro) c.1483G>C (p.Ala495Pro) c.1345G>C (p.Ala449Pro) c.3907G>C (p.Ala1303Pro) c.4672G>C (p.Ala1558Pro) c.4861G>C (p.Ala1621Pro) c.4654G>C (p.Ala1552Pro) c.1357G>C (p.Ala453Pro) c.1402G>C (p.Ala468Pro) c.4858G>C (p.Ala1620Pro) c.1182G>C c.1369G>C (p.Ala457Pro) c.*4578G>C (n.*4578G>C) c.1108G>C (p.Ala370Pro) c.5-7168G>C (n.5-7168G>C) c.268G>C (p.Ala90Pro) c.-98-20929G>C (n.-98-20929G>C) n.4931G>C n.4972G>C | dbSNP |
17 | g.43071119C>T | CA10591931 | BRCA1 | c.4792G>A (p.Ala1598Thr) c.4795G>A (p.Ala1599Thr) c.4669G>A (p.Ala1557Thr) c.4789G>A (p.Ala1597Thr) c.4717G>A (p.Ala1573Thr) c.1483G>A (p.Ala495Thr) c.1345G>A (p.Ala449Thr) c.3907G>A (p.Ala1303Thr) c.4672G>A (p.Ala1558Thr) c.4861G>A (p.Ala1621Thr) c.4654G>A (p.Ala1552Thr) c.1357G>A (p.Ala453Thr) c.1402G>A (p.Ala468Thr) c.4858G>A (p.Ala1620Thr) c.1182G>A c.1369G>A (p.Ala457Thr) c.*4578G>A (n.*4578G>A) c.1108G>A (p.Ala370Thr) c.5-7168G>A (n.5-7168G>A) c.268G>A (p.Ala90Thr) c.-98-20929G>A (n.-98-20929G>A) n.4931G>A n.4972G>A | ClinVar dbSNP gnomAD v4 |
17 | g.43071120del | CA2697559921 | BRCA1 | c.4791del (p.Ala1598HisfsTer2) c.4794del (p.Ala1599HisfsTer2) c.4668del (p.Ala1557HisfsTer2) c.4788del (p.Ala1597HisfsTer2) c.4716del (p.Ala1573HisfsTer2) c.1482del (p.Ala495HisfsTer2) c.1344del (p.Ala449HisfsTer2) c.3906del (p.Ala1303HisfsTer2) c.4671del (p.Ala1558HisfsTer2) c.4860del (p.Ala1621HisfsTer2) c.4653del (p.Ala1552HisfsTer2) c.1356del (p.Ala453HisfsTer2) c.1401del (p.Ala468HisfsTer2) c.4857del (p.Ala1620HisfsTer2) c.1181del c.1368del (p.Ala457HisfsTer2) c.*4577del (n.*4577del) c.1107del (p.Ala370HisfsTer2) c.5-7169del (n.5-7169del) c.267del (p.Ala90HisfsTer2) c.-98-20930del (n.-98-20930del) n.4930del n.4971del | ClinVar |
17 | g.43071120A= | CA2260772933 | BRCA1 | c.4791T= (p.Ser1597=) c.4794T= (p.Ser1598=) c.4668T= (p.Ser1556=) c.4788T= (p.Ser1596=) c.4716T= (p.Ser1572=) c.1482T= (p.Ser494=) c.1344T= (p.Ser448=) c.3906T= (p.Ser1302=) c.4671T= (p.Ser1557=) c.4860T= (p.Ser1620=) c.4653T= (p.Ser1551=) c.1356T= (p.Ser452=) c.1401T= (p.Ser467=) c.4857T= (p.Ser1619=) c.1181T= c.1368T= (p.Ser456=) c.*4577T= (n.*4577T=) c.1107T= (p.Ser369=) c.5-7169T= (n.5-7169T=) c.267T= (p.Ser89=) c.-98-20930T= (n.-98-20930T=) n.4930T= n.4971T= | |
17 | g.43071120A>C | CA500231831 | BRCA1 | c.4791T>G (p.Ser1597=) c.4794T>G (p.Ser1598=) c.4668T>G (p.Ser1556=) c.4788T>G (p.Ser1596=) c.4716T>G (p.Ser1572=) c.1482T>G (p.Ser494=) c.1344T>G (p.Ser448=) c.3906T>G (p.Ser1302=) c.4671T>G (p.Ser1557=) c.4860T>G (p.Ser1620=) c.4653T>G (p.Ser1551=) c.1356T>G (p.Ser452=) c.1401T>G (p.Ser467=) c.4857T>G (p.Ser1619=) c.1181T>G c.1368T>G (p.Ser456=) c.*4577T>G (n.*4577T>G) c.1107T>G (p.Ser369=) c.5-7169T>G (n.5-7169T>G) c.267T>G (p.Ser89=) c.-98-20930T>G (n.-98-20930T>G) n.4930T>G n.4971T>G | |
17 | g.43071120A>G | CA500231833 | BRCA1 | c.4791T>C (p.Ser1597=) c.4794T>C (p.Ser1598=) c.4668T>C (p.Ser1556=) c.4788T>C (p.Ser1596=) c.4716T>C (p.Ser1572=) c.1482T>C (p.Ser494=) c.1344T>C (p.Ser448=) c.3906T>C (p.Ser1302=) c.4671T>C (p.Ser1557=) c.4860T>C (p.Ser1620=) c.4653T>C (p.Ser1551=) c.1356T>C (p.Ser452=) c.1401T>C (p.Ser467=) c.4857T>C (p.Ser1619=) c.1181T>C c.1368T>C (p.Ser456=) c.*4577T>C (n.*4577T>C) c.1107T>C (p.Ser369=) c.5-7169T>C (n.5-7169T>C) c.267T>C (p.Ser89=) c.-98-20930T>C (n.-98-20930T>C) n.4930T>C n.4971T>C | dbSNP |
17 | g.43071120A>T | CA500231832 | BRCA1 | c.4791T>A (p.Ser1597=) c.4794T>A (p.Ser1598=) c.4668T>A (p.Ser1556=) c.4788T>A (p.Ser1596=) c.4716T>A (p.Ser1572=) c.1482T>A (p.Ser494=) c.1344T>A (p.Ser448=) c.3906T>A (p.Ser1302=) c.4671T>A (p.Ser1557=) c.4860T>A (p.Ser1620=) c.4653T>A (p.Ser1551=) c.1356T>A (p.Ser452=) c.1401T>A (p.Ser467=) c.4857T>A (p.Ser1619=) c.1181T>A c.1368T>A (p.Ser456=) c.*4577T>A (n.*4577T>A) c.1107T>A (p.Ser369=) c.5-7169T>A (n.5-7169T>A) c.267T>A (p.Ser89=) c.-98-20930T>A (n.-98-20930T>A) n.4930T>A n.4971T>A | ClinVar dbSNP gnomAD v4 |
17 | g.43071121G>A | CA10591932 | BRCA1 | c.4790C>T (p.Ser1597Phe) c.4793C>T (p.Ser1598Phe) c.4667C>T (p.Ser1556Phe) c.4787C>T (p.Ser1596Phe) c.4715C>T (p.Ser1572Phe) c.1481C>T (p.Ser494Phe) c.1343C>T (p.Ser448Phe) c.3905C>T (p.Ser1302Phe) c.4670C>T (p.Ser1557Phe) c.4859C>T (p.Ser1620Phe) c.4652C>T (p.Ser1551Phe) c.1355C>T (p.Ser452Phe) c.1400C>T (p.Ser467Phe) c.4856C>T (p.Ser1619Phe) c.1180C>T c.1367C>T (p.Ser456Phe) c.*4576C>T (n.*4576C>T) c.1106C>T (p.Ser369Phe) c.5-7170C>T (n.5-7170C>T) c.266C>T (p.Ser89Phe) c.-98-20931C>T (n.-98-20931C>T) n.4929C>T n.4970C>T | ClinVar dbSNP gnomAD v4 |
17 | g.43071121G>C | CA10591933 | BRCA1 | c.4790C>G (p.Ser1597Cys) c.4793C>G (p.Ser1598Cys) c.4667C>G (p.Ser1556Cys) c.4787C>G (p.Ser1596Cys) c.4715C>G (p.Ser1572Cys) c.1481C>G (p.Ser494Cys) c.1343C>G (p.Ser448Cys) c.3905C>G (p.Ser1302Cys) c.4670C>G (p.Ser1557Cys) c.4859C>G (p.Ser1620Cys) c.4652C>G (p.Ser1551Cys) c.1355C>G (p.Ser452Cys) c.1400C>G (p.Ser467Cys) c.4856C>G (p.Ser1619Cys) c.1180C>G c.1367C>G (p.Ser456Cys) c.*4576C>G (n.*4576C>G) c.1106C>G (p.Ser369Cys) c.5-7170C>G (n.5-7170C>G) c.266C>G (p.Ser89Cys) c.-98-20931C>G (n.-98-20931C>G) n.4929C>G n.4970C>G | dbSNP |
17 | g.43071121G>T | CA10591934 | BRCA1 | c.4790C>A (p.Ser1597Tyr) c.4793C>A (p.Ser1598Tyr) c.4667C>A (p.Ser1556Tyr) c.4787C>A (p.Ser1596Tyr) c.4715C>A (p.Ser1572Tyr) c.1481C>A (p.Ser494Tyr) c.1343C>A (p.Ser448Tyr) c.3905C>A (p.Ser1302Tyr) c.4670C>A (p.Ser1557Tyr) c.4859C>A (p.Ser1620Tyr) c.4652C>A (p.Ser1551Tyr) c.1355C>A (p.Ser452Tyr) c.1400C>A (p.Ser467Tyr) c.4856C>A (p.Ser1619Tyr) c.1180C>A c.1367C>A (p.Ser456Tyr) c.*4576C>A (n.*4576C>A) c.1106C>A (p.Ser369Tyr) c.5-7170C>A (n.5-7170C>A) c.266C>A (p.Ser89Tyr) c.-98-20931C>A (n.-98-20931C>A) n.4929C>A n.4970C>A | dbSNP |
17 | g.43071121_43071134del | CA2499224397 | BRCA1 | c.4777_4790del (p.Pro1593CysfsTer23) c.4780_4793del (p.Pro1594CysfsTer23) c.4654_4667del (p.Pro1552CysfsTer23) c.4774_4787del (p.Pro1592CysfsTer23) c.4702_4715del (p.Pro1568CysfsTer23) c.1468_1481del (p.Pro490CysfsTer23) c.1330_1343del (p.Pro444CysfsTer23) c.3892_3905del (p.Pro1298CysfsTer23) c.4657_4670del (p.Pro1553CysfsTer23) c.4846_4859del (p.Pro1616CysfsTer23) c.4639_4652del (p.Pro1547CysfsTer23) c.1342_1355del (p.Pro448CysfsTer23) c.1387_1400del (p.Pro463CysfsTer23) c.4843_4856del (p.Pro1615CysfsTer23) c.1167_1180del c.1354_1367del (p.Pro452CysfsTer23) c.*4563_*4576del (n.*4563_*4576del) c.1093_1106del (p.Pro365CysfsTer23) c.5-7183_5-7170del (n.5-7183_5-7170del) c.253_266del (p.Pro85CysfsTer23) c.-98-20944_-98-20931del (n.-98-20944_-98-20931del) n.4916_4929del n.4957_4970del | |
17 | g.43071121_43071134dup | CA919844206 | BRCA1 | c.4777_4790dup (p.Ala1598HisfsTer7) c.4780_4793dup (p.Ala1599HisfsTer7) c.4654_4667dup (p.Ala1557HisfsTer7) c.4774_4787dup (p.Ala1597HisfsTer7) c.4702_4715dup (p.Ala1573HisfsTer7) c.1468_1481dup (p.Ala495HisfsTer7) c.1330_1343dup (p.Ala449HisfsTer7) c.3892_3905dup (p.Ala1303HisfsTer7) c.4657_4670dup (p.Ala1558HisfsTer7) c.4846_4859dup (p.Ala1621HisfsTer7) c.4639_4652dup (p.Ala1552HisfsTer7) c.1342_1355dup (p.Ala453HisfsTer7) c.1387_1400dup (p.Ala468HisfsTer7) c.4843_4856dup (p.Ala1620HisfsTer7) c.1167_1180dup c.1354_1367dup (p.Ala457HisfsTer7) c.*4563_*4576dup (n.*4563_*4576dup) c.1093_1106dup (p.Ala370HisfsTer7) c.5-7183_5-7170dup (n.5-7183_5-7170dup) c.253_266dup (p.Ala90HisfsTer7) c.-98-20944_-98-20931dup (n.-98-20944_-98-20931dup) n.4916_4929dup n.4957_4970dup | dbSNP |
17 | g.43071122A>C | CA10591935 | BRCA1 | c.4789T>G (p.Ser1597Ala) c.4792T>G (p.Ser1598Ala) c.4666T>G (p.Ser1556Ala) c.4786T>G (p.Ser1596Ala) c.4714T>G (p.Ser1572Ala) c.1480T>G (p.Ser494Ala) c.1342T>G (p.Ser448Ala) c.3904T>G (p.Ser1302Ala) c.4669T>G (p.Ser1557Ala) c.4858T>G (p.Ser1620Ala) c.4651T>G (p.Ser1551Ala) c.1354T>G (p.Ser452Ala) c.1399T>G (p.Ser467Ala) c.4855T>G (p.Ser1619Ala) c.1179T>G c.1366T>G (p.Ser456Ala) c.*4575T>G (n.*4575T>G) c.1105T>G (p.Ser369Ala) c.5-7171T>G (n.5-7171T>G) c.265T>G (p.Ser89Ala) c.-98-20932T>G (n.-98-20932T>G) n.4928T>G n.4969T>G | |
17 | g.43071122A>G | CA10591936 | BRCA1 | c.4789T>C (p.Ser1597Pro) c.4792T>C (p.Ser1598Pro) c.4666T>C (p.Ser1556Pro) c.4786T>C (p.Ser1596Pro) c.4714T>C (p.Ser1572Pro) c.1480T>C (p.Ser494Pro) c.1342T>C (p.Ser448Pro) c.3904T>C (p.Ser1302Pro) c.4669T>C (p.Ser1557Pro) c.4858T>C (p.Ser1620Pro) c.4651T>C (p.Ser1551Pro) c.1354T>C (p.Ser452Pro) c.1399T>C (p.Ser467Pro) c.4855T>C (p.Ser1619Pro) c.1179T>C c.1366T>C (p.Ser456Pro) c.*4575T>C (n.*4575T>C) c.1105T>C (p.Ser369Pro) c.5-7171T>C (n.5-7171T>C) c.265T>C (p.Ser89Pro) c.-98-20932T>C (n.-98-20932T>C) n.4928T>C n.4969T>C | dbSNP |
17 | g.43071122A>T | CA10591937 | BRCA1 | c.4789T>A (p.Ser1597Thr) c.4792T>A (p.Ser1598Thr) c.4666T>A (p.Ser1556Thr) c.4786T>A (p.Ser1596Thr) c.4714T>A (p.Ser1572Thr) c.1480T>A (p.Ser494Thr) c.1342T>A (p.Ser448Thr) c.3904T>A (p.Ser1302Thr) c.4669T>A (p.Ser1557Thr) c.4858T>A (p.Ser1620Thr) c.4651T>A (p.Ser1551Thr) c.1354T>A (p.Ser452Thr) c.1399T>A (p.Ser467Thr) c.4855T>A (p.Ser1619Thr) c.1179T>A c.1366T>A (p.Ser456Thr) c.*4575T>A (n.*4575T>A) c.1105T>A (p.Ser369Thr) c.5-7171T>A (n.5-7171T>A) c.265T>A (p.Ser89Thr) c.-98-20932T>A (n.-98-20932T>A) n.4928T>A n.4969T>A | dbSNP |
17 | g.43071122_43071123delinsAG | CA2260772934 | BRCA1 | c.4788_4789delinsCT (p.Thr1596=) c.4791_4792delinsCT (p.Thr1597=) c.4665_4666delinsCT (p.Thr1555=) c.4785_4786delinsCT (p.Thr1595=) c.4713_4714delinsCT (p.Thr1571=) c.1479_1480delinsCT (p.Thr493=) c.1341_1342delinsCT (p.Thr447=) c.3903_3904delinsCT (p.Thr1301=) c.4668_4669delinsCT (p.Thr1556=) c.4857_4858delinsCT (p.Thr1619=) c.4650_4651delinsCT (p.Thr1550=) c.1353_1354delinsCT (p.Thr451=) c.1398_1399delinsCT (p.Thr466=) c.4854_4855delinsCT (p.Thr1618=) c.1178_1179delinsCT c.1365_1366delinsCT (p.Thr455=) c.*4574_*4575delinsCT (n.*4574_*4575delinsCT) c.1104_1105delinsCT (p.Thr368=) c.5-7172_5-7171delinsCT (n.5-7172_5-7171delinsCT) c.264_265delinsCT (p.Thr88=) c.-98-20933_-98-20932delinsCT (n.-98-20933_-98-20932delinsCT) n.4927_4928delinsCT n.4968_4969delinsCT | |
17 | g.43071123G>A | CA500231834 | BRCA1 | c.4788C>T (p.Thr1596=) c.4791C>T (p.Thr1597=) c.4665C>T (p.Thr1555=) c.4785C>T (p.Thr1595=) c.4713C>T (p.Thr1571=) c.1479C>T (p.Thr493=) c.1341C>T (p.Thr447=) c.3903C>T (p.Thr1301=) c.4668C>T (p.Thr1556=) c.4857C>T (p.Thr1619=) c.4650C>T (p.Thr1550=) c.1353C>T (p.Thr451=) c.1398C>T (p.Thr466=) c.4854C>T (p.Thr1618=) c.1178C>T c.1365C>T (p.Thr455=) c.*4574C>T (n.*4574C>T) c.1104C>T (p.Thr368=) c.5-7172C>T (n.5-7172C>T) c.264C>T (p.Thr88=) c.-98-20933C>T (n.-98-20933C>T) n.4927C>T n.4968C>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
17 | g.43071123G>C | CA500231835 | BRCA1 | c.4788C>G (p.Thr1596=) c.4791C>G (p.Thr1597=) c.4665C>G (p.Thr1555=) c.4785C>G (p.Thr1595=) c.4713C>G (p.Thr1571=) c.1479C>G (p.Thr493=) c.1341C>G (p.Thr447=) c.3903C>G (p.Thr1301=) c.4668C>G (p.Thr1556=) c.4857C>G (p.Thr1619=) c.4650C>G (p.Thr1550=) c.1353C>G (p.Thr451=) c.1398C>G (p.Thr466=) c.4854C>G (p.Thr1618=) c.1178C>G c.1365C>G (p.Thr455=) c.*4574C>G (n.*4574C>G) c.1104C>G (p.Thr368=) c.5-7172C>G (n.5-7172C>G) c.264C>G (p.Thr88=) c.-98-20933C>G (n.-98-20933C>G) n.4927C>G n.4968C>G | ClinVar COSMIC COSMIC |
17 | g.43071123G= | CA2260772935 | BRCA1 | c.4788C= (p.Thr1596=) c.4791C= (p.Thr1597=) c.4665C= (p.Thr1555=) c.4785C= (p.Thr1595=) c.4713C= (p.Thr1571=) c.1479C= (p.Thr493=) c.1341C= (p.Thr447=) c.3903C= (p.Thr1301=) c.4668C= (p.Thr1556=) c.4857C= (p.Thr1619=) c.4650C= (p.Thr1550=) c.1353C= (p.Thr451=) c.1398C= (p.Thr466=) c.4854C= (p.Thr1618=) c.1178C= c.1365C= (p.Thr455=) c.*4574C= (n.*4574C=) c.1104C= (p.Thr368=) c.5-7172C= (n.5-7172C=) c.264C= (p.Thr88=) c.-98-20933C= (n.-98-20933C=) n.4927C= n.4968C= | |
17 | g.43071123G>T | CA500231836 | BRCA1 | c.4788C>A (p.Thr1596=) c.4791C>A (p.Thr1597=) c.4665C>A (p.Thr1555=) c.4785C>A (p.Thr1595=) c.4713C>A (p.Thr1571=) c.1479C>A (p.Thr493=) c.1341C>A (p.Thr447=) c.3903C>A (p.Thr1301=) c.4668C>A (p.Thr1556=) c.4857C>A (p.Thr1619=) c.4650C>A (p.Thr1550=) c.1353C>A (p.Thr451=) c.1398C>A (p.Thr466=) c.4854C>A (p.Thr1618=) c.1178C>A c.1365C>A (p.Thr455=) c.*4574C>A (n.*4574C>A) c.1104C>A (p.Thr368=) c.5-7172C>A (n.5-7172C>A) c.264C>A (p.Thr88=) c.-98-20933C>A (n.-98-20933C>A) n.4927C>A n.4968C>A | ClinVar |
17 | g.43071124del | CA1139665580 | BRCA1 | c.4788del (p.Ser1597LeufsTer3) c.4791del (p.Ser1598LeufsTer3) c.4665del (p.Ser1556LeufsTer3) c.4785del (p.Ser1596LeufsTer3) c.4713del (p.Ser1572LeufsTer3) c.1479del (p.Ser494LeufsTer3) c.1341del (p.Ser448LeufsTer3) c.3903del (p.Ser1302LeufsTer3) c.4668del (p.Ser1557LeufsTer3) c.4857del (p.Ser1620LeufsTer3) c.4650del (p.Ser1551LeufsTer3) c.1353del (p.Ser452LeufsTer3) c.1398del (p.Ser467LeufsTer3) c.4854del (p.Ser1619LeufsTer3) c.1178del c.1365del (p.Ser456LeufsTer3) c.*4574del (n.*4574del) c.1104del (p.Ser369LeufsTer3) c.5-7172del (n.5-7172del) c.264del (p.Ser89LeufsTer3) c.-98-20933del (n.-98-20933del) n.4927del n.4968del | ClinVar dbSNP |
17 | g.43071124G>A | CA053224 | BRCA1 | c.4787C>T (p.Thr1596Ile) c.4790C>T (p.Thr1597Ile) c.4664C>T (p.Thr1555Ile) c.4784C>T (p.Thr1595Ile) c.4712C>T (p.Thr1571Ile) c.1478C>T (p.Thr493Ile) c.1340C>T (p.Thr447Ile) c.3902C>T (p.Thr1301Ile) c.4667C>T (p.Thr1556Ile) c.4856C>T (p.Thr1619Ile) c.4649C>T (p.Thr1550Ile) c.1352C>T (p.Thr451Ile) c.1397C>T (p.Thr466Ile) c.4853C>T (p.Thr1618Ile) c.1177C>T c.1364C>T (p.Thr455Ile) c.*4573C>T (n.*4573C>T) c.1103C>T (p.Thr368Ile) c.5-7173C>T (n.5-7173C>T) c.263C>T (p.Thr88Ile) c.-98-20934C>T (n.-98-20934C>T) n.4926C>T n.4967C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071124G>C | CA10591938 | BRCA1 | c.4787C>G (p.Thr1596Ser) c.4790C>G (p.Thr1597Ser) c.4664C>G (p.Thr1555Ser) c.4784C>G (p.Thr1595Ser) c.4712C>G (p.Thr1571Ser) c.1478C>G (p.Thr493Ser) c.1340C>G (p.Thr447Ser) c.3902C>G (p.Thr1301Ser) c.4667C>G (p.Thr1556Ser) c.4856C>G (p.Thr1619Ser) c.4649C>G (p.Thr1550Ser) c.1352C>G (p.Thr451Ser) c.1397C>G (p.Thr466Ser) c.4853C>G (p.Thr1618Ser) c.1177C>G c.1364C>G (p.Thr455Ser) c.*4573C>G (n.*4573C>G) c.1103C>G (p.Thr368Ser) c.5-7173C>G (n.5-7173C>G) c.263C>G (p.Thr88Ser) c.-98-20934C>G (n.-98-20934C>G) n.4926C>G n.4967C>G | ClinVar dbSNP |
17 | g.43071124G= | CA2260772936 | BRCA1 | c.4787C= (p.Thr1596=) c.4790C= (p.Thr1597=) c.4664C= (p.Thr1555=) c.4784C= (p.Thr1595=) c.4712C= (p.Thr1571=) c.1478C= (p.Thr493=) c.1340C= (p.Thr447=) c.3902C= (p.Thr1301=) c.4667C= (p.Thr1556=) c.4856C= (p.Thr1619=) c.4649C= (p.Thr1550=) c.1352C= (p.Thr451=) c.1397C= (p.Thr466=) c.4853C= (p.Thr1618=) c.1177C= c.1364C= (p.Thr455=) c.*4573C= (n.*4573C=) c.1103C= (p.Thr368=) c.5-7173C= (n.5-7173C=) c.263C= (p.Thr88=) c.-98-20934C= (n.-98-20934C=) n.4926C= n.4967C= | |
17 | g.43071124G>T | CA003024 | BRCA1 | c.4787C>A (p.Thr1596Asn) c.4790C>A (p.Thr1597Asn) c.4664C>A (p.Thr1555Asn) c.4784C>A (p.Thr1595Asn) c.4712C>A (p.Thr1571Asn) c.1478C>A (p.Thr493Asn) c.1340C>A (p.Thr447Asn) c.3902C>A (p.Thr1301Asn) c.4667C>A (p.Thr1556Asn) c.4856C>A (p.Thr1619Asn) c.4649C>A (p.Thr1550Asn) c.1352C>A (p.Thr451Asn) c.1397C>A (p.Thr466Asn) c.4853C>A (p.Thr1618Asn) c.1177C>A c.1364C>A (p.Thr455Asn) c.*4573C>A (n.*4573C>A) c.1103C>A (p.Thr368Asn) c.5-7173C>A (n.5-7173C>A) c.263C>A (p.Thr88Asn) c.-98-20934C>A (n.-98-20934C>A) n.4926C>A n.4967C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071125_43071130del | CA645578304 | BRCA1 | c.4782_4787del (p.Ser1595_Thr1596del) c.4785_4790del (p.Ser1596_Thr1597del) c.4659_4664del (p.Ser1554_Thr1555del) c.4779_4784del (p.Ser1594_Thr1595del) c.4707_4712del (p.Ser1570_Thr1571del) c.1473_1478del (p.Ser492_Thr493del) c.1335_1340del (p.Ser446_Thr447del) c.3897_3902del (p.Ser1300_Thr1301del) c.4662_4667del (p.Ser1555_Thr1556del) c.4851_4856del (p.Ser1618_Thr1619del) c.4644_4649del (p.Ser1549_Thr1550del) c.1347_1352del (p.Ser450_Thr451del) c.1392_1397del (p.Ser465_Thr466del) c.4848_4853del (p.Ser1617_Thr1618del) c.1172_1177del c.1359_1364del (p.Ser454_Thr455del) c.*4568_*4573del (n.*4568_*4573del) c.1098_1103del (p.Ser367_Thr368del) c.5-7178_5-7173del (n.5-7178_5-7173del) c.258_263del (p.Ser87_Thr88del) c.-98-20939_-98-20934del (n.-98-20939_-98-20934del) n.4921_4926del n.4962_4967del | COSMIC COSMIC |
17 | g.43071125T>A | CA10591939 | BRCA1 | c.4786A>T (p.Thr1596Ser) c.4789A>T (p.Thr1597Ser) c.4663A>T (p.Thr1555Ser) c.4783A>T (p.Thr1595Ser) c.4711A>T (p.Thr1571Ser) c.1477A>T (p.Thr493Ser) c.1339A>T (p.Thr447Ser) c.3901A>T (p.Thr1301Ser) c.4666A>T (p.Thr1556Ser) c.4855A>T (p.Thr1619Ser) c.4648A>T (p.Thr1550Ser) c.1351A>T (p.Thr451Ser) c.1396A>T (p.Thr466Ser) c.4852A>T (p.Thr1618Ser) c.1176A>T c.1363A>T (p.Thr455Ser) c.*4572A>T (n.*4572A>T) c.1102A>T (p.Thr368Ser) c.5-7174A>T (n.5-7174A>T) c.262A>T (p.Thr88Ser) c.-98-20935A>T (n.-98-20935A>T) n.4925A>T n.4966A>T | dbSNP |
17 | g.43071125T>C | CA003023 | BRCA1 | c.4786A>G (p.Thr1596Ala) c.4789A>G (p.Thr1597Ala) c.4663A>G (p.Thr1555Ala) c.4783A>G (p.Thr1595Ala) c.4711A>G (p.Thr1571Ala) c.1477A>G (p.Thr493Ala) c.1339A>G (p.Thr447Ala) c.3901A>G (p.Thr1301Ala) c.4666A>G (p.Thr1556Ala) c.4855A>G (p.Thr1619Ala) c.4648A>G (p.Thr1550Ala) c.1351A>G (p.Thr451Ala) c.1396A>G (p.Thr466Ala) c.4852A>G (p.Thr1618Ala) c.1176A>G c.1363A>G (p.Thr455Ala) c.*4572A>G (n.*4572A>G) c.1102A>G (p.Thr368Ala) c.5-7174A>G (n.5-7174A>G) c.262A>G (p.Thr88Ala) c.-98-20935A>G (n.-98-20935A>G) n.4925A>G n.4966A>G | ClinVar dbSNP gnomAD v4 |
17 | g.43071125T>G | CA10591940 | BRCA1 | c.4786A>C (p.Thr1596Pro) c.4789A>C (p.Thr1597Pro) c.4663A>C (p.Thr1555Pro) c.4783A>C (p.Thr1595Pro) c.4711A>C (p.Thr1571Pro) c.1477A>C (p.Thr493Pro) c.1339A>C (p.Thr447Pro) c.3901A>C (p.Thr1301Pro) c.4666A>C (p.Thr1556Pro) c.4855A>C (p.Thr1619Pro) c.4648A>C (p.Thr1550Pro) c.1351A>C (p.Thr451Pro) c.1396A>C (p.Thr466Pro) c.4852A>C (p.Thr1618Pro) c.1176A>C c.1363A>C (p.Thr455Pro) c.*4572A>C (n.*4572A>C) c.1102A>C (p.Thr368Pro) c.5-7174A>C (n.5-7174A>C) c.262A>C (p.Thr88Pro) c.-98-20935A>C (n.-98-20935A>C) n.4925A>C n.4966A>C | dbSNP |
17 | g.43071125T= | CA2260772937 | BRCA1 | c.4786A= (p.Thr1596=) c.4789A= (p.Thr1597=) c.4663A= (p.Thr1555=) c.4783A= (p.Thr1595=) c.4711A= (p.Thr1571=) c.1477A= (p.Thr493=) c.1339A= (p.Thr447=) c.3901A= (p.Thr1301=) c.4666A= (p.Thr1556=) c.4855A= (p.Thr1619=) c.4648A= (p.Thr1550=) c.1351A= (p.Thr451=) c.1396A= (p.Thr466=) c.4852A= (p.Thr1618=) c.1176A= c.1363A= (p.Thr455=) c.*4572A= (n.*4572A=) c.1102A= (p.Thr368=) c.5-7174A= (n.5-7174A=) c.262A= (p.Thr88=) c.-98-20935A= (n.-98-20935A=) n.4925A= n.4966A= | |
17 | g.43071126T>A | CA500231837 | BRCA1 | c.4785A>T (p.Ser1595=) c.4788A>T (p.Ser1596=) c.4662A>T (p.Ser1554=) c.4782A>T (p.Ser1594=) c.4710A>T (p.Ser1570=) c.1476A>T (p.Ser492=) c.1338A>T (p.Ser446=) c.3900A>T (p.Ser1300=) c.4665A>T (p.Ser1555=) c.4854A>T (p.Ser1618=) c.4647A>T (p.Ser1549=) c.1350A>T (p.Ser450=) c.1395A>T (p.Ser465=) c.4851A>T (p.Ser1617=) c.1175A>T c.1362A>T (p.Ser454=) c.*4571A>T (n.*4571A>T) c.1101A>T (p.Ser367=) c.5-7175A>T (n.5-7175A>T) c.261A>T (p.Ser87=) c.-98-20936A>T (n.-98-20936A>T) n.4924A>T n.4965A>T | dbSNP |
17 | g.43071126T>C | CA500231838 | BRCA1 | c.4785A>G (p.Ser1595=) c.4788A>G (p.Ser1596=) c.4662A>G (p.Ser1554=) c.4782A>G (p.Ser1594=) c.4710A>G (p.Ser1570=) c.1476A>G (p.Ser492=) c.1338A>G (p.Ser446=) c.3900A>G (p.Ser1300=) c.4665A>G (p.Ser1555=) c.4854A>G (p.Ser1618=) c.4647A>G (p.Ser1549=) c.1350A>G (p.Ser450=) c.1395A>G (p.Ser465=) c.4851A>G (p.Ser1617=) c.1175A>G c.1362A>G (p.Ser454=) c.*4571A>G (n.*4571A>G) c.1101A>G (p.Ser367=) c.5-7175A>G (n.5-7175A>G) c.261A>G (p.Ser87=) c.-98-20936A>G (n.-98-20936A>G) n.4924A>G n.4965A>G | gnomAD v4 |
17 | g.43071126T>G | CA500231839 | BRCA1 | c.4785A>C (p.Ser1595=) c.4788A>C (p.Ser1596=) c.4662A>C (p.Ser1554=) c.4782A>C (p.Ser1594=) c.4710A>C (p.Ser1570=) c.1476A>C (p.Ser492=) c.1338A>C (p.Ser446=) c.3900A>C (p.Ser1300=) c.4665A>C (p.Ser1555=) c.4854A>C (p.Ser1618=) c.4647A>C (p.Ser1549=) c.1350A>C (p.Ser450=) c.1395A>C (p.Ser465=) c.4851A>C (p.Ser1617=) c.1175A>C c.1362A>C (p.Ser454=) c.*4571A>C (n.*4571A>C) c.1101A>C (p.Ser367=) c.5-7175A>C (n.5-7175A>C) c.261A>C (p.Ser87=) c.-98-20936A>C (n.-98-20936A>C) n.4924A>C n.4965A>C | ClinVar |
17 | g.43071127G>A | CA003022 | BRCA1 | c.4784C>T (p.Ser1595Leu) c.4787C>T (p.Ser1596Leu) c.4661C>T (p.Ser1554Leu) c.4781C>T (p.Ser1594Leu) c.4709C>T (p.Ser1570Leu) c.1475C>T (p.Ser492Leu) c.1337C>T (p.Ser446Leu) c.3899C>T (p.Ser1300Leu) c.4664C>T (p.Ser1555Leu) c.4853C>T (p.Ser1618Leu) c.4646C>T (p.Ser1549Leu) c.1349C>T (p.Ser450Leu) c.1394C>T (p.Ser465Leu) c.4850C>T (p.Ser1617Leu) c.1174C>T c.1361C>T (p.Ser454Leu) c.*4570C>T (n.*4570C>T) c.1100C>T (p.Ser367Leu) c.5-7176C>T (n.5-7176C>T) c.260C>T (p.Ser87Leu) c.-98-20937C>T (n.-98-20937C>T) n.4923C>T n.4964C>T | ClinVar dbSNP |
17 | g.43071127G>C | CA10591941 | BRCA1 | c.4784C>G (p.Ser1595Ter) c.4787C>G (p.Ser1596Ter) c.4661C>G (p.Ser1554Ter) c.4781C>G (p.Ser1594Ter) c.4709C>G (p.Ser1570Ter) c.1475C>G (p.Ser492Ter) c.1337C>G (p.Ser446Ter) c.3899C>G (p.Ser1300Ter) c.4664C>G (p.Ser1555Ter) c.4853C>G (p.Ser1618Ter) c.4646C>G (p.Ser1549Ter) c.1349C>G (p.Ser450Ter) c.1394C>G (p.Ser465Ter) c.4850C>G (p.Ser1617Ter) c.1174C>G c.1361C>G (p.Ser454Ter) c.*4570C>G (n.*4570C>G) c.1100C>G (p.Ser367Ter) c.5-7176C>G (n.5-7176C>G) c.260C>G (p.Ser87Ter) c.-98-20937C>G (n.-98-20937C>G) n.4923C>G n.4964C>G | dbSNP |
17 | g.43071127G= | CA2260772938 | BRCA1 | c.4784C= (p.Ser1595=) c.4787C= (p.Ser1596=) c.4661C= (p.Ser1554=) c.4781C= (p.Ser1594=) c.4709C= (p.Ser1570=) c.1475C= (p.Ser492=) c.1337C= (p.Ser446=) c.3899C= (p.Ser1300=) c.4664C= (p.Ser1555=) c.4853C= (p.Ser1618=) c.4646C= (p.Ser1549=) c.1349C= (p.Ser450=) c.1394C= (p.Ser465=) c.4850C= (p.Ser1617=) c.1174C= c.1361C= (p.Ser454=) c.*4570C= (n.*4570C=) c.1100C= (p.Ser367=) c.5-7176C= (n.5-7176C=) c.260C= (p.Ser87=) c.-98-20937C= (n.-98-20937C=) n.4923C= n.4964C= | |
17 | g.43071127G>T | CA10591942 | BRCA1 | c.4784C>A (p.Ser1595Ter) c.4787C>A (p.Ser1596Ter) c.4661C>A (p.Ser1554Ter) c.4781C>A (p.Ser1594Ter) c.4709C>A (p.Ser1570Ter) c.1475C>A (p.Ser492Ter) c.1337C>A (p.Ser446Ter) c.3899C>A (p.Ser1300Ter) c.4664C>A (p.Ser1555Ter) c.4853C>A (p.Ser1618Ter) c.4646C>A (p.Ser1549Ter) c.1349C>A (p.Ser450Ter) c.1394C>A (p.Ser465Ter) c.4850C>A (p.Ser1617Ter) c.1174C>A c.1361C>A (p.Ser454Ter) c.*4570C>A (n.*4570C>A) c.1100C>A (p.Ser367Ter) c.5-7176C>A (n.5-7176C>A) c.260C>A (p.Ser87Ter) c.-98-20937C>A (n.-98-20937C>A) n.4923C>A n.4964C>A | ClinVar dbSNP COSMIC COSMIC |
17 | g.43071128A= | CA2260772939 | BRCA1 | c.4783T= (p.Ser1595=) c.4786T= (p.Ser1596=) c.4660T= (p.Ser1554=) c.4780T= (p.Ser1594=) c.4708T= (p.Ser1570=) c.1474T= (p.Ser492=) c.1336T= (p.Ser446=) c.3898T= (p.Ser1300=) c.4663T= (p.Ser1555=) c.4852T= (p.Ser1618=) c.4645T= (p.Ser1549=) c.1348T= (p.Ser450=) c.1393T= (p.Ser465=) c.4849T= (p.Ser1617=) c.1173T= c.1360T= (p.Ser454=) c.*4569T= (n.*4569T=) c.1099T= (p.Ser367=) c.5-7177T= (n.5-7177T=) c.259T= (p.Ser87=) c.-98-20938T= (n.-98-20938T=) n.4922T= n.4963T= | |
17 | g.43071128A>C | CA10591943 | BRCA1 | c.4783T>G (p.Ser1595Ala) c.4786T>G (p.Ser1596Ala) c.4660T>G (p.Ser1554Ala) c.4780T>G (p.Ser1594Ala) c.4708T>G (p.Ser1570Ala) c.1474T>G (p.Ser492Ala) c.1336T>G (p.Ser446Ala) c.3898T>G (p.Ser1300Ala) c.4663T>G (p.Ser1555Ala) c.4852T>G (p.Ser1618Ala) c.4645T>G (p.Ser1549Ala) c.1348T>G (p.Ser450Ala) c.1393T>G (p.Ser465Ala) c.4849T>G (p.Ser1617Ala) c.1173T>G c.1360T>G (p.Ser454Ala) c.*4569T>G (n.*4569T>G) c.1099T>G (p.Ser367Ala) c.5-7177T>G (n.5-7177T>G) c.259T>G (p.Ser87Ala) c.-98-20938T>G (n.-98-20938T>G) n.4922T>G n.4963T>G | ClinVar dbSNP |
17 | g.43071128A>G | CA10591944 | BRCA1 | c.4783T>C (p.Ser1595Pro) c.4786T>C (p.Ser1596Pro) c.4660T>C (p.Ser1554Pro) c.4780T>C (p.Ser1594Pro) c.4708T>C (p.Ser1570Pro) c.1474T>C (p.Ser492Pro) c.1336T>C (p.Ser446Pro) c.3898T>C (p.Ser1300Pro) c.4663T>C (p.Ser1555Pro) c.4852T>C (p.Ser1618Pro) c.4645T>C (p.Ser1549Pro) c.1348T>C (p.Ser450Pro) c.1393T>C (p.Ser465Pro) c.4849T>C (p.Ser1617Pro) c.1173T>C c.1360T>C (p.Ser454Pro) c.*4569T>C (n.*4569T>C) c.1099T>C (p.Ser367Pro) c.5-7177T>C (n.5-7177T>C) c.259T>C (p.Ser87Pro) c.-98-20938T>C (n.-98-20938T>C) n.4922T>C n.4963T>C | dbSNP |
17 | g.43071128A>T | CA10591945 | BRCA1 | c.4783T>A (p.Ser1595Thr) c.4786T>A (p.Ser1596Thr) c.4660T>A (p.Ser1554Thr) c.4780T>A (p.Ser1594Thr) c.4708T>A (p.Ser1570Thr) c.1474T>A (p.Ser492Thr) c.1336T>A (p.Ser446Thr) c.3898T>A (p.Ser1300Thr) c.4663T>A (p.Ser1555Thr) c.4852T>A (p.Ser1618Thr) c.4645T>A (p.Ser1549Thr) c.1348T>A (p.Ser450Thr) c.1393T>A (p.Ser465Thr) c.4849T>A (p.Ser1617Thr) c.1173T>A c.1360T>A (p.Ser454Thr) c.*4569T>A (n.*4569T>A) c.1099T>A (p.Ser367Thr) c.5-7177T>A (n.5-7177T>A) c.259T>A (p.Ser87Thr) c.-98-20938T>A (n.-98-20938T>A) n.4922T>A n.4963T>A | dbSNP |
17 | g.43071129A>C | CA500231840 | BRCA1 | c.4782T>G (p.Ser1594=) c.4785T>G (p.Ser1595=) c.4659T>G (p.Ser1553=) c.4779T>G (p.Ser1593=) c.4707T>G (p.Ser1569=) c.1473T>G (p.Ser491=) c.1335T>G (p.Ser445=) c.3897T>G (p.Ser1299=) c.4662T>G (p.Ser1554=) c.4851T>G (p.Ser1617=) c.4644T>G (p.Ser1548=) c.1347T>G (p.Ser449=) c.1392T>G (p.Ser464=) c.4848T>G (p.Ser1616=) c.1172T>G c.1359T>G (p.Ser453=) c.*4568T>G (n.*4568T>G) c.1098T>G (p.Ser366=) c.5-7178T>G (n.5-7178T>G) c.258T>G (p.Ser86=) c.-98-20939T>G (n.-98-20939T>G) n.4921T>G n.4962T>G | |
17 | g.43071129A>G | CA500231841 | BRCA1 | c.4782T>C (p.Ser1594=) c.4785T>C (p.Ser1595=) c.4659T>C (p.Ser1553=) c.4779T>C (p.Ser1593=) c.4707T>C (p.Ser1569=) c.1473T>C (p.Ser491=) c.1335T>C (p.Ser445=) c.3897T>C (p.Ser1299=) c.4662T>C (p.Ser1554=) c.4851T>C (p.Ser1617=) c.4644T>C (p.Ser1548=) c.1347T>C (p.Ser449=) c.1392T>C (p.Ser464=) c.4848T>C (p.Ser1616=) c.1172T>C c.1359T>C (p.Ser453=) c.*4568T>C (n.*4568T>C) c.1098T>C (p.Ser366=) c.5-7178T>C (n.5-7178T>C) c.258T>C (p.Ser86=) c.-98-20939T>C (n.-98-20939T>C) n.4921T>C n.4962T>C | |
17 | g.43071129A>T | CA500231842 | BRCA1 | c.4782T>A (p.Ser1594=) c.4785T>A (p.Ser1595=) c.4659T>A (p.Ser1553=) c.4779T>A (p.Ser1593=) c.4707T>A (p.Ser1569=) c.1473T>A (p.Ser491=) c.1335T>A (p.Ser445=) c.3897T>A (p.Ser1299=) c.4662T>A (p.Ser1554=) c.4851T>A (p.Ser1617=) c.4644T>A (p.Ser1548=) c.1347T>A (p.Ser449=) c.1392T>A (p.Ser464=) c.4848T>A (p.Ser1616=) c.1172T>A c.1359T>A (p.Ser453=) c.*4568T>A (n.*4568T>A) c.1098T>A (p.Ser366=) c.5-7178T>A (n.5-7178T>A) c.258T>A (p.Ser86=) c.-98-20939T>A (n.-98-20939T>A) n.4921T>A n.4962T>A | dbSNP |
17 | g.43071129_43071130delinsAG | CA2260772940 | BRCA1 | c.4781_4782delinsCT (p.Ser1594=) c.4784_4785delinsCT (p.Ser1595=) c.4658_4659delinsCT (p.Ser1553=) c.4778_4779delinsCT (p.Ser1593=) c.4706_4707delinsCT (p.Ser1569=) c.1472_1473delinsCT (p.Ser491=) c.1334_1335delinsCT (p.Ser445=) c.3896_3897delinsCT (p.Ser1299=) c.4661_4662delinsCT (p.Ser1554=) c.4850_4851delinsCT (p.Ser1617=) c.4643_4644delinsCT (p.Ser1548=) c.1346_1347delinsCT (p.Ser449=) c.1391_1392delinsCT (p.Ser464=) c.4847_4848delinsCT (p.Ser1616=) c.1171_1172delinsCT c.1358_1359delinsCT (p.Ser453=) c.*4567_*4568delinsCT (n.*4567_*4568delinsCT) c.1097_1098delinsCT (p.Ser366=) c.5-7179_5-7178delinsCT (n.5-7179_5-7178delinsCT) c.257_258delinsCT (p.Ser86=) c.-98-20940_-98-20939delinsCT (n.-98-20940_-98-20939delinsCT) n.4920_4921delinsCT n.4961_4962delinsCT | |
17 | g.43071130del | CA10589644 | BRCA1 | c.4781del (p.Ser1594PhefsTer6) c.4784del (p.Ser1595PhefsTer6) c.4658del (p.Ser1553PhefsTer6) c.4778del (p.Ser1593PhefsTer6) c.4706del (p.Ser1569PhefsTer6) c.1472del (p.Ser491PhefsTer6) c.1334del (p.Ser445PhefsTer6) c.3896del (p.Ser1299PhefsTer6) c.4661del (p.Ser1554PhefsTer6) c.4850del (p.Ser1617PhefsTer6) c.4643del (p.Ser1548PhefsTer6) c.1346del (p.Ser449PhefsTer6) c.1391del (p.Ser464PhefsTer6) c.4847del (p.Ser1616PhefsTer6) c.1171del c.1358del (p.Ser453PhefsTer6) c.*4567del (n.*4567del) c.1097del (p.Ser366PhefsTer6) c.5-7179del (n.5-7179del) c.257del (p.Ser86PhefsTer6) c.-98-20940del (n.-98-20940del) n.4920del n.4961del | ClinVar dbSNP |
17 | g.43071130G>A | CA10591946 | BRCA1 | c.4781C>T (p.Ser1594Phe) c.4784C>T (p.Ser1595Phe) c.4658C>T (p.Ser1553Phe) c.4778C>T (p.Ser1593Phe) c.4706C>T (p.Ser1569Phe) c.1472C>T (p.Ser491Phe) c.1334C>T (p.Ser445Phe) c.3896C>T (p.Ser1299Phe) c.4661C>T (p.Ser1554Phe) c.4850C>T (p.Ser1617Phe) c.4643C>T (p.Ser1548Phe) c.1346C>T (p.Ser449Phe) c.1391C>T (p.Ser464Phe) c.4847C>T (p.Ser1616Phe) c.1171C>T c.1358C>T (p.Ser453Phe) c.*4567C>T (n.*4567C>T) c.1097C>T (p.Ser366Phe) c.5-7179C>T (n.5-7179C>T) c.257C>T (p.Ser86Phe) c.-98-20940C>T (n.-98-20940C>T) n.4920C>T n.4961C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
17 | g.43071130G>C | CA10591947 | BRCA1 | c.4781C>G (p.Ser1594Cys) c.4784C>G (p.Ser1595Cys) c.4658C>G (p.Ser1553Cys) c.4778C>G (p.Ser1593Cys) c.4706C>G (p.Ser1569Cys) c.1472C>G (p.Ser491Cys) c.1334C>G (p.Ser445Cys) c.3896C>G (p.Ser1299Cys) c.4661C>G (p.Ser1554Cys) c.4850C>G (p.Ser1617Cys) c.4643C>G (p.Ser1548Cys) c.1346C>G (p.Ser449Cys) c.1391C>G (p.Ser464Cys) c.4847C>G (p.Ser1616Cys) c.1171C>G c.1358C>G (p.Ser453Cys) c.*4567C>G (n.*4567C>G) c.1097C>G (p.Ser366Cys) c.5-7179C>G (n.5-7179C>G) c.257C>G (p.Ser86Cys) c.-98-20940C>G (n.-98-20940C>G) n.4920C>G n.4961C>G | dbSNP |
17 | g.43071130G= | CA2260772941 | BRCA1 | c.4781C= (p.Ser1594=) c.4784C= (p.Ser1595=) c.4658C= (p.Ser1553=) c.4778C= (p.Ser1593=) c.4706C= (p.Ser1569=) c.1472C= (p.Ser491=) c.1334C= (p.Ser445=) c.3896C= (p.Ser1299=) c.4661C= (p.Ser1554=) c.4850C= (p.Ser1617=) c.4643C= (p.Ser1548=) c.1346C= (p.Ser449=) c.1391C= (p.Ser464=) c.4847C= (p.Ser1616=) c.1171C= c.1358C= (p.Ser453=) c.*4567C= (n.*4567C=) c.1097C= (p.Ser366=) c.5-7179C= (n.5-7179C=) c.257C= (p.Ser86=) c.-98-20940C= (n.-98-20940C=) n.4920C= n.4961C= | |
17 | g.43071130G>T | CA10591948 | BRCA1 | c.4781C>A (p.Ser1594Tyr) c.4784C>A (p.Ser1595Tyr) c.4658C>A (p.Ser1553Tyr) c.4778C>A (p.Ser1593Tyr) c.4706C>A (p.Ser1569Tyr) c.1472C>A (p.Ser491Tyr) c.1334C>A (p.Ser445Tyr) c.3896C>A (p.Ser1299Tyr) c.4661C>A (p.Ser1554Tyr) c.4850C>A (p.Ser1617Tyr) c.4643C>A (p.Ser1548Tyr) c.1346C>A (p.Ser449Tyr) c.1391C>A (p.Ser464Tyr) c.4847C>A (p.Ser1616Tyr) c.1171C>A c.1358C>A (p.Ser453Tyr) c.*4567C>A (n.*4567C>A) c.1097C>A (p.Ser366Tyr) c.5-7179C>A (n.5-7179C>A) c.257C>A (p.Ser86Tyr) c.-98-20940C>A (n.-98-20940C>A) n.4920C>A n.4961C>A | |
17 | g.43071131A= | CA2260772943 | BRCA1 | c.4780T= (p.Ser1594=) c.4783T= (p.Ser1595=) c.4657T= (p.Ser1553=) c.4777T= (p.Ser1593=) c.4705T= (p.Ser1569=) c.1471T= (p.Ser491=) c.1333T= (p.Ser445=) c.3895T= (p.Ser1299=) c.4660T= (p.Ser1554=) c.4849T= (p.Ser1617=) c.4642T= (p.Ser1548=) c.1345T= (p.Ser449=) c.1390T= (p.Ser464=) c.4846T= (p.Ser1616=) c.1170T= c.1357T= (p.Ser453=) c.*4566T= (n.*4566T=) c.1096T= (p.Ser366=) c.5-7180T= (n.5-7180T=) c.256T= (p.Ser86=) c.-98-20941T= (n.-98-20941T=) n.4919T= n.4960T= | |
17 | g.43071131A>C | CA10591949 | BRCA1 | c.4780T>G (p.Ser1594Ala) c.4783T>G (p.Ser1595Ala) c.4657T>G (p.Ser1553Ala) c.4777T>G (p.Ser1593Ala) c.4705T>G (p.Ser1569Ala) c.1471T>G (p.Ser491Ala) c.1333T>G (p.Ser445Ala) c.3895T>G (p.Ser1299Ala) c.4660T>G (p.Ser1554Ala) c.4849T>G (p.Ser1617Ala) c.4642T>G (p.Ser1548Ala) c.1345T>G (p.Ser449Ala) c.1390T>G (p.Ser464Ala) c.4846T>G (p.Ser1616Ala) c.1170T>G c.1357T>G (p.Ser453Ala) c.*4566T>G (n.*4566T>G) c.1096T>G (p.Ser366Ala) c.5-7180T>G (n.5-7180T>G) c.256T>G (p.Ser86Ala) c.-98-20941T>G (n.-98-20941T>G) n.4919T>G n.4960T>G | ClinVar |
17 | g.43071131A>G | CA10591950 | BRCA1 | c.4780T>C (p.Ser1594Pro) c.4783T>C (p.Ser1595Pro) c.4657T>C (p.Ser1553Pro) c.4777T>C (p.Ser1593Pro) c.4705T>C (p.Ser1569Pro) c.1471T>C (p.Ser491Pro) c.1333T>C (p.Ser445Pro) c.3895T>C (p.Ser1299Pro) c.4660T>C (p.Ser1554Pro) c.4849T>C (p.Ser1617Pro) c.4642T>C (p.Ser1548Pro) c.1345T>C (p.Ser449Pro) c.1390T>C (p.Ser464Pro) c.4846T>C (p.Ser1616Pro) c.1170T>C c.1357T>C (p.Ser453Pro) c.*4566T>C (n.*4566T>C) c.1096T>C (p.Ser366Pro) c.5-7180T>C (n.5-7180T>C) c.256T>C (p.Ser86Pro) c.-98-20941T>C (n.-98-20941T>C) n.4919T>C n.4960T>C | ClinVar dbSNP |
17 | g.43071131A>T | CA10591951 | BRCA1 | c.4780T>A (p.Ser1594Thr) c.4783T>A (p.Ser1595Thr) c.4657T>A (p.Ser1553Thr) c.4777T>A (p.Ser1593Thr) c.4705T>A (p.Ser1569Thr) c.1471T>A (p.Ser491Thr) c.1333T>A (p.Ser445Thr) c.3895T>A (p.Ser1299Thr) c.4660T>A (p.Ser1554Thr) c.4849T>A (p.Ser1617Thr) c.4642T>A (p.Ser1548Thr) c.1345T>A (p.Ser449Thr) c.1390T>A (p.Ser464Thr) c.4846T>A (p.Ser1616Thr) c.1170T>A c.1357T>A (p.Ser453Thr) c.*4566T>A (n.*4566T>A) c.1096T>A (p.Ser366Thr) c.5-7180T>A (n.5-7180T>A) c.256T>A (p.Ser86Thr) c.-98-20941T>A (n.-98-20941T>A) n.4919T>A n.4960T>A | ClinVar dbSNP |
17 | g.43071131_43071132delinsAT | CA2260772942 | BRCA1 | c.4779_4780delinsAT (p.Pro1593=) c.4782_4783delinsAT (p.Pro1594=) c.4656_4657delinsAT (p.Pro1552=) c.4776_4777delinsAT (p.Pro1592=) c.4704_4705delinsAT (p.Pro1568=) c.1470_1471delinsAT (p.Pro490=) c.1332_1333delinsAT (p.Pro444=) c.3894_3895delinsAT (p.Pro1298=) c.4659_4660delinsAT (p.Pro1553=) c.4848_4849delinsAT (p.Pro1616=) c.4641_4642delinsAT (p.Pro1547=) c.1344_1345delinsAT (p.Pro448=) c.1389_1390delinsAT (p.Pro463=) c.4845_4846delinsAT (p.Pro1615=) c.1169_1170delinsAT c.1356_1357delinsAT (p.Pro452=) c.*4565_*4566delinsAT (n.*4565_*4566delinsAT) c.1095_1096delinsAT (p.Pro365=) c.5-7181_5-7180delinsAT (n.5-7181_5-7180delinsAT) c.255_256delinsAT (p.Pro85=) c.-98-20942_-98-20941delinsAT (n.-98-20942_-98-20941delinsAT) n.4918_4919delinsAT n.4959_4960delinsAT | |
17 | g.43071132del | CA915950108 | BRCA1 | c.4779del (p.Ser1594LeufsTer6) c.4782del (p.Ser1595LeufsTer6) c.4656del (p.Ser1553LeufsTer6) c.4776del (p.Ser1593LeufsTer6) c.4704del (p.Ser1569LeufsTer6) c.1470del (p.Ser491LeufsTer6) c.1332del (p.Ser445LeufsTer6) c.3894del (p.Ser1299LeufsTer6) c.4659del (p.Ser1554LeufsTer6) c.4848del (p.Ser1617LeufsTer6) c.4641del (p.Ser1548LeufsTer6) c.1344del (p.Ser449LeufsTer6) c.1389del (p.Ser464LeufsTer6) c.4845del (p.Ser1616LeufsTer6) c.1169del c.1356del (p.Ser453LeufsTer6) c.*4565del (n.*4565del) c.1095del (p.Ser366LeufsTer6) c.5-7181del (n.5-7181del) c.255del (p.Ser86LeufsTer6) c.-98-20942del (n.-98-20942del) n.4918del n.4959del | ClinVar dbSNP |
17 | g.43071132T>A | CA500231844 | BRCA1 | c.4779A>T (p.Pro1593=) c.4782A>T (p.Pro1594=) c.4656A>T (p.Pro1552=) c.4776A>T (p.Pro1592=) c.4704A>T (p.Pro1568=) c.1470A>T (p.Pro490=) c.1332A>T (p.Pro444=) c.3894A>T (p.Pro1298=) c.4659A>T (p.Pro1553=) c.4848A>T (p.Pro1616=) c.4641A>T (p.Pro1547=) c.1344A>T (p.Pro448=) c.1389A>T (p.Pro463=) c.4845A>T (p.Pro1615=) c.1169A>T c.1356A>T (p.Pro452=) c.*4565A>T (n.*4565A>T) c.1095A>T (p.Pro365=) c.5-7181A>T (n.5-7181A>T) c.255A>T (p.Pro85=) c.-98-20942A>T (n.-98-20942A>T) n.4918A>T n.4959A>T | |
17 | g.43071132T>C | CA10580508 | BRCA1 | c.4779A>G (p.Pro1593=) c.4782A>G (p.Pro1594=) c.4656A>G (p.Pro1552=) c.4776A>G (p.Pro1592=) c.4704A>G (p.Pro1568=) c.1470A>G (p.Pro490=) c.1332A>G (p.Pro444=) c.3894A>G (p.Pro1298=) c.4659A>G (p.Pro1553=) c.4848A>G (p.Pro1616=) c.4641A>G (p.Pro1547=) c.1344A>G (p.Pro448=) c.1389A>G (p.Pro463=) c.4845A>G (p.Pro1615=) c.1169A>G c.1356A>G (p.Pro452=) c.*4565A>G (n.*4565A>G) c.1095A>G (p.Pro365=) c.5-7181A>G (n.5-7181A>G) c.255A>G (p.Pro85=) c.-98-20942A>G (n.-98-20942A>G) n.4918A>G n.4959A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.43071132T>G | CA500231843 | BRCA1 | c.4779A>C (p.Pro1593=) c.4782A>C (p.Pro1594=) c.4656A>C (p.Pro1552=) c.4776A>C (p.Pro1592=) c.4704A>C (p.Pro1568=) c.1470A>C (p.Pro490=) c.1332A>C (p.Pro444=) c.3894A>C (p.Pro1298=) c.4659A>C (p.Pro1553=) c.4848A>C (p.Pro1616=) c.4641A>C (p.Pro1547=) c.1344A>C (p.Pro448=) c.1389A>C (p.Pro463=) c.4845A>C (p.Pro1615=) c.1169A>C c.1356A>C (p.Pro452=) c.*4565A>C (n.*4565A>C) c.1095A>C (p.Pro365=) c.5-7181A>C (n.5-7181A>C) c.255A>C (p.Pro85=) c.-98-20942A>C (n.-98-20942A>C) n.4918A>C n.4959A>C | |
17 | g.43071132T= | CA2260772944 | BRCA1 | c.4779A= (p.Pro1593=) c.4782A= (p.Pro1594=) c.4656A= (p.Pro1552=) c.4776A= (p.Pro1592=) c.4704A= (p.Pro1568=) c.1470A= (p.Pro490=) c.1332A= (p.Pro444=) c.3894A= (p.Pro1298=) c.4659A= (p.Pro1553=) c.4848A= (p.Pro1616=) c.4641A= (p.Pro1547=) c.1344A= (p.Pro448=) c.1389A= (p.Pro463=) c.4845A= (p.Pro1615=) c.1169A= c.1356A= (p.Pro452=) c.*4565A= (n.*4565A=) c.1095A= (p.Pro365=) c.5-7181A= (n.5-7181A=) c.255A= (p.Pro85=) c.-98-20942A= (n.-98-20942A=) n.4918A= n.4959A= | |
17 | g.43071132_43071133delinsTG | CA2260772945 | BRCA1 | c.4778_4779delinsCA (p.Pro1593=) c.4781_4782delinsCA (p.Pro1594=) c.4655_4656delinsCA (p.Pro1552=) c.4775_4776delinsCA (p.Pro1592=) c.4703_4704delinsCA (p.Pro1568=) c.1469_1470delinsCA (p.Pro490=) c.1331_1332delinsCA (p.Pro444=) c.3893_3894delinsCA (p.Pro1298=) c.4658_4659delinsCA (p.Pro1553=) c.4847_4848delinsCA (p.Pro1616=) c.4640_4641delinsCA (p.Pro1547=) c.1343_1344delinsCA (p.Pro448=) c.1388_1389delinsCA (p.Pro463=) c.4844_4845delinsCA (p.Pro1615=) c.1168_1169delinsCA c.1355_1356delinsCA (p.Pro452=) c.*4564_*4565delinsCA (n.*4564_*4565delinsCA) c.1094_1095delinsCA (p.Pro365=) c.5-7182_5-7181delinsCA (n.5-7182_5-7181delinsCA) c.254_255delinsCA (p.Pro85=) c.-98-20943_-98-20942delinsCA (n.-98-20943_-98-20942delinsCA) n.4917_4918delinsCA n.4958_4959delinsCA | |
17 | g.43071133G>A | CA10591952 | BRCA1 | c.4778C>T (p.Pro1593Leu) c.4781C>T (p.Pro1594Leu) c.4655C>T (p.Pro1552Leu) c.4775C>T (p.Pro1592Leu) c.4703C>T (p.Pro1568Leu) c.1469C>T (p.Pro490Leu) c.1331C>T (p.Pro444Leu) c.3893C>T (p.Pro1298Leu) c.4658C>T (p.Pro1553Leu) c.4847C>T (p.Pro1616Leu) c.4640C>T (p.Pro1547Leu) c.1343C>T (p.Pro448Leu) c.1388C>T (p.Pro463Leu) c.4844C>T (p.Pro1615Leu) c.1168C>T c.1355C>T (p.Pro452Leu) c.*4564C>T (n.*4564C>T) c.1094C>T (p.Pro365Leu) c.5-7182C>T (n.5-7182C>T) c.254C>T (p.Pro85Leu) c.-98-20943C>T (n.-98-20943C>T) n.4917C>T n.4958C>T | ClinVar dbSNP |
17 | g.43071133G>C | CA10591953 | BRCA1 | c.4778C>G (p.Pro1593Arg) c.4781C>G (p.Pro1594Arg) c.4655C>G (p.Pro1552Arg) c.4775C>G (p.Pro1592Arg) c.4703C>G (p.Pro1568Arg) c.1469C>G (p.Pro490Arg) c.1331C>G (p.Pro444Arg) c.3893C>G (p.Pro1298Arg) c.4658C>G (p.Pro1553Arg) c.4847C>G (p.Pro1616Arg) c.4640C>G (p.Pro1547Arg) c.1343C>G (p.Pro448Arg) c.1388C>G (p.Pro463Arg) c.4844C>G (p.Pro1615Arg) c.1168C>G c.1355C>G (p.Pro452Arg) c.*4564C>G (n.*4564C>G) c.1094C>G (p.Pro365Arg) c.5-7182C>G (n.5-7182C>G) c.254C>G (p.Pro85Arg) c.-98-20943C>G (n.-98-20943C>G) n.4917C>G n.4958C>G | dbSNP gnomAD v2 gnomAD v4 |
17 | g.43071133G= | CA2260772946 | BRCA1 | c.4778C= (p.Pro1593=) c.4781C= (p.Pro1594=) c.4655C= (p.Pro1552=) c.4775C= (p.Pro1592=) c.4703C= (p.Pro1568=) c.1469C= (p.Pro490=) c.1331C= (p.Pro444=) c.3893C= (p.Pro1298=) c.4658C= (p.Pro1553=) c.4847C= (p.Pro1616=) c.4640C= (p.Pro1547=) c.1343C= (p.Pro448=) c.1388C= (p.Pro463=) c.4844C= (p.Pro1615=) c.1168C= c.1355C= (p.Pro452=) c.*4564C= (n.*4564C=) c.1094C= (p.Pro365=) c.5-7182C= (n.5-7182C=) c.254C= (p.Pro85=) c.-98-20943C= (n.-98-20943C=) n.4917C= n.4958C= | |
17 | g.43071133G>T | CA10591954 | BRCA1 | c.4778C>A (p.Pro1593Gln) c.4781C>A (p.Pro1594Gln) c.4655C>A (p.Pro1552Gln) c.4775C>A (p.Pro1592Gln) c.4703C>A (p.Pro1568Gln) c.1469C>A (p.Pro490Gln) c.1331C>A (p.Pro444Gln) c.3893C>A (p.Pro1298Gln) c.4658C>A (p.Pro1553Gln) c.4847C>A (p.Pro1616Gln) c.4640C>A (p.Pro1547Gln) c.1343C>A (p.Pro448Gln) c.1388C>A (p.Pro463Gln) c.4844C>A (p.Pro1615Gln) c.1168C>A c.1355C>A (p.Pro452Gln) c.*4564C>A (n.*4564C>A) c.1094C>A (p.Pro365Gln) c.5-7182C>A (n.5-7182C>A) c.254C>A (p.Pro85Gln) c.-98-20943C>A (n.-98-20943C>A) n.4917C>A n.4958C>A | ClinVar dbSNP |
17 | g.43071134del | CA1139665581 | BRCA1 | c.4778del (p.Pro1593HisfsTer7) c.4781del (p.Pro1594HisfsTer7) c.4655del (p.Pro1552HisfsTer7) c.4775del (p.Pro1592HisfsTer7) c.4703del (p.Pro1568HisfsTer7) c.1469del (p.Pro490HisfsTer7) c.1331del (p.Pro444HisfsTer7) c.3893del (p.Pro1298HisfsTer7) c.4658del (p.Pro1553HisfsTer7) c.4847del (p.Pro1616HisfsTer7) c.4640del (p.Pro1547HisfsTer7) c.1343del (p.Pro448HisfsTer7) c.1388del (p.Pro463HisfsTer7) c.4844del (p.Pro1615HisfsTer7) c.1168del c.1355del (p.Pro452HisfsTer7) c.*4564del (n.*4564del) c.1094del (p.Pro365HisfsTer7) c.5-7182del (n.5-7182del) c.254del (p.Pro85HisfsTer7) c.-98-20943del (n.-98-20943del) n.4917del n.4958del | ClinVar dbSNP |
17 | g.43071134G>A | CA10591955 | BRCA1 | c.4777C>T (p.Pro1593Ser) c.4780C>T (p.Pro1594Ser) c.4654C>T (p.Pro1552Ser) c.4774C>T (p.Pro1592Ser) c.4702C>T (p.Pro1568Ser) c.1468C>T (p.Pro490Ser) c.1330C>T (p.Pro444Ser) c.3892C>T (p.Pro1298Ser) c.4657C>T (p.Pro1553Ser) c.4846C>T (p.Pro1616Ser) c.4639C>T (p.Pro1547Ser) c.1342C>T (p.Pro448Ser) c.1387C>T (p.Pro463Ser) c.4843C>T (p.Pro1615Ser) c.1167C>T c.1354C>T (p.Pro452Ser) c.*4563C>T (n.*4563C>T) c.1093C>T (p.Pro365Ser) c.5-7183C>T (n.5-7183C>T) c.253C>T (p.Pro85Ser) c.-98-20944C>T (n.-98-20944C>T) n.4916C>T n.4957C>T | ClinVar dbSNP |
17 | g.43071134G>C | CA003021 | BRCA1 | c.4777C>G (p.Pro1593Ala) c.4780C>G (p.Pro1594Ala) c.4654C>G (p.Pro1552Ala) c.4774C>G (p.Pro1592Ala) c.4702C>G (p.Pro1568Ala) c.1468C>G (p.Pro490Ala) c.1330C>G (p.Pro444Ala) c.3892C>G (p.Pro1298Ala) c.4657C>G (p.Pro1553Ala) c.4846C>G (p.Pro1616Ala) c.4639C>G (p.Pro1547Ala) c.1342C>G (p.Pro448Ala) c.1387C>G (p.Pro463Ala) c.4843C>G (p.Pro1615Ala) c.1167C>G c.1354C>G (p.Pro452Ala) c.*4563C>G (n.*4563C>G) c.1093C>G (p.Pro365Ala) c.5-7183C>G (n.5-7183C>G) c.253C>G (p.Pro85Ala) c.-98-20944C>G (n.-98-20944C>G) n.4916C>G n.4957C>G | ClinVar dbSNP |
17 | g.43071134G= | CA2260772948 | BRCA1 | c.4777C= (p.Pro1593=) c.4780C= (p.Pro1594=) c.4654C= (p.Pro1552=) c.4774C= (p.Pro1592=) c.4702C= (p.Pro1568=) c.1468C= (p.Pro490=) c.1330C= (p.Pro444=) c.3892C= (p.Pro1298=) c.4657C= (p.Pro1553=) c.4846C= (p.Pro1616=) c.4639C= (p.Pro1547=) c.1342C= (p.Pro448=) c.1387C= (p.Pro463=) c.4843C= (p.Pro1615=) c.1167C= c.1354C= (p.Pro452=) c.*4563C= (n.*4563C=) c.1093C= (p.Pro365=) c.5-7183C= (n.5-7183C=) c.253C= (p.Pro85=) c.-98-20944C= (n.-98-20944C=) n.4916C= n.4957C= | |
17 | g.43071134G>T | CA10591956 | BRCA1 | c.4777C>A (p.Pro1593Thr) c.4780C>A (p.Pro1594Thr) c.4654C>A (p.Pro1552Thr) c.4774C>A (p.Pro1592Thr) c.4702C>A (p.Pro1568Thr) c.1468C>A (p.Pro490Thr) c.1330C>A (p.Pro444Thr) c.3892C>A (p.Pro1298Thr) c.4657C>A (p.Pro1553Thr) c.4846C>A (p.Pro1616Thr) c.4639C>A (p.Pro1547Thr) c.1342C>A (p.Pro448Thr) c.1387C>A (p.Pro463Thr) c.4843C>A (p.Pro1615Thr) c.1167C>A c.1354C>A (p.Pro452Thr) c.*4563C>A (n.*4563C>A) c.1093C>A (p.Pro365Thr) c.5-7183C>A (n.5-7183C>A) c.253C>A (p.Pro85Thr) c.-98-20944C>A (n.-98-20944C>A) n.4916C>A n.4957C>A | ClinVar |
17 | g.43071134_43071139delinsGTATGT | CA2260772947 | BRCA1 | c.4772_4777delinsACATAC (p.Asn1591=) c.4775_4780delinsACATAC (p.Asn1592=) c.4649_4654delinsACATAC (p.Asn1550=) c.4769_4774delinsACATAC (p.Asn1590=) c.4697_4702delinsACATAC (p.Asn1566=) c.1463_1468delinsACATAC (p.Asn488=) c.1325_1330delinsACATAC (p.Asn442=) c.3887_3892delinsACATAC (p.Asn1296=) c.4652_4657delinsACATAC (p.Asn1551=) c.4841_4846delinsACATAC (p.Asn1614=) c.4634_4639delinsACATAC (p.Asn1545=) c.1337_1342delinsACATAC (p.Asn446=) c.1382_1387delinsACATAC (p.Asn461=) c.4838_4843delinsACATAC (p.Asn1613=) c.1162_1167delinsACATAC c.1349_1354delinsACATAC (p.Asn450=) c.*4558_*4563delinsACATAC (n.*4558_*4563delinsACATAC) c.1088_1093delinsACATAC (p.Asn363=) c.5-7188_5-7183delinsACATAC (n.5-7188_5-7183delinsACATAC) c.248_253delinsACATAC (p.Asn83=) c.-98-20949_-98-20944delinsACATAC (n.-98-20949_-98-20944delinsACATAC) n.4911_4916delinsACATAC n.4952_4957delinsACATAC | |
17 | g.43071135T>A | CA500231845 | BRCA1 | c.4776A>T (p.Ile1592=) c.4779A>T (p.Ile1593=) c.4653A>T (p.Ile1551=) c.4773A>T (p.Ile1591=) c.4701A>T (p.Ile1567=) c.1467A>T (p.Ile489=) c.1329A>T (p.Ile443=) c.3891A>T (p.Ile1297=) c.4656A>T (p.Ile1552=) c.4845A>T (p.Ile1615=) c.4638A>T (p.Ile1546=) c.1341A>T (p.Ile447=) c.1386A>T (p.Ile462=) c.4842A>T (p.Ile1614=) c.1166A>T c.1353A>T (p.Ile451=) c.*4562A>T (n.*4562A>T) c.1092A>T (p.Ile364=) c.5-7184A>T (n.5-7184A>T) c.252A>T (p.Ile84=) c.-98-20945A>T (n.-98-20945A>T) n.4915A>T n.4956A>T | dbSNP |
17 | g.43071135T>C | CA10591957 | BRCA1 | c.4776A>G (p.Ile1592Met) c.4779A>G (p.Ile1593Met) c.4653A>G (p.Ile1551Met) c.4773A>G (p.Ile1591Met) c.4701A>G (p.Ile1567Met) c.1467A>G (p.Ile489Met) c.1329A>G (p.Ile443Met) c.3891A>G (p.Ile1297Met) c.4656A>G (p.Ile1552Met) c.4845A>G (p.Ile1615Met) c.4638A>G (p.Ile1546Met) c.1341A>G (p.Ile447Met) c.1386A>G (p.Ile462Met) c.4842A>G (p.Ile1614Met) c.1166A>G c.1353A>G (p.Ile451Met) c.*4562A>G (n.*4562A>G) c.1092A>G (p.Ile364Met) c.5-7184A>G (n.5-7184A>G) c.252A>G (p.Ile84Met) c.-98-20945A>G (n.-98-20945A>G) n.4915A>G n.4956A>G | |
17 | g.43071135T>G | CA500231846 | BRCA1 | c.4776A>C (p.Ile1592=) c.4779A>C (p.Ile1593=) c.4653A>C (p.Ile1551=) c.4773A>C (p.Ile1591=) c.4701A>C (p.Ile1567=) c.1467A>C (p.Ile489=) c.1329A>C (p.Ile443=) c.3891A>C (p.Ile1297=) c.4656A>C (p.Ile1552=) c.4845A>C (p.Ile1615=) c.4638A>C (p.Ile1546=) c.1341A>C (p.Ile447=) c.1386A>C (p.Ile462=) c.4842A>C (p.Ile1614=) c.1166A>C c.1353A>C (p.Ile451=) c.*4562A>C (n.*4562A>C) c.1092A>C (p.Ile364=) c.5-7184A>C (n.5-7184A>C) c.252A>C (p.Ile84=) c.-98-20945A>C (n.-98-20945A>C) n.4915A>C n.4956A>C | dbSNP |
17 | g.43071135_43071139delinsG | CA003016 | BRCA1 | c.4772_4776delinsC (p.Asn1591ThrfsTer8) c.4775_4779delinsC (p.Asn1592ThrfsTer8) c.4649_4653delinsC (p.Asn1550ThrfsTer8) c.4769_4773delinsC (p.Asn1590ThrfsTer8) c.4697_4701delinsC (p.Asn1566ThrfsTer8) c.1463_1467delinsC (p.Asn488ThrfsTer8) c.1325_1329delinsC (p.Asn442ThrfsTer8) c.3887_3891delinsC (p.Asn1296ThrfsTer8) c.4652_4656delinsC (p.Asn1551ThrfsTer8) c.4841_4845delinsC (p.Asn1614ThrfsTer8) c.4634_4638delinsC (p.Asn1545ThrfsTer8) c.1337_1341delinsC (p.Asn446ThrfsTer8) c.1382_1386delinsC (p.Asn461ThrfsTer8) c.4838_4842delinsC (p.Asn1613ThrfsTer8) c.1162_1166delinsC c.1349_1353delinsC (p.Asn450ThrfsTer8) c.*4558_*4562delinsC (n.*4558_*4562delinsC) c.1088_1092delinsC (p.Asn363ThrfsTer8) c.5-7188_5-7184delinsC (n.5-7188_5-7184delinsC) c.248_252delinsC (p.Asn83ThrfsTer8) c.-98-20949_-98-20945delinsC (n.-98-20949_-98-20945delinsC) n.4911_4915delinsC n.4952_4956delinsC | ClinVar dbSNP |
17 | g.43071136A>C | CA10591958 | BRCA1 | c.4775T>G (p.Ile1592Arg) c.4778T>G (p.Ile1593Arg) c.4652T>G (p.Ile1551Arg) c.4772T>G (p.Ile1591Arg) c.4700T>G (p.Ile1567Arg) c.1466T>G (p.Ile489Arg) c.1328T>G (p.Ile443Arg) c.3890T>G (p.Ile1297Arg) c.4655T>G (p.Ile1552Arg) c.4844T>G (p.Ile1615Arg) c.4637T>G (p.Ile1546Arg) c.1340T>G (p.Ile447Arg) c.1385T>G (p.Ile462Arg) c.4841T>G (p.Ile1614Arg) c.1165T>G c.1352T>G (p.Ile451Arg) c.*4561T>G (n.*4561T>G) c.1091T>G (p.Ile364Arg) c.5-7185T>G (n.5-7185T>G) c.251T>G (p.Ile84Arg) c.-98-20946T>G (n.-98-20946T>G) n.4914T>G n.4955T>G | dbSNP |
17 | g.43071136A>G | CA10591959 | BRCA1 | c.4775T>C (p.Ile1592Thr) c.4778T>C (p.Ile1593Thr) c.4652T>C (p.Ile1551Thr) c.4772T>C (p.Ile1591Thr) c.4700T>C (p.Ile1567Thr) c.1466T>C (p.Ile489Thr) c.1328T>C (p.Ile443Thr) c.3890T>C (p.Ile1297Thr) c.4655T>C (p.Ile1552Thr) c.4844T>C (p.Ile1615Thr) c.4637T>C (p.Ile1546Thr) c.1340T>C (p.Ile447Thr) c.1385T>C (p.Ile462Thr) c.4841T>C (p.Ile1614Thr) c.1165T>C c.1352T>C (p.Ile451Thr) c.*4561T>C (n.*4561T>C) c.1091T>C (p.Ile364Thr) c.5-7185T>C (n.5-7185T>C) c.251T>C (p.Ile84Thr) c.-98-20946T>C (n.-98-20946T>C) n.4914T>C n.4955T>C | ClinVar dbSNP |
17 | g.43071136A>T | CA10591960 | BRCA1 | c.4775T>A (p.Ile1592Lys) c.4778T>A (p.Ile1593Lys) c.4652T>A (p.Ile1551Lys) c.4772T>A (p.Ile1591Lys) c.4700T>A (p.Ile1567Lys) c.1466T>A (p.Ile489Lys) c.1328T>A (p.Ile443Lys) c.3890T>A (p.Ile1297Lys) c.4655T>A (p.Ile1552Lys) c.4844T>A (p.Ile1615Lys) c.4637T>A (p.Ile1546Lys) c.1340T>A (p.Ile447Lys) c.1385T>A (p.Ile462Lys) c.4841T>A (p.Ile1614Lys) c.1165T>A c.1352T>A (p.Ile451Lys) c.*4561T>A (n.*4561T>A) c.1091T>A (p.Ile364Lys) c.5-7185T>A (n.5-7185T>A) c.251T>A (p.Ile84Lys) c.-98-20946T>A (n.-98-20946T>A) n.4914T>A n.4955T>A | dbSNP |
17 | g.43071136dup | CA645578305 | BRCA1 | c.4775dup (p.Pro1593ThrfsTer28) c.4778dup (p.Pro1594ThrfsTer28) c.4652dup (p.Pro1552ThrfsTer28) c.4772dup (p.Pro1592ThrfsTer28) c.4700dup (p.Pro1568ThrfsTer28) c.1466dup (p.Pro490ThrfsTer28) c.1328dup (p.Pro444ThrfsTer28) c.3890dup (p.Pro1298ThrfsTer28) c.4655dup (p.Pro1553ThrfsTer28) c.4844dup (p.Pro1616ThrfsTer28) c.4637dup (p.Pro1547ThrfsTer28) c.1340dup (p.Pro448ThrfsTer28) c.1385dup (p.Pro463ThrfsTer28) c.4841dup (p.Pro1615ThrfsTer28) c.1165dup c.1352dup (p.Pro452ThrfsTer28) c.*4561dup (n.*4561dup) c.1091dup (p.Pro365ThrfsTer28) c.5-7185dup (n.5-7185dup) c.251dup (p.Pro85ThrfsTer28) c.-98-20946dup (n.-98-20946dup) n.4914dup n.4955dup | COSMIC COSMIC |
17 | g.43071137_43071147del | CA2695225908 | BRCA1 | c.4765_4775del (p.Val1589ThrfsTer28) c.4768_4778del (p.Val1590ThrfsTer28) c.4642_4652del (p.Val1548ThrfsTer28) c.4762_4772del (p.Val1588ThrfsTer28) c.4690_4700del (p.Val1564ThrfsTer28) c.1456_1466del (p.Val486ThrfsTer28) c.1318_1328del (p.Val440ThrfsTer28) c.3880_3890del (p.Val1294ThrfsTer28) c.4645_4655del (p.Val1549ThrfsTer28) c.4834_4844del (p.Val1612ThrfsTer28) c.4627_4637del (p.Val1543ThrfsTer28) c.1330_1340del (p.Val444ThrfsTer28) c.1375_1385del (p.Val459ThrfsTer28) c.4831_4841del (p.Val1611ThrfsTer28) c.1155_1165del c.1342_1352del (p.Val448ThrfsTer28) c.*4551_*4561del (n.*4551_*4561del) c.1081_1091del (p.Val361ThrfsTer28) c.5-7195_5-7185del (n.5-7195_5-7185del) c.241_251del (p.Val81ThrfsTer28) c.-98-20956_-98-20946del (n.-98-20956_-98-20946del) n.4904_4914del n.4945_4955del | |
17 | g.43071137T>A | CA003020 | BRCA1 | c.4774A>T (p.Ile1592Leu) c.4777A>T (p.Ile1593Leu) c.4651A>T (p.Ile1551Leu) c.4771A>T (p.Ile1591Leu) c.4699A>T (p.Ile1567Leu) c.1465A>T (p.Ile489Leu) c.1327A>T (p.Ile443Leu) c.3889A>T (p.Ile1297Leu) c.4654A>T (p.Ile1552Leu) c.4843A>T (p.Ile1615Leu) c.4636A>T (p.Ile1546Leu) c.1339A>T (p.Ile447Leu) c.1384A>T (p.Ile462Leu) c.4840A>T (p.Ile1614Leu) c.1164A>T c.1351A>T (p.Ile451Leu) c.*4560A>T (n.*4560A>T) c.1090A>T (p.Ile364Leu) c.5-7186A>T (n.5-7186A>T) c.250A>T (p.Ile84Leu) c.-98-20947A>T (n.-98-20947A>T) n.4913A>T n.4954A>T | ClinVar dbSNP |
17 | g.43071137T>C | CA003019 | BRCA1 | c.4774A>G (p.Ile1592Val) c.4777A>G (p.Ile1593Val) c.4651A>G (p.Ile1551Val) c.4771A>G (p.Ile1591Val) c.4699A>G (p.Ile1567Val) c.1465A>G (p.Ile489Val) c.1327A>G (p.Ile443Val) c.3889A>G (p.Ile1297Val) c.4654A>G (p.Ile1552Val) c.4843A>G (p.Ile1615Val) c.4636A>G (p.Ile1546Val) c.1339A>G (p.Ile447Val) c.1384A>G (p.Ile462Val) c.4840A>G (p.Ile1614Val) c.1164A>G c.1351A>G (p.Ile451Val) c.*4560A>G (n.*4560A>G) c.1090A>G (p.Ile364Val) c.5-7186A>G (n.5-7186A>G) c.250A>G (p.Ile84Val) c.-98-20947A>G (n.-98-20947A>G) n.4913A>G n.4954A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.43071137T>G | CA10591961 | BRCA1 | c.4774A>C (p.Ile1592Leu) c.4777A>C (p.Ile1593Leu) c.4651A>C (p.Ile1551Leu) c.4771A>C (p.Ile1591Leu) c.4699A>C (p.Ile1567Leu) c.1465A>C (p.Ile489Leu) c.1327A>C (p.Ile443Leu) c.3889A>C (p.Ile1297Leu) c.4654A>C (p.Ile1552Leu) c.4843A>C (p.Ile1615Leu) c.4636A>C (p.Ile1546Leu) c.1339A>C (p.Ile447Leu) c.1384A>C (p.Ile462Leu) c.4840A>C (p.Ile1614Leu) c.1164A>C c.1351A>C (p.Ile451Leu) c.*4560A>C (n.*4560A>C) c.1090A>C (p.Ile364Leu) c.5-7186A>C (n.5-7186A>C) c.250A>C (p.Ile84Leu) c.-98-20947A>C (n.-98-20947A>C) n.4913A>C n.4954A>C | dbSNP |
17 | g.43071137T= | CA2260772949 | BRCA1 | c.4774A= (p.Ile1592=) c.4777A= (p.Ile1593=) c.4651A= (p.Ile1551=) c.4771A= (p.Ile1591=) c.4699A= (p.Ile1567=) c.1465A= (p.Ile489=) c.1327A= (p.Ile443=) c.3889A= (p.Ile1297=) c.4654A= (p.Ile1552=) c.4843A= (p.Ile1615=) c.4636A= (p.Ile1546=) c.1339A= (p.Ile447=) c.1384A= (p.Ile462=) c.4840A= (p.Ile1614=) c.1164A= c.1351A= (p.Ile451=) c.*4560A= (n.*4560A=) c.1090A= (p.Ile364=) c.5-7186A= (n.5-7186A=) c.250A= (p.Ile84=) c.-98-20947A= (n.-98-20947A=) n.4913A= n.4954A= | |
17 | g.43071138G>A | CA500231847 | BRCA1 | c.4773C>T (p.Asn1591=) c.4776C>T (p.Asn1592=) c.4650C>T (p.Asn1550=) c.4770C>T (p.Asn1590=) c.4698C>T (p.Asn1566=) c.1464C>T (p.Asn488=) c.1326C>T (p.Asn442=) c.3888C>T (p.Asn1296=) c.4653C>T (p.Asn1551=) c.4842C>T (p.Asn1614=) c.4635C>T (p.Asn1545=) c.1338C>T (p.Asn446=) c.1383C>T (p.Asn461=) c.4839C>T (p.Asn1613=) c.1163C>T c.1350C>T (p.Asn450=) c.*4559C>T (n.*4559C>T) c.1089C>T (p.Asn363=) c.5-7187C>T (n.5-7187C>T) c.249C>T (p.Asn83=) c.-98-20948C>T (n.-98-20948C>T) n.4912C>T n.4953C>T | ClinVar dbSNP |
17 | g.43071138G>C | CA003018 | BRCA1 | c.4773C>G (p.Asn1591Lys) c.4776C>G (p.Asn1592Lys) c.4650C>G (p.Asn1550Lys) c.4770C>G (p.Asn1590Lys) c.4698C>G (p.Asn1566Lys) c.1464C>G (p.Asn488Lys) c.1326C>G (p.Asn442Lys) c.3888C>G (p.Asn1296Lys) c.4653C>G (p.Asn1551Lys) c.4842C>G (p.Asn1614Lys) c.4635C>G (p.Asn1545Lys) c.1338C>G (p.Asn446Lys) c.1383C>G (p.Asn461Lys) c.4839C>G (p.Asn1613Lys) c.1163C>G c.1350C>G (p.Asn450Lys) c.*4559C>G (n.*4559C>G) c.1089C>G (p.Asn363Lys) c.5-7187C>G (n.5-7187C>G) c.249C>G (p.Asn83Lys) c.-98-20948C>G (n.-98-20948C>G) n.4912C>G n.4953C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071138G= | CA2260772950 | BRCA1 | c.4773C= (p.Asn1591=) c.4776C= (p.Asn1592=) c.4650C= (p.Asn1550=) c.4770C= (p.Asn1590=) c.4698C= (p.Asn1566=) c.1464C= (p.Asn488=) c.1326C= (p.Asn442=) c.3888C= (p.Asn1296=) c.4653C= (p.Asn1551=) c.4842C= (p.Asn1614=) c.4635C= (p.Asn1545=) c.1338C= (p.Asn446=) c.1383C= (p.Asn461=) c.4839C= (p.Asn1613=) c.1163C= c.1350C= (p.Asn450=) c.*4559C= (n.*4559C=) c.1089C= (p.Asn363=) c.5-7187C= (n.5-7187C=) c.249C= (p.Asn83=) c.-98-20948C= (n.-98-20948C=) n.4912C= n.4953C= | |
17 | g.43071138G>T | CA10591962 | BRCA1 | c.4773C>A (p.Asn1591Lys) c.4776C>A (p.Asn1592Lys) c.4650C>A (p.Asn1550Lys) c.4770C>A (p.Asn1590Lys) c.4698C>A (p.Asn1566Lys) c.1464C>A (p.Asn488Lys) c.1326C>A (p.Asn442Lys) c.3888C>A (p.Asn1296Lys) c.4653C>A (p.Asn1551Lys) c.4842C>A (p.Asn1614Lys) c.4635C>A (p.Asn1545Lys) c.1338C>A (p.Asn446Lys) c.1383C>A (p.Asn461Lys) c.4839C>A (p.Asn1613Lys) c.1163C>A c.1350C>A (p.Asn450Lys) c.*4559C>A (n.*4559C>A) c.1089C>A (p.Asn363Lys) c.5-7187C>A (n.5-7187C>A) c.249C>A (p.Asn83Lys) c.-98-20948C>A (n.-98-20948C>A) n.4912C>A n.4953C>A | |
17 | g.43071139T>A | CA10591963 | BRCA1 | c.4772A>T (p.Asn1591Ile) c.4775A>T (p.Asn1592Ile) c.4649A>T (p.Asn1550Ile) c.4769A>T (p.Asn1590Ile) c.4697A>T (p.Asn1566Ile) c.1463A>T (p.Asn488Ile) c.1325A>T (p.Asn442Ile) c.3887A>T (p.Asn1296Ile) c.4652A>T (p.Asn1551Ile) c.4841A>T (p.Asn1614Ile) c.4634A>T (p.Asn1545Ile) c.1337A>T (p.Asn446Ile) c.1382A>T (p.Asn461Ile) c.4838A>T (p.Asn1613Ile) c.1162A>T c.1349A>T (p.Asn450Ile) c.*4558A>T (n.*4558A>T) c.1088A>T (p.Asn363Ile) c.5-7188A>T (n.5-7188A>T) c.248A>T (p.Asn83Ile) c.-98-20949A>T (n.-98-20949A>T) n.4911A>T n.4952A>T | |
17 | g.43071139T>C | CA003017 | BRCA1 | c.4772A>G (p.Asn1591Ser) c.4775A>G (p.Asn1592Ser) c.4649A>G (p.Asn1550Ser) c.4769A>G (p.Asn1590Ser) c.4697A>G (p.Asn1566Ser) c.1463A>G (p.Asn488Ser) c.1325A>G (p.Asn442Ser) c.3887A>G (p.Asn1296Ser) c.4652A>G (p.Asn1551Ser) c.4841A>G (p.Asn1614Ser) c.4634A>G (p.Asn1545Ser) c.1337A>G (p.Asn446Ser) c.1382A>G (p.Asn461Ser) c.4838A>G (p.Asn1613Ser) c.1162A>G c.1349A>G (p.Asn450Ser) c.*4558A>G (n.*4558A>G) c.1088A>G (p.Asn363Ser) c.5-7188A>G (n.5-7188A>G) c.248A>G (p.Asn83Ser) c.-98-20949A>G (n.-98-20949A>G) n.4911A>G n.4952A>G | ClinVar dbSNP gnomAD v4 |
17 | g.43071139T>G | CA10591964 | BRCA1 | c.4772A>C (p.Asn1591Thr) c.4775A>C (p.Asn1592Thr) c.4649A>C (p.Asn1550Thr) c.4769A>C (p.Asn1590Thr) c.4697A>C (p.Asn1566Thr) c.1463A>C (p.Asn488Thr) c.1325A>C (p.Asn442Thr) c.3887A>C (p.Asn1296Thr) c.4652A>C (p.Asn1551Thr) c.4841A>C (p.Asn1614Thr) c.4634A>C (p.Asn1545Thr) c.1337A>C (p.Asn446Thr) c.1382A>C (p.Asn461Thr) c.4838A>C (p.Asn1613Thr) c.1162A>C c.1349A>C (p.Asn450Thr) c.*4558A>C (n.*4558A>C) c.1088A>C (p.Asn363Thr) c.5-7188A>C (n.5-7188A>C) c.248A>C (p.Asn83Thr) c.-98-20949A>C (n.-98-20949A>C) n.4911A>C n.4952A>C | |
17 | g.43071139T= | CA2260772951 | BRCA1 | c.4772A= (p.Asn1591=) c.4775A= (p.Asn1592=) c.4649A= (p.Asn1550=) c.4769A= (p.Asn1590=) c.4697A= (p.Asn1566=) c.1463A= (p.Asn488=) c.1325A= (p.Asn442=) c.3887A= (p.Asn1296=) c.4652A= (p.Asn1551=) c.4841A= (p.Asn1614=) c.4634A= (p.Asn1545=) c.1337A= (p.Asn446=) c.1382A= (p.Asn461=) c.4838A= (p.Asn1613=) c.1162A= c.1349A= (p.Asn450=) c.*4558A= (n.*4558A=) c.1088A= (p.Asn363=) c.5-7188A= (n.5-7188A=) c.248A= (p.Asn83=) c.-98-20949A= (n.-98-20949A=) n.4911A= n.4952A= | |
17 | g.43071140del | CA2695225909 | BRCA1 | c.4772del (p.Asn1591ThrfsTer9) c.4775del (p.Asn1592ThrfsTer9) c.4649del (p.Asn1550ThrfsTer9) c.4769del (p.Asn1590ThrfsTer9) c.4697del (p.Asn1566ThrfsTer9) c.1463del (p.Asn488ThrfsTer9) c.1325del (p.Asn442ThrfsTer9) c.3887del (p.Asn1296ThrfsTer9) c.4652del (p.Asn1551ThrfsTer9) c.4841del (p.Asn1614ThrfsTer9) c.4634del (p.Asn1545ThrfsTer9) c.1337del (p.Asn446ThrfsTer9) c.1382del (p.Asn461ThrfsTer9) c.4838del (p.Asn1613ThrfsTer9) c.1162del c.1349del (p.Asn450ThrfsTer9) c.*4558del (n.*4558del) c.1088del (p.Asn363ThrfsTer9) c.5-7188del (n.5-7188del) c.248del (p.Asn83ThrfsTer9) c.-98-20949del (n.-98-20949del) n.4911del n.4952del | |
17 | g.43071140T>A | CA10591965 | BRCA1 | c.4771A>T (p.Asn1591Tyr) c.4774A>T (p.Asn1592Tyr) c.4648A>T (p.Asn1550Tyr) c.4768A>T (p.Asn1590Tyr) c.4696A>T (p.Asn1566Tyr) c.1462A>T (p.Asn488Tyr) c.1324A>T (p.Asn442Tyr) c.3886A>T (p.Asn1296Tyr) c.4651A>T (p.Asn1551Tyr) c.4840A>T (p.Asn1614Tyr) c.4633A>T (p.Asn1545Tyr) c.1336A>T (p.Asn446Tyr) c.1381A>T (p.Asn461Tyr) c.4837A>T (p.Asn1613Tyr) c.1161A>T c.1348A>T (p.Asn450Tyr) c.*4557A>T (n.*4557A>T) c.1087A>T (p.Asn363Tyr) c.5-7189A>T (n.5-7189A>T) c.247A>T (p.Asn83Tyr) c.-98-20950A>T (n.-98-20950A>T) n.4910A>T n.4951A>T | dbSNP |
17 | g.43071140T>C | CA10591966 | BRCA1 | c.4771A>G (p.Asn1591Asp) c.4774A>G (p.Asn1592Asp) c.4648A>G (p.Asn1550Asp) c.4768A>G (p.Asn1590Asp) c.4696A>G (p.Asn1566Asp) c.1462A>G (p.Asn488Asp) c.1324A>G (p.Asn442Asp) c.3886A>G (p.Asn1296Asp) c.4651A>G (p.Asn1551Asp) c.4840A>G (p.Asn1614Asp) c.4633A>G (p.Asn1545Asp) c.1336A>G (p.Asn446Asp) c.1381A>G (p.Asn461Asp) c.4837A>G (p.Asn1613Asp) c.1161A>G c.1348A>G (p.Asn450Asp) c.*4557A>G (n.*4557A>G) c.1087A>G (p.Asn363Asp) c.5-7189A>G (n.5-7189A>G) c.247A>G (p.Asn83Asp) c.-98-20950A>G (n.-98-20950A>G) n.4910A>G n.4951A>G | gnomAD v4 |
17 | g.43071140T>G | CA10591967 | BRCA1 | c.4771A>C (p.Asn1591His) c.4774A>C (p.Asn1592His) c.4648A>C (p.Asn1550His) c.4768A>C (p.Asn1590His) c.4696A>C (p.Asn1566His) c.1462A>C (p.Asn488His) c.1324A>C (p.Asn442His) c.3886A>C (p.Asn1296His) c.4651A>C (p.Asn1551His) c.4840A>C (p.Asn1614His) c.4633A>C (p.Asn1545His) c.1336A>C (p.Asn446His) c.1381A>C (p.Asn461His) c.4837A>C (p.Asn1613His) c.1161A>C c.1348A>C (p.Asn450His) c.*4557A>C (n.*4557A>C) c.1087A>C (p.Asn363His) c.5-7189A>C (n.5-7189A>C) c.247A>C (p.Asn83His) c.-98-20950A>C (n.-98-20950A>C) n.4910A>C n.4951A>C | ClinVar dbSNP gnomAD v4 |
17 | g.43071140T= | CA2260772952 | BRCA1 | c.4771A= (p.Asn1591=) c.4774A= (p.Asn1592=) c.4648A= (p.Asn1550=) c.4768A= (p.Asn1590=) c.4696A= (p.Asn1566=) c.1462A= (p.Asn488=) c.1324A= (p.Asn442=) c.3886A= (p.Asn1296=) c.4651A= (p.Asn1551=) c.4840A= (p.Asn1614=) c.4633A= (p.Asn1545=) c.1336A= (p.Asn446=) c.1381A= (p.Asn461=) c.4837A= (p.Asn1613=) c.1161A= c.1348A= (p.Asn450=) c.*4557A= (n.*4557A=) c.1087A= (p.Asn363=) c.5-7189A= (n.5-7189A=) c.247A= (p.Asn83=) c.-98-20950A= (n.-98-20950A=) n.4910A= n.4951A= | |
17 | g.43071141G>A | CA500231850 | BRCA1 | c.4770C>T (p.Gly1590=) c.4773C>T (p.Gly1591=) c.4647C>T (p.Gly1549=) c.4767C>T (p.Gly1589=) c.4695C>T (p.Gly1565=) c.1461C>T (p.Gly487=) c.1323C>T (p.Gly441=) c.3885C>T (p.Gly1295=) c.4650C>T (p.Gly1550=) c.4839C>T (p.Gly1613=) c.4632C>T (p.Gly1544=) c.1335C>T (p.Gly445=) c.1380C>T (p.Gly460=) c.4836C>T (p.Gly1612=) c.1160C>T c.1347C>T (p.Gly449=) c.*4556C>T (n.*4556C>T) c.1086C>T (p.Gly362=) c.5-7190C>T (n.5-7190C>T) c.246C>T (p.Gly82=) c.-98-20951C>T (n.-98-20951C>T) n.4909C>T n.4950C>T | ClinVar dbSNP |
17 | g.43071141G>C | CA500231848 | BRCA1 | c.4770C>G (p.Gly1590=) c.4773C>G (p.Gly1591=) c.4647C>G (p.Gly1549=) c.4767C>G (p.Gly1589=) c.4695C>G (p.Gly1565=) c.1461C>G (p.Gly487=) c.1323C>G (p.Gly441=) c.3885C>G (p.Gly1295=) c.4650C>G (p.Gly1550=) c.4839C>G (p.Gly1613=) c.4632C>G (p.Gly1544=) c.1335C>G (p.Gly445=) c.1380C>G (p.Gly460=) c.4836C>G (p.Gly1612=) c.1160C>G c.1347C>G (p.Gly449=) c.*4556C>G (n.*4556C>G) c.1086C>G (p.Gly362=) c.5-7190C>G (n.5-7190C>G) c.246C>G (p.Gly82=) c.-98-20951C>G (n.-98-20951C>G) n.4909C>G n.4950C>G | ClinVar |
17 | g.43071141G>T | CA500231849 | BRCA1 | c.4770C>A (p.Gly1590=) c.4773C>A (p.Gly1591=) c.4647C>A (p.Gly1549=) c.4767C>A (p.Gly1589=) c.4695C>A (p.Gly1565=) c.1461C>A (p.Gly487=) c.1323C>A (p.Gly441=) c.3885C>A (p.Gly1295=) c.4650C>A (p.Gly1550=) c.4839C>A (p.Gly1613=) c.4632C>A (p.Gly1544=) c.1335C>A (p.Gly445=) c.1380C>A (p.Gly460=) c.4836C>A (p.Gly1612=) c.1160C>A c.1347C>A (p.Gly449=) c.*4556C>A (n.*4556C>A) c.1086C>A (p.Gly362=) c.5-7190C>A (n.5-7190C>A) c.246C>A (p.Gly82=) c.-98-20951C>A (n.-98-20951C>A) n.4909C>A n.4950C>A | |
17 | g.43071142C>A | CA10591968 | BRCA1 | c.4769G>T (p.Gly1590Val) c.4772G>T (p.Gly1591Val) c.4646G>T (p.Gly1549Val) c.4766G>T (p.Gly1589Val) c.4694G>T (p.Gly1565Val) c.1460G>T (p.Gly487Val) c.1322G>T (p.Gly441Val) c.3884G>T (p.Gly1295Val) c.4649G>T (p.Gly1550Val) c.4838G>T (p.Gly1613Val) c.4631G>T (p.Gly1544Val) c.1334G>T (p.Gly445Val) c.1379G>T (p.Gly460Val) c.4835G>T (p.Gly1612Val) c.1159G>T c.1346G>T (p.Gly449Val) c.*4555G>T (n.*4555G>T) c.1085G>T (p.Gly362Val) c.5-7191G>T (n.5-7191G>T) c.245G>T (p.Gly82Val) c.-98-20952G>T (n.-98-20952G>T) n.4908G>T n.4949G>T | dbSNP |
17 | g.43071142C= | CA2260772953 | BRCA1 | c.4769G= (p.Gly1590=) c.4772G= (p.Gly1591=) c.4646G= (p.Gly1549=) c.4766G= (p.Gly1589=) c.4694G= (p.Gly1565=) c.1460G= (p.Gly487=) c.1322G= (p.Gly441=) c.3884G= (p.Gly1295=) c.4649G= (p.Gly1550=) c.4838G= (p.Gly1613=) c.4631G= (p.Gly1544=) c.1334G= (p.Gly445=) c.1379G= (p.Gly460=) c.4835G= (p.Gly1612=) c.1159G= c.1346G= (p.Gly449=) c.*4555G= (n.*4555G=) c.1085G= (p.Gly362=) c.5-7191G= (n.5-7191G=) c.245G= (p.Gly82=) c.-98-20952G= (n.-98-20952G=) n.4908G= n.4949G= | |
17 | g.43071142C>G | CA10591969 | BRCA1 | c.4769G>C (p.Gly1590Ala) c.4772G>C (p.Gly1591Ala) c.4646G>C (p.Gly1549Ala) c.4766G>C (p.Gly1589Ala) c.4694G>C (p.Gly1565Ala) c.1460G>C (p.Gly487Ala) c.1322G>C (p.Gly441Ala) c.3884G>C (p.Gly1295Ala) c.4649G>C (p.Gly1550Ala) c.4838G>C (p.Gly1613Ala) c.4631G>C (p.Gly1544Ala) c.1334G>C (p.Gly445Ala) c.1379G>C (p.Gly460Ala) c.4835G>C (p.Gly1612Ala) c.1159G>C c.1346G>C (p.Gly449Ala) c.*4555G>C (n.*4555G>C) c.1085G>C (p.Gly362Ala) c.5-7191G>C (n.5-7191G>C) c.245G>C (p.Gly82Ala) c.-98-20952G>C (n.-98-20952G>C) n.4908G>C n.4949G>C | dbSNP |
17 | g.43071142C>T | CA10591970 | BRCA1 | c.4769G>A (p.Gly1590Asp) c.4772G>A (p.Gly1591Asp) c.4646G>A (p.Gly1549Asp) c.4766G>A (p.Gly1589Asp) c.4694G>A (p.Gly1565Asp) c.1460G>A (p.Gly487Asp) c.1322G>A (p.Gly441Asp) c.3884G>A (p.Gly1295Asp) c.4649G>A (p.Gly1550Asp) c.4838G>A (p.Gly1613Asp) c.4631G>A (p.Gly1544Asp) c.1334G>A (p.Gly445Asp) c.1379G>A (p.Gly460Asp) c.4835G>A (p.Gly1612Asp) c.1159G>A c.1346G>A (p.Gly449Asp) c.*4555G>A (n.*4555G>A) c.1085G>A (p.Gly362Asp) c.5-7191G>A (n.5-7191G>A) c.245G>A (p.Gly82Asp) c.-98-20952G>A (n.-98-20952G>A) n.4908G>A n.4949G>A | ClinVar dbSNP |
17 | g.43071142_43071143delinsCC | CA2260772954 | BRCA1 | c.4768_4769delinsGG (p.Gly1590=) c.4771_4772delinsGG (p.Gly1591=) c.4645_4646delinsGG (p.Gly1549=) c.4765_4766delinsGG (p.Gly1589=) c.4693_4694delinsGG (p.Gly1565=) c.1459_1460delinsGG (p.Gly487=) c.1321_1322delinsGG (p.Gly441=) c.3883_3884delinsGG (p.Gly1295=) c.4648_4649delinsGG (p.Gly1550=) c.4837_4838delinsGG (p.Gly1613=) c.4630_4631delinsGG (p.Gly1544=) c.1333_1334delinsGG (p.Gly445=) c.1378_1379delinsGG (p.Gly460=) c.4834_4835delinsGG (p.Gly1612=) c.1158_1159delinsGG c.1345_1346delinsGG (p.Gly449=) c.*4554_*4555delinsGG (n.*4554_*4555delinsGG) c.1084_1085delinsGG (p.Gly362=) c.5-7192_5-7191delinsGG (n.5-7192_5-7191delinsGG) c.244_245delinsGG (p.Gly82=) c.-98-20953_-98-20952delinsGG (n.-98-20953_-98-20952delinsGG) n.4907_4908delinsGG n.4948_4949delinsGG | |
17 | g.43071142_43071143delinsTT | CA915950109 | BRCA1 | c.4768_4769delinsAA (p.Gly1590Asn) c.4771_4772delinsAA (p.Gly1591Asn) c.4645_4646delinsAA (p.Gly1549Asn) c.4765_4766delinsAA (p.Gly1589Asn) c.4693_4694delinsAA (p.Gly1565Asn) c.1459_1460delinsAA (p.Gly487Asn) c.1321_1322delinsAA (p.Gly441Asn) c.3883_3884delinsAA (p.Gly1295Asn) c.4648_4649delinsAA (p.Gly1550Asn) c.4837_4838delinsAA (p.Gly1613Asn) c.4630_4631delinsAA (p.Gly1544Asn) c.1333_1334delinsAA (p.Gly445Asn) c.1378_1379delinsAA (p.Gly460Asn) c.4834_4835delinsAA (p.Gly1612Asn) c.1158_1159delinsAA c.1345_1346delinsAA (p.Gly449Asn) c.*4554_*4555delinsAA (n.*4554_*4555delinsAA) c.1084_1085delinsAA (p.Gly362Asn) c.5-7192_5-7191delinsAA (n.5-7192_5-7191delinsAA) c.244_245delinsAA (p.Gly82Asn) c.-98-20953_-98-20952delinsAA (n.-98-20953_-98-20952delinsAA) n.4907_4908delinsAA n.4948_4949delinsAA | ClinVar dbSNP |
17 | g.43071143C>A | CA10591971 | BRCA1 | c.4768G>T (p.Gly1590Cys) c.4771G>T (p.Gly1591Cys) c.4645G>T (p.Gly1549Cys) c.4765G>T (p.Gly1589Cys) c.4693G>T (p.Gly1565Cys) c.1459G>T (p.Gly487Cys) c.1321G>T (p.Gly441Cys) c.3883G>T (p.Gly1295Cys) c.4648G>T (p.Gly1550Cys) c.4837G>T (p.Gly1613Cys) c.4630G>T (p.Gly1544Cys) c.1333G>T (p.Gly445Cys) c.1378G>T (p.Gly460Cys) c.4834G>T (p.Gly1612Cys) c.1158G>T c.1345G>T (p.Gly449Cys) c.*4554G>T (n.*4554G>T) c.1084G>T (p.Gly362Cys) c.5-7192G>T (n.5-7192G>T) c.244G>T (p.Gly82Cys) c.-98-20953G>T (n.-98-20953G>T) n.4907G>T n.4948G>T | dbSNP |
17 | g.43071143C= | CA2260772955 | BRCA1 | c.4768G= (p.Gly1590=) c.4771G= (p.Gly1591=) c.4645G= (p.Gly1549=) c.4765G= (p.Gly1589=) c.4693G= (p.Gly1565=) c.1459G= (p.Gly487=) c.1321G= (p.Gly441=) c.3883G= (p.Gly1295=) c.4648G= (p.Gly1550=) c.4837G= (p.Gly1613=) c.4630G= (p.Gly1544=) c.1333G= (p.Gly445=) c.1378G= (p.Gly460=) c.4834G= (p.Gly1612=) c.1158G= c.1345G= (p.Gly449=) c.*4554G= (n.*4554G=) c.1084G= (p.Gly362=) c.5-7192G= (n.5-7192G=) c.244G= (p.Gly82=) c.-98-20953G= (n.-98-20953G=) n.4907G= n.4948G= | |
17 | g.43071143C>G | CA10591972 | BRCA1 | c.4768G>C (p.Gly1590Arg) c.4771G>C (p.Gly1591Arg) c.4645G>C (p.Gly1549Arg) c.4765G>C (p.Gly1589Arg) c.4693G>C (p.Gly1565Arg) c.1459G>C (p.Gly487Arg) c.1321G>C (p.Gly441Arg) c.3883G>C (p.Gly1295Arg) c.4648G>C (p.Gly1550Arg) c.4837G>C (p.Gly1613Arg) c.4630G>C (p.Gly1544Arg) c.1333G>C (p.Gly445Arg) c.1378G>C (p.Gly460Arg) c.4834G>C (p.Gly1612Arg) c.1158G>C c.1345G>C (p.Gly449Arg) c.*4554G>C (n.*4554G>C) c.1084G>C (p.Gly362Arg) c.5-7192G>C (n.5-7192G>C) c.244G>C (p.Gly82Arg) c.-98-20953G>C (n.-98-20953G>C) n.4907G>C n.4948G>C | dbSNP |
17 | g.43071143C>T | CA003015 | BRCA1 | c.4768G>A (p.Gly1590Ser) c.4771G>A (p.Gly1591Ser) c.4645G>A (p.Gly1549Ser) c.4765G>A (p.Gly1589Ser) c.4693G>A (p.Gly1565Ser) c.1459G>A (p.Gly487Ser) c.1321G>A (p.Gly441Ser) c.3883G>A (p.Gly1295Ser) c.4648G>A (p.Gly1550Ser) c.4837G>A (p.Gly1613Ser) c.4630G>A (p.Gly1544Ser) c.1333G>A (p.Gly445Ser) c.1378G>A (p.Gly460Ser) c.4834G>A (p.Gly1612Ser) c.1158G>A c.1345G>A (p.Gly449Ser) c.*4554G>A (n.*4554G>A) c.1084G>A (p.Gly362Ser) c.5-7192G>A (n.5-7192G>A) c.244G>A (p.Gly82Ser) c.-98-20953G>A (n.-98-20953G>A) n.4907G>A n.4948G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071144A>C | CA500231851 | BRCA1 | c.4767T>G (p.Val1589=) c.4770T>G (p.Val1590=) c.4644T>G (p.Val1548=) c.4764T>G (p.Val1588=) c.4692T>G (p.Val1564=) c.1458T>G (p.Val486=) c.1320T>G (p.Val440=) c.3882T>G (p.Val1294=) c.4647T>G (p.Val1549=) c.4836T>G (p.Val1612=) c.4629T>G (p.Val1543=) c.1332T>G (p.Val444=) c.1377T>G (p.Val459=) c.4833T>G (p.Val1611=) c.1157T>G c.1344T>G (p.Val448=) c.*4553T>G (n.*4553T>G) c.1083T>G (p.Val361=) c.5-7193T>G (n.5-7193T>G) c.243T>G (p.Val81=) c.-98-20954T>G (n.-98-20954T>G) n.4906T>G n.4947T>G | dbSNP |
17 | g.43071144A>G | CA500231852 | BRCA1 | c.4767T>C (p.Val1589=) c.4770T>C (p.Val1590=) c.4644T>C (p.Val1548=) c.4764T>C (p.Val1588=) c.4692T>C (p.Val1564=) c.1458T>C (p.Val486=) c.1320T>C (p.Val440=) c.3882T>C (p.Val1294=) c.4647T>C (p.Val1549=) c.4836T>C (p.Val1612=) c.4629T>C (p.Val1543=) c.1332T>C (p.Val444=) c.1377T>C (p.Val459=) c.4833T>C (p.Val1611=) c.1157T>C c.1344T>C (p.Val448=) c.*4553T>C (n.*4553T>C) c.1083T>C (p.Val361=) c.5-7193T>C (n.5-7193T>C) c.243T>C (p.Val81=) c.-98-20954T>C (n.-98-20954T>C) n.4906T>C n.4947T>C | ClinVar dbSNP |
17 | g.43071144A>T | CA500231853 | BRCA1 | c.4767T>A (p.Val1589=) c.4770T>A (p.Val1590=) c.4644T>A (p.Val1548=) c.4764T>A (p.Val1588=) c.4692T>A (p.Val1564=) c.1458T>A (p.Val486=) c.1320T>A (p.Val440=) c.3882T>A (p.Val1294=) c.4647T>A (p.Val1549=) c.4836T>A (p.Val1612=) c.4629T>A (p.Val1543=) c.1332T>A (p.Val444=) c.1377T>A (p.Val459=) c.4833T>A (p.Val1611=) c.1157T>A c.1344T>A (p.Val448=) c.*4553T>A (n.*4553T>A) c.1083T>A (p.Val361=) c.5-7193T>A (n.5-7193T>A) c.243T>A (p.Val81=) c.-98-20954T>A (n.-98-20954T>A) n.4906T>A n.4947T>A | dbSNP |
17 | g.43071145A= | CA2260772956 | BRCA1 | c.4766T= (p.Val1589=) c.4769T= (p.Val1590=) c.4643T= (p.Val1548=) c.4763T= (p.Val1588=) c.4691T= (p.Val1564=) c.1457T= (p.Val486=) c.1319T= (p.Val440=) c.3881T= (p.Val1294=) c.4646T= (p.Val1549=) c.4835T= (p.Val1612=) c.4628T= (p.Val1543=) c.1331T= (p.Val444=) c.1376T= (p.Val459=) c.4832T= (p.Val1611=) c.1156T= c.1343T= (p.Val448=) c.*4552T= (n.*4552T=) c.1082T= (p.Val361=) c.5-7194T= (n.5-7194T=) c.242T= (p.Val81=) c.-98-20955T= (n.-98-20955T=) n.4905T= n.4946T= | |
17 | g.43071145A>C | CA10591973 | BRCA1 | c.4766T>G (p.Val1589Gly) c.4769T>G (p.Val1590Gly) c.4643T>G (p.Val1548Gly) c.4763T>G (p.Val1588Gly) c.4691T>G (p.Val1564Gly) c.1457T>G (p.Val486Gly) c.1319T>G (p.Val440Gly) c.3881T>G (p.Val1294Gly) c.4646T>G (p.Val1549Gly) c.4835T>G (p.Val1612Gly) c.4628T>G (p.Val1543Gly) c.1331T>G (p.Val444Gly) c.1376T>G (p.Val459Gly) c.4832T>G (p.Val1611Gly) c.1156T>G c.1343T>G (p.Val448Gly) c.*4552T>G (n.*4552T>G) c.1082T>G (p.Val361Gly) c.5-7194T>G (n.5-7194T>G) c.242T>G (p.Val81Gly) c.-98-20955T>G (n.-98-20955T>G) n.4905T>G n.4946T>G | ClinVar dbSNP |
17 | g.43071145A>G | CA053026 | BRCA1 | c.4766T>C (p.Val1589Ala) c.4769T>C (p.Val1590Ala) c.4643T>C (p.Val1548Ala) c.4763T>C (p.Val1588Ala) c.4691T>C (p.Val1564Ala) c.1457T>C (p.Val486Ala) c.1319T>C (p.Val440Ala) c.3881T>C (p.Val1294Ala) c.4646T>C (p.Val1549Ala) c.4835T>C (p.Val1612Ala) c.4628T>C (p.Val1543Ala) c.1331T>C (p.Val444Ala) c.1376T>C (p.Val459Ala) c.4832T>C (p.Val1611Ala) c.1156T>C c.1343T>C (p.Val448Ala) c.*4552T>C (n.*4552T>C) c.1082T>C (p.Val361Ala) c.5-7194T>C (n.5-7194T>C) c.242T>C (p.Val81Ala) c.-98-20955T>C (n.-98-20955T>C) n.4905T>C n.4946T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071145A>T | CA10591974 | BRCA1 | c.4766T>A (p.Val1589Asp) c.4769T>A (p.Val1590Asp) c.4643T>A (p.Val1548Asp) c.4763T>A (p.Val1588Asp) c.4691T>A (p.Val1564Asp) c.1457T>A (p.Val486Asp) c.1319T>A (p.Val440Asp) c.3881T>A (p.Val1294Asp) c.4646T>A (p.Val1549Asp) c.4835T>A (p.Val1612Asp) c.4628T>A (p.Val1543Asp) c.1331T>A (p.Val444Asp) c.1376T>A (p.Val459Asp) c.4832T>A (p.Val1611Asp) c.1156T>A c.1343T>A (p.Val448Asp) c.*4552T>A (n.*4552T>A) c.1082T>A (p.Val361Asp) c.5-7194T>A (n.5-7194T>A) c.242T>A (p.Val81Asp) c.-98-20955T>A (n.-98-20955T>A) n.4905T>A n.4946T>A | dbSNP |
17 | g.43071146del | CA2573154035 | BRCA1 | c.4765del (p.Val1589LeufsTer11) c.4768del (p.Val1590LeufsTer11) c.4642del (p.Val1548LeufsTer11) c.4762del (p.Val1588LeufsTer11) c.4690del (p.Val1564LeufsTer11) c.1456del (p.Val486LeufsTer11) c.1318del (p.Val440LeufsTer11) c.3880del (p.Val1294LeufsTer11) c.4645del (p.Val1549LeufsTer11) c.4834del (p.Val1612LeufsTer11) c.4627del (p.Val1543LeufsTer11) c.1330del (p.Val444LeufsTer11) c.1375del (p.Val459LeufsTer11) c.4831del (p.Val1611LeufsTer11) c.1155del c.1342del (p.Val448LeufsTer11) c.*4551del (n.*4551del) c.1081del (p.Val361LeufsTer11) c.5-7195del (n.5-7195del) c.241del (p.Val81LeufsTer11) c.-98-20956del (n.-98-20956del) n.4904del n.4945del | ClinVar dbSNP |
17 | g.43071146C>A | CA10591975 | BRCA1 | c.4765G>T (p.Val1589Phe) c.4768G>T (p.Val1590Phe) c.4642G>T (p.Val1548Phe) c.4762G>T (p.Val1588Phe) c.4690G>T (p.Val1564Phe) c.1456G>T (p.Val486Phe) c.1318G>T (p.Val440Phe) c.3880G>T (p.Val1294Phe) c.4645G>T (p.Val1549Phe) c.4834G>T (p.Val1612Phe) c.4627G>T (p.Val1543Phe) c.1330G>T (p.Val444Phe) c.1375G>T (p.Val459Phe) c.4831G>T (p.Val1611Phe) c.1155G>T c.1342G>T (p.Val448Phe) c.*4551G>T (n.*4551G>T) c.1081G>T (p.Val361Phe) c.5-7195G>T (n.5-7195G>T) c.241G>T (p.Val81Phe) c.-98-20956G>T (n.-98-20956G>T) n.4904G>T n.4945G>T | dbSNP |
17 | g.43071146C>G | CA10591976 | BRCA1 | c.4765G>C (p.Val1589Leu) c.4768G>C (p.Val1590Leu) c.4642G>C (p.Val1548Leu) c.4762G>C (p.Val1588Leu) c.4690G>C (p.Val1564Leu) c.1456G>C (p.Val486Leu) c.1318G>C (p.Val440Leu) c.3880G>C (p.Val1294Leu) c.4645G>C (p.Val1549Leu) c.4834G>C (p.Val1612Leu) c.4627G>C (p.Val1543Leu) c.1330G>C (p.Val444Leu) c.1375G>C (p.Val459Leu) c.4831G>C (p.Val1611Leu) c.1155G>C c.1342G>C (p.Val448Leu) c.*4551G>C (n.*4551G>C) c.1081G>C (p.Val361Leu) c.5-7195G>C (n.5-7195G>C) c.241G>C (p.Val81Leu) c.-98-20956G>C (n.-98-20956G>C) n.4904G>C n.4945G>C | dbSNP |
17 | g.43071146C>T | CA10591977 | BRCA1 | c.4765G>A (p.Val1589Ile) c.4768G>A (p.Val1590Ile) c.4642G>A (p.Val1548Ile) c.4762G>A (p.Val1588Ile) c.4690G>A (p.Val1564Ile) c.1456G>A (p.Val486Ile) c.1318G>A (p.Val440Ile) c.3880G>A (p.Val1294Ile) c.4645G>A (p.Val1549Ile) c.4834G>A (p.Val1612Ile) c.4627G>A (p.Val1543Ile) c.1330G>A (p.Val444Ile) c.1375G>A (p.Val459Ile) c.4831G>A (p.Val1611Ile) c.1155G>A c.1342G>A (p.Val448Ile) c.*4551G>A (n.*4551G>A) c.1081G>A (p.Val361Ile) c.5-7195G>A (n.5-7195G>A) c.241G>A (p.Val81Ile) c.-98-20956G>A (n.-98-20956G>A) n.4904G>A n.4945G>A | ClinVar |
17 | g.43071147A= | CA2260772957 | BRCA1 | c.4764T= (p.Arg1588=) c.4767T= (p.Arg1589=) c.4641T= (p.Arg1547=) c.4761T= (p.Arg1587=) c.4689T= (p.Arg1563=) c.1455T= (p.Arg485=) c.1317T= (p.Arg439=) c.3879T= (p.Arg1293=) c.4644T= (p.Arg1548=) c.4833T= (p.Arg1611=) c.4626T= (p.Arg1542=) c.1329T= (p.Arg443=) c.1374T= (p.Arg458=) c.4830T= (p.Arg1610=) c.1154T= c.1341T= (p.Arg447=) c.*4550T= (n.*4550T=) c.1080T= (p.Arg360=) c.5-7196T= (n.5-7196T=) c.240T= (p.Arg80=) c.-98-20957T= (n.-98-20957T=) n.4903T= n.4944T= | |
17 | g.43071147A>C | CA003014 | BRCA1 | c.4764T>G (p.Arg1588=) c.4767T>G (p.Arg1589=) c.4641T>G (p.Arg1547=) c.4761T>G (p.Arg1587=) c.4689T>G (p.Arg1563=) c.1455T>G (p.Arg485=) c.1317T>G (p.Arg439=) c.3879T>G (p.Arg1293=) c.4644T>G (p.Arg1548=) c.4833T>G (p.Arg1611=) c.4626T>G (p.Arg1542=) c.1329T>G (p.Arg443=) c.1374T>G (p.Arg458=) c.4830T>G (p.Arg1610=) c.1154T>G c.1341T>G (p.Arg447=) c.*4550T>G (n.*4550T>G) c.1080T>G (p.Arg360=) c.5-7196T>G (n.5-7196T>G) c.240T>G (p.Arg80=) c.-98-20957T>G (n.-98-20957T>G) n.4903T>G n.4944T>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.43071147A>G | CA500231854 | BRCA1 | c.4764T>C (p.Arg1588=) c.4767T>C (p.Arg1589=) c.4641T>C (p.Arg1547=) c.4761T>C (p.Arg1587=) c.4689T>C (p.Arg1563=) c.1455T>C (p.Arg485=) c.1317T>C (p.Arg439=) c.3879T>C (p.Arg1293=) c.4644T>C (p.Arg1548=) c.4833T>C (p.Arg1611=) c.4626T>C (p.Arg1542=) c.1329T>C (p.Arg443=) c.1374T>C (p.Arg458=) c.4830T>C (p.Arg1610=) c.1154T>C c.1341T>C (p.Arg447=) c.*4550T>C (n.*4550T>C) c.1080T>C (p.Arg360=) c.5-7196T>C (n.5-7196T>C) c.240T>C (p.Arg80=) c.-98-20957T>C (n.-98-20957T>C) n.4903T>C n.4944T>C | dbSNP |
17 | g.43071147A>T | CA500231855 | BRCA1 | c.4764T>A (p.Arg1588=) c.4767T>A (p.Arg1589=) c.4641T>A (p.Arg1547=) c.4761T>A (p.Arg1587=) c.4689T>A (p.Arg1563=) c.1455T>A (p.Arg485=) c.1317T>A (p.Arg439=) c.3879T>A (p.Arg1293=) c.4644T>A (p.Arg1548=) c.4833T>A (p.Arg1611=) c.4626T>A (p.Arg1542=) c.1329T>A (p.Arg443=) c.1374T>A (p.Arg458=) c.4830T>A (p.Arg1610=) c.1154T>A c.1341T>A (p.Arg447=) c.*4550T>A (n.*4550T>A) c.1080T>A (p.Arg360=) c.5-7196T>A (n.5-7196T>A) c.240T>A (p.Arg80=) c.-98-20957T>A (n.-98-20957T>A) n.4903T>A n.4944T>A | ClinVar dbSNP |
17 | g.43071148C>A | CA10591978 | BRCA1 | c.4763G>T (p.Arg1588Leu) c.4766G>T (p.Arg1589Leu) c.4640G>T (p.Arg1547Leu) c.4760G>T (p.Arg1587Leu) c.4688G>T (p.Arg1563Leu) c.1454G>T (p.Arg485Leu) c.1316G>T (p.Arg439Leu) c.3878G>T (p.Arg1293Leu) c.4643G>T (p.Arg1548Leu) c.4832G>T (p.Arg1611Leu) c.4625G>T (p.Arg1542Leu) c.1328G>T (p.Arg443Leu) c.1373G>T (p.Arg458Leu) c.4829G>T (p.Arg1610Leu) c.1153G>T c.1340G>T (p.Arg447Leu) c.*4549G>T (n.*4549G>T) c.1079G>T (p.Arg360Leu) c.5-7197G>T (n.5-7197G>T) c.239G>T (p.Arg80Leu) c.-98-20958G>T (n.-98-20958G>T) n.4902G>T n.4943G>T | dbSNP |
17 | g.43071148C= | CA2260772958 | BRCA1 | c.4763G= (p.Arg1588=) c.4766G= (p.Arg1589=) c.4640G= (p.Arg1547=) c.4760G= (p.Arg1587=) c.4688G= (p.Arg1563=) c.1454G= (p.Arg485=) c.1316G= (p.Arg439=) c.3878G= (p.Arg1293=) c.4643G= (p.Arg1548=) c.4832G= (p.Arg1611=) c.4625G= (p.Arg1542=) c.1328G= (p.Arg443=) c.1373G= (p.Arg458=) c.4829G= (p.Arg1610=) c.1153G= c.1340G= (p.Arg447=) c.*4549G= (n.*4549G=) c.1079G= (p.Arg360=) c.5-7197G= (n.5-7197G=) c.239G= (p.Arg80=) c.-98-20958G= (n.-98-20958G=) n.4902G= n.4943G= | |
17 | g.43071148C>G | CA10591979 | BRCA1 | c.4763G>C (p.Arg1588Pro) c.4766G>C (p.Arg1589Pro) c.4640G>C (p.Arg1547Pro) c.4760G>C (p.Arg1587Pro) c.4688G>C (p.Arg1563Pro) c.1454G>C (p.Arg485Pro) c.1316G>C (p.Arg439Pro) c.3878G>C (p.Arg1293Pro) c.4643G>C (p.Arg1548Pro) c.4832G>C (p.Arg1611Pro) c.4625G>C (p.Arg1542Pro) c.1328G>C (p.Arg443Pro) c.1373G>C (p.Arg458Pro) c.4829G>C (p.Arg1610Pro) c.1153G>C c.1340G>C (p.Arg447Pro) c.*4549G>C (n.*4549G>C) c.1079G>C (p.Arg360Pro) c.5-7197G>C (n.5-7197G>C) c.239G>C (p.Arg80Pro) c.-98-20958G>C (n.-98-20958G>C) n.4902G>C n.4943G>C | ClinVar dbSNP |
17 | g.43071148C>T | CA003013 | BRCA1 | c.4763G>A (p.Arg1588His) c.4766G>A (p.Arg1589His) c.4640G>A (p.Arg1547His) c.4760G>A (p.Arg1587His) c.4688G>A (p.Arg1563His) c.1454G>A (p.Arg485His) c.1316G>A (p.Arg439His) c.3878G>A (p.Arg1293His) c.4643G>A (p.Arg1548His) c.4832G>A (p.Arg1611His) c.4625G>A (p.Arg1542His) c.1328G>A (p.Arg443His) c.1373G>A (p.Arg458His) c.4829G>A (p.Arg1610His) c.1153G>A c.1340G>A (p.Arg447His) c.*4549G>A (n.*4549G>A) c.1079G>A (p.Arg360His) c.5-7197G>A (n.5-7197G>A) c.239G>A (p.Arg80His) c.-98-20958G>A (n.-98-20958G>A) n.4902G>A n.4943G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
17 | g.43071148_43071150delinsCGA | CA2260772959 | BRCA1 | c.4761_4763delinsTCG (p.Ala1587=) c.4764_4766delinsTCG (p.Ala1588=) c.4638_4640delinsTCG (p.Ala1546=) c.4758_4760delinsTCG (p.Ala1586=) c.4686_4688delinsTCG (p.Ala1562=) c.1452_1454delinsTCG (p.Ala484=) c.1314_1316delinsTCG (p.Ala438=) c.3876_3878delinsTCG (p.Ala1292=) c.4641_4643delinsTCG (p.Ala1547=) c.4830_4832delinsTCG (p.Ala1610=) c.4623_4625delinsTCG (p.Ala1541=) c.1326_1328delinsTCG (p.Ala442=) c.1371_1373delinsTCG (p.Ala457=) c.4827_4829delinsTCG (p.Ala1609=) c.1151_1153delinsTCG c.1338_1340delinsTCG (p.Ala446=) c.*4547_*4549delinsTCG (n.*4547_*4549delinsTCG) c.1077_1079delinsTCG (p.Ala359=) c.5-7199_5-7197delinsTCG (n.5-7199_5-7197delinsTCG) c.237_239delinsTCG (p.Ala79=) c.-98-20960_-98-20958delinsTCG (n.-98-20960_-98-20958delinsTCG) n.4900_4902delinsTCG n.4941_4943delinsTCG | |
17 | g.43071149G>A | CA003012 | BRCA1 | c.4762C>T (p.Arg1588Cys) c.4765C>T (p.Arg1589Cys) c.4639C>T (p.Arg1547Cys) c.4759C>T (p.Arg1587Cys) c.4687C>T (p.Arg1563Cys) c.1453C>T (p.Arg485Cys) c.1315C>T (p.Arg439Cys) c.3877C>T (p.Arg1293Cys) c.4642C>T (p.Arg1548Cys) c.4831C>T (p.Arg1611Cys) c.4624C>T (p.Arg1542Cys) c.1327C>T (p.Arg443Cys) c.1372C>T (p.Arg458Cys) c.4828C>T (p.Arg1610Cys) c.1152C>T c.1339C>T (p.Arg447Cys) c.*4548C>T (n.*4548C>T) c.1078C>T (p.Arg360Cys) c.5-7198C>T (n.5-7198C>T) c.238C>T (p.Arg80Cys) c.-98-20959C>T (n.-98-20959C>T) n.4901C>T n.4942C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
17 | g.43071149G>C | CA10591980 | BRCA1 | c.4762C>G (p.Arg1588Gly) c.4765C>G (p.Arg1589Gly) c.4639C>G (p.Arg1547Gly) c.4759C>G (p.Arg1587Gly) c.4687C>G (p.Arg1563Gly) c.1453C>G (p.Arg485Gly) c.1315C>G (p.Arg439Gly) c.3877C>G (p.Arg1293Gly) c.4642C>G (p.Arg1548Gly) c.4831C>G (p.Arg1611Gly) c.4624C>G (p.Arg1542Gly) c.1327C>G (p.Arg443Gly) c.1372C>G (p.Arg458Gly) c.4828C>G (p.Arg1610Gly) c.1152C>G c.1339C>G (p.Arg447Gly) c.*4548C>G (n.*4548C>G) c.1078C>G (p.Arg360Gly) c.5-7198C>G (n.5-7198C>G) c.238C>G (p.Arg80Gly) c.-98-20959C>G (n.-98-20959C>G) n.4901C>G n.4942C>G | ClinVar dbSNP |
17 | g.43071149G= | CA2260772960 | BRCA1 | c.4762C= (p.Arg1588=) c.4765C= (p.Arg1589=) c.4639C= (p.Arg1547=) c.4759C= (p.Arg1587=) c.4687C= (p.Arg1563=) c.1453C= (p.Arg485=) c.1315C= (p.Arg439=) c.3877C= (p.Arg1293=) c.4642C= (p.Arg1548=) c.4831C= (p.Arg1611=) c.4624C= (p.Arg1542=) c.1327C= (p.Arg443=) c.1372C= (p.Arg458=) c.4828C= (p.Arg1610=) c.1152C= c.1339C= (p.Arg447=) c.*4548C= (n.*4548C=) c.1078C= (p.Arg360=) c.5-7198C= (n.5-7198C=) c.238C= (p.Arg80=) c.-98-20959C= (n.-98-20959C=) n.4901C= n.4942C= | |
17 | g.43071149G>T | CA10591981 | BRCA1 | c.4762C>A (p.Arg1588Ser) c.4765C>A (p.Arg1589Ser) c.4639C>A (p.Arg1547Ser) c.4759C>A (p.Arg1587Ser) c.4687C>A (p.Arg1563Ser) c.1453C>A (p.Arg485Ser) c.1315C>A (p.Arg439Ser) c.3877C>A (p.Arg1293Ser) c.4642C>A (p.Arg1548Ser) c.4831C>A (p.Arg1611Ser) c.4624C>A (p.Arg1542Ser) c.1327C>A (p.Arg443Ser) c.1372C>A (p.Arg458Ser) c.4828C>A (p.Arg1610Ser) c.1152C>A c.1339C>A (p.Arg447Ser) c.*4548C>A (n.*4548C>A) c.1078C>A (p.Arg360Ser) c.5-7198C>A (n.5-7198C>A) c.238C>A (p.Arg80Ser) c.-98-20959C>A (n.-98-20959C>A) n.4901C>A n.4942C>A | |
17 | g.43071149_43071150delinsGA | CA2260772961 | BRCA1 | c.4761_4762delinsTC (p.Ala1587=) c.4764_4765delinsTC (p.Ala1588=) c.4638_4639delinsTC (p.Ala1546=) c.4758_4759delinsTC (p.Ala1586=) c.4686_4687delinsTC (p.Ala1562=) c.1452_1453delinsTC (p.Ala484=) c.1314_1315delinsTC (p.Ala438=) c.3876_3877delinsTC (p.Ala1292=) c.4641_4642delinsTC (p.Ala1547=) c.4830_4831delinsTC (p.Ala1610=) c.4623_4624delinsTC (p.Ala1541=) c.1326_1327delinsTC (p.Ala442=) c.1371_1372delinsTC (p.Ala457=) c.4827_4828delinsTC (p.Ala1609=) c.1151_1152delinsTC c.1338_1339delinsTC (p.Ala446=) c.*4547_*4548delinsTC (n.*4547_*4548delinsTC) c.1077_1078delinsTC (p.Ala359=) c.5-7199_5-7198delinsTC (n.5-7199_5-7198delinsTC) c.237_238delinsTC (p.Ala79=) c.-98-20960_-98-20959delinsTC (n.-98-20960_-98-20959delinsTC) n.4900_4901delinsTC n.4941_4942delinsTC | |
17 | g.43071150_43071151del | CA003009 | BRCA1 | c.4761_4762del (p.Arg1588CysfsTer?) c.4764_4765del (p.Arg1589CysfsTer?) c.4638_4639del (p.Arg1547CysfsTer?) c.4758_4759del (p.Arg1587CysfsTer?) c.4686_4687del (p.Arg1563CysfsTer?) c.1452_1453del (p.Arg485CysfsTer?) c.1314_1315del (p.Arg439CysfsTer?) c.3876_3877del (p.Arg1293CysfsTer?) c.4641_4642del (p.Arg1548CysfsTer?) c.4830_4831del (p.Arg1611CysfsTer?) c.4623_4624del (p.Arg1542CysfsTer?) c.1326_1327del (p.Arg443CysfsTer?) c.1371_1372del (p.Arg458CysfsTer?) c.4827_4828del (p.Arg1610CysfsTer?) c.1151_1152del c.1338_1339del (p.Arg447CysfsTer?) c.*4547_*4548del (n.*4547_*4548del) c.1077_1078del (p.Arg360CysfsTer?) c.5-7199_5-7198del (n.5-7199_5-7198del) c.237_238del (p.Arg80CysfsTer?) c.-98-20960_-98-20959del (n.-98-20960_-98-20959del) n.4900_4901del n.4941_4942del | ClinVar dbSNP |
17 | g.43071150del | CA003010 | BRCA1 | c.4761del (p.Arg1588ValfsTer12) c.4764del (p.Arg1589ValfsTer12) c.4638del (p.Arg1547ValfsTer12) c.4758del (p.Arg1587ValfsTer12) c.4686del (p.Arg1563ValfsTer12) c.1452del (p.Arg485ValfsTer12) c.1314del (p.Arg439ValfsTer12) c.3876del (p.Arg1293ValfsTer12) c.4641del (p.Arg1548ValfsTer12) c.4830del (p.Arg1611ValfsTer12) c.4623del (p.Arg1542ValfsTer12) c.1326del (p.Arg443ValfsTer12) c.1371del (p.Arg458ValfsTer12) c.4827del (p.Arg1610ValfsTer12) c.1151del c.1338del (p.Arg447ValfsTer12) c.*4547del (n.*4547del) c.1077del (p.Arg360ValfsTer12) c.5-7199del (n.5-7199del) c.237del (p.Arg80ValfsTer12) c.-98-20960del (n.-98-20960del) n.4900del n.4941del | ClinVar dbSNP |
17 | g.43071150A= | CA2260772962 | BRCA1 | c.4761T= (p.Ala1587=) c.4764T= (p.Ala1588=) c.4638T= (p.Ala1546=) c.4758T= (p.Ala1586=) c.4686T= (p.Ala1562=) c.1452T= (p.Ala484=) c.1314T= (p.Ala438=) c.3876T= (p.Ala1292=) c.4641T= (p.Ala1547=) c.4830T= (p.Ala1610=) c.4623T= (p.Ala1541=) c.1326T= (p.Ala442=) c.1371T= (p.Ala457=) c.4827T= (p.Ala1609=) c.1151T= c.1338T= (p.Ala446=) c.*4547T= (n.*4547T=) c.1077T= (p.Ala359=) c.5-7199T= (n.5-7199T=) c.237T= (p.Ala79=) c.-98-20960T= (n.-98-20960T=) n.4900T= n.4941T= | |
17 | g.43071150A>C | CA500231856 | BRCA1 | c.4761T>G (p.Ala1587=) c.4764T>G (p.Ala1588=) c.4638T>G (p.Ala1546=) c.4758T>G (p.Ala1586=) c.4686T>G (p.Ala1562=) c.1452T>G (p.Ala484=) c.1314T>G (p.Ala438=) c.3876T>G (p.Ala1292=) c.4641T>G (p.Ala1547=) c.4830T>G (p.Ala1610=) c.4623T>G (p.Ala1541=) c.1326T>G (p.Ala442=) c.1371T>G (p.Ala457=) c.4827T>G (p.Ala1609=) c.1151T>G c.1338T>G (p.Ala446=) c.*4547T>G (n.*4547T>G) c.1077T>G (p.Ala359=) c.5-7199T>G (n.5-7199T>G) c.237T>G (p.Ala79=) c.-98-20960T>G (n.-98-20960T>G) n.4900T>G n.4941T>G | |
17 | g.43071150A>G | CA003011 | BRCA1 | c.4761T>C (p.Ala1587=) c.4764T>C (p.Ala1588=) c.4638T>C (p.Ala1546=) c.4758T>C (p.Ala1586=) c.4686T>C (p.Ala1562=) c.1452T>C (p.Ala484=) c.1314T>C (p.Ala438=) c.3876T>C (p.Ala1292=) c.4641T>C (p.Ala1547=) c.4830T>C (p.Ala1610=) c.4623T>C (p.Ala1541=) c.1326T>C (p.Ala442=) c.1371T>C (p.Ala457=) c.4827T>C (p.Ala1609=) c.1151T>C c.1338T>C (p.Ala446=) c.*4547T>C (n.*4547T>C) c.1077T>C (p.Ala359=) c.5-7199T>C (n.5-7199T>C) c.237T>C (p.Ala79=) c.-98-20960T>C (n.-98-20960T>C) n.4900T>C n.4941T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071150A>T | CA10580509 | BRCA1 | c.4761T>A (p.Ala1587=) c.4764T>A (p.Ala1588=) c.4638T>A (p.Ala1546=) c.4758T>A (p.Ala1586=) c.4686T>A (p.Ala1562=) c.1452T>A (p.Ala484=) c.1314T>A (p.Ala438=) c.3876T>A (p.Ala1292=) c.4641T>A (p.Ala1547=) c.4830T>A (p.Ala1610=) c.4623T>A (p.Ala1541=) c.1326T>A (p.Ala442=) c.1371T>A (p.Ala457=) c.4827T>A (p.Ala1609=) c.1151T>A c.1338T>A (p.Ala446=) c.*4547T>A (n.*4547T>A) c.1077T>A (p.Ala359=) c.5-7199T>A (n.5-7199T>A) c.237T>A (p.Ala79=) c.-98-20960T>A (n.-98-20960T>A) n.4900T>A n.4941T>A | ClinVar dbSNP gnomAD v4 |
17 | g.43071151G>A | CA052948 | BRCA1 | c.4760C>T (p.Ala1587Val) c.4763C>T (p.Ala1588Val) c.4637C>T (p.Ala1546Val) c.4757C>T (p.Ala1586Val) c.4685C>T (p.Ala1562Val) c.1451C>T (p.Ala484Val) c.1313C>T (p.Ala438Val) c.3875C>T (p.Ala1292Val) c.4640C>T (p.Ala1547Val) c.4829C>T (p.Ala1610Val) c.4622C>T (p.Ala1541Val) c.1325C>T (p.Ala442Val) c.1370C>T (p.Ala457Val) c.4826C>T (p.Ala1609Val) c.1150C>T c.1337C>T (p.Ala446Val) c.*4546C>T (n.*4546C>T) c.1076C>T (p.Ala359Val) c.5-7200C>T (n.5-7200C>T) c.236C>T (p.Ala79Val) c.-98-20961C>T (n.-98-20961C>T) n.4899C>T n.4940C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071151G>C | CA10591982 | BRCA1 | c.4760C>G (p.Ala1587Gly) c.4763C>G (p.Ala1588Gly) c.4637C>G (p.Ala1546Gly) c.4757C>G (p.Ala1586Gly) c.4685C>G (p.Ala1562Gly) c.1451C>G (p.Ala484Gly) c.1313C>G (p.Ala438Gly) c.3875C>G (p.Ala1292Gly) c.4640C>G (p.Ala1547Gly) c.4829C>G (p.Ala1610Gly) c.4622C>G (p.Ala1541Gly) c.1325C>G (p.Ala442Gly) c.1370C>G (p.Ala457Gly) c.4826C>G (p.Ala1609Gly) c.1150C>G c.1337C>G (p.Ala446Gly) c.*4546C>G (n.*4546C>G) c.1076C>G (p.Ala359Gly) c.5-7200C>G (n.5-7200C>G) c.236C>G (p.Ala79Gly) c.-98-20961C>G (n.-98-20961C>G) n.4899C>G n.4940C>G | dbSNP |
17 | g.43071151G= | CA2260772963 | BRCA1 | c.4760C= (p.Ala1587=) c.4763C= (p.Ala1588=) c.4637C= (p.Ala1546=) c.4757C= (p.Ala1586=) c.4685C= (p.Ala1562=) c.1451C= (p.Ala484=) c.1313C= (p.Ala438=) c.3875C= (p.Ala1292=) c.4640C= (p.Ala1547=) c.4829C= (p.Ala1610=) c.4622C= (p.Ala1541=) c.1325C= (p.Ala442=) c.1370C= (p.Ala457=) c.4826C= (p.Ala1609=) c.1150C= c.1337C= (p.Ala446=) c.*4546C= (n.*4546C=) c.1076C= (p.Ala359=) c.5-7200C= (n.5-7200C=) c.236C= (p.Ala79=) c.-98-20961C= (n.-98-20961C=) n.4899C= n.4940C= | |
17 | g.43071151G>T | CA10591983 | BRCA1 | c.4760C>A (p.Ala1587Asp) c.4763C>A (p.Ala1588Asp) c.4637C>A (p.Ala1546Asp) c.4757C>A (p.Ala1586Asp) c.4685C>A (p.Ala1562Asp) c.1451C>A (p.Ala484Asp) c.1313C>A (p.Ala438Asp) c.3875C>A (p.Ala1292Asp) c.4640C>A (p.Ala1547Asp) c.4829C>A (p.Ala1610Asp) c.4622C>A (p.Ala1541Asp) c.1325C>A (p.Ala442Asp) c.1370C>A (p.Ala457Asp) c.4826C>A (p.Ala1609Asp) c.1150C>A c.1337C>A (p.Ala446Asp) c.*4546C>A (n.*4546C>A) c.1076C>A (p.Ala359Asp) c.5-7200C>A (n.5-7200C>A) c.236C>A (p.Ala79Asp) c.-98-20961C>A (n.-98-20961C>A) n.4899C>A n.4940C>A | dbSNP |
17 | g.43071152C>A | CA10591984 | BRCA1 | c.4759G>T (p.Ala1587Ser) c.4762G>T (p.Ala1588Ser) c.4636G>T (p.Ala1546Ser) c.4756G>T (p.Ala1586Ser) c.4684G>T (p.Ala1562Ser) c.1450G>T (p.Ala484Ser) c.1312G>T (p.Ala438Ser) c.3874G>T (p.Ala1292Ser) c.4639G>T (p.Ala1547Ser) c.4828G>T (p.Ala1610Ser) c.4621G>T (p.Ala1541Ser) c.1324G>T (p.Ala442Ser) c.1369G>T (p.Ala457Ser) c.4825G>T (p.Ala1609Ser) c.1149G>T c.1336G>T (p.Ala446Ser) c.*4545G>T (n.*4545G>T) c.1075G>T (p.Ala359Ser) c.5-7201G>T (n.5-7201G>T) c.235G>T (p.Ala79Ser) c.-98-20962G>T (n.-98-20962G>T) n.4898G>T n.4939G>T | dbSNP |
17 | g.43071152C>G | CA10591985 | BRCA1 | c.4759G>C (p.Ala1587Pro) c.4762G>C (p.Ala1588Pro) c.4636G>C (p.Ala1546Pro) c.4756G>C (p.Ala1586Pro) c.4684G>C (p.Ala1562Pro) c.1450G>C (p.Ala484Pro) c.1312G>C (p.Ala438Pro) c.3874G>C (p.Ala1292Pro) c.4639G>C (p.Ala1547Pro) c.4828G>C (p.Ala1610Pro) c.4621G>C (p.Ala1541Pro) c.1324G>C (p.Ala442Pro) c.1369G>C (p.Ala457Pro) c.4825G>C (p.Ala1609Pro) c.1149G>C c.1336G>C (p.Ala446Pro) c.*4545G>C (n.*4545G>C) c.1075G>C (p.Ala359Pro) c.5-7201G>C (n.5-7201G>C) c.235G>C (p.Ala79Pro) c.-98-20962G>C (n.-98-20962G>C) n.4898G>C n.4939G>C | dbSNP |
17 | g.43071152C>T | CA10591986 | BRCA1 | c.4759G>A (p.Ala1587Thr) c.4762G>A (p.Ala1588Thr) c.4636G>A (p.Ala1546Thr) c.4756G>A (p.Ala1586Thr) c.4684G>A (p.Ala1562Thr) c.1450G>A (p.Ala484Thr) c.1312G>A (p.Ala438Thr) c.3874G>A (p.Ala1292Thr) c.4639G>A (p.Ala1547Thr) c.4828G>A (p.Ala1610Thr) c.4621G>A (p.Ala1541Thr) c.1324G>A (p.Ala442Thr) c.1369G>A (p.Ala457Thr) c.4825G>A (p.Ala1609Thr) c.1149G>A c.1336G>A (p.Ala446Thr) c.*4545G>A (n.*4545G>A) c.1075G>A (p.Ala359Thr) c.5-7201G>A (n.5-7201G>A) c.235G>A (p.Ala79Thr) c.-98-20962G>A (n.-98-20962G>A) n.4898G>A n.4939G>A | dbSNP |
17 | g.43071153T>A | CA500231857 | BRCA1 | c.4758A>T (p.Ser1586=) c.4761A>T (p.Ser1587=) c.4635A>T (p.Ser1545=) c.4755A>T (p.Ser1585=) c.4683A>T (p.Ser1561=) c.1449A>T (p.Ser483=) c.1311A>T (p.Ser437=) c.3873A>T (p.Ser1291=) c.4638A>T (p.Ser1546=) c.4827A>T (p.Ser1609=) c.4620A>T (p.Ser1540=) c.1323A>T (p.Ser441=) c.1368A>T (p.Ser456=) c.4824A>T (p.Ser1608=) c.1148A>T c.1335A>T (p.Ser445=) c.*4544A>T (n.*4544A>T) c.1074A>T (p.Ser358=) c.5-7202A>T (n.5-7202A>T) c.234A>T (p.Ser78=) c.-98-20963A>T (n.-98-20963A>T) n.4897A>T n.4938A>T | dbSNP |
17 | g.43071153T>C | CA500231858 | BRCA1 | c.4758A>G (p.Ser1586=) c.4761A>G (p.Ser1587=) c.4635A>G (p.Ser1545=) c.4755A>G (p.Ser1585=) c.4683A>G (p.Ser1561=) c.1449A>G (p.Ser483=) c.1311A>G (p.Ser437=) c.3873A>G (p.Ser1291=) c.4638A>G (p.Ser1546=) c.4827A>G (p.Ser1609=) c.4620A>G (p.Ser1540=) c.1323A>G (p.Ser441=) c.1368A>G (p.Ser456=) c.4824A>G (p.Ser1608=) c.1148A>G c.1335A>G (p.Ser445=) c.*4544A>G (n.*4544A>G) c.1074A>G (p.Ser358=) c.5-7202A>G (n.5-7202A>G) c.234A>G (p.Ser78=) c.-98-20963A>G (n.-98-20963A>G) n.4897A>G n.4938A>G | ClinVar dbSNP |
17 | g.43071153T>G | CA500231859 | BRCA1 | c.4758A>C (p.Ser1586=) c.4761A>C (p.Ser1587=) c.4635A>C (p.Ser1545=) c.4755A>C (p.Ser1585=) c.4683A>C (p.Ser1561=) c.1449A>C (p.Ser483=) c.1311A>C (p.Ser437=) c.3873A>C (p.Ser1291=) c.4638A>C (p.Ser1546=) c.4827A>C (p.Ser1609=) c.4620A>C (p.Ser1540=) c.1323A>C (p.Ser441=) c.1368A>C (p.Ser456=) c.4824A>C (p.Ser1608=) c.1148A>C c.1335A>C (p.Ser445=) c.*4544A>C (n.*4544A>C) c.1074A>C (p.Ser358=) c.5-7202A>C (n.5-7202A>C) c.234A>C (p.Ser78=) c.-98-20963A>C (n.-98-20963A>C) n.4897A>C n.4938A>C | |
17 | g.43071154G>A | CA10591987 | BRCA1 | c.4757C>T (p.Ser1586Leu) c.4760C>T (p.Ser1587Leu) c.4634C>T (p.Ser1545Leu) c.4754C>T (p.Ser1585Leu) c.4682C>T (p.Ser1561Leu) c.1448C>T (p.Ser483Leu) c.1310C>T (p.Ser437Leu) c.3872C>T (p.Ser1291Leu) c.4637C>T (p.Ser1546Leu) c.4826C>T (p.Ser1609Leu) c.4619C>T (p.Ser1540Leu) c.1322C>T (p.Ser441Leu) c.1367C>T (p.Ser456Leu) c.4823C>T (p.Ser1608Leu) c.1147C>T c.1334C>T (p.Ser445Leu) c.*4543C>T (n.*4543C>T) c.1073C>T (p.Ser358Leu) c.5-7203C>T (n.5-7203C>T) c.233C>T (p.Ser78Leu) c.-98-20964C>T (n.-98-20964C>T) n.4896C>T n.4937C>T | ClinVar dbSNP gnomAD v4 |
17 | g.43071154G>C | CA003008 | BRCA1 | c.4757C>G (p.Ser1586Ter) c.4760C>G (p.Ser1587Ter) c.4634C>G (p.Ser1545Ter) c.4754C>G (p.Ser1585Ter) c.4682C>G (p.Ser1561Ter) c.1448C>G (p.Ser483Ter) c.1310C>G (p.Ser437Ter) c.3872C>G (p.Ser1291Ter) c.4637C>G (p.Ser1546Ter) c.4826C>G (p.Ser1609Ter) c.4619C>G (p.Ser1540Ter) c.1322C>G (p.Ser441Ter) c.1367C>G (p.Ser456Ter) c.4823C>G (p.Ser1608Ter) c.1147C>G c.1334C>G (p.Ser445Ter) c.*4543C>G (n.*4543C>G) c.1073C>G (p.Ser358Ter) c.5-7203C>G (n.5-7203C>G) c.233C>G (p.Ser78Ter) c.-98-20964C>G (n.-98-20964C>G) n.4896C>G n.4937C>G | ClinVar dbSNP |
17 | g.43071154G= | CA2260772964 | BRCA1 | c.4757C= (p.Ser1586=) c.4760C= (p.Ser1587=) c.4634C= (p.Ser1545=) c.4754C= (p.Ser1585=) c.4682C= (p.Ser1561=) c.1448C= (p.Ser483=) c.1310C= (p.Ser437=) c.3872C= (p.Ser1291=) c.4637C= (p.Ser1546=) c.4826C= (p.Ser1609=) c.4619C= (p.Ser1540=) c.1322C= (p.Ser441=) c.1367C= (p.Ser456=) c.4823C= (p.Ser1608=) c.1147C= c.1334C= (p.Ser445=) c.*4543C= (n.*4543C=) c.1073C= (p.Ser358=) c.5-7203C= (n.5-7203C=) c.233C= (p.Ser78=) c.-98-20964C= (n.-98-20964C=) n.4896C= n.4937C= | |
17 | g.43071154G>T | CA10591988 | BRCA1 | c.4757C>A (p.Ser1586Ter) c.4760C>A (p.Ser1587Ter) c.4634C>A (p.Ser1545Ter) c.4754C>A (p.Ser1585Ter) c.4682C>A (p.Ser1561Ter) c.1448C>A (p.Ser483Ter) c.1310C>A (p.Ser437Ter) c.3872C>A (p.Ser1291Ter) c.4637C>A (p.Ser1546Ter) c.4826C>A (p.Ser1609Ter) c.4619C>A (p.Ser1540Ter) c.1322C>A (p.Ser441Ter) c.1367C>A (p.Ser456Ter) c.4823C>A (p.Ser1608Ter) c.1147C>A c.1334C>A (p.Ser445Ter) c.*4543C>A (n.*4543C>A) c.1073C>A (p.Ser358Ter) c.5-7203C>A (n.5-7203C>A) c.233C>A (p.Ser78Ter) c.-98-20964C>A (n.-98-20964C>A) n.4896C>A n.4937C>A | |
17 | g.43071154_43071155insT | CA658825008 | BRCA1 | c.4756_4757insA (p.Ser1586TyrfsTer?) c.4759_4760insA (p.Ser1587TyrfsTer?) c.4633_4634insA (p.Ser1545TyrfsTer?) c.4753_4754insA (p.Ser1585TyrfsTer?) c.4681_4682insA (p.Ser1561TyrfsTer?) c.1447_1448insA (p.Ser483TyrfsTer?) c.1309_1310insA (p.Ser437TyrfsTer?) c.3871_3872insA (p.Ser1291TyrfsTer?) c.4636_4637insA (p.Ser1546TyrfsTer?) c.4825_4826insA (p.Ser1609TyrfsTer?) c.4618_4619insA (p.Ser1540TyrfsTer?) c.1321_1322insA (p.Ser441TyrfsTer?) c.1366_1367insA (p.Ser456TyrfsTer?) c.4822_4823insA (p.Ser1608TyrfsTer?) c.1146_1147insA c.1333_1334insA (p.Ser445TyrfsTer?) c.*4542_*4543insA (n.*4542_*4543insA) c.1072_1073insA (p.Ser358TyrfsTer?) c.5-7204_5-7203insA (n.5-7204_5-7203insA) c.232_233insA (p.Ser78TyrfsTer?) c.-98-20965_-98-20964insA (n.-98-20965_-98-20964insA) n.4895_4896insA n.4936_4937insA | ClinVar dbSNP |
17 | g.43071155A= | CA2260772965 | BRCA1 | c.4756T= (p.Ser1586=) c.4759T= (p.Ser1587=) c.4633T= (p.Ser1545=) c.4753T= (p.Ser1585=) c.4681T= (p.Ser1561=) c.1447T= (p.Ser483=) c.1309T= (p.Ser437=) c.3871T= (p.Ser1291=) c.4636T= (p.Ser1546=) c.4825T= (p.Ser1609=) c.4618T= (p.Ser1540=) c.1321T= (p.Ser441=) c.1366T= (p.Ser456=) c.4822T= (p.Ser1608=) c.1146T= c.1333T= (p.Ser445=) c.*4542T= (n.*4542T=) c.1072T= (p.Ser358=) c.5-7204T= (n.5-7204T=) c.232T= (p.Ser78=) c.-98-20965T= (n.-98-20965T=) n.4895T= n.4936T= | |
17 | g.43071155A>C | CA10591989 | BRCA1 | c.4756T>G (p.Ser1586Ala) c.4759T>G (p.Ser1587Ala) c.4633T>G (p.Ser1545Ala) c.4753T>G (p.Ser1585Ala) c.4681T>G (p.Ser1561Ala) c.1447T>G (p.Ser483Ala) c.1309T>G (p.Ser437Ala) c.3871T>G (p.Ser1291Ala) c.4636T>G (p.Ser1546Ala) c.4825T>G (p.Ser1609Ala) c.4618T>G (p.Ser1540Ala) c.1321T>G (p.Ser441Ala) c.1366T>G (p.Ser456Ala) c.4822T>G (p.Ser1608Ala) c.1146T>G c.1333T>G (p.Ser445Ala) c.*4542T>G (n.*4542T>G) c.1072T>G (p.Ser358Ala) c.5-7204T>G (n.5-7204T>G) c.232T>G (p.Ser78Ala) c.-98-20965T>G (n.-98-20965T>G) n.4895T>G n.4936T>G | dbSNP |
17 | g.43071155A>G | CA10591990 | BRCA1 | c.4756T>C (p.Ser1586Pro) c.4759T>C (p.Ser1587Pro) c.4633T>C (p.Ser1545Pro) c.4753T>C (p.Ser1585Pro) c.4681T>C (p.Ser1561Pro) c.1447T>C (p.Ser483Pro) c.1309T>C (p.Ser437Pro) c.3871T>C (p.Ser1291Pro) c.4636T>C (p.Ser1546Pro) c.4825T>C (p.Ser1609Pro) c.4618T>C (p.Ser1540Pro) c.1321T>C (p.Ser441Pro) c.1366T>C (p.Ser456Pro) c.4822T>C (p.Ser1608Pro) c.1146T>C c.1333T>C (p.Ser445Pro) c.*4542T>C (n.*4542T>C) c.1072T>C (p.Ser358Pro) c.5-7204T>C (n.5-7204T>C) c.232T>C (p.Ser78Pro) c.-98-20965T>C (n.-98-20965T>C) n.4895T>C n.4936T>C | dbSNP gnomAD v4 COSMIC COSMIC |
17 | g.43071155A>T | CA10591991 | BRCA1 | c.4756T>A (p.Ser1586Thr) c.4759T>A (p.Ser1587Thr) c.4633T>A (p.Ser1545Thr) c.4753T>A (p.Ser1585Thr) c.4681T>A (p.Ser1561Thr) c.1447T>A (p.Ser483Thr) c.1309T>A (p.Ser437Thr) c.3871T>A (p.Ser1291Thr) c.4636T>A (p.Ser1546Thr) c.4825T>A (p.Ser1609Thr) c.4618T>A (p.Ser1540Thr) c.1321T>A (p.Ser441Thr) c.1366T>A (p.Ser456Thr) c.4822T>A (p.Ser1608Thr) c.1146T>A c.1333T>A (p.Ser445Thr) c.*4542T>A (n.*4542T>A) c.1072T>A (p.Ser358Thr) c.5-7204T>A (n.5-7204T>A) c.232T>A (p.Ser78Thr) c.-98-20965T>A (n.-98-20965T>A) n.4895T>A n.4936T>A | dbSNP |
17 | g.43071155_43071156insT | CA10589645 | BRCA1 | c.4755_4756insA (p.Ser1586IlefsTer?) c.4758_4759insA (p.Ser1587IlefsTer?) c.4632_4633insA (p.Ser1545IlefsTer?) c.4752_4753insA (p.Ser1585IlefsTer?) c.4680_4681insA (p.Ser1561IlefsTer?) c.1446_1447insA (p.Ser483IlefsTer?) c.1308_1309insA (p.Ser437IlefsTer?) c.3870_3871insA (p.Ser1291IlefsTer?) c.4635_4636insA (p.Ser1546IlefsTer?) c.4824_4825insA (p.Ser1609IlefsTer?) c.4617_4618insA (p.Ser1540IlefsTer?) c.1320_1321insA (p.Ser441IlefsTer?) c.1365_1366insA (p.Ser456IlefsTer?) c.4821_4822insA (p.Ser1608IlefsTer?) c.1145_1146insA c.1332_1333insA (p.Ser445IlefsTer?) c.*4541_*4542insA (n.*4541_*4542insA) c.1071_1072insA (p.Ser358IlefsTer?) c.5-7205_5-7204insA (n.5-7205_5-7204insA) c.231_232insA (p.Ser78IlefsTer?) c.-98-20966_-98-20965insA (n.-98-20966_-98-20965insA) n.4894_4895insA n.4935_4936insA | ClinVar dbSNP |
17 | g.43071156C>A | CA10591992 | BRCA1 | c.4755G>T (p.Glu1585Asp) c.4758G>T (p.Glu1586Asp) c.4632G>T (p.Glu1544Asp) c.4752G>T (p.Glu1584Asp) c.4680G>T (p.Glu1560Asp) c.1446G>T (p.Glu482Asp) c.1308G>T (p.Glu436Asp) c.3870G>T (p.Glu1290Asp) c.4635G>T (p.Glu1545Asp) c.4824G>T (p.Glu1608Asp) c.4617G>T (p.Glu1539Asp) c.1320G>T (p.Glu440Asp) c.1365G>T (p.Glu455Asp) c.4821G>T (p.Glu1607Asp) c.1145G>T c.1332G>T (p.Glu444Asp) c.*4541G>T (n.*4541G>T) c.1071G>T (p.Glu357Asp) c.5-7205G>T (n.5-7205G>T) c.231G>T (p.Glu77Asp) c.-98-20966G>T (n.-98-20966G>T) n.4894G>T n.4935G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071156C= | CA2260772966 | BRCA1 | c.4755G= (p.Glu1585=) c.4758G= (p.Glu1586=) c.4632G= (p.Glu1544=) c.4752G= (p.Glu1584=) c.4680G= (p.Glu1560=) c.1446G= (p.Glu482=) c.1308G= (p.Glu436=) c.3870G= (p.Glu1290=) c.4635G= (p.Glu1545=) c.4824G= (p.Glu1608=) c.4617G= (p.Glu1539=) c.1320G= (p.Glu440=) c.1365G= (p.Glu455=) c.4821G= (p.Glu1607=) c.1145G= c.1332G= (p.Glu444=) c.*4541G= (n.*4541G=) c.1071G= (p.Glu357=) c.5-7205G= (n.5-7205G=) c.231G= (p.Glu77=) c.-98-20966G= (n.-98-20966G=) n.4894G= n.4935G= | |
17 | g.43071156C>G | CA10591993 | BRCA1 | c.4755G>C (p.Glu1585Asp) c.4758G>C (p.Glu1586Asp) c.4632G>C (p.Glu1544Asp) c.4752G>C (p.Glu1584Asp) c.4680G>C (p.Glu1560Asp) c.1446G>C (p.Glu482Asp) c.1308G>C (p.Glu436Asp) c.3870G>C (p.Glu1290Asp) c.4635G>C (p.Glu1545Asp) c.4824G>C (p.Glu1608Asp) c.4617G>C (p.Glu1539Asp) c.1320G>C (p.Glu440Asp) c.1365G>C (p.Glu455Asp) c.4821G>C (p.Glu1607Asp) c.1145G>C c.1332G>C (p.Glu444Asp) c.*4541G>C (n.*4541G>C) c.1071G>C (p.Glu357Asp) c.5-7205G>C (n.5-7205G>C) c.231G>C (p.Glu77Asp) c.-98-20966G>C (n.-98-20966G>C) n.4894G>C n.4935G>C | dbSNP |
17 | g.43071156C>T | CA500231860 | BRCA1 | c.4755G>A (p.Glu1585=) c.4758G>A (p.Glu1586=) c.4632G>A (p.Glu1544=) c.4752G>A (p.Glu1584=) c.4680G>A (p.Glu1560=) c.1446G>A (p.Glu482=) c.1308G>A (p.Glu436=) c.3870G>A (p.Glu1290=) c.4635G>A (p.Glu1545=) c.4824G>A (p.Glu1608=) c.4617G>A (p.Glu1539=) c.1320G>A (p.Glu440=) c.1365G>A (p.Glu455=) c.4821G>A (p.Glu1607=) c.1145G>A c.1332G>A (p.Glu444=) c.*4541G>A (n.*4541G>A) c.1071G>A (p.Glu357=) c.5-7205G>A (n.5-7205G>A) c.231G>A (p.Glu77=) c.-98-20966G>A (n.-98-20966G>A) n.4894G>A n.4935G>A | |
17 | g.43071157T>A | CA10591994 | BRCA1 | c.4754A>T (p.Glu1585Val) c.4757A>T (p.Glu1586Val) c.4631A>T (p.Glu1544Val) c.4751A>T (p.Glu1584Val) c.4679A>T (p.Glu1560Val) c.1445A>T (p.Glu482Val) c.1307A>T (p.Glu436Val) c.3869A>T (p.Glu1290Val) c.4634A>T (p.Glu1545Val) c.4823A>T (p.Glu1608Val) c.4616A>T (p.Glu1539Val) c.1319A>T (p.Glu440Val) c.1364A>T (p.Glu455Val) c.4820A>T (p.Glu1607Val) c.1144A>T c.1331A>T (p.Glu444Val) c.*4540A>T (n.*4540A>T) c.1070A>T (p.Glu357Val) c.5-7206A>T (n.5-7206A>T) c.230A>T (p.Glu77Val) c.-98-20967A>T (n.-98-20967A>T) n.4893A>T n.4934A>T | ClinVar dbSNP |
17 | g.43071157T>C | CA10591995 | BRCA1 | c.4754A>G (p.Glu1585Gly) c.4757A>G (p.Glu1586Gly) c.4631A>G (p.Glu1544Gly) c.4751A>G (p.Glu1584Gly) c.4679A>G (p.Glu1560Gly) c.1445A>G (p.Glu482Gly) c.1307A>G (p.Glu436Gly) c.3869A>G (p.Glu1290Gly) c.4634A>G (p.Glu1545Gly) c.4823A>G (p.Glu1608Gly) c.4616A>G (p.Glu1539Gly) c.1319A>G (p.Glu440Gly) c.1364A>G (p.Glu455Gly) c.4820A>G (p.Glu1607Gly) c.1144A>G c.1331A>G (p.Glu444Gly) c.*4540A>G (n.*4540A>G) c.1070A>G (p.Glu357Gly) c.5-7206A>G (n.5-7206A>G) c.230A>G (p.Glu77Gly) c.-98-20967A>G (n.-98-20967A>G) n.4893A>G n.4934A>G | |
17 | g.43071157T>G | CA052929 | BRCA1 | c.4754A>C (p.Glu1585Ala) c.4757A>C (p.Glu1586Ala) c.4631A>C (p.Glu1544Ala) c.4751A>C (p.Glu1584Ala) c.4679A>C (p.Glu1560Ala) c.1445A>C (p.Glu482Ala) c.1307A>C (p.Glu436Ala) c.3869A>C (p.Glu1290Ala) c.4634A>C (p.Glu1545Ala) c.4823A>C (p.Glu1608Ala) c.4616A>C (p.Glu1539Ala) c.1319A>C (p.Glu440Ala) c.1364A>C (p.Glu455Ala) c.4820A>C (p.Glu1607Ala) c.1144A>C c.1331A>C (p.Glu444Ala) c.*4540A>C (n.*4540A>C) c.1070A>C (p.Glu357Ala) c.5-7206A>C (n.5-7206A>C) c.230A>C (p.Glu77Ala) c.-98-20967A>C (n.-98-20967A>C) n.4893A>C n.4934A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071157T= | CA2260772967 | BRCA1 | c.4754A= (p.Glu1585=) c.4757A= (p.Glu1586=) c.4631A= (p.Glu1544=) c.4751A= (p.Glu1584=) c.4679A= (p.Glu1560=) c.1445A= (p.Glu482=) c.1307A= (p.Glu436=) c.3869A= (p.Glu1290=) c.4634A= (p.Glu1545=) c.4823A= (p.Glu1608=) c.4616A= (p.Glu1539=) c.1319A= (p.Glu440=) c.1364A= (p.Glu455=) c.4820A= (p.Glu1607=) c.1144A= c.1331A= (p.Glu444=) c.*4540A= (n.*4540A=) c.1070A= (p.Glu357=) c.5-7206A= (n.5-7206A=) c.230A= (p.Glu77=) c.-98-20967A= (n.-98-20967A=) n.4893A= n.4934A= | |
17 | g.43071157dup | CA658761204 | BRCA1 | c.4754dup (p.Ser1586ValfsTer?) c.4757dup (p.Ser1587ValfsTer?) c.4631dup (p.Ser1545ValfsTer?) c.4751dup (p.Ser1585ValfsTer?) c.4679dup (p.Ser1561ValfsTer?) c.1445dup (p.Ser483ValfsTer?) c.1307dup (p.Ser437ValfsTer?) c.3869dup (p.Ser1291ValfsTer?) c.4634dup (p.Ser1546ValfsTer?) c.4823dup (p.Ser1609ValfsTer?) c.4616dup (p.Ser1540ValfsTer?) c.1319dup (p.Ser441ValfsTer?) c.1364dup (p.Ser456ValfsTer?) c.4820dup (p.Ser1608ValfsTer?) c.1144dup c.1331dup (p.Ser445ValfsTer?) c.*4540dup (n.*4540dup) c.1070dup (p.Ser358ValfsTer?) c.5-7206dup (n.5-7206dup) c.230dup (p.Ser78ValfsTer?) c.-98-20967dup (n.-98-20967dup) n.4893dup n.4934dup | |
17 | g.43071158C>A | CA10591996 | BRCA1 | c.4753G>T (p.Glu1585Ter) c.4756G>T (p.Glu1586Ter) c.4630G>T (p.Glu1544Ter) c.4750G>T (p.Glu1584Ter) c.4678G>T (p.Glu1560Ter) c.1444G>T (p.Glu482Ter) c.1306G>T (p.Glu436Ter) c.3868G>T (p.Glu1290Ter) c.4633G>T (p.Glu1545Ter) c.4822G>T (p.Glu1608Ter) c.4615G>T (p.Glu1539Ter) c.1318G>T (p.Glu440Ter) c.1363G>T (p.Glu455Ter) c.4819G>T (p.Glu1607Ter) c.1143G>T c.1330G>T (p.Glu444Ter) c.*4539G>T (n.*4539G>T) c.1069G>T (p.Glu357Ter) c.5-7207G>T (n.5-7207G>T) c.229G>T (p.Glu77Ter) c.-98-20968G>T (n.-98-20968G>T) n.4892G>T n.4933G>T | ClinVar dbSNP |
17 | g.43071158C= | CA2260772970 | BRCA1 | c.4753G= (p.Glu1585=) c.4756G= (p.Glu1586=) c.4630G= (p.Glu1544=) c.4750G= (p.Glu1584=) c.4678G= (p.Glu1560=) c.1444G= (p.Glu482=) c.1306G= (p.Glu436=) c.3868G= (p.Glu1290=) c.4633G= (p.Glu1545=) c.4822G= (p.Glu1608=) c.4615G= (p.Glu1539=) c.1318G= (p.Glu440=) c.1363G= (p.Glu455=) c.4819G= (p.Glu1607=) c.1143G= c.1330G= (p.Glu444=) c.*4539G= (n.*4539G=) c.1069G= (p.Glu357=) c.5-7207G= (n.5-7207G=) c.229G= (p.Glu77=) c.-98-20968G= (n.-98-20968G=) n.4892G= n.4933G= | |
17 | g.43071158C>G | CA10591997 | BRCA1 | c.4753G>C (p.Glu1585Gln) c.4756G>C (p.Glu1586Gln) c.4630G>C (p.Glu1544Gln) c.4750G>C (p.Glu1584Gln) c.4678G>C (p.Glu1560Gln) c.1444G>C (p.Glu482Gln) c.1306G>C (p.Glu436Gln) c.3868G>C (p.Glu1290Gln) c.4633G>C (p.Glu1545Gln) c.4822G>C (p.Glu1608Gln) c.4615G>C (p.Glu1539Gln) c.1318G>C (p.Glu440Gln) c.1363G>C (p.Glu455Gln) c.4819G>C (p.Glu1607Gln) c.1143G>C c.1330G>C (p.Glu444Gln) c.*4539G>C (n.*4539G>C) c.1069G>C (p.Glu357Gln) c.5-7207G>C (n.5-7207G>C) c.229G>C (p.Glu77Gln) c.-98-20968G>C (n.-98-20968G>C) n.4892G>C n.4933G>C | dbSNP |
17 | g.43071158C>T | CA10591998 | BRCA1 | c.4753G>A (p.Glu1585Lys) c.4756G>A (p.Glu1586Lys) c.4630G>A (p.Glu1544Lys) c.4750G>A (p.Glu1584Lys) c.4678G>A (p.Glu1560Lys) c.1444G>A (p.Glu482Lys) c.1306G>A (p.Glu436Lys) c.3868G>A (p.Glu1290Lys) c.4633G>A (p.Glu1545Lys) c.4822G>A (p.Glu1608Lys) c.4615G>A (p.Glu1539Lys) c.1318G>A (p.Glu440Lys) c.1363G>A (p.Glu455Lys) c.4819G>A (p.Glu1607Lys) c.1143G>A c.1330G>A (p.Glu444Lys) c.*4539G>A (n.*4539G>A) c.1069G>A (p.Glu357Lys) c.5-7207G>A (n.5-7207G>A) c.229G>A (p.Glu77Lys) c.-98-20968G>A (n.-98-20968G>A) n.4892G>A n.4933G>A | dbSNP |
17 | g.43071158_43071159delinsCT | CA2260772969 | BRCA1 | c.4752_4753delinsAG (p.Pro1584=) c.4755_4756delinsAG (p.Pro1585=) c.4629_4630delinsAG (p.Pro1543=) c.4749_4750delinsAG (p.Pro1583=) c.4677_4678delinsAG (p.Pro1559=) c.1443_1444delinsAG (p.Pro481=) c.1305_1306delinsAG (p.Pro435=) c.3867_3868delinsAG (p.Pro1289=) c.4632_4633delinsAG (p.Pro1544=) c.4821_4822delinsAG (p.Pro1607=) c.4614_4615delinsAG (p.Pro1538=) c.1317_1318delinsAG (p.Pro439=) c.1362_1363delinsAG (p.Pro454=) c.4818_4819delinsAG (p.Pro1606=) c.1142_1143delinsAG c.1329_1330delinsAG (p.Pro443=) c.*4538_*4539delinsAG (n.*4538_*4539delinsAG) c.1068_1069delinsAG (p.Pro356=) c.5-7208_5-7207delinsAG (n.5-7208_5-7207delinsAG) c.228_229delinsAG (p.Pro76=) c.-98-20969_-98-20968delinsAG (n.-98-20969_-98-20968delinsAG) n.4891_4892delinsAG n.4932_4933delinsAG | |
17 | g.43071158_43071160delinsCTG | CA2260772968 | BRCA1 | c.4751_4753delinsCAG (p.Pro1584=) c.4754_4756delinsCAG (p.Pro1585=) c.4628_4630delinsCAG (p.Pro1543=) c.4748_4750delinsCAG (p.Pro1583=) c.4676_4678delinsCAG (p.Pro1559=) c.1442_1444delinsCAG (p.Pro481=) c.1304_1306delinsCAG (p.Pro435=) c.3866_3868delinsCAG (p.Pro1289=) c.4631_4633delinsCAG (p.Pro1544=) c.4820_4822delinsCAG (p.Pro1607=) c.4613_4615delinsCAG (p.Pro1538=) c.1316_1318delinsCAG (p.Pro439=) c.1361_1363delinsCAG (p.Pro454=) c.4817_4819delinsCAG (p.Pro1606=) c.1141_1143delinsCAG c.1328_1330delinsCAG (p.Pro443=) c.*4537_*4539delinsCAG (n.*4537_*4539delinsCAG) c.1067_1069delinsCAG (p.Pro356=) c.5-7209_5-7207delinsCAG (n.5-7209_5-7207delinsCAG) c.227_229delinsCAG (p.Pro76=) c.-98-20970_-98-20968delinsCAG (n.-98-20970_-98-20968delinsCAG) n.4890_4892delinsCAG n.4931_4933delinsCAG | |
17 | g.43071159del | CA10575940 | BRCA1 | c.4752del (p.Glu1585SerfsTer15) c.4755del (p.Glu1586SerfsTer15) c.4629del (p.Glu1544SerfsTer15) c.4749del (p.Glu1584SerfsTer15) c.4677del (p.Glu1560SerfsTer15) c.1443del (p.Glu482SerfsTer15) c.1305del (p.Glu436SerfsTer15) c.3867del (p.Glu1290SerfsTer15) c.4632del (p.Glu1545SerfsTer15) c.4821del (p.Glu1608SerfsTer15) c.4614del (p.Glu1539SerfsTer15) c.1317del (p.Glu440SerfsTer15) c.1362del (p.Glu455SerfsTer15) c.4818del (p.Glu1607SerfsTer15) c.1142del c.1329del (p.Glu444SerfsTer15) c.*4538del (n.*4538del) c.1068del (p.Glu357SerfsTer15) c.5-7208del (n.5-7208del) c.228del (p.Glu77SerfsTer15) c.-98-20969del (n.-98-20969del) n.4891del n.4932del | ClinVar dbSNP |
17 | g.43071159T>A | CA500231861 | BRCA1 | c.4752A>T (p.Pro1584=) c.4755A>T (p.Pro1585=) c.4629A>T (p.Pro1543=) c.4749A>T (p.Pro1583=) c.4677A>T (p.Pro1559=) c.1443A>T (p.Pro481=) c.1305A>T (p.Pro435=) c.3867A>T (p.Pro1289=) c.4632A>T (p.Pro1544=) c.4821A>T (p.Pro1607=) c.4614A>T (p.Pro1538=) c.1317A>T (p.Pro439=) c.1362A>T (p.Pro454=) c.4818A>T (p.Pro1606=) c.1142A>T c.1329A>T (p.Pro443=) c.*4538A>T (n.*4538A>T) c.1068A>T (p.Pro356=) c.5-7208A>T (n.5-7208A>T) c.228A>T (p.Pro76=) c.-98-20969A>T (n.-98-20969A>T) n.4891A>T n.4932A>T | |
17 | g.43071159T>C | CA500231862 | BRCA1 | c.4752A>G (p.Pro1584=) c.4755A>G (p.Pro1585=) c.4629A>G (p.Pro1543=) c.4749A>G (p.Pro1583=) c.4677A>G (p.Pro1559=) c.1443A>G (p.Pro481=) c.1305A>G (p.Pro435=) c.3867A>G (p.Pro1289=) c.4632A>G (p.Pro1544=) c.4821A>G (p.Pro1607=) c.4614A>G (p.Pro1538=) c.1317A>G (p.Pro439=) c.1362A>G (p.Pro454=) c.4818A>G (p.Pro1606=) c.1142A>G c.1329A>G (p.Pro443=) c.*4538A>G (n.*4538A>G) c.1068A>G (p.Pro356=) c.5-7208A>G (n.5-7208A>G) c.228A>G (p.Pro76=) c.-98-20969A>G (n.-98-20969A>G) n.4891A>G n.4932A>G | |
17 | g.43071159T>G | CA500231863 | BRCA1 | c.4752A>C (p.Pro1584=) c.4755A>C (p.Pro1585=) c.4629A>C (p.Pro1543=) c.4749A>C (p.Pro1583=) c.4677A>C (p.Pro1559=) c.1443A>C (p.Pro481=) c.1305A>C (p.Pro435=) c.3867A>C (p.Pro1289=) c.4632A>C (p.Pro1544=) c.4821A>C (p.Pro1607=) c.4614A>C (p.Pro1538=) c.1317A>C (p.Pro439=) c.1362A>C (p.Pro454=) c.4818A>C (p.Pro1606=) c.1142A>C c.1329A>C (p.Pro443=) c.*4538A>C (n.*4538A>C) c.1068A>C (p.Pro356=) c.5-7208A>C (n.5-7208A>C) c.228A>C (p.Pro76=) c.-98-20969A>C (n.-98-20969A>C) n.4891A>C n.4932A>C | ClinVar dbSNP |
17 | g.43071159T= | CA2260772971 | BRCA1 | c.4752A= (p.Pro1584=) c.4755A= (p.Pro1585=) c.4629A= (p.Pro1543=) c.4749A= (p.Pro1583=) c.4677A= (p.Pro1559=) c.1443A= (p.Pro481=) c.1305A= (p.Pro435=) c.3867A= (p.Pro1289=) c.4632A= (p.Pro1544=) c.4821A= (p.Pro1607=) c.4614A= (p.Pro1538=) c.1317A= (p.Pro439=) c.1362A= (p.Pro454=) c.4818A= (p.Pro1606=) c.1142A= c.1329A= (p.Pro443=) c.*4538A= (n.*4538A=) c.1068A= (p.Pro356=) c.5-7208A= (n.5-7208A=) c.228A= (p.Pro76=) c.-98-20969A= (n.-98-20969A=) n.4891A= n.4932A= | |
17 | g.43071159_43071160del | CA003007 | BRCA1 | c.4751_4752del (p.Pro1584ArgfsTer?) c.4754_4755del (p.Pro1585ArgfsTer?) c.4628_4629del (p.Pro1543ArgfsTer?) c.4748_4749del (p.Pro1583ArgfsTer?) c.4676_4677del (p.Pro1559ArgfsTer?) c.1442_1443del (p.Pro481ArgfsTer?) c.1304_1305del (p.Pro435ArgfsTer?) c.3866_3867del (p.Pro1289ArgfsTer?) c.4631_4632del (p.Pro1544ArgfsTer?) c.4820_4821del (p.Pro1607ArgfsTer?) c.4613_4614del (p.Pro1538ArgfsTer?) c.1316_1317del (p.Pro439ArgfsTer?) c.1361_1362del (p.Pro454ArgfsTer?) c.4817_4818del (p.Pro1606ArgfsTer?) c.1141_1142del c.1328_1329del (p.Pro443ArgfsTer?) c.*4537_*4538del (n.*4537_*4538del) c.1067_1068del (p.Pro356ArgfsTer?) c.5-7209_5-7208del (n.5-7209_5-7208del) c.227_228del (p.Pro76ArgfsTer?) c.-98-20970_-98-20969del (n.-98-20970_-98-20969del) n.4890_4891del n.4931_4932del | ClinVar dbSNP |
17 | g.43071160G>A | CA10591999 | BRCA1 | c.4751C>T (p.Pro1584Leu) c.4754C>T (p.Pro1585Leu) c.4628C>T (p.Pro1543Leu) c.4748C>T (p.Pro1583Leu) c.4676C>T (p.Pro1559Leu) c.1442C>T (p.Pro481Leu) c.1304C>T (p.Pro435Leu) c.3866C>T (p.Pro1289Leu) c.4631C>T (p.Pro1544Leu) c.4820C>T (p.Pro1607Leu) c.4613C>T (p.Pro1538Leu) c.1316C>T (p.Pro439Leu) c.1361C>T (p.Pro454Leu) c.4817C>T (p.Pro1606Leu) c.1141C>T c.1328C>T (p.Pro443Leu) c.*4537C>T (n.*4537C>T) c.1067C>T (p.Pro356Leu) c.5-7209C>T (n.5-7209C>T) c.227C>T (p.Pro76Leu) c.-98-20970C>T (n.-98-20970C>T) n.4890C>T n.4931C>T | ClinVar dbSNP |
17 | g.43071160G>C | CA10592000 | BRCA1 | c.4751C>G (p.Pro1584Arg) c.4754C>G (p.Pro1585Arg) c.4628C>G (p.Pro1543Arg) c.4748C>G (p.Pro1583Arg) c.4676C>G (p.Pro1559Arg) c.1442C>G (p.Pro481Arg) c.1304C>G (p.Pro435Arg) c.3866C>G (p.Pro1289Arg) c.4631C>G (p.Pro1544Arg) c.4820C>G (p.Pro1607Arg) c.4613C>G (p.Pro1538Arg) c.1316C>G (p.Pro439Arg) c.1361C>G (p.Pro454Arg) c.4817C>G (p.Pro1606Arg) c.1141C>G c.1328C>G (p.Pro443Arg) c.*4537C>G (n.*4537C>G) c.1067C>G (p.Pro356Arg) c.5-7209C>G (n.5-7209C>G) c.227C>G (p.Pro76Arg) c.-98-20970C>G (n.-98-20970C>G) n.4890C>G n.4931C>G | dbSNP |
17 | g.43071160G>T | CA10592001 | BRCA1 | c.4751C>A (p.Pro1584Gln) c.4754C>A (p.Pro1585Gln) c.4628C>A (p.Pro1543Gln) c.4748C>A (p.Pro1583Gln) c.4676C>A (p.Pro1559Gln) c.1442C>A (p.Pro481Gln) c.1304C>A (p.Pro435Gln) c.3866C>A (p.Pro1289Gln) c.4631C>A (p.Pro1544Gln) c.4820C>A (p.Pro1607Gln) c.4613C>A (p.Pro1538Gln) c.1316C>A (p.Pro439Gln) c.1361C>A (p.Pro454Gln) c.4817C>A (p.Pro1606Gln) c.1141C>A c.1328C>A (p.Pro443Gln) c.*4537C>A (n.*4537C>A) c.1067C>A (p.Pro356Gln) c.5-7209C>A (n.5-7209C>A) c.227C>A (p.Pro76Gln) c.-98-20970C>A (n.-98-20970C>A) n.4890C>A n.4931C>A | |
17 | g.43071163dup | CA915950112 | BRCA1 | c.4751dup (p.Glu1585ArgfsTer?) c.4754dup (p.Glu1586ArgfsTer?) c.4628dup (p.Glu1544ArgfsTer?) c.4748dup (p.Glu1584ArgfsTer?) c.4676dup (p.Glu1560ArgfsTer?) c.1442dup (p.Glu482ArgfsTer?) c.1304dup (p.Glu436ArgfsTer?) c.3866dup (p.Glu1290ArgfsTer?) c.4631dup (p.Glu1545ArgfsTer?) c.4820dup (p.Glu1608ArgfsTer?) c.4613dup (p.Glu1539ArgfsTer?) c.1316dup (p.Glu440ArgfsTer?) c.1361dup (p.Glu455ArgfsTer?) c.4817dup (p.Glu1607ArgfsTer?) c.1141dup c.1328dup (p.Glu444ArgfsTer?) c.*4537dup (n.*4537dup) c.1067dup (p.Glu357ArgfsTer?) c.5-7209dup (n.5-7209dup) c.227dup (p.Glu77ArgfsTer?) c.-98-20970dup (n.-98-20970dup) n.4890dup n.4931dup | ClinVar dbSNP |
17 | g.43071161G>A | CA10592002 | BRCA1 | c.4750C>T (p.Pro1584Ser) c.4753C>T (p.Pro1585Ser) c.4627C>T (p.Pro1543Ser) c.4747C>T (p.Pro1583Ser) c.4675C>T (p.Pro1559Ser) c.1441C>T (p.Pro481Ser) c.1303C>T (p.Pro435Ser) c.3865C>T (p.Pro1289Ser) c.4630C>T (p.Pro1544Ser) c.4819C>T (p.Pro1607Ser) c.4612C>T (p.Pro1538Ser) c.1315C>T (p.Pro439Ser) c.1360C>T (p.Pro454Ser) c.4816C>T (p.Pro1606Ser) c.1140C>T c.1327C>T (p.Pro443Ser) c.*4536C>T (n.*4536C>T) c.1066C>T (p.Pro356Ser) c.5-7210C>T (n.5-7210C>T) c.226C>T (p.Pro76Ser) c.-98-20971C>T (n.-98-20971C>T) n.4889C>T n.4930C>T | ClinVar dbSNP gnomAD v4 |
17 | g.43071161G>C | CA10592003 | BRCA1 | c.4750C>G (p.Pro1584Ala) c.4753C>G (p.Pro1585Ala) c.4627C>G (p.Pro1543Ala) c.4747C>G (p.Pro1583Ala) c.4675C>G (p.Pro1559Ala) c.1441C>G (p.Pro481Ala) c.1303C>G (p.Pro435Ala) c.3865C>G (p.Pro1289Ala) c.4630C>G (p.Pro1544Ala) c.4819C>G (p.Pro1607Ala) c.4612C>G (p.Pro1538Ala) c.1315C>G (p.Pro439Ala) c.1360C>G (p.Pro454Ala) c.4816C>G (p.Pro1606Ala) c.1140C>G c.1327C>G (p.Pro443Ala) c.*4536C>G (n.*4536C>G) c.1066C>G (p.Pro356Ala) c.5-7210C>G (n.5-7210C>G) c.226C>G (p.Pro76Ala) c.-98-20971C>G (n.-98-20971C>G) n.4889C>G n.4930C>G | ClinVar dbSNP |
17 | g.43071161G= | CA2260772972 | BRCA1 | c.4750C= (p.Pro1584=) c.4753C= (p.Pro1585=) c.4627C= (p.Pro1543=) c.4747C= (p.Pro1583=) c.4675C= (p.Pro1559=) c.1441C= (p.Pro481=) c.1303C= (p.Pro435=) c.3865C= (p.Pro1289=) c.4630C= (p.Pro1544=) c.4819C= (p.Pro1607=) c.4612C= (p.Pro1538=) c.1315C= (p.Pro439=) c.1360C= (p.Pro454=) c.4816C= (p.Pro1606=) c.1140C= c.1327C= (p.Pro443=) c.*4536C= (n.*4536C=) c.1066C= (p.Pro356=) c.5-7210C= (n.5-7210C=) c.226C= (p.Pro76=) c.-98-20971C= (n.-98-20971C=) n.4889C= n.4930C= | |
17 | g.43071161G>T | CA10592004 | BRCA1 | c.4750C>A (p.Pro1584Thr) c.4753C>A (p.Pro1585Thr) c.4627C>A (p.Pro1543Thr) c.4747C>A (p.Pro1583Thr) c.4675C>A (p.Pro1559Thr) c.1441C>A (p.Pro481Thr) c.1303C>A (p.Pro435Thr) c.3865C>A (p.Pro1289Thr) c.4630C>A (p.Pro1544Thr) c.4819C>A (p.Pro1607Thr) c.4612C>A (p.Pro1538Thr) c.1315C>A (p.Pro439Thr) c.1360C>A (p.Pro454Thr) c.4816C>A (p.Pro1606Thr) c.1140C>A c.1327C>A (p.Pro443Thr) c.*4536C>A (n.*4536C>A) c.1066C>A (p.Pro356Thr) c.5-7210C>A (n.5-7210C>A) c.226C>A (p.Pro76Thr) c.-98-20971C>A (n.-98-20971C>A) n.4889C>A n.4930C>A | dbSNP |
17 | g.43071162G>A | CA003006 | BRCA1 | c.4749C>T (p.Ala1583=) c.4752C>T (p.Ala1584=) c.4626C>T (p.Ala1542=) c.4746C>T (p.Ala1582=) c.4674C>T (p.Ala1558=) c.1440C>T (p.Ala480=) c.1302C>T (p.Ala434=) c.3864C>T (p.Ala1288=) c.4629C>T (p.Ala1543=) c.4818C>T (p.Ala1606=) c.4611C>T (p.Ala1537=) c.1314C>T (p.Ala438=) c.1359C>T (p.Ala453=) c.4815C>T (p.Ala1605=) c.1139C>T c.1326C>T (p.Ala442=) c.*4535C>T (n.*4535C>T) c.1065C>T (p.Ala355=) c.5-7211C>T (n.5-7211C>T) c.225C>T (p.Ala75=) c.-98-20972C>T (n.-98-20972C>T) n.4888C>T n.4929C>T | ClinVar dbSNP |
17 | g.43071162G>C | CA500231864 | BRCA1 | c.4749C>G (p.Ala1583=) c.4752C>G (p.Ala1584=) c.4626C>G (p.Ala1542=) c.4746C>G (p.Ala1582=) c.4674C>G (p.Ala1558=) c.1440C>G (p.Ala480=) c.1302C>G (p.Ala434=) c.3864C>G (p.Ala1288=) c.4629C>G (p.Ala1543=) c.4818C>G (p.Ala1606=) c.4611C>G (p.Ala1537=) c.1314C>G (p.Ala438=) c.1359C>G (p.Ala453=) c.4815C>G (p.Ala1605=) c.1139C>G c.1326C>G (p.Ala442=) c.*4535C>G (n.*4535C>G) c.1065C>G (p.Ala355=) c.5-7211C>G (n.5-7211C>G) c.225C>G (p.Ala75=) c.-98-20972C>G (n.-98-20972C>G) n.4888C>G n.4929C>G | dbSNP |
17 | g.43071162G= | CA2260772973 | BRCA1 | c.4749C= (p.Ala1583=) c.4752C= (p.Ala1584=) c.4626C= (p.Ala1542=) c.4746C= (p.Ala1582=) c.4674C= (p.Ala1558=) c.1440C= (p.Ala480=) c.1302C= (p.Ala434=) c.3864C= (p.Ala1288=) c.4629C= (p.Ala1543=) c.4818C= (p.Ala1606=) c.4611C= (p.Ala1537=) c.1314C= (p.Ala438=) c.1359C= (p.Ala453=) c.4815C= (p.Ala1605=) c.1139C= c.1326C= (p.Ala442=) c.*4535C= (n.*4535C=) c.1065C= (p.Ala355=) c.5-7211C= (n.5-7211C=) c.225C= (p.Ala75=) c.-98-20972C= (n.-98-20972C=) n.4888C= n.4929C= | |
17 | g.43071162G>T | CA500231865 | BRCA1 | c.4749C>A (p.Ala1583=) c.4752C>A (p.Ala1584=) c.4626C>A (p.Ala1542=) c.4746C>A (p.Ala1582=) c.4674C>A (p.Ala1558=) c.1440C>A (p.Ala480=) c.1302C>A (p.Ala434=) c.3864C>A (p.Ala1288=) c.4629C>A (p.Ala1543=) c.4818C>A (p.Ala1606=) c.4611C>A (p.Ala1537=) c.1314C>A (p.Ala438=) c.1359C>A (p.Ala453=) c.4815C>A (p.Ala1605=) c.1139C>A c.1326C>A (p.Ala442=) c.*4535C>A (n.*4535C>A) c.1065C>A (p.Ala355=) c.5-7211C>A (n.5-7211C>A) c.225C>A (p.Ala75=) c.-98-20972C>A (n.-98-20972C>A) n.4888C>A n.4929C>A | dbSNP |
17 | g.43071163G>A | CA10592005 | BRCA1 | c.4748C>T (p.Ala1583Val) c.4751C>T (p.Ala1584Val) c.4625C>T (p.Ala1542Val) c.4745C>T (p.Ala1582Val) c.4673C>T (p.Ala1558Val) c.1439C>T (p.Ala480Val) c.1301C>T (p.Ala434Val) c.3863C>T (p.Ala1288Val) c.4628C>T (p.Ala1543Val) c.4817C>T (p.Ala1606Val) c.4610C>T (p.Ala1537Val) c.1313C>T (p.Ala438Val) c.1358C>T (p.Ala453Val) c.4814C>T (p.Ala1605Val) c.1138C>T c.1325C>T (p.Ala442Val) c.*4534C>T (n.*4534C>T) c.1064C>T (p.Ala355Val) c.5-7212C>T (n.5-7212C>T) c.224C>T (p.Ala75Val) c.-98-20973C>T (n.-98-20973C>T) n.4887C>T n.4928C>T | ClinVar dbSNP |
17 | g.43071163G>C | CA10592006 | BRCA1 | c.4748C>G (p.Ala1583Gly) c.4751C>G (p.Ala1584Gly) c.4625C>G (p.Ala1542Gly) c.4745C>G (p.Ala1582Gly) c.4673C>G (p.Ala1558Gly) c.1439C>G (p.Ala480Gly) c.1301C>G (p.Ala434Gly) c.3863C>G (p.Ala1288Gly) c.4628C>G (p.Ala1543Gly) c.4817C>G (p.Ala1606Gly) c.4610C>G (p.Ala1537Gly) c.1313C>G (p.Ala438Gly) c.1358C>G (p.Ala453Gly) c.4814C>G (p.Ala1605Gly) c.1138C>G c.1325C>G (p.Ala442Gly) c.*4534C>G (n.*4534C>G) c.1064C>G (p.Ala355Gly) c.5-7212C>G (n.5-7212C>G) c.224C>G (p.Ala75Gly) c.-98-20973C>G (n.-98-20973C>G) n.4887C>G n.4928C>G | ClinVar dbSNP |
17 | g.43071163G= | CA2260772975 | BRCA1 | c.4748C= (p.Ala1583=) c.4751C= (p.Ala1584=) c.4625C= (p.Ala1542=) c.4745C= (p.Ala1582=) c.4673C= (p.Ala1558=) c.1439C= (p.Ala480=) c.1301C= (p.Ala434=) c.3863C= (p.Ala1288=) c.4628C= (p.Ala1543=) c.4817C= (p.Ala1606=) c.4610C= (p.Ala1537=) c.1313C= (p.Ala438=) c.1358C= (p.Ala453=) c.4814C= (p.Ala1605=) c.1138C= c.1325C= (p.Ala442=) c.*4534C= (n.*4534C=) c.1064C= (p.Ala355=) c.5-7212C= (n.5-7212C=) c.224C= (p.Ala75=) c.-98-20973C= (n.-98-20973C=) n.4887C= n.4928C= | |
17 | g.43071163G>T | CA10592007 | BRCA1 | c.4748C>A (p.Ala1583Asp) c.4751C>A (p.Ala1584Asp) c.4625C>A (p.Ala1542Asp) c.4745C>A (p.Ala1582Asp) c.4673C>A (p.Ala1558Asp) c.1439C>A (p.Ala480Asp) c.1301C>A (p.Ala434Asp) c.3863C>A (p.Ala1288Asp) c.4628C>A (p.Ala1543Asp) c.4817C>A (p.Ala1606Asp) c.4610C>A (p.Ala1537Asp) c.1313C>A (p.Ala438Asp) c.1358C>A (p.Ala453Asp) c.4814C>A (p.Ala1605Asp) c.1138C>A c.1325C>A (p.Ala442Asp) c.*4534C>A (n.*4534C>A) c.1064C>A (p.Ala355Asp) c.5-7212C>A (n.5-7212C>A) c.224C>A (p.Ala75Asp) c.-98-20973C>A (n.-98-20973C>A) n.4887C>A n.4928C>A | dbSNP |
17 | g.43071163_43071164delinsGC | CA2260772976 | BRCA1 | c.4747_4748delinsGC (p.Ala1583=) c.4750_4751delinsGC (p.Ala1584=) c.4624_4625delinsGC (p.Ala1542=) c.4744_4745delinsGC (p.Ala1582=) c.4672_4673delinsGC (p.Ala1558=) c.1438_1439delinsGC (p.Ala480=) c.1300_1301delinsGC (p.Ala434=) c.3862_3863delinsGC (p.Ala1288=) c.4627_4628delinsGC (p.Ala1543=) c.4816_4817delinsGC (p.Ala1606=) c.4609_4610delinsGC (p.Ala1537=) c.1312_1313delinsGC (p.Ala438=) c.1357_1358delinsGC (p.Ala453=) c.4813_4814delinsGC (p.Ala1605=) c.1137_1138delinsGC c.1324_1325delinsGC (p.Ala442=) c.*4533_*4534delinsGC (n.*4533_*4534delinsGC) c.1063_1064delinsGC (p.Ala355=) c.5-7213_5-7212delinsGC (n.5-7213_5-7212delinsGC) c.223_224delinsGC (p.Ala75=) c.-98-20974_-98-20973delinsGC (n.-98-20974_-98-20973delinsGC) n.4886_4887delinsGC n.4927_4928delinsGC | |
17 | g.43071163_43071165delinsGCT | CA2260772974 | BRCA1 | c.4746_4748delinsAGC (p.Arg1582=) c.4749_4751delinsAGC (p.Arg1583=) c.4623_4625delinsAGC (p.Arg1541=) c.4743_4745delinsAGC (p.Arg1581=) c.4671_4673delinsAGC (p.Arg1557=) c.1437_1439delinsAGC (p.Arg479=) c.1299_1301delinsAGC (p.Arg433=) c.3861_3863delinsAGC (p.Arg1287=) c.4626_4628delinsAGC (p.Arg1542=) c.4815_4817delinsAGC (p.Arg1605=) c.4608_4610delinsAGC (p.Arg1536=) c.1311_1313delinsAGC (p.Arg437=) c.1356_1358delinsAGC (p.Arg452=) c.4812_4814delinsAGC (p.Arg1604=) c.1136_1138delinsAGC c.1323_1325delinsAGC (p.Arg441=) c.*4532_*4534delinsAGC (n.*4532_*4534delinsAGC) c.1062_1064delinsAGC (p.Arg354=) c.5-7214_5-7212delinsAGC (n.5-7214_5-7212delinsAGC) c.222_224delinsAGC (p.Arg74=) c.-98-20975_-98-20973delinsAGC (n.-98-20975_-98-20973delinsAGC) n.4885_4887delinsAGC n.4926_4928delinsAGC | |
17 | g.43071164del | CA1139665582 | BRCA1 | c.4747del (p.Ala1583ProfsTer17) c.4750del (p.Ala1584ProfsTer17) c.4624del (p.Ala1542ProfsTer17) c.4744del (p.Ala1582ProfsTer17) c.4672del (p.Ala1558ProfsTer17) c.1438del (p.Ala480ProfsTer17) c.1300del (p.Ala434ProfsTer17) c.3862del (p.Ala1288ProfsTer17) c.4627del (p.Ala1543ProfsTer17) c.4816del (p.Ala1606ProfsTer17) c.4609del (p.Ala1537ProfsTer17) c.1312del (p.Ala438ProfsTer17) c.1357del (p.Ala453ProfsTer17) c.4813del (p.Ala1605ProfsTer17) c.1137del c.1324del (p.Ala442ProfsTer17) c.*4533del (n.*4533del) c.1063del (p.Ala355ProfsTer17) c.5-7213del (n.5-7213del) c.223del (p.Ala75ProfsTer17) c.-98-20974del (n.-98-20974del) n.4886del n.4927del | ClinVar dbSNP |
17 | g.43071164C>A | CA003005 | BRCA1 | c.4747G>T (p.Ala1583Ser) c.4750G>T (p.Ala1584Ser) c.4624G>T (p.Ala1542Ser) c.4744G>T (p.Ala1582Ser) c.4672G>T (p.Ala1558Ser) c.1438G>T (p.Ala480Ser) c.1300G>T (p.Ala434Ser) c.3862G>T (p.Ala1288Ser) c.4627G>T (p.Ala1543Ser) c.4816G>T (p.Ala1606Ser) c.4609G>T (p.Ala1537Ser) c.1312G>T (p.Ala438Ser) c.1357G>T (p.Ala453Ser) c.4813G>T (p.Ala1605Ser) c.1137G>T c.1324G>T (p.Ala442Ser) c.*4533G>T (n.*4533G>T) c.1063G>T (p.Ala355Ser) c.5-7213G>T (n.5-7213G>T) c.223G>T (p.Ala75Ser) c.-98-20974G>T (n.-98-20974G>T) n.4886G>T n.4927G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.43071164C= | CA2260772977 | BRCA1 | c.4747G= (p.Ala1583=) c.4750G= (p.Ala1584=) c.4624G= (p.Ala1542=) c.4744G= (p.Ala1582=) c.4672G= (p.Ala1558=) c.1438G= (p.Ala480=) c.1300G= (p.Ala434=) c.3862G= (p.Ala1288=) c.4627G= (p.Ala1543=) c.4816G= (p.Ala1606=) c.4609G= (p.Ala1537=) c.1312G= (p.Ala438=) c.1357G= (p.Ala453=) c.4813G= (p.Ala1605=) c.1137G= c.1324G= (p.Ala442=) c.*4533G= (n.*4533G=) c.1063G= (p.Ala355=) c.5-7213G= (n.5-7213G=) c.223G= (p.Ala75=) c.-98-20974G= (n.-98-20974G=) n.4886G= n.4927G= | |
17 | g.43071164C>G | CA10592008 | BRCA1 | c.4747G>C (p.Ala1583Pro) c.4750G>C (p.Ala1584Pro) c.4624G>C (p.Ala1542Pro) c.4744G>C (p.Ala1582Pro) c.4672G>C (p.Ala1558Pro) c.1438G>C (p.Ala480Pro) c.1300G>C (p.Ala434Pro) c.3862G>C (p.Ala1288Pro) c.4627G>C (p.Ala1543Pro) c.4816G>C (p.Ala1606Pro) c.4609G>C (p.Ala1537Pro) c.1312G>C (p.Ala438Pro) c.1357G>C (p.Ala453Pro) c.4813G>C (p.Ala1605Pro) c.1137G>C c.1324G>C (p.Ala442Pro) c.*4533G>C (n.*4533G>C) c.1063G>C (p.Ala355Pro) c.5-7213G>C (n.5-7213G>C) c.223G>C (p.Ala75Pro) c.-98-20974G>C (n.-98-20974G>C) n.4886G>C n.4927G>C | dbSNP |
17 | g.43071164C>T | CA10592009 | BRCA1 | c.4747G>A (p.Ala1583Thr) c.4750G>A (p.Ala1584Thr) c.4624G>A (p.Ala1542Thr) c.4744G>A (p.Ala1582Thr) c.4672G>A (p.Ala1558Thr) c.1438G>A (p.Ala480Thr) c.1300G>A (p.Ala434Thr) c.3862G>A (p.Ala1288Thr) c.4627G>A (p.Ala1543Thr) c.4816G>A (p.Ala1606Thr) c.4609G>A (p.Ala1537Thr) c.1312G>A (p.Ala438Thr) c.1357G>A (p.Ala453Thr) c.4813G>A (p.Ala1605Thr) c.1137G>A c.1324G>A (p.Ala442Thr) c.*4533G>A (n.*4533G>A) c.1063G>A (p.Ala355Thr) c.5-7213G>A (n.5-7213G>A) c.223G>A (p.Ala75Thr) c.-98-20974G>A (n.-98-20974G>A) n.4886G>A n.4927G>A | dbSNP |
17 | g.43071166_43071167del | CA003004 | BRCA1 | c.4746_4747del (p.Arg1582SerfsTer?) c.4749_4750del (p.Arg1583SerfsTer?) c.4623_4624del (p.Arg1541SerfsTer?) c.4743_4744del (p.Arg1581SerfsTer?) c.4671_4672del (p.Arg1557SerfsTer?) c.1437_1438del (p.Arg479SerfsTer?) c.1299_1300del (p.Arg433SerfsTer?) c.3861_3862del (p.Arg1287SerfsTer?) c.4626_4627del (p.Arg1542SerfsTer?) c.4815_4816del (p.Arg1605SerfsTer?) c.4608_4609del (p.Arg1536SerfsTer?) c.1311_1312del (p.Arg437SerfsTer?) c.1356_1357del (p.Arg452SerfsTer?) c.4812_4813del (p.Arg1604SerfsTer?) c.1136_1137del c.1323_1324del (p.Arg441SerfsTer?) c.*4532_*4533del (n.*4532_*4533del) c.1062_1063del (p.Arg354SerfsTer?) c.5-7214_5-7213del (n.5-7214_5-7213del) c.222_223del (p.Arg74SerfsTer?) c.-98-20975_-98-20974del (n.-98-20975_-98-20974del) n.4885_4886del n.4926_4927del | ClinVar dbSNP |
17 | g.43071165T>A | CA10592010 | BRCA1 | c.4746A>T (p.Arg1582Ser) c.4749A>T (p.Arg1583Ser) c.4623A>T (p.Arg1541Ser) c.4743A>T (p.Arg1581Ser) c.4671A>T (p.Arg1557Ser) c.1437A>T (p.Arg479Ser) c.1299A>T (p.Arg433Ser) c.3861A>T (p.Arg1287Ser) c.4626A>T (p.Arg1542Ser) c.4815A>T (p.Arg1605Ser) c.4608A>T (p.Arg1536Ser) c.1311A>T (p.Arg437Ser) c.1356A>T (p.Arg452Ser) c.4812A>T (p.Arg1604Ser) c.1136A>T c.1323A>T (p.Arg441Ser) c.*4532A>T (n.*4532A>T) c.1062A>T (p.Arg354Ser) c.5-7214A>T (n.5-7214A>T) c.222A>T (p.Arg74Ser) c.-98-20975A>T (n.-98-20975A>T) n.4885A>T n.4926A>T | ClinVar dbSNP |
17 | g.43071165T>C | CA500231866 | BRCA1 | c.4746A>G (p.Arg1582=) c.4749A>G (p.Arg1583=) c.4623A>G (p.Arg1541=) c.4743A>G (p.Arg1581=) c.4671A>G (p.Arg1557=) c.1437A>G (p.Arg479=) c.1299A>G (p.Arg433=) c.3861A>G (p.Arg1287=) c.4626A>G (p.Arg1542=) c.4815A>G (p.Arg1605=) c.4608A>G (p.Arg1536=) c.1311A>G (p.Arg437=) c.1356A>G (p.Arg452=) c.4812A>G (p.Arg1604=) c.1136A>G c.1323A>G (p.Arg441=) c.*4532A>G (n.*4532A>G) c.1062A>G (p.Arg354=) c.5-7214A>G (n.5-7214A>G) c.222A>G (p.Arg74=) c.-98-20975A>G (n.-98-20975A>G) n.4885A>G n.4926A>G | ClinVar dbSNP |
17 | g.43071165T>G | CA10592011 | BRCA1 | c.4746A>C (p.Arg1582Ser) c.4749A>C (p.Arg1583Ser) c.4623A>C (p.Arg1541Ser) c.4743A>C (p.Arg1581Ser) c.4671A>C (p.Arg1557Ser) c.1437A>C (p.Arg479Ser) c.1299A>C (p.Arg433Ser) c.3861A>C (p.Arg1287Ser) c.4626A>C (p.Arg1542Ser) c.4815A>C (p.Arg1605Ser) c.4608A>C (p.Arg1536Ser) c.1311A>C (p.Arg437Ser) c.1356A>C (p.Arg452Ser) c.4812A>C (p.Arg1604Ser) c.1136A>C c.1323A>C (p.Arg441Ser) c.*4532A>C (n.*4532A>C) c.1062A>C (p.Arg354Ser) c.5-7214A>C (n.5-7214A>C) c.222A>C (p.Arg74Ser) c.-98-20975A>C (n.-98-20975A>C) n.4885A>C n.4926A>C | |
17 | g.43071165T= | CA2260772978 | BRCA1 | c.4746A= (p.Arg1582=) c.4749A= (p.Arg1583=) c.4623A= (p.Arg1541=) c.4743A= (p.Arg1581=) c.4671A= (p.Arg1557=) c.1437A= (p.Arg479=) c.1299A= (p.Arg433=) c.3861A= (p.Arg1287=) c.4626A= (p.Arg1542=) c.4815A= (p.Arg1605=) c.4608A= (p.Arg1536=) c.1311A= (p.Arg437=) c.1356A= (p.Arg452=) c.4812A= (p.Arg1604=) c.1136A= c.1323A= (p.Arg441=) c.*4532A= (n.*4532A=) c.1062A= (p.Arg354=) c.5-7214A= (n.5-7214A=) c.222A= (p.Arg74=) c.-98-20975A= (n.-98-20975A=) n.4885A= n.4926A= | |
17 | g.43071166C>A | CA10592012 | BRCA1 | c.4745G>T (p.Arg1582Ile) c.4748G>T (p.Arg1583Ile) c.4622G>T (p.Arg1541Ile) c.4742G>T (p.Arg1581Ile) c.4670G>T (p.Arg1557Ile) c.1436G>T (p.Arg479Ile) c.1298G>T (p.Arg433Ile) c.3860G>T (p.Arg1287Ile) c.4625G>T (p.Arg1542Ile) c.4814G>T (p.Arg1605Ile) c.4607G>T (p.Arg1536Ile) c.1310G>T (p.Arg437Ile) c.1355G>T (p.Arg452Ile) c.4811G>T (p.Arg1604Ile) c.1135G>T c.1322G>T (p.Arg441Ile) c.*4531G>T (n.*4531G>T) c.1061G>T (p.Arg354Ile) c.5-7215G>T (n.5-7215G>T) c.221G>T (p.Arg74Ile) c.-98-20976G>T (n.-98-20976G>T) n.4884G>T n.4925G>T | dbSNP |
17 | g.43071166C= | CA2260772979 | BRCA1 | c.4745G= (p.Arg1582=) c.4748G= (p.Arg1583=) c.4622G= (p.Arg1541=) c.4742G= (p.Arg1581=) c.4670G= (p.Arg1557=) c.1436G= (p.Arg479=) c.1298G= (p.Arg433=) c.3860G= (p.Arg1287=) c.4625G= (p.Arg1542=) c.4814G= (p.Arg1605=) c.4607G= (p.Arg1536=) c.1310G= (p.Arg437=) c.1355G= (p.Arg452=) c.4811G= (p.Arg1604=) c.1135G= c.1322G= (p.Arg441=) c.*4531G= (n.*4531G=) c.1061G= (p.Arg354=) c.5-7215G= (n.5-7215G=) c.221G= (p.Arg74=) c.-98-20976G= (n.-98-20976G=) n.4884G= n.4925G= | |
17 | g.43071166C>G | CA10592013 | BRCA1 | c.4745G>C (p.Arg1582Thr) c.4748G>C (p.Arg1583Thr) c.4622G>C (p.Arg1541Thr) c.4742G>C (p.Arg1581Thr) c.4670G>C (p.Arg1557Thr) c.1436G>C (p.Arg479Thr) c.1298G>C (p.Arg433Thr) c.3860G>C (p.Arg1287Thr) c.4625G>C (p.Arg1542Thr) c.4814G>C (p.Arg1605Thr) c.4607G>C (p.Arg1536Thr) c.1310G>C (p.Arg437Thr) c.1355G>C (p.Arg452Thr) c.4811G>C (p.Arg1604Thr) c.1135G>C c.1322G>C (p.Arg441Thr) c.*4531G>C (n.*4531G>C) c.1061G>C (p.Arg354Thr) c.5-7215G>C (n.5-7215G>C) c.221G>C (p.Arg74Thr) c.-98-20976G>C (n.-98-20976G>C) n.4884G>C n.4925G>C | ClinVar dbSNP gnomAD v4 |
17 | g.43071166C>T | CA052895 | BRCA1 | c.4745G>A (p.Arg1582Lys) c.4748G>A (p.Arg1583Lys) c.4622G>A (p.Arg1541Lys) c.4742G>A (p.Arg1581Lys) c.4670G>A (p.Arg1557Lys) c.1436G>A (p.Arg479Lys) c.1298G>A (p.Arg433Lys) c.3860G>A (p.Arg1287Lys) c.4625G>A (p.Arg1542Lys) c.4814G>A (p.Arg1605Lys) c.4607G>A (p.Arg1536Lys) c.1310G>A (p.Arg437Lys) c.1355G>A (p.Arg452Lys) c.4811G>A (p.Arg1604Lys) c.1135G>A c.1322G>A (p.Arg441Lys) c.*4531G>A (n.*4531G>A) c.1061G>A (p.Arg354Lys) c.5-7215G>A (n.5-7215G>A) c.221G>A (p.Arg74Lys) c.-98-20976G>A (n.-98-20976G>A) n.4884G>A n.4925G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071167T>A | CA10592014 | BRCA1 | c.4744A>T (p.Arg1582Ter) c.4747A>T (p.Arg1583Ter) c.4621A>T (p.Arg1541Ter) c.4741A>T (p.Arg1581Ter) c.4669A>T (p.Arg1557Ter) c.1435A>T (p.Arg479Ter) c.1297A>T (p.Arg433Ter) c.3859A>T (p.Arg1287Ter) c.4624A>T (p.Arg1542Ter) c.4813A>T (p.Arg1605Ter) c.4606A>T (p.Arg1536Ter) c.1309A>T (p.Arg437Ter) c.1354A>T (p.Arg452Ter) c.4810A>T (p.Arg1604Ter) c.1134A>T c.1321A>T (p.Arg441Ter) c.*4530A>T (n.*4530A>T) c.1060A>T (p.Arg354Ter) c.5-7216A>T (n.5-7216A>T) c.220A>T (p.Arg74Ter) c.-98-20977A>T (n.-98-20977A>T) n.4883A>T n.4924A>T | dbSNP |
17 | g.43071167T>C | CA10592015 | BRCA1 | c.4744A>G (p.Arg1582Gly) c.4747A>G (p.Arg1583Gly) c.4621A>G (p.Arg1541Gly) c.4741A>G (p.Arg1581Gly) c.4669A>G (p.Arg1557Gly) c.1435A>G (p.Arg479Gly) c.1297A>G (p.Arg433Gly) c.3859A>G (p.Arg1287Gly) c.4624A>G (p.Arg1542Gly) c.4813A>G (p.Arg1605Gly) c.4606A>G (p.Arg1536Gly) c.1309A>G (p.Arg437Gly) c.1354A>G (p.Arg452Gly) c.4810A>G (p.Arg1604Gly) c.1134A>G c.1321A>G (p.Arg441Gly) c.*4530A>G (n.*4530A>G) c.1060A>G (p.Arg354Gly) c.5-7216A>G (n.5-7216A>G) c.220A>G (p.Arg74Gly) c.-98-20977A>G (n.-98-20977A>G) n.4883A>G n.4924A>G | ClinVar dbSNP |
17 | g.43071167T>G | CA500231867 | BRCA1 | c.4744A>C (p.Arg1582=) c.4747A>C (p.Arg1583=) c.4621A>C (p.Arg1541=) c.4741A>C (p.Arg1581=) c.4669A>C (p.Arg1557=) c.1435A>C (p.Arg479=) c.1297A>C (p.Arg433=) c.3859A>C (p.Arg1287=) c.4624A>C (p.Arg1542=) c.4813A>C (p.Arg1605=) c.4606A>C (p.Arg1536=) c.1309A>C (p.Arg437=) c.1354A>C (p.Arg452=) c.4810A>C (p.Arg1604=) c.1134A>C c.1321A>C (p.Arg441=) c.*4530A>C (n.*4530A>C) c.1060A>C (p.Arg354=) c.5-7216A>C (n.5-7216A>C) c.220A>C (p.Arg74=) c.-98-20977A>C (n.-98-20977A>C) n.4883A>C n.4924A>C | dbSNP |
17 | g.43071167T= | CA2260772980 | BRCA1 | c.4744A= (p.Arg1582=) c.4747A= (p.Arg1583=) c.4621A= (p.Arg1541=) c.4741A= (p.Arg1581=) c.4669A= (p.Arg1557=) c.1435A= (p.Arg479=) c.1297A= (p.Arg433=) c.3859A= (p.Arg1287=) c.4624A= (p.Arg1542=) c.4813A= (p.Arg1605=) c.4606A= (p.Arg1536=) c.1309A= (p.Arg437=) c.1354A= (p.Arg452=) c.4810A= (p.Arg1604=) c.1134A= c.1321A= (p.Arg441=) c.*4530A= (n.*4530A=) c.1060A= (p.Arg354=) c.5-7216A= (n.5-7216A=) c.220A= (p.Arg74=) c.-98-20977A= (n.-98-20977A=) n.4883A= n.4924A= | |
17 | g.43071168G>A | CA500231868 | BRCA1 | c.4743C>T (p.Asp1581=) c.4746C>T (p.Asp1582=) c.4620C>T (p.Asp1540=) c.4740C>T (p.Asp1580=) c.4668C>T (p.Asp1556=) c.1434C>T (p.Asp478=) c.1296C>T (p.Asp432=) c.3858C>T (p.Asp1286=) c.4623C>T (p.Asp1541=) c.4812C>T (p.Asp1604=) c.4605C>T (p.Asp1535=) c.1308C>T (p.Asp436=) c.1353C>T (p.Asp451=) c.4809C>T (p.Asp1603=) c.1133C>T c.1320C>T (p.Asp440=) c.*4529C>T (n.*4529C>T) c.1059C>T (p.Asp353=) c.5-7217C>T (n.5-7217C>T) c.219C>T (p.Asp73=) c.-98-20978C>T (n.-98-20978C>T) n.4882C>T n.4923C>T | ClinVar dbSNP gnomAD v2 |
17 | g.43071168G>C | CA10592016 | BRCA1 | c.4743C>G (p.Asp1581Glu) c.4746C>G (p.Asp1582Glu) c.4620C>G (p.Asp1540Glu) c.4740C>G (p.Asp1580Glu) c.4668C>G (p.Asp1556Glu) c.1434C>G (p.Asp478Glu) c.1296C>G (p.Asp432Glu) c.3858C>G (p.Asp1286Glu) c.4623C>G (p.Asp1541Glu) c.4812C>G (p.Asp1604Glu) c.4605C>G (p.Asp1535Glu) c.1308C>G (p.Asp436Glu) c.1353C>G (p.Asp451Glu) c.4809C>G (p.Asp1603Glu) c.1133C>G c.1320C>G (p.Asp440Glu) c.*4529C>G (n.*4529C>G) c.1059C>G (p.Asp353Glu) c.5-7217C>G (n.5-7217C>G) c.219C>G (p.Asp73Glu) c.-98-20978C>G (n.-98-20978C>G) n.4882C>G n.4923C>G | ClinVar dbSNP |
17 | g.43071168G>T | CA10592017 | BRCA1 | c.4743C>A (p.Asp1581Glu) c.4746C>A (p.Asp1582Glu) c.4620C>A (p.Asp1540Glu) c.4740C>A (p.Asp1580Glu) c.4668C>A (p.Asp1556Glu) c.1434C>A (p.Asp478Glu) c.1296C>A (p.Asp432Glu) c.3858C>A (p.Asp1286Glu) c.4623C>A (p.Asp1541Glu) c.4812C>A (p.Asp1604Glu) c.4605C>A (p.Asp1535Glu) c.1308C>A (p.Asp436Glu) c.1353C>A (p.Asp451Glu) c.4809C>A (p.Asp1603Glu) c.1133C>A c.1320C>A (p.Asp440Glu) c.*4529C>A (n.*4529C>A) c.1059C>A (p.Asp353Glu) c.5-7217C>A (n.5-7217C>A) c.219C>A (p.Asp73Glu) c.-98-20978C>A (n.-98-20978C>A) n.4882C>A n.4923C>A | COSMIC COSMIC |
17 | g.43071168_43071169delinsGT | CA2260772981 | BRCA1 | c.4742_4743delinsAC (p.Asp1581=) c.4745_4746delinsAC (p.Asp1582=) c.4619_4620delinsAC (p.Asp1540=) c.4739_4740delinsAC (p.Asp1580=) c.4667_4668delinsAC (p.Asp1556=) c.1433_1434delinsAC (p.Asp478=) c.1295_1296delinsAC (p.Asp432=) c.3857_3858delinsAC (p.Asp1286=) c.4622_4623delinsAC (p.Asp1541=) c.4811_4812delinsAC (p.Asp1604=) c.4604_4605delinsAC (p.Asp1535=) c.1307_1308delinsAC (p.Asp436=) c.1352_1353delinsAC (p.Asp451=) c.4808_4809delinsAC (p.Asp1603=) c.1132_1133delinsAC c.1319_1320delinsAC (p.Asp440=) c.*4528_*4529delinsAC (n.*4528_*4529delinsAC) c.1058_1059delinsAC (p.Asp353=) c.5-7218_5-7217delinsAC (n.5-7218_5-7217delinsAC) c.218_219delinsAC (p.Asp73=) c.-98-20979_-98-20978delinsAC (n.-98-20979_-98-20978delinsAC) n.4881_4882delinsAC n.4922_4923delinsAC | |
17 | g.43071169del | CA003003 | BRCA1 | c.4742del (p.Asp1581AlafsTer19) c.4745del (p.Asp1582AlafsTer19) c.4619del (p.Asp1540AlafsTer19) c.4739del (p.Asp1580AlafsTer19) c.4667del (p.Asp1556AlafsTer19) c.1433del (p.Asp478AlafsTer19) c.1295del (p.Asp432AlafsTer19) c.3857del (p.Asp1286AlafsTer19) c.4622del (p.Asp1541AlafsTer19) c.4811del (p.Asp1604AlafsTer19) c.4604del (p.Asp1535AlafsTer19) c.1307del (p.Asp436AlafsTer19) c.1352del (p.Asp451AlafsTer19) c.4808del (p.Asp1603AlafsTer19) c.1132del c.1319del (p.Asp440AlafsTer19) c.*4528del (n.*4528del) c.1058del (p.Asp353AlafsTer19) c.5-7218del (n.5-7218del) c.218del (p.Asp73AlafsTer19) c.-98-20979del (n.-98-20979del) n.4881del n.4922del | ClinVar dbSNP gnomAD v2 |
17 | g.43071169T>A | CA10592018 | BRCA1 | c.4742A>T (p.Asp1581Val) c.4745A>T (p.Asp1582Val) c.4619A>T (p.Asp1540Val) c.4739A>T (p.Asp1580Val) c.4667A>T (p.Asp1556Val) c.1433A>T (p.Asp478Val) c.1295A>T (p.Asp432Val) c.3857A>T (p.Asp1286Val) c.4622A>T (p.Asp1541Val) c.4811A>T (p.Asp1604Val) c.4604A>T (p.Asp1535Val) c.1307A>T (p.Asp436Val) c.1352A>T (p.Asp451Val) c.4808A>T (p.Asp1603Val) c.1132A>T c.1319A>T (p.Asp440Val) c.*4528A>T (n.*4528A>T) c.1058A>T (p.Asp353Val) c.5-7218A>T (n.5-7218A>T) c.218A>T (p.Asp73Val) c.-98-20979A>T (n.-98-20979A>T) n.4881A>T n.4922A>T | dbSNP |
17 | g.43071169T>C | CA10592019 | BRCA1 | c.4742A>G (p.Asp1581Gly) c.4745A>G (p.Asp1582Gly) c.4619A>G (p.Asp1540Gly) c.4739A>G (p.Asp1580Gly) c.4667A>G (p.Asp1556Gly) c.1433A>G (p.Asp478Gly) c.1295A>G (p.Asp432Gly) c.3857A>G (p.Asp1286Gly) c.4622A>G (p.Asp1541Gly) c.4811A>G (p.Asp1604Gly) c.4604A>G (p.Asp1535Gly) c.1307A>G (p.Asp436Gly) c.1352A>G (p.Asp451Gly) c.4808A>G (p.Asp1603Gly) c.1132A>G c.1319A>G (p.Asp440Gly) c.*4528A>G (n.*4528A>G) c.1058A>G (p.Asp353Gly) c.5-7218A>G (n.5-7218A>G) c.218A>G (p.Asp73Gly) c.-98-20979A>G (n.-98-20979A>G) n.4881A>G n.4922A>G | ClinVar |
17 | g.43071169T>G | CA10592020 | BRCA1 | c.4742A>C (p.Asp1581Ala) c.4745A>C (p.Asp1582Ala) c.4619A>C (p.Asp1540Ala) c.4739A>C (p.Asp1580Ala) c.4667A>C (p.Asp1556Ala) c.1433A>C (p.Asp478Ala) c.1295A>C (p.Asp432Ala) c.3857A>C (p.Asp1286Ala) c.4622A>C (p.Asp1541Ala) c.4811A>C (p.Asp1604Ala) c.4604A>C (p.Asp1535Ala) c.1307A>C (p.Asp436Ala) c.1352A>C (p.Asp451Ala) c.4808A>C (p.Asp1603Ala) c.1132A>C c.1319A>C (p.Asp440Ala) c.*4528A>C (n.*4528A>C) c.1058A>C (p.Asp353Ala) c.5-7218A>C (n.5-7218A>C) c.218A>C (p.Asp73Ala) c.-98-20979A>C (n.-98-20979A>C) n.4881A>C n.4922A>C | dbSNP |
17 | g.43071169T= | CA2581309321 | BRCA1 | c.4742A= (p.Asp1581=) c.4745A= (p.Asp1582=) c.4619A= (p.Asp1540=) c.4739A= (p.Asp1580=) c.4667A= (p.Asp1556=) c.1433A= (p.Asp478=) c.1295A= (p.Asp432=) c.3857A= (p.Asp1286=) c.4622A= (p.Asp1541=) c.4811A= (p.Asp1604=) c.4604A= (p.Asp1535=) c.1307A= (p.Asp436=) c.1352A= (p.Asp451=) c.4808A= (p.Asp1603=) c.1132A= c.1319A= (p.Asp440=) c.*4528A= (n.*4528A=) c.1058A= (p.Asp353=) c.5-7218A= (n.5-7218A=) c.218A= (p.Asp73=) c.-98-20979A= (n.-98-20979A=) n.4881A= n.4922A= | |
17 | g.43071170C>A | CA10592021 | BRCA1 | c.4741G>T (p.Asp1581Tyr) c.4744G>T (p.Asp1582Tyr) c.4618G>T (p.Asp1540Tyr) c.4738G>T (p.Asp1580Tyr) c.4666G>T (p.Asp1556Tyr) c.1432G>T (p.Asp478Tyr) c.1294G>T (p.Asp432Tyr) c.3856G>T (p.Asp1286Tyr) c.4621G>T (p.Asp1541Tyr) c.4810G>T (p.Asp1604Tyr) c.4603G>T (p.Asp1535Tyr) c.1306G>T (p.Asp436Tyr) c.1351G>T (p.Asp451Tyr) c.4807G>T (p.Asp1603Tyr) c.1131G>T c.1318G>T (p.Asp440Tyr) c.*4527G>T (n.*4527G>T) c.1057G>T (p.Asp353Tyr) c.5-7219G>T (n.5-7219G>T) c.217G>T (p.Asp73Tyr) c.-98-20980G>T (n.-98-20980G>T) n.4880G>T n.4921G>T | gnomAD v4 |
17 | g.43071170C>G | CA10592022 | BRCA1 | c.4741G>C (p.Asp1581His) c.4744G>C (p.Asp1582His) c.4618G>C (p.Asp1540His) c.4738G>C (p.Asp1580His) c.4666G>C (p.Asp1556His) c.1432G>C (p.Asp478His) c.1294G>C (p.Asp432His) c.3856G>C (p.Asp1286His) c.4621G>C (p.Asp1541His) c.4810G>C (p.Asp1604His) c.4603G>C (p.Asp1535His) c.1306G>C (p.Asp436His) c.1351G>C (p.Asp451His) c.4807G>C (p.Asp1603His) c.1131G>C c.1318G>C (p.Asp440His) c.*4527G>C (n.*4527G>C) c.1057G>C (p.Asp353His) c.5-7219G>C (n.5-7219G>C) c.217G>C (p.Asp73His) c.-98-20980G>C (n.-98-20980G>C) n.4880G>C n.4921G>C | dbSNP |
17 | g.43071170C>T | CA10592023 | BRCA1 | c.4741G>A (p.Asp1581Asn) c.4744G>A (p.Asp1582Asn) c.4618G>A (p.Asp1540Asn) c.4738G>A (p.Asp1580Asn) c.4666G>A (p.Asp1556Asn) c.1432G>A (p.Asp478Asn) c.1294G>A (p.Asp432Asn) c.3856G>A (p.Asp1286Asn) c.4621G>A (p.Asp1541Asn) c.4810G>A (p.Asp1604Asn) c.4603G>A (p.Asp1535Asn) c.1306G>A (p.Asp436Asn) c.1351G>A (p.Asp451Asn) c.4807G>A (p.Asp1603Asn) c.1131G>A c.1318G>A (p.Asp440Asn) c.*4527G>A (n.*4527G>A) c.1057G>A (p.Asp353Asn) c.5-7219G>A (n.5-7219G>A) c.217G>A (p.Asp73Asn) c.-98-20980G>A (n.-98-20980G>A) n.4880G>A n.4921G>A | ClinVar dbSNP |
17 | g.43071170delinsGG | CA2580094180 | BRCA1 | c.4741delinsCC (p.Asp1581ProfsTer?) c.4744delinsCC (p.Asp1582ProfsTer?) c.4618delinsCC (p.Asp1540ProfsTer?) c.4738delinsCC (p.Asp1580ProfsTer?) c.4666delinsCC (p.Asp1556ProfsTer?) c.1432delinsCC (p.Asp478ProfsTer?) c.1294delinsCC (p.Asp432ProfsTer?) c.3856delinsCC (p.Asp1286ProfsTer?) c.4621delinsCC (p.Asp1541ProfsTer?) c.4810delinsCC (p.Asp1604ProfsTer?) c.4603delinsCC (p.Asp1535ProfsTer?) c.1306delinsCC (p.Asp436ProfsTer?) c.1351delinsCC (p.Asp451ProfsTer?) c.4807delinsCC (p.Asp1603ProfsTer?) c.1131delinsCC c.1318delinsCC (p.Asp440ProfsTer?) c.*4527delinsCC (n.*4527delinsCC) c.1057delinsCC (p.Asp353ProfsTer?) c.5-7219delinsCC (n.5-7219delinsCC) c.217delinsCC (p.Asp73ProfsTer?) c.-98-20980delinsCC (n.-98-20980delinsCC) n.4880delinsCC n.4921delinsCC | ClinVar |
17 | g.43071170_43071171delinsCT | CA2260772982 | BRCA1 | c.4740_4741delinsAG (p.Glu1580=) c.4743_4744delinsAG (p.Glu1581=) c.4617_4618delinsAG (p.Glu1539=) c.4737_4738delinsAG (p.Glu1579=) c.4665_4666delinsAG (p.Glu1555=) c.1431_1432delinsAG (p.Glu477=) c.1293_1294delinsAG (p.Glu431=) c.3855_3856delinsAG (p.Glu1285=) c.4620_4621delinsAG (p.Glu1540=) c.4809_4810delinsAG (p.Glu1603=) c.4602_4603delinsAG (p.Glu1534=) c.1305_1306delinsAG (p.Glu435=) c.1350_1351delinsAG (p.Glu450=) c.4806_4807delinsAG (p.Glu1602=) c.1130_1131delinsAG c.1317_1318delinsAG (p.Glu439=) c.*4526_*4527delinsAG (n.*4526_*4527delinsAG) c.1056_1057delinsAG (p.Glu352=) c.5-7220_5-7219delinsAG (n.5-7220_5-7219delinsAG) c.216_217delinsAG (p.Glu72=) c.-98-20981_-98-20980delinsAG (n.-98-20981_-98-20980delinsAG) n.4879_4880delinsAG n.4920_4921delinsAG | |
17 | g.43071170_43071200del | CA2695225910 | BRCA1 | c.4711_4741del (p.Ser1571ThrfsTer19) c.4714_4744del (p.Ser1572ThrfsTer19) c.4588_4618del (p.Ser1530ThrfsTer19) c.4708_4738del (p.Ser1570ThrfsTer19) c.4636_4666del (p.Ser1546ThrfsTer19) c.1402_1432del (p.Ser468ThrfsTer19) c.1264_1294del (p.Ser422ThrfsTer19) c.3826_3856del (p.Ser1276ThrfsTer19) c.4591_4621del (p.Ser1531ThrfsTer19) c.4780_4810del (p.Ser1594ThrfsTer19) c.4573_4603del (p.Ser1525ThrfsTer19) c.1276_1306del (p.Ser426ThrfsTer19) c.1321_1351del (p.Ser441ThrfsTer19) c.4777_4807del (p.Ser1593ThrfsTer19) c.1101_1131del c.1288_1318del (p.Ser430ThrfsTer19) c.*4497_*4527del (n.*4497_*4527del) c.1027_1057del (p.Ser343ThrfsTer19) c.5-7249_5-7219del (n.5-7249_5-7219del) c.187_217del (p.Ser63ThrfsTer19) c.-98-21010_-98-20980del (n.-98-21010_-98-20980del) n.4850_4880del n.4891_4921del | |
17 | g.43071171T>A | CA10592024 | BRCA1 | c.4740A>T (p.Glu1580Asp) c.4743A>T (p.Glu1581Asp) c.4617A>T (p.Glu1539Asp) c.4737A>T (p.Glu1579Asp) c.4665A>T (p.Glu1555Asp) c.1431A>T (p.Glu477Asp) c.1293A>T (p.Glu431Asp) c.3855A>T (p.Glu1285Asp) c.4620A>T (p.Glu1540Asp) c.4809A>T (p.Glu1603Asp) c.4602A>T (p.Glu1534Asp) c.1305A>T (p.Glu435Asp) c.1350A>T (p.Glu450Asp) c.4806A>T (p.Glu1602Asp) c.1130A>T c.1317A>T (p.Glu439Asp) c.*4526A>T (n.*4526A>T) c.1056A>T (p.Glu352Asp) c.5-7220A>T (n.5-7220A>T) c.216A>T (p.Glu72Asp) c.-98-20981A>T (n.-98-20981A>T) n.4879A>T n.4920A>T | dbSNP |
17 | g.43071171T>C | CA003002 | BRCA1 | c.4740A>G (p.Glu1580=) c.4743A>G (p.Glu1581=) c.4617A>G (p.Glu1539=) c.4737A>G (p.Glu1579=) c.4665A>G (p.Glu1555=) c.1431A>G (p.Glu477=) c.1293A>G (p.Glu431=) c.3855A>G (p.Glu1285=) c.4620A>G (p.Glu1540=) c.4809A>G (p.Glu1603=) c.4602A>G (p.Glu1534=) c.1305A>G (p.Glu435=) c.1350A>G (p.Glu450=) c.4806A>G (p.Glu1602=) c.1130A>G c.1317A>G (p.Glu439=) c.*4526A>G (n.*4526A>G) c.1056A>G (p.Glu352=) c.5-7220A>G (n.5-7220A>G) c.216A>G (p.Glu72=) c.-98-20981A>G (n.-98-20981A>G) n.4879A>G n.4920A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071171T>G | CA003001 | BRCA1 | c.4740A>C (p.Glu1580Asp) c.4743A>C (p.Glu1581Asp) c.4617A>C (p.Glu1539Asp) c.4737A>C (p.Glu1579Asp) c.4665A>C (p.Glu1555Asp) c.1431A>C (p.Glu477Asp) c.1293A>C (p.Glu431Asp) c.3855A>C (p.Glu1285Asp) c.4620A>C (p.Glu1540Asp) c.4809A>C (p.Glu1603Asp) c.4602A>C (p.Glu1534Asp) c.1305A>C (p.Glu435Asp) c.1350A>C (p.Glu450Asp) c.4806A>C (p.Glu1602Asp) c.1130A>C c.1317A>C (p.Glu439Asp) c.*4526A>C (n.*4526A>C) c.1056A>C (p.Glu352Asp) c.5-7220A>C (n.5-7220A>C) c.216A>C (p.Glu72Asp) c.-98-20981A>C (n.-98-20981A>C) n.4879A>C n.4920A>C | ClinVar dbSNP |
17 | g.43071171T= | CA2260772983 | BRCA1 | c.4740A= (p.Glu1580=) c.4743A= (p.Glu1581=) c.4617A= (p.Glu1539=) c.4737A= (p.Glu1579=) c.4665A= (p.Glu1555=) c.1431A= (p.Glu477=) c.1293A= (p.Glu431=) c.3855A= (p.Glu1285=) c.4620A= (p.Glu1540=) c.4809A= (p.Glu1603=) c.4602A= (p.Glu1534=) c.1305A= (p.Glu435=) c.1350A= (p.Glu450=) c.4806A= (p.Glu1602=) c.1130A= c.1317A= (p.Glu439=) c.*4526A= (n.*4526A=) c.1056A= (p.Glu352=) c.5-7220A= (n.5-7220A=) c.216A= (p.Glu72=) c.-98-20981A= (n.-98-20981A=) n.4879A= n.4920A= | |
17 | g.43071172del | CA10589646 | BRCA1 | c.4740del (p.Asp1581ThrfsTer19) c.4743del (p.Asp1582ThrfsTer19) c.4617del (p.Asp1540ThrfsTer19) c.4737del (p.Asp1580ThrfsTer19) c.4665del (p.Asp1556ThrfsTer19) c.1431del (p.Asp478ThrfsTer19) c.1293del (p.Asp432ThrfsTer19) c.3855del (p.Asp1286ThrfsTer19) c.4620del (p.Asp1541ThrfsTer19) c.4809del (p.Asp1604ThrfsTer19) c.4602del (p.Asp1535ThrfsTer19) c.1305del (p.Asp436ThrfsTer19) c.1350del (p.Asp451ThrfsTer19) c.4806del (p.Asp1603ThrfsTer19) c.1130del c.1317del (p.Asp440ThrfsTer19) c.*4526del (n.*4526del) c.1056del (p.Asp353ThrfsTer19) c.5-7220del (n.5-7220del) c.216del (p.Asp73ThrfsTer19) c.-98-20981del (n.-98-20981del) n.4879del n.4920del | ClinVar dbSNP |
17 | g.43071172T>A | CA10592025 | BRCA1 | c.4739A>T (p.Glu1580Val) c.4742A>T (p.Glu1581Val) c.4616A>T (p.Glu1539Val) c.4736A>T (p.Glu1579Val) c.4664A>T (p.Glu1555Val) c.1430A>T (p.Glu477Val) c.1292A>T (p.Glu431Val) c.3854A>T (p.Glu1285Val) c.4619A>T (p.Glu1540Val) c.4808A>T (p.Glu1603Val) c.4601A>T (p.Glu1534Val) c.1304A>T (p.Glu435Val) c.1349A>T (p.Glu450Val) c.4805A>T (p.Glu1602Val) c.1129A>T c.1316A>T (p.Glu439Val) c.*4525A>T (n.*4525A>T) c.1055A>T (p.Glu352Val) c.5-7221A>T (n.5-7221A>T) c.215A>T (p.Glu72Val) c.-98-20982A>T (n.-98-20982A>T) n.4878A>T n.4919A>T | dbSNP |
17 | g.43071172T>C | CA10592026 | BRCA1 | c.4739A>G (p.Glu1580Gly) c.4742A>G (p.Glu1581Gly) c.4616A>G (p.Glu1539Gly) c.4736A>G (p.Glu1579Gly) c.4664A>G (p.Glu1555Gly) c.1430A>G (p.Glu477Gly) c.1292A>G (p.Glu431Gly) c.3854A>G (p.Glu1285Gly) c.4619A>G (p.Glu1540Gly) c.4808A>G (p.Glu1603Gly) c.4601A>G (p.Glu1534Gly) c.1304A>G (p.Glu435Gly) c.1349A>G (p.Glu450Gly) c.4805A>G (p.Glu1602Gly) c.1129A>G c.1316A>G (p.Glu439Gly) c.*4525A>G (n.*4525A>G) c.1055A>G (p.Glu352Gly) c.5-7221A>G (n.5-7221A>G) c.215A>G (p.Glu72Gly) c.-98-20982A>G (n.-98-20982A>G) n.4878A>G n.4919A>G | |
17 | g.43071172T>G | CA10592027 | BRCA1 | c.4739A>C (p.Glu1580Ala) c.4742A>C (p.Glu1581Ala) c.4616A>C (p.Glu1539Ala) c.4736A>C (p.Glu1579Ala) c.4664A>C (p.Glu1555Ala) c.1430A>C (p.Glu477Ala) c.1292A>C (p.Glu431Ala) c.3854A>C (p.Glu1285Ala) c.4619A>C (p.Glu1540Ala) c.4808A>C (p.Glu1603Ala) c.4601A>C (p.Glu1534Ala) c.1304A>C (p.Glu435Ala) c.1349A>C (p.Glu450Ala) c.4805A>C (p.Glu1602Ala) c.1129A>C c.1316A>C (p.Glu439Ala) c.*4525A>C (n.*4525A>C) c.1055A>C (p.Glu352Ala) c.5-7221A>C (n.5-7221A>C) c.215A>C (p.Glu72Ala) c.-98-20982A>C (n.-98-20982A>C) n.4878A>C n.4919A>C | |
17 | g.43071173C>A | CA003000 | BRCA1 | c.4738G>T (p.Glu1580Ter) c.4741G>T (p.Glu1581Ter) c.4615G>T (p.Glu1539Ter) c.4735G>T (p.Glu1579Ter) c.4663G>T (p.Glu1555Ter) c.1429G>T (p.Glu477Ter) c.1291G>T (p.Glu431Ter) c.3853G>T (p.Glu1285Ter) c.4618G>T (p.Glu1540Ter) c.4807G>T (p.Glu1603Ter) c.4600G>T (p.Glu1534Ter) c.1303G>T (p.Glu435Ter) c.1348G>T (p.Glu450Ter) c.4804G>T (p.Glu1602Ter) c.1128G>T c.1315G>T (p.Glu439Ter) c.*4524G>T (n.*4524G>T) c.1054G>T (p.Glu352Ter) c.5-7222G>T (n.5-7222G>T) c.214G>T (p.Glu72Ter) c.-98-20983G>T (n.-98-20983G>T) n.4877G>T n.4918G>T | ClinVar dbSNP |
17 | g.43071173C= | CA2260772984 | BRCA1 | c.4738G= (p.Glu1580=) c.4741G= (p.Glu1581=) c.4615G= (p.Glu1539=) c.4735G= (p.Glu1579=) c.4663G= (p.Glu1555=) c.1429G= (p.Glu477=) c.1291G= (p.Glu431=) c.3853G= (p.Glu1285=) c.4618G= (p.Glu1540=) c.4807G= (p.Glu1603=) c.4600G= (p.Glu1534=) c.1303G= (p.Glu435=) c.1348G= (p.Glu450=) c.4804G= (p.Glu1602=) c.1128G= c.1315G= (p.Glu439=) c.*4524G= (n.*4524G=) c.1054G= (p.Glu352=) c.5-7222G= (n.5-7222G=) c.214G= (p.Glu72=) c.-98-20983G= (n.-98-20983G=) n.4877G= n.4918G= | |
17 | g.43071173C>G | CA10592028 | BRCA1 | c.4738G>C (p.Glu1580Gln) c.4741G>C (p.Glu1581Gln) c.4615G>C (p.Glu1539Gln) c.4735G>C (p.Glu1579Gln) c.4663G>C (p.Glu1555Gln) c.1429G>C (p.Glu477Gln) c.1291G>C (p.Glu431Gln) c.3853G>C (p.Glu1285Gln) c.4618G>C (p.Glu1540Gln) c.4807G>C (p.Glu1603Gln) c.4600G>C (p.Glu1534Gln) c.1303G>C (p.Glu435Gln) c.1348G>C (p.Glu450Gln) c.4804G>C (p.Glu1602Gln) c.1128G>C c.1315G>C (p.Glu439Gln) c.*4524G>C (n.*4524G>C) c.1054G>C (p.Glu352Gln) c.5-7222G>C (n.5-7222G>C) c.214G>C (p.Glu72Gln) c.-98-20983G>C (n.-98-20983G>C) n.4877G>C n.4918G>C | ClinVar dbSNP gnomAD v4 |
17 | g.43071173C>T | CA10592029 | BRCA1 | c.4738G>A (p.Glu1580Lys) c.4741G>A (p.Glu1581Lys) c.4615G>A (p.Glu1539Lys) c.4735G>A (p.Glu1579Lys) c.4663G>A (p.Glu1555Lys) c.1429G>A (p.Glu477Lys) c.1291G>A (p.Glu431Lys) c.3853G>A (p.Glu1285Lys) c.4618G>A (p.Glu1540Lys) c.4807G>A (p.Glu1603Lys) c.4600G>A (p.Glu1534Lys) c.1303G>A (p.Glu435Lys) c.1348G>A (p.Glu450Lys) c.4804G>A (p.Glu1602Lys) c.1128G>A c.1315G>A (p.Glu439Lys) c.*4524G>A (n.*4524G>A) c.1054G>A (p.Glu352Lys) c.5-7222G>A (n.5-7222G>A) c.214G>A (p.Glu72Lys) c.-98-20983G>A (n.-98-20983G>A) n.4877G>A n.4918G>A | ClinVar dbSNP gnomAD v4 |
17 | g.43071174A= | CA2260772985 | BRCA1 | c.4737T= (p.Ser1579=) c.4740T= (p.Ser1580=) c.4614T= (p.Ser1538=) c.4734T= (p.Ser1578=) c.4662T= (p.Ser1554=) c.1428T= (p.Ser476=) c.1290T= (p.Ser430=) c.3852T= (p.Ser1284=) c.4617T= (p.Ser1539=) c.4806T= (p.Ser1602=) c.4599T= (p.Ser1533=) c.1302T= (p.Ser434=) c.1347T= (p.Ser449=) c.4803T= (p.Ser1601=) c.1127T= c.1314T= (p.Ser438=) c.*4523T= (n.*4523T=) c.1053T= (p.Ser351=) c.5-7223T= (n.5-7223T=) c.213T= (p.Ser71=) c.-98-20984T= (n.-98-20984T=) n.4876T= n.4917T= | |
17 | g.43071174A>C | CA500231869 | BRCA1 | c.4737T>G (p.Ser1579=) c.4740T>G (p.Ser1580=) c.4614T>G (p.Ser1538=) c.4734T>G (p.Ser1578=) c.4662T>G (p.Ser1554=) c.1428T>G (p.Ser476=) c.1290T>G (p.Ser430=) c.3852T>G (p.Ser1284=) c.4617T>G (p.Ser1539=) c.4806T>G (p.Ser1602=) c.4599T>G (p.Ser1533=) c.1302T>G (p.Ser434=) c.1347T>G (p.Ser449=) c.4803T>G (p.Ser1601=) c.1127T>G c.1314T>G (p.Ser438=) c.*4523T>G (n.*4523T>G) c.1053T>G (p.Ser351=) c.5-7223T>G (n.5-7223T>G) c.213T>G (p.Ser71=) c.-98-20984T>G (n.-98-20984T>G) n.4876T>G n.4917T>G | |
17 | g.43071174A>G | CA052880 | BRCA1 | c.4737T>C (p.Ser1579=) c.4740T>C (p.Ser1580=) c.4614T>C (p.Ser1538=) c.4734T>C (p.Ser1578=) c.4662T>C (p.Ser1554=) c.1428T>C (p.Ser476=) c.1290T>C (p.Ser430=) c.3852T>C (p.Ser1284=) c.4617T>C (p.Ser1539=) c.4806T>C (p.Ser1602=) c.4599T>C (p.Ser1533=) c.1302T>C (p.Ser434=) c.1347T>C (p.Ser449=) c.4803T>C (p.Ser1601=) c.1127T>C c.1314T>C (p.Ser438=) c.*4523T>C (n.*4523T>C) c.1053T>C (p.Ser351=) c.5-7223T>C (n.5-7223T>C) c.213T>C (p.Ser71=) c.-98-20984T>C (n.-98-20984T>C) n.4876T>C n.4917T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071174A>T | CA500231870 | BRCA1 | c.4737T>A (p.Ser1579=) c.4740T>A (p.Ser1580=) c.4614T>A (p.Ser1538=) c.4734T>A (p.Ser1578=) c.4662T>A (p.Ser1554=) c.1428T>A (p.Ser476=) c.1290T>A (p.Ser430=) c.3852T>A (p.Ser1284=) c.4617T>A (p.Ser1539=) c.4806T>A (p.Ser1602=) c.4599T>A (p.Ser1533=) c.1302T>A (p.Ser434=) c.1347T>A (p.Ser449=) c.4803T>A (p.Ser1601=) c.1127T>A c.1314T>A (p.Ser438=) c.*4523T>A (n.*4523T>A) c.1053T>A (p.Ser351=) c.5-7223T>A (n.5-7223T>A) c.213T>A (p.Ser71=) c.-98-20984T>A (n.-98-20984T>A) n.4876T>A n.4917T>A | dbSNP |
17 | g.43071174_43071178delinsAGAAG | CA2260772986 | BRCA1 | c.4733_4737delinsCTTCT (p.Pro1578=) c.4736_4740delinsCTTCT (p.Pro1579=) c.4610_4614delinsCTTCT (p.Pro1537=) c.4730_4734delinsCTTCT (p.Pro1577=) c.4658_4662delinsCTTCT (p.Pro1553=) c.1424_1428delinsCTTCT (p.Pro475=) c.1286_1290delinsCTTCT (p.Pro429=) c.3848_3852delinsCTTCT (p.Pro1283=) c.4613_4617delinsCTTCT (p.Pro1538=) c.4802_4806delinsCTTCT (p.Pro1601=) c.4595_4599delinsCTTCT (p.Pro1532=) c.1298_1302delinsCTTCT (p.Pro433=) c.1343_1347delinsCTTCT (p.Pro448=) c.4799_4803delinsCTTCT (p.Pro1600=) c.1123_1127delinsCTTCT c.1310_1314delinsCTTCT (p.Pro437=) c.*4519_*4523delinsCTTCT (n.*4519_*4523delinsCTTCT) c.1049_1053delinsCTTCT (p.Pro350=) c.5-7227_5-7223delinsCTTCT (n.5-7227_5-7223delinsCTTCT) c.209_213delinsCTTCT (p.Pro70=) c.-98-20988_-98-20984delinsCTTCT (n.-98-20988_-98-20984delinsCTTCT) n.4872_4876delinsCTTCT n.4913_4917delinsCTTCT | |
17 | g.43071176_43071206dup | CA2573154037 | BRCA1 | c.4707_4737dup (p.Glu1580LeufsTer3) c.4710_4740dup (p.Glu1581LeufsTer3) c.4584_4614dup (p.Glu1539LeufsTer3) c.4704_4734dup (p.Glu1579LeufsTer3) c.4632_4662dup (p.Glu1555LeufsTer3) c.1398_1428dup (p.Glu477LeufsTer3) c.1260_1290dup (p.Glu431LeufsTer3) c.3822_3852dup (p.Glu1285LeufsTer3) c.4587_4617dup (p.Glu1540LeufsTer3) c.4776_4806dup (p.Glu1603LeufsTer3) c.4569_4599dup (p.Glu1534LeufsTer3) c.1272_1302dup (p.Glu435LeufsTer3) c.1317_1347dup (p.Glu450LeufsTer3) c.4773_4803dup (p.Glu1602LeufsTer3) c.1097_1127dup c.1284_1314dup (p.Glu439LeufsTer3) c.*4493_*4523dup (n.*4493_*4523dup) c.1023_1053dup (p.Glu352LeufsTer3) c.5-7253_5-7223dup (n.5-7253_5-7223dup) c.183_213dup (p.Glu72LeufsTer3) c.-98-21014_-98-20984dup (n.-98-21014_-98-20984dup) n.4846_4876dup n.4887_4917dup | ClinVar dbSNP |
17 | g.43071175G>A | CA002999 | BRCA1 | c.4736C>T (p.Ser1579Phe) c.4739C>T (p.Ser1580Phe) c.4613C>T (p.Ser1538Phe) c.4733C>T (p.Ser1578Phe) c.4661C>T (p.Ser1554Phe) c.1427C>T (p.Ser476Phe) c.1289C>T (p.Ser430Phe) c.3851C>T (p.Ser1284Phe) c.4616C>T (p.Ser1539Phe) c.4805C>T (p.Ser1602Phe) c.4598C>T (p.Ser1533Phe) c.1301C>T (p.Ser434Phe) c.1346C>T (p.Ser449Phe) c.4802C>T (p.Ser1601Phe) c.1126C>T c.1313C>T (p.Ser438Phe) c.*4522C>T (n.*4522C>T) c.1052C>T (p.Ser351Phe) c.5-7224C>T (n.5-7224C>T) c.212C>T (p.Ser71Phe) c.-98-20985C>T (n.-98-20985C>T) n.4875C>T n.4916C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071175G>C | CA10592030 | BRCA1 | c.4736C>G (p.Ser1579Cys) c.4739C>G (p.Ser1580Cys) c.4613C>G (p.Ser1538Cys) c.4733C>G (p.Ser1578Cys) c.4661C>G (p.Ser1554Cys) c.1427C>G (p.Ser476Cys) c.1289C>G (p.Ser430Cys) c.3851C>G (p.Ser1284Cys) c.4616C>G (p.Ser1539Cys) c.4805C>G (p.Ser1602Cys) c.4598C>G (p.Ser1533Cys) c.1301C>G (p.Ser434Cys) c.1346C>G (p.Ser449Cys) c.4802C>G (p.Ser1601Cys) c.1126C>G c.1313C>G (p.Ser438Cys) c.*4522C>G (n.*4522C>G) c.1052C>G (p.Ser351Cys) c.5-7224C>G (n.5-7224C>G) c.212C>G (p.Ser71Cys) c.-98-20985C>G (n.-98-20985C>G) n.4875C>G n.4916C>G | dbSNP |
17 | g.43071175G= | CA2260772987 | BRCA1 | c.4736C= (p.Ser1579=) c.4739C= (p.Ser1580=) c.4613C= (p.Ser1538=) c.4733C= (p.Ser1578=) c.4661C= (p.Ser1554=) c.1427C= (p.Ser476=) c.1289C= (p.Ser430=) c.3851C= (p.Ser1284=) c.4616C= (p.Ser1539=) c.4805C= (p.Ser1602=) c.4598C= (p.Ser1533=) c.1301C= (p.Ser434=) c.1346C= (p.Ser449=) c.4802C= (p.Ser1601=) c.1126C= c.1313C= (p.Ser438=) c.*4522C= (n.*4522C=) c.1052C= (p.Ser351=) c.5-7224C= (n.5-7224C=) c.212C= (p.Ser71=) c.-98-20985C= (n.-98-20985C=) n.4875C= n.4916C= | |
17 | g.43071175G>T | CA10592031 | BRCA1 | c.4736C>A (p.Ser1579Tyr) c.4739C>A (p.Ser1580Tyr) c.4613C>A (p.Ser1538Tyr) c.4733C>A (p.Ser1578Tyr) c.4661C>A (p.Ser1554Tyr) c.1427C>A (p.Ser476Tyr) c.1289C>A (p.Ser430Tyr) c.3851C>A (p.Ser1284Tyr) c.4616C>A (p.Ser1539Tyr) c.4805C>A (p.Ser1602Tyr) c.4598C>A (p.Ser1533Tyr) c.1301C>A (p.Ser434Tyr) c.1346C>A (p.Ser449Tyr) c.4802C>A (p.Ser1601Tyr) c.1126C>A c.1313C>A (p.Ser438Tyr) c.*4522C>A (n.*4522C>A) c.1052C>A (p.Ser351Tyr) c.5-7224C>A (n.5-7224C>A) c.212C>A (p.Ser71Tyr) c.-98-20985C>A (n.-98-20985C>A) n.4875C>A n.4916C>A | ClinVar dbSNP gnomAD v4 |
17 | g.43071177_43071180del | CA658684116 | BRCA1 | c.4733_4736del (p.Pro1578LeufsTer21) c.4736_4739del (p.Pro1579LeufsTer21) c.4610_4613del (p.Pro1537LeufsTer21) c.4730_4733del (p.Pro1577LeufsTer21) c.4658_4661del (p.Pro1553LeufsTer21) c.1424_1427del (p.Pro475LeufsTer21) c.1286_1289del (p.Pro429LeufsTer21) c.3848_3851del (p.Pro1283LeufsTer21) c.4613_4616del (p.Pro1538LeufsTer21) c.4802_4805del (p.Pro1601LeufsTer21) c.4595_4598del (p.Pro1532LeufsTer21) c.1298_1301del (p.Pro433LeufsTer21) c.1343_1346del (p.Pro448LeufsTer21) c.4799_4802del (p.Pro1600LeufsTer21) c.1123_1126del c.1310_1313del (p.Pro437LeufsTer21) c.*4519_*4522del (n.*4519_*4522del) c.1049_1052del (p.Pro350LeufsTer21) c.5-7227_5-7224del (n.5-7227_5-7224del) c.209_212del (p.Pro70LeufsTer21) c.-98-20988_-98-20985del (n.-98-20988_-98-20985del) n.4872_4875del n.4913_4916del | ClinVar dbSNP |
17 | g.43071176A>C | CA10592032 | BRCA1 | c.4735T>G (p.Ser1579Ala) c.4738T>G (p.Ser1580Ala) c.4612T>G (p.Ser1538Ala) c.4732T>G (p.Ser1578Ala) c.4660T>G (p.Ser1554Ala) c.1426T>G (p.Ser476Ala) c.1288T>G (p.Ser430Ala) c.3850T>G (p.Ser1284Ala) c.4615T>G (p.Ser1539Ala) c.4804T>G (p.Ser1602Ala) c.4597T>G (p.Ser1533Ala) c.1300T>G (p.Ser434Ala) c.1345T>G (p.Ser449Ala) c.4801T>G (p.Ser1601Ala) c.1125T>G c.1312T>G (p.Ser438Ala) c.*4521T>G (n.*4521T>G) c.1051T>G (p.Ser351Ala) c.5-7225T>G (n.5-7225T>G) c.211T>G (p.Ser71Ala) c.-98-20986T>G (n.-98-20986T>G) n.4874T>G n.4915T>G | |
17 | g.43071176A>G | CA10592033 | BRCA1 | c.4735T>C (p.Ser1579Pro) c.4738T>C (p.Ser1580Pro) c.4612T>C (p.Ser1538Pro) c.4732T>C (p.Ser1578Pro) c.4660T>C (p.Ser1554Pro) c.1426T>C (p.Ser476Pro) c.1288T>C (p.Ser430Pro) c.3850T>C (p.Ser1284Pro) c.4615T>C (p.Ser1539Pro) c.4804T>C (p.Ser1602Pro) c.4597T>C (p.Ser1533Pro) c.1300T>C (p.Ser434Pro) c.1345T>C (p.Ser449Pro) c.4801T>C (p.Ser1601Pro) c.1125T>C c.1312T>C (p.Ser438Pro) c.*4521T>C (n.*4521T>C) c.1051T>C (p.Ser351Pro) c.5-7225T>C (n.5-7225T>C) c.211T>C (p.Ser71Pro) c.-98-20986T>C (n.-98-20986T>C) n.4874T>C n.4915T>C | dbSNP gnomAD v4 |
17 | g.43071176A>T | CA10592034 | BRCA1 | c.4735T>A (p.Ser1579Thr) c.4738T>A (p.Ser1580Thr) c.4612T>A (p.Ser1538Thr) c.4732T>A (p.Ser1578Thr) c.4660T>A (p.Ser1554Thr) c.1426T>A (p.Ser476Thr) c.1288T>A (p.Ser430Thr) c.3850T>A (p.Ser1284Thr) c.4615T>A (p.Ser1539Thr) c.4804T>A (p.Ser1602Thr) c.4597T>A (p.Ser1533Thr) c.1300T>A (p.Ser434Thr) c.1345T>A (p.Ser449Thr) c.4801T>A (p.Ser1601Thr) c.1125T>A c.1312T>A (p.Ser438Thr) c.*4521T>A (n.*4521T>A) c.1051T>A (p.Ser351Thr) c.5-7225T>A (n.5-7225T>A) c.211T>A (p.Ser71Thr) c.-98-20986T>A (n.-98-20986T>A) n.4874T>A n.4915T>A | |
17 | g.43071177A= | CA2260772988 | BRCA1 | c.4734T= (p.Pro1578=) c.4737T= (p.Pro1579=) c.4611T= (p.Pro1537=) c.4731T= (p.Pro1577=) c.4659T= (p.Pro1553=) c.1425T= (p.Pro475=) c.1287T= (p.Pro429=) c.3849T= (p.Pro1283=) c.4614T= (p.Pro1538=) c.4803T= (p.Pro1601=) c.4596T= (p.Pro1532=) c.1299T= (p.Pro433=) c.1344T= (p.Pro448=) c.4800T= (p.Pro1600=) c.1124T= c.1311T= (p.Pro437=) c.*4520T= (n.*4520T=) c.1050T= (p.Pro350=) c.5-7226T= (n.5-7226T=) c.210T= (p.Pro70=) c.-98-20987T= (n.-98-20987T=) n.4873T= n.4914T= | |
17 | g.43071177A>C | CA500231872 | BRCA1 | c.4734T>G (p.Pro1578=) c.4737T>G (p.Pro1579=) c.4611T>G (p.Pro1537=) c.4731T>G (p.Pro1577=) c.4659T>G (p.Pro1553=) c.1425T>G (p.Pro475=) c.1287T>G (p.Pro429=) c.3849T>G (p.Pro1283=) c.4614T>G (p.Pro1538=) c.4803T>G (p.Pro1601=) c.4596T>G (p.Pro1532=) c.1299T>G (p.Pro433=) c.1344T>G (p.Pro448=) c.4800T>G (p.Pro1600=) c.1124T>G c.1311T>G (p.Pro437=) c.*4520T>G (n.*4520T>G) c.1050T>G (p.Pro350=) c.5-7226T>G (n.5-7226T>G) c.210T>G (p.Pro70=) c.-98-20987T>G (n.-98-20987T>G) n.4873T>G n.4914T>G | |
17 | g.43071177A>G | CA10583557 | BRCA1 | c.4734T>C (p.Pro1578=) c.4737T>C (p.Pro1579=) c.4611T>C (p.Pro1537=) c.4731T>C (p.Pro1577=) c.4659T>C (p.Pro1553=) c.1425T>C (p.Pro475=) c.1287T>C (p.Pro429=) c.3849T>C (p.Pro1283=) c.4614T>C (p.Pro1538=) c.4803T>C (p.Pro1601=) c.4596T>C (p.Pro1532=) c.1299T>C (p.Pro433=) c.1344T>C (p.Pro448=) c.4800T>C (p.Pro1600=) c.1124T>C c.1311T>C (p.Pro437=) c.*4520T>C (n.*4520T>C) c.1050T>C (p.Pro350=) c.5-7226T>C (n.5-7226T>C) c.210T>C (p.Pro70=) c.-98-20987T>C (n.-98-20987T>C) n.4873T>C n.4914T>C | ClinVar dbSNP |
17 | g.43071177A>T | CA500231871 | BRCA1 | c.4734T>A (p.Pro1578=) c.4737T>A (p.Pro1579=) c.4611T>A (p.Pro1537=) c.4731T>A (p.Pro1577=) c.4659T>A (p.Pro1553=) c.1425T>A (p.Pro475=) c.1287T>A (p.Pro429=) c.3849T>A (p.Pro1283=) c.4614T>A (p.Pro1538=) c.4803T>A (p.Pro1601=) c.4596T>A (p.Pro1532=) c.1299T>A (p.Pro433=) c.1344T>A (p.Pro448=) c.4800T>A (p.Pro1600=) c.1124T>A c.1311T>A (p.Pro437=) c.*4520T>A (n.*4520T>A) c.1050T>A (p.Pro350=) c.5-7226T>A (n.5-7226T>A) c.210T>A (p.Pro70=) c.-98-20987T>A (n.-98-20987T>A) n.4873T>A n.4914T>A | dbSNP |
17 | g.43071178G>A | CA10592035 | BRCA1 | c.4733C>T (p.Pro1578Leu) c.4736C>T (p.Pro1579Leu) c.4610C>T (p.Pro1537Leu) c.4730C>T (p.Pro1577Leu) c.4658C>T (p.Pro1553Leu) c.1424C>T (p.Pro475Leu) c.1286C>T (p.Pro429Leu) c.3848C>T (p.Pro1283Leu) c.4613C>T (p.Pro1538Leu) c.4802C>T (p.Pro1601Leu) c.4595C>T (p.Pro1532Leu) c.1298C>T (p.Pro433Leu) c.1343C>T (p.Pro448Leu) c.4799C>T (p.Pro1600Leu) c.1123C>T c.1310C>T (p.Pro437Leu) c.*4519C>T (n.*4519C>T) c.1049C>T (p.Pro350Leu) c.5-7227C>T (n.5-7227C>T) c.209C>T (p.Pro70Leu) c.-98-20988C>T (n.-98-20988C>T) n.4872C>T n.4913C>T | ClinVar dbSNP |
17 | g.43071178G>C | CA10592036 | BRCA1 | c.4733C>G (p.Pro1578Arg) c.4736C>G (p.Pro1579Arg) c.4610C>G (p.Pro1537Arg) c.4730C>G (p.Pro1577Arg) c.4658C>G (p.Pro1553Arg) c.1424C>G (p.Pro475Arg) c.1286C>G (p.Pro429Arg) c.3848C>G (p.Pro1283Arg) c.4613C>G (p.Pro1538Arg) c.4802C>G (p.Pro1601Arg) c.4595C>G (p.Pro1532Arg) c.1298C>G (p.Pro433Arg) c.1343C>G (p.Pro448Arg) c.4799C>G (p.Pro1600Arg) c.1123C>G c.1310C>G (p.Pro437Arg) c.*4519C>G (n.*4519C>G) c.1049C>G (p.Pro350Arg) c.5-7227C>G (n.5-7227C>G) c.209C>G (p.Pro70Arg) c.-98-20988C>G (n.-98-20988C>G) n.4872C>G n.4913C>G | dbSNP |
17 | g.43071178G= | CA2260772989 | BRCA1 | c.4733C= (p.Pro1578=) c.4736C= (p.Pro1579=) c.4610C= (p.Pro1537=) c.4730C= (p.Pro1577=) c.4658C= (p.Pro1553=) c.1424C= (p.Pro475=) c.1286C= (p.Pro429=) c.3848C= (p.Pro1283=) c.4613C= (p.Pro1538=) c.4802C= (p.Pro1601=) c.4595C= (p.Pro1532=) c.1298C= (p.Pro433=) c.1343C= (p.Pro448=) c.4799C= (p.Pro1600=) c.1123C= c.1310C= (p.Pro437=) c.*4519C= (n.*4519C=) c.1049C= (p.Pro350=) c.5-7227C= (n.5-7227C=) c.209C= (p.Pro70=) c.-98-20988C= (n.-98-20988C=) n.4872C= n.4913C= | |
17 | g.43071178G>T | CA10592037 | BRCA1 | c.4733C>A (p.Pro1578His) c.4736C>A (p.Pro1579His) c.4610C>A (p.Pro1537His) c.4730C>A (p.Pro1577His) c.4658C>A (p.Pro1553His) c.1424C>A (p.Pro475His) c.1286C>A (p.Pro429His) c.3848C>A (p.Pro1283His) c.4613C>A (p.Pro1538His) c.4802C>A (p.Pro1601His) c.4595C>A (p.Pro1532His) c.1298C>A (p.Pro433His) c.1343C>A (p.Pro448His) c.4799C>A (p.Pro1600His) c.1123C>A c.1310C>A (p.Pro437His) c.*4519C>A (n.*4519C>A) c.1049C>A (p.Pro350His) c.5-7227C>A (n.5-7227C>A) c.209C>A (p.Pro70His) c.-98-20988C>A (n.-98-20988C>A) n.4872C>A n.4913C>A | dbSNP |
17 | g.43071179G>A | CA052875 | BRCA1 | c.4732C>T (p.Pro1578Ser) c.4735C>T (p.Pro1579Ser) c.4609C>T (p.Pro1537Ser) c.4729C>T (p.Pro1577Ser) c.4657C>T (p.Pro1553Ser) c.1423C>T (p.Pro475Ser) c.1285C>T (p.Pro429Ser) c.3847C>T (p.Pro1283Ser) c.4612C>T (p.Pro1538Ser) c.4801C>T (p.Pro1601Ser) c.4594C>T (p.Pro1532Ser) c.1297C>T (p.Pro433Ser) c.1342C>T (p.Pro448Ser) c.4798C>T (p.Pro1600Ser) c.1122C>T c.1309C>T (p.Pro437Ser) c.*4518C>T (n.*4518C>T) c.1048C>T (p.Pro350Ser) c.5-7228C>T (n.5-7228C>T) c.208C>T (p.Pro70Ser) c.-98-20989C>T (n.-98-20989C>T) n.4871C>T n.4912C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071179G>C | CA002998 | BRCA1 | c.4732C>G (p.Pro1578Ala) c.4735C>G (p.Pro1579Ala) c.4609C>G (p.Pro1537Ala) c.4729C>G (p.Pro1577Ala) c.4657C>G (p.Pro1553Ala) c.1423C>G (p.Pro475Ala) c.1285C>G (p.Pro429Ala) c.3847C>G (p.Pro1283Ala) c.4612C>G (p.Pro1538Ala) c.4801C>G (p.Pro1601Ala) c.4594C>G (p.Pro1532Ala) c.1297C>G (p.Pro433Ala) c.1342C>G (p.Pro448Ala) c.4798C>G (p.Pro1600Ala) c.1122C>G c.1309C>G (p.Pro437Ala) c.*4518C>G (n.*4518C>G) c.1048C>G (p.Pro350Ala) c.5-7228C>G (n.5-7228C>G) c.208C>G (p.Pro70Ala) c.-98-20989C>G (n.-98-20989C>G) n.4871C>G n.4912C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071179G= | CA2260772990 | BRCA1 | c.4732C= (p.Pro1578=) c.4735C= (p.Pro1579=) c.4609C= (p.Pro1537=) c.4729C= (p.Pro1577=) c.4657C= (p.Pro1553=) c.1423C= (p.Pro475=) c.1285C= (p.Pro429=) c.3847C= (p.Pro1283=) c.4612C= (p.Pro1538=) c.4801C= (p.Pro1601=) c.4594C= (p.Pro1532=) c.1297C= (p.Pro433=) c.1342C= (p.Pro448=) c.4798C= (p.Pro1600=) c.1122C= c.1309C= (p.Pro437=) c.*4518C= (n.*4518C=) c.1048C= (p.Pro350=) c.5-7228C= (n.5-7228C=) c.208C= (p.Pro70=) c.-98-20989C= (n.-98-20989C=) n.4871C= n.4912C= | |
17 | g.43071179G>T | CA10592038 | BRCA1 | c.4732C>A (p.Pro1578Thr) c.4735C>A (p.Pro1579Thr) c.4609C>A (p.Pro1537Thr) c.4729C>A (p.Pro1577Thr) c.4657C>A (p.Pro1553Thr) c.1423C>A (p.Pro475Thr) c.1285C>A (p.Pro429Thr) c.3847C>A (p.Pro1283Thr) c.4612C>A (p.Pro1538Thr) c.4801C>A (p.Pro1601Thr) c.4594C>A (p.Pro1532Thr) c.1297C>A (p.Pro433Thr) c.1342C>A (p.Pro448Thr) c.4798C>A (p.Pro1600Thr) c.1122C>A c.1309C>A (p.Pro437Thr) c.*4518C>A (n.*4518C>A) c.1048C>A (p.Pro350Thr) c.5-7228C>A (n.5-7228C>A) c.208C>A (p.Pro70Thr) c.-98-20989C>A (n.-98-20989C>A) n.4871C>A n.4912C>A | dbSNP |
17 | g.43071180A>C | CA10592039 | BRCA1 | c.4731T>G (p.Asp1577Glu) c.4734T>G (p.Asp1578Glu) c.4608T>G (p.Asp1536Glu) c.4728T>G (p.Asp1576Glu) c.4656T>G (p.Asp1552Glu) c.1422T>G (p.Asp474Glu) c.1284T>G (p.Asp428Glu) c.3846T>G (p.Asp1282Glu) c.4611T>G (p.Asp1537Glu) c.4800T>G (p.Asp1600Glu) c.4593T>G (p.Asp1531Glu) c.1296T>G (p.Asp432Glu) c.1341T>G (p.Asp447Glu) c.4797T>G (p.Asp1599Glu) c.1121T>G c.1308T>G (p.Asp436Glu) c.*4517T>G (n.*4517T>G) c.1047T>G (p.Asp349Glu) c.5-7229T>G (n.5-7229T>G) c.207T>G (p.Asp69Glu) c.-98-20990T>G (n.-98-20990T>G) n.4870T>G n.4911T>G | dbSNP |
17 | g.43071180A>G | CA500231873 | BRCA1 | c.4731T>C (p.Asp1577=) c.4734T>C (p.Asp1578=) c.4608T>C (p.Asp1536=) c.4728T>C (p.Asp1576=) c.4656T>C (p.Asp1552=) c.1422T>C (p.Asp474=) c.1284T>C (p.Asp428=) c.3846T>C (p.Asp1282=) c.4611T>C (p.Asp1537=) c.4800T>C (p.Asp1600=) c.4593T>C (p.Asp1531=) c.1296T>C (p.Asp432=) c.1341T>C (p.Asp447=) c.4797T>C (p.Asp1599=) c.1121T>C c.1308T>C (p.Asp436=) c.*4517T>C (n.*4517T>C) c.1047T>C (p.Asp349=) c.5-7229T>C (n.5-7229T>C) c.207T>C (p.Asp69=) c.-98-20990T>C (n.-98-20990T>C) n.4870T>C n.4911T>C | |
17 | g.43071180A>T | CA10592040 | BRCA1 | c.4731T>A (p.Asp1577Glu) c.4734T>A (p.Asp1578Glu) c.4608T>A (p.Asp1536Glu) c.4728T>A (p.Asp1576Glu) c.4656T>A (p.Asp1552Glu) c.1422T>A (p.Asp474Glu) c.1284T>A (p.Asp428Glu) c.3846T>A (p.Asp1282Glu) c.4611T>A (p.Asp1537Glu) c.4800T>A (p.Asp1600Glu) c.4593T>A (p.Asp1531Glu) c.1296T>A (p.Asp432Glu) c.1341T>A (p.Asp447Glu) c.4797T>A (p.Asp1599Glu) c.1121T>A c.1308T>A (p.Asp436Glu) c.*4517T>A (n.*4517T>A) c.1047T>A (p.Asp349Glu) c.5-7229T>A (n.5-7229T>A) c.207T>A (p.Asp69Glu) c.-98-20990T>A (n.-98-20990T>A) n.4870T>A n.4911T>A | dbSNP |
17 | g.43071181T>A | CA10592041 | BRCA1 | c.4730A>T (p.Asp1577Val) c.4733A>T (p.Asp1578Val) c.4607A>T (p.Asp1536Val) c.4727A>T (p.Asp1576Val) c.4655A>T (p.Asp1552Val) c.1421A>T (p.Asp474Val) c.1283A>T (p.Asp428Val) c.3845A>T (p.Asp1282Val) c.4610A>T (p.Asp1537Val) c.4799A>T (p.Asp1600Val) c.4592A>T (p.Asp1531Val) c.1295A>T (p.Asp432Val) c.1340A>T (p.Asp447Val) c.4796A>T (p.Asp1599Val) c.1120A>T c.1307A>T (p.Asp436Val) c.*4516A>T (n.*4516A>T) c.1046A>T (p.Asp349Val) c.5-7230A>T (n.5-7230A>T) c.206A>T (p.Asp69Val) c.-98-20991A>T (n.-98-20991A>T) n.4869A>T n.4910A>T | dbSNP |
17 | g.43071181T>C | CA002997 | BRCA1 | c.4730A>G (p.Asp1577Gly) c.4733A>G (p.Asp1578Gly) c.4607A>G (p.Asp1536Gly) c.4727A>G (p.Asp1576Gly) c.4655A>G (p.Asp1552Gly) c.1421A>G (p.Asp474Gly) c.1283A>G (p.Asp428Gly) c.3845A>G (p.Asp1282Gly) c.4610A>G (p.Asp1537Gly) c.4799A>G (p.Asp1600Gly) c.4592A>G (p.Asp1531Gly) c.1295A>G (p.Asp432Gly) c.1340A>G (p.Asp447Gly) c.4796A>G (p.Asp1599Gly) c.1120A>G c.1307A>G (p.Asp436Gly) c.*4516A>G (n.*4516A>G) c.1046A>G (p.Asp349Gly) c.5-7230A>G (n.5-7230A>G) c.206A>G (p.Asp69Gly) c.-98-20991A>G (n.-98-20991A>G) n.4869A>G n.4910A>G | ClinVar dbSNP gnomAD v4 |
17 | g.43071181T>G | CA10592042 | BRCA1 | c.4730A>C (p.Asp1577Ala) c.4733A>C (p.Asp1578Ala) c.4607A>C (p.Asp1536Ala) c.4727A>C (p.Asp1576Ala) c.4655A>C (p.Asp1552Ala) c.1421A>C (p.Asp474Ala) c.1283A>C (p.Asp428Ala) c.3845A>C (p.Asp1282Ala) c.4610A>C (p.Asp1537Ala) c.4799A>C (p.Asp1600Ala) c.4592A>C (p.Asp1531Ala) c.1295A>C (p.Asp432Ala) c.1340A>C (p.Asp447Ala) c.4796A>C (p.Asp1599Ala) c.1120A>C c.1307A>C (p.Asp436Ala) c.*4516A>C (n.*4516A>C) c.1046A>C (p.Asp349Ala) c.5-7230A>C (n.5-7230A>C) c.206A>C (p.Asp69Ala) c.-98-20991A>C (n.-98-20991A>C) n.4869A>C n.4910A>C | dbSNP |
17 | g.43071181T= | CA2260772991 | BRCA1 | c.4730A= (p.Asp1577=) c.4733A= (p.Asp1578=) c.4607A= (p.Asp1536=) c.4727A= (p.Asp1576=) c.4655A= (p.Asp1552=) c.1421A= (p.Asp474=) c.1283A= (p.Asp428=) c.3845A= (p.Asp1282=) c.4610A= (p.Asp1537=) c.4799A= (p.Asp1600=) c.4592A= (p.Asp1531=) c.1295A= (p.Asp432=) c.1340A= (p.Asp447=) c.4796A= (p.Asp1599=) c.1120A= c.1307A= (p.Asp436=) c.*4516A= (n.*4516A=) c.1046A= (p.Asp349=) c.5-7230A= (n.5-7230A=) c.206A= (p.Asp69=) c.-98-20991A= (n.-98-20991A=) n.4869A= n.4910A= | |
17 | g.43071182C>A | CA10592043 | BRCA1 | c.4729G>T (p.Asp1577Tyr) c.4732G>T (p.Asp1578Tyr) c.4606G>T (p.Asp1536Tyr) c.4726G>T (p.Asp1576Tyr) c.4654G>T (p.Asp1552Tyr) c.1420G>T (p.Asp474Tyr) c.1282G>T (p.Asp428Tyr) c.3844G>T (p.Asp1282Tyr) c.4609G>T (p.Asp1537Tyr) c.4798G>T (p.Asp1600Tyr) c.4591G>T (p.Asp1531Tyr) c.1294G>T (p.Asp432Tyr) c.1339G>T (p.Asp447Tyr) c.4795G>T (p.Asp1599Tyr) c.1119G>T c.1306G>T (p.Asp436Tyr) c.*4515G>T (n.*4515G>T) c.1045G>T (p.Asp349Tyr) c.5-7231G>T (n.5-7231G>T) c.205G>T (p.Asp69Tyr) c.-98-20992G>T (n.-98-20992G>T) n.4868G>T n.4909G>T | dbSNP |
17 | g.43071182C>G | CA10592044 | BRCA1 | c.4729G>C (p.Asp1577His) c.4732G>C (p.Asp1578His) c.4606G>C (p.Asp1536His) c.4726G>C (p.Asp1576His) c.4654G>C (p.Asp1552His) c.1420G>C (p.Asp474His) c.1282G>C (p.Asp428His) c.3844G>C (p.Asp1282His) c.4609G>C (p.Asp1537His) c.4798G>C (p.Asp1600His) c.4591G>C (p.Asp1531His) c.1294G>C (p.Asp432His) c.1339G>C (p.Asp447His) c.4795G>C (p.Asp1599His) c.1119G>C c.1306G>C (p.Asp436His) c.*4515G>C (n.*4515G>C) c.1045G>C (p.Asp349His) c.5-7231G>C (n.5-7231G>C) c.205G>C (p.Asp69His) c.-98-20992G>C (n.-98-20992G>C) n.4868G>C n.4909G>C | dbSNP |
17 | g.43071182C>T | CA10592045 | BRCA1 | c.4729G>A (p.Asp1577Asn) c.4732G>A (p.Asp1578Asn) c.4606G>A (p.Asp1536Asn) c.4726G>A (p.Asp1576Asn) c.4654G>A (p.Asp1552Asn) c.1420G>A (p.Asp474Asn) c.1282G>A (p.Asp428Asn) c.3844G>A (p.Asp1282Asn) c.4609G>A (p.Asp1537Asn) c.4798G>A (p.Asp1600Asn) c.4591G>A (p.Asp1531Asn) c.1294G>A (p.Asp432Asn) c.1339G>A (p.Asp447Asn) c.4795G>A (p.Asp1599Asn) c.1119G>A c.1306G>A (p.Asp436Asn) c.*4515G>A (n.*4515G>A) c.1045G>A (p.Asp349Asn) c.5-7231G>A (n.5-7231G>A) c.205G>A (p.Asp69Asn) c.-98-20992G>A (n.-98-20992G>A) n.4868G>A n.4909G>A | dbSNP |
17 | g.43071183A= | CA2260772992 | BRCA1 | c.4728T= (p.Ser1576=) c.4731T= (p.Ser1577=) c.4605T= (p.Ser1535=) c.4725T= (p.Ser1575=) c.4653T= (p.Ser1551=) c.1419T= (p.Ser473=) c.1281T= (p.Ser427=) c.3843T= (p.Ser1281=) c.4608T= (p.Ser1536=) c.4797T= (p.Ser1599=) c.4590T= (p.Ser1530=) c.1293T= (p.Ser431=) c.1338T= (p.Ser446=) c.4794T= (p.Ser1598=) c.1118T= c.1305T= (p.Ser435=) c.*4514T= (n.*4514T=) c.1044T= (p.Ser348=) c.5-7232T= (n.5-7232T=) c.204T= (p.Ser68=) c.-98-20993T= (n.-98-20993T=) n.4867T= n.4908T= | |
17 | g.43071183A>C | CA500231874 | BRCA1 | c.4728T>G (p.Ser1576=) c.4731T>G (p.Ser1577=) c.4605T>G (p.Ser1535=) c.4725T>G (p.Ser1575=) c.4653T>G (p.Ser1551=) c.1419T>G (p.Ser473=) c.1281T>G (p.Ser427=) c.3843T>G (p.Ser1281=) c.4608T>G (p.Ser1536=) c.4797T>G (p.Ser1599=) c.4590T>G (p.Ser1530=) c.1293T>G (p.Ser431=) c.1338T>G (p.Ser446=) c.4794T>G (p.Ser1598=) c.1118T>G c.1305T>G (p.Ser435=) c.*4514T>G (n.*4514T>G) c.1044T>G (p.Ser348=) c.5-7232T>G (n.5-7232T>G) c.204T>G (p.Ser68=) c.-98-20993T>G (n.-98-20993T>G) n.4867T>G n.4908T>G | |
17 | g.43071183A>G | CA500231875 | BRCA1 | c.4728T>C (p.Ser1576=) c.4731T>C (p.Ser1577=) c.4605T>C (p.Ser1535=) c.4725T>C (p.Ser1575=) c.4653T>C (p.Ser1551=) c.1419T>C (p.Ser473=) c.1281T>C (p.Ser427=) c.3843T>C (p.Ser1281=) c.4608T>C (p.Ser1536=) c.4797T>C (p.Ser1599=) c.4590T>C (p.Ser1530=) c.1293T>C (p.Ser431=) c.1338T>C (p.Ser446=) c.4794T>C (p.Ser1598=) c.1118T>C c.1305T>C (p.Ser435=) c.*4514T>C (n.*4514T>C) c.1044T>C (p.Ser348=) c.5-7232T>C (n.5-7232T>C) c.204T>C (p.Ser68=) c.-98-20993T>C (n.-98-20993T>C) n.4867T>C n.4908T>C | ClinVar dbSNP |
17 | g.43071183A>T | CA500231876 | BRCA1 | c.4728T>A (p.Ser1576=) c.4731T>A (p.Ser1577=) c.4605T>A (p.Ser1535=) c.4725T>A (p.Ser1575=) c.4653T>A (p.Ser1551=) c.1419T>A (p.Ser473=) c.1281T>A (p.Ser427=) c.3843T>A (p.Ser1281=) c.4608T>A (p.Ser1536=) c.4797T>A (p.Ser1599=) c.4590T>A (p.Ser1530=) c.1293T>A (p.Ser431=) c.1338T>A (p.Ser446=) c.4794T>A (p.Ser1598=) c.1118T>A c.1305T>A (p.Ser435=) c.*4514T>A (n.*4514T>A) c.1044T>A (p.Ser348=) c.5-7232T>A (n.5-7232T>A) c.204T>A (p.Ser68=) c.-98-20993T>A (n.-98-20993T>A) n.4867T>A n.4908T>A | ClinVar dbSNP |
17 | g.43071184G>A | CA10592046 | BRCA1 | c.4727C>T (p.Ser1576Phe) c.4730C>T (p.Ser1577Phe) c.4604C>T (p.Ser1535Phe) c.4724C>T (p.Ser1575Phe) c.4652C>T (p.Ser1551Phe) c.1418C>T (p.Ser473Phe) c.1280C>T (p.Ser427Phe) c.3842C>T (p.Ser1281Phe) c.4607C>T (p.Ser1536Phe) c.4796C>T (p.Ser1599Phe) c.4589C>T (p.Ser1530Phe) c.1292C>T (p.Ser431Phe) c.1337C>T (p.Ser446Phe) c.4793C>T (p.Ser1598Phe) c.1117C>T c.1304C>T (p.Ser435Phe) c.*4513C>T (n.*4513C>T) c.1043C>T (p.Ser348Phe) c.5-7233C>T (n.5-7233C>T) c.203C>T (p.Ser68Phe) c.-98-20994C>T (n.-98-20994C>T) n.4866C>T n.4907C>T | ClinVar dbSNP gnomAD v4 |
17 | g.43071184G>C | CA10592047 | BRCA1 | c.4727C>G (p.Ser1576Cys) c.4730C>G (p.Ser1577Cys) c.4604C>G (p.Ser1535Cys) c.4724C>G (p.Ser1575Cys) c.4652C>G (p.Ser1551Cys) c.1418C>G (p.Ser473Cys) c.1280C>G (p.Ser427Cys) c.3842C>G (p.Ser1281Cys) c.4607C>G (p.Ser1536Cys) c.4796C>G (p.Ser1599Cys) c.4589C>G (p.Ser1530Cys) c.1292C>G (p.Ser431Cys) c.1337C>G (p.Ser446Cys) c.4793C>G (p.Ser1598Cys) c.1117C>G c.1304C>G (p.Ser435Cys) c.*4513C>G (n.*4513C>G) c.1043C>G (p.Ser348Cys) c.5-7233C>G (n.5-7233C>G) c.203C>G (p.Ser68Cys) c.-98-20994C>G (n.-98-20994C>G) n.4866C>G n.4907C>G | dbSNP |
17 | g.43071184G= | CA2260772993 | BRCA1 | c.4727C= (p.Ser1576=) c.4730C= (p.Ser1577=) c.4604C= (p.Ser1535=) c.4724C= (p.Ser1575=) c.4652C= (p.Ser1551=) c.1418C= (p.Ser473=) c.1280C= (p.Ser427=) c.3842C= (p.Ser1281=) c.4607C= (p.Ser1536=) c.4796C= (p.Ser1599=) c.4589C= (p.Ser1530=) c.1292C= (p.Ser431=) c.1337C= (p.Ser446=) c.4793C= (p.Ser1598=) c.1117C= c.1304C= (p.Ser435=) c.*4513C= (n.*4513C=) c.1043C= (p.Ser348=) c.5-7233C= (n.5-7233C=) c.203C= (p.Ser68=) c.-98-20994C= (n.-98-20994C=) n.4866C= n.4907C= | |
17 | g.43071184G>T | CA002996 | BRCA1 | c.4727C>A (p.Ser1576Tyr) c.4730C>A (p.Ser1577Tyr) c.4604C>A (p.Ser1535Tyr) c.4724C>A (p.Ser1575Tyr) c.4652C>A (p.Ser1551Tyr) c.1418C>A (p.Ser473Tyr) c.1280C>A (p.Ser427Tyr) c.3842C>A (p.Ser1281Tyr) c.4607C>A (p.Ser1536Tyr) c.4796C>A (p.Ser1599Tyr) c.4589C>A (p.Ser1530Tyr) c.1292C>A (p.Ser431Tyr) c.1337C>A (p.Ser446Tyr) c.4793C>A (p.Ser1598Tyr) c.1117C>A c.1304C>A (p.Ser435Tyr) c.*4513C>A (n.*4513C>A) c.1043C>A (p.Ser348Tyr) c.5-7233C>A (n.5-7233C>A) c.203C>A (p.Ser68Tyr) c.-98-20994C>A (n.-98-20994C>A) n.4866C>A n.4907C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071185A= | CA2260772994 | BRCA1 | c.4726T= (p.Ser1576=) c.4729T= (p.Ser1577=) c.4603T= (p.Ser1535=) c.4723T= (p.Ser1575=) c.4651T= (p.Ser1551=) c.1417T= (p.Ser473=) c.1279T= (p.Ser427=) c.3841T= (p.Ser1281=) c.4606T= (p.Ser1536=) c.4795T= (p.Ser1599=) c.4588T= (p.Ser1530=) c.1291T= (p.Ser431=) c.1336T= (p.Ser446=) c.4792T= (p.Ser1598=) c.1116T= c.1303T= (p.Ser435=) c.*4512T= (n.*4512T=) c.1042T= (p.Ser348=) c.5-7234T= (n.5-7234T=) c.202T= (p.Ser68=) c.-98-20995T= (n.-98-20995T=) n.4865T= n.4906T= | |
17 | g.43071185A>C | CA10592048 | BRCA1 | c.4726T>G (p.Ser1576Ala) c.4729T>G (p.Ser1577Ala) c.4603T>G (p.Ser1535Ala) c.4723T>G (p.Ser1575Ala) c.4651T>G (p.Ser1551Ala) c.1417T>G (p.Ser473Ala) c.1279T>G (p.Ser427Ala) c.3841T>G (p.Ser1281Ala) c.4606T>G (p.Ser1536Ala) c.4795T>G (p.Ser1599Ala) c.4588T>G (p.Ser1530Ala) c.1291T>G (p.Ser431Ala) c.1336T>G (p.Ser446Ala) c.4792T>G (p.Ser1598Ala) c.1116T>G c.1303T>G (p.Ser435Ala) c.*4512T>G (n.*4512T>G) c.1042T>G (p.Ser348Ala) c.5-7234T>G (n.5-7234T>G) c.202T>G (p.Ser68Ala) c.-98-20995T>G (n.-98-20995T>G) n.4865T>G n.4906T>G | ClinVar dbSNP |
17 | g.43071185A>G | CA002994 | BRCA1 | c.4726T>C (p.Ser1576Pro) c.4729T>C (p.Ser1577Pro) c.4603T>C (p.Ser1535Pro) c.4723T>C (p.Ser1575Pro) c.4651T>C (p.Ser1551Pro) c.1417T>C (p.Ser473Pro) c.1279T>C (p.Ser427Pro) c.3841T>C (p.Ser1281Pro) c.4606T>C (p.Ser1536Pro) c.4795T>C (p.Ser1599Pro) c.4588T>C (p.Ser1530Pro) c.1291T>C (p.Ser431Pro) c.1336T>C (p.Ser446Pro) c.4792T>C (p.Ser1598Pro) c.1116T>C c.1303T>C (p.Ser435Pro) c.*4512T>C (n.*4512T>C) c.1042T>C (p.Ser348Pro) c.5-7234T>C (n.5-7234T>C) c.202T>C (p.Ser68Pro) c.-98-20995T>C (n.-98-20995T>C) n.4865T>C n.4906T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071185A>T | CA10592049 | BRCA1 | c.4726T>A (p.Ser1576Thr) c.4729T>A (p.Ser1577Thr) c.4603T>A (p.Ser1535Thr) c.4723T>A (p.Ser1575Thr) c.4651T>A (p.Ser1551Thr) c.1417T>A (p.Ser473Thr) c.1279T>A (p.Ser427Thr) c.3841T>A (p.Ser1281Thr) c.4606T>A (p.Ser1536Thr) c.4795T>A (p.Ser1599Thr) c.4588T>A (p.Ser1530Thr) c.1291T>A (p.Ser431Thr) c.1336T>A (p.Ser446Thr) c.4792T>A (p.Ser1598Thr) c.1116T>A c.1303T>A (p.Ser435Thr) c.*4512T>A (n.*4512T>A) c.1042T>A (p.Ser348Thr) c.5-7234T>A (n.5-7234T>A) c.202T>A (p.Ser68Thr) c.-98-20995T>A (n.-98-20995T>A) n.4865T>A n.4906T>A | dbSNP |
17 | g.43071186T>A | CA10592050 | BRCA1 | c.4725A>T (p.Glu1575Asp) c.4728A>T (p.Glu1576Asp) c.4602A>T (p.Glu1534Asp) c.4722A>T (p.Glu1574Asp) c.4650A>T (p.Glu1550Asp) c.1416A>T (p.Glu472Asp) c.1278A>T (p.Glu426Asp) c.3840A>T (p.Glu1280Asp) c.4605A>T (p.Glu1535Asp) c.4794A>T (p.Glu1598Asp) c.4587A>T (p.Glu1529Asp) c.1290A>T (p.Glu430Asp) c.1335A>T (p.Glu445Asp) c.4791A>T (p.Glu1597Asp) c.1115A>T c.1302A>T (p.Glu434Asp) c.*4511A>T (n.*4511A>T) c.1041A>T (p.Glu347Asp) c.5-7235A>T (n.5-7235A>T) c.201A>T (p.Glu67Asp) c.-98-20996A>T (n.-98-20996A>T) n.4864A>T n.4905A>T | dbSNP |
17 | g.43071186T>C | CA500231877 | BRCA1 | c.4725A>G (p.Glu1575=) c.4728A>G (p.Glu1576=) c.4602A>G (p.Glu1534=) c.4722A>G (p.Glu1574=) c.4650A>G (p.Glu1550=) c.1416A>G (p.Glu472=) c.1278A>G (p.Glu426=) c.3840A>G (p.Glu1280=) c.4605A>G (p.Glu1535=) c.4794A>G (p.Glu1598=) c.4587A>G (p.Glu1529=) c.1290A>G (p.Glu430=) c.1335A>G (p.Glu445=) c.4791A>G (p.Glu1597=) c.1115A>G c.1302A>G (p.Glu434=) c.*4511A>G (n.*4511A>G) c.1041A>G (p.Glu347=) c.5-7235A>G (n.5-7235A>G) c.201A>G (p.Glu67=) c.-98-20996A>G (n.-98-20996A>G) n.4864A>G n.4905A>G | ClinVar dbSNP gnomAD v4 |
17 | g.43071186T>G | CA10592051 | BRCA1 | c.4725A>C (p.Glu1575Asp) c.4728A>C (p.Glu1576Asp) c.4602A>C (p.Glu1534Asp) c.4722A>C (p.Glu1574Asp) c.4650A>C (p.Glu1550Asp) c.1416A>C (p.Glu472Asp) c.1278A>C (p.Glu426Asp) c.3840A>C (p.Glu1280Asp) c.4605A>C (p.Glu1535Asp) c.4794A>C (p.Glu1598Asp) c.4587A>C (p.Glu1529Asp) c.1290A>C (p.Glu430Asp) c.1335A>C (p.Glu445Asp) c.4791A>C (p.Glu1597Asp) c.1115A>C c.1302A>C (p.Glu434Asp) c.*4511A>C (n.*4511A>C) c.1041A>C (p.Glu347Asp) c.5-7235A>C (n.5-7235A>C) c.201A>C (p.Glu67Asp) c.-98-20996A>C (n.-98-20996A>C) n.4864A>C n.4905A>C | dbSNP |
17 | g.43071186T= | CA2260772995 | BRCA1 | c.4725A= (p.Glu1575=) c.4728A= (p.Glu1576=) c.4602A= (p.Glu1534=) c.4722A= (p.Glu1574=) c.4650A= (p.Glu1550=) c.1416A= (p.Glu472=) c.1278A= (p.Glu426=) c.3840A= (p.Glu1280=) c.4605A= (p.Glu1535=) c.4794A= (p.Glu1598=) c.4587A= (p.Glu1529=) c.1290A= (p.Glu430=) c.1335A= (p.Glu445=) c.4791A= (p.Glu1597=) c.1115A= c.1302A= (p.Glu434=) c.*4511A= (n.*4511A=) c.1041A= (p.Glu347=) c.5-7235A= (n.5-7235A=) c.201A= (p.Glu67=) c.-98-20996A= (n.-98-20996A=) n.4864A= n.4905A= | |
17 | g.43071187T>A | CA10592052 | BRCA1 | c.4724A>T (p.Glu1575Val) c.4727A>T (p.Glu1576Val) c.4601A>T (p.Glu1534Val) c.4721A>T (p.Glu1574Val) c.4649A>T (p.Glu1550Val) c.1415A>T (p.Glu472Val) c.1277A>T (p.Glu426Val) c.3839A>T (p.Glu1280Val) c.4604A>T (p.Glu1535Val) c.4793A>T (p.Glu1598Val) c.4586A>T (p.Glu1529Val) c.1289A>T (p.Glu430Val) c.1334A>T (p.Glu445Val) c.4790A>T (p.Glu1597Val) c.1114A>T c.1301A>T (p.Glu434Val) c.*4510A>T (n.*4510A>T) c.1040A>T (p.Glu347Val) c.5-7236A>T (n.5-7236A>T) c.200A>T (p.Glu67Val) c.-98-20997A>T (n.-98-20997A>T) n.4863A>T n.4904A>T | dbSNP |
17 | g.43071187T>C | CA10580510 | BRCA1 | c.4724A>G (p.Glu1575Gly) c.4727A>G (p.Glu1576Gly) c.4601A>G (p.Glu1534Gly) c.4721A>G (p.Glu1574Gly) c.4649A>G (p.Glu1550Gly) c.1415A>G (p.Glu472Gly) c.1277A>G (p.Glu426Gly) c.3839A>G (p.Glu1280Gly) c.4604A>G (p.Glu1535Gly) c.4793A>G (p.Glu1598Gly) c.4586A>G (p.Glu1529Gly) c.1289A>G (p.Glu430Gly) c.1334A>G (p.Glu445Gly) c.4790A>G (p.Glu1597Gly) c.1114A>G c.1301A>G (p.Glu434Gly) c.*4510A>G (n.*4510A>G) c.1040A>G (p.Glu347Gly) c.5-7236A>G (n.5-7236A>G) c.200A>G (p.Glu67Gly) c.-98-20997A>G (n.-98-20997A>G) n.4863A>G n.4904A>G | ClinVar dbSNP |
17 | g.43071187T>G | CA10592053 | BRCA1 | c.4724A>C (p.Glu1575Ala) c.4727A>C (p.Glu1576Ala) c.4601A>C (p.Glu1534Ala) c.4721A>C (p.Glu1574Ala) c.4649A>C (p.Glu1550Ala) c.1415A>C (p.Glu472Ala) c.1277A>C (p.Glu426Ala) c.3839A>C (p.Glu1280Ala) c.4604A>C (p.Glu1535Ala) c.4793A>C (p.Glu1598Ala) c.4586A>C (p.Glu1529Ala) c.1289A>C (p.Glu430Ala) c.1334A>C (p.Glu445Ala) c.4790A>C (p.Glu1597Ala) c.1114A>C c.1301A>C (p.Glu434Ala) c.*4510A>C (n.*4510A>C) c.1040A>C (p.Glu347Ala) c.5-7236A>C (n.5-7236A>C) c.200A>C (p.Glu67Ala) c.-98-20997A>C (n.-98-20997A>C) n.4863A>C n.4904A>C | |
17 | g.43071187T= | CA2260772996 | BRCA1 | c.4724A= (p.Glu1575=) c.4727A= (p.Glu1576=) c.4601A= (p.Glu1534=) c.4721A= (p.Glu1574=) c.4649A= (p.Glu1550=) c.1415A= (p.Glu472=) c.1277A= (p.Glu426=) c.3839A= (p.Glu1280=) c.4604A= (p.Glu1535=) c.4793A= (p.Glu1598=) c.4586A= (p.Glu1529=) c.1289A= (p.Glu430=) c.1334A= (p.Glu445=) c.4790A= (p.Glu1597=) c.1114A= c.1301A= (p.Glu434=) c.*4510A= (n.*4510A=) c.1040A= (p.Glu347=) c.5-7236A= (n.5-7236A=) c.200A= (p.Glu67=) c.-98-20997A= (n.-98-20997A=) n.4863A= n.4904A= | |
17 | g.43071188C>A | CA10592054 | BRCA1 | c.4723G>T (p.Glu1575Ter) c.4726G>T (p.Glu1576Ter) c.4600G>T (p.Glu1534Ter) c.4720G>T (p.Glu1574Ter) c.4648G>T (p.Glu1550Ter) c.1414G>T (p.Glu472Ter) c.1276G>T (p.Glu426Ter) c.3838G>T (p.Glu1280Ter) c.4603G>T (p.Glu1535Ter) c.4792G>T (p.Glu1598Ter) c.4585G>T (p.Glu1529Ter) c.1288G>T (p.Glu430Ter) c.1333G>T (p.Glu445Ter) c.4789G>T (p.Glu1597Ter) c.1113G>T c.1300G>T (p.Glu434Ter) c.*4509G>T (n.*4509G>T) c.1039G>T (p.Glu347Ter) c.5-7237G>T (n.5-7237G>T) c.199G>T (p.Glu67Ter) c.-98-20998G>T (n.-98-20998G>T) n.4862G>T n.4903G>T | dbSNP |
17 | g.43071188C= | CA2260772997 | BRCA1 | c.4723G= (p.Glu1575=) c.4726G= (p.Glu1576=) c.4600G= (p.Glu1534=) c.4720G= (p.Glu1574=) c.4648G= (p.Glu1550=) c.1414G= (p.Glu472=) c.1276G= (p.Glu426=) c.3838G= (p.Glu1280=) c.4603G= (p.Glu1535=) c.4792G= (p.Glu1598=) c.4585G= (p.Glu1529=) c.1288G= (p.Glu430=) c.1333G= (p.Glu445=) c.4789G= (p.Glu1597=) c.1113G= c.1300G= (p.Glu434=) c.*4509G= (n.*4509G=) c.1039G= (p.Glu347=) c.5-7237G= (n.5-7237G=) c.199G= (p.Glu67=) c.-98-20998G= (n.-98-20998G=) n.4862G= n.4903G= | |
17 | g.43071188C>G | CA10592055 | BRCA1 | c.4723G>C (p.Glu1575Gln) c.4726G>C (p.Glu1576Gln) c.4600G>C (p.Glu1534Gln) c.4720G>C (p.Glu1574Gln) c.4648G>C (p.Glu1550Gln) c.1414G>C (p.Glu472Gln) c.1276G>C (p.Glu426Gln) c.3838G>C (p.Glu1280Gln) c.4603G>C (p.Glu1535Gln) c.4792G>C (p.Glu1598Gln) c.4585G>C (p.Glu1529Gln) c.1288G>C (p.Glu430Gln) c.1333G>C (p.Glu445Gln) c.4789G>C (p.Glu1597Gln) c.1113G>C c.1300G>C (p.Glu434Gln) c.*4509G>C (n.*4509G>C) c.1039G>C (p.Glu347Gln) c.5-7237G>C (n.5-7237G>C) c.199G>C (p.Glu67Gln) c.-98-20998G>C (n.-98-20998G>C) n.4862G>C n.4903G>C | ClinVar dbSNP |
17 | g.43071188C>T | CA10592056 | BRCA1 | c.4723G>A (p.Glu1575Lys) c.4726G>A (p.Glu1576Lys) c.4600G>A (p.Glu1534Lys) c.4720G>A (p.Glu1574Lys) c.4648G>A (p.Glu1550Lys) c.1414G>A (p.Glu472Lys) c.1276G>A (p.Glu426Lys) c.3838G>A (p.Glu1280Lys) c.4603G>A (p.Glu1535Lys) c.4792G>A (p.Glu1598Lys) c.4585G>A (p.Glu1529Lys) c.1288G>A (p.Glu430Lys) c.1333G>A (p.Glu445Lys) c.4789G>A (p.Glu1597Lys) c.1113G>A c.1300G>A (p.Glu434Lys) c.*4509G>A (n.*4509G>A) c.1039G>A (p.Glu347Lys) c.5-7237G>A (n.5-7237G>A) c.199G>A (p.Glu67Lys) c.-98-20998G>A (n.-98-20998G>A) n.4862G>A n.4903G>A | ClinVar dbSNP |
17 | g.43071189A= | CA2260772999 | BRCA1 | c.4722T= (p.Pro1574=) c.4725T= (p.Pro1575=) c.4599T= (p.Pro1533=) c.4719T= (p.Pro1573=) c.4647T= (p.Pro1549=) c.1413T= (p.Pro471=) c.1275T= (p.Pro425=) c.3837T= (p.Pro1279=) c.4602T= (p.Pro1534=) c.4791T= (p.Pro1597=) c.4584T= (p.Pro1528=) c.1287T= (p.Pro429=) c.1332T= (p.Pro444=) c.4788T= (p.Pro1596=) c.1112T= c.1299T= (p.Pro433=) c.*4508T= (n.*4508T=) c.1038T= (p.Pro346=) c.5-7238T= (n.5-7238T=) c.198T= (p.Pro66=) c.-98-20999T= (n.-98-20999T=) n.4861T= n.4902T= | |
17 | g.43071189A>C | CA10583558 | BRCA1 | c.4722T>G (p.Pro1574=) c.4725T>G (p.Pro1575=) c.4599T>G (p.Pro1533=) c.4719T>G (p.Pro1573=) c.4647T>G (p.Pro1549=) c.1413T>G (p.Pro471=) c.1275T>G (p.Pro425=) c.3837T>G (p.Pro1279=) c.4602T>G (p.Pro1534=) c.4791T>G (p.Pro1597=) c.4584T>G (p.Pro1528=) c.1287T>G (p.Pro429=) c.1332T>G (p.Pro444=) c.4788T>G (p.Pro1596=) c.1112T>G c.1299T>G (p.Pro433=) c.*4508T>G (n.*4508T>G) c.1038T>G (p.Pro346=) c.5-7238T>G (n.5-7238T>G) c.198T>G (p.Pro66=) c.-98-20999T>G (n.-98-20999T>G) n.4861T>G n.4902T>G | ClinVar dbSNP |
17 | g.43071189A>G | CA500231878 | BRCA1 | c.4722T>C (p.Pro1574=) c.4725T>C (p.Pro1575=) c.4599T>C (p.Pro1533=) c.4719T>C (p.Pro1573=) c.4647T>C (p.Pro1549=) c.1413T>C (p.Pro471=) c.1275T>C (p.Pro425=) c.3837T>C (p.Pro1279=) c.4602T>C (p.Pro1534=) c.4791T>C (p.Pro1597=) c.4584T>C (p.Pro1528=) c.1287T>C (p.Pro429=) c.1332T>C (p.Pro444=) c.4788T>C (p.Pro1596=) c.1112T>C c.1299T>C (p.Pro433=) c.*4508T>C (n.*4508T>C) c.1038T>C (p.Pro346=) c.5-7238T>C (n.5-7238T>C) c.198T>C (p.Pro66=) c.-98-20999T>C (n.-98-20999T>C) n.4861T>C n.4902T>C | ClinVar dbSNP |
17 | g.43071189A>T | CA500231879 | BRCA1 | c.4722T>A (p.Pro1574=) c.4725T>A (p.Pro1575=) c.4599T>A (p.Pro1533=) c.4719T>A (p.Pro1573=) c.4647T>A (p.Pro1549=) c.1413T>A (p.Pro471=) c.1275T>A (p.Pro425=) c.3837T>A (p.Pro1279=) c.4602T>A (p.Pro1534=) c.4791T>A (p.Pro1597=) c.4584T>A (p.Pro1528=) c.1287T>A (p.Pro429=) c.1332T>A (p.Pro444=) c.4788T>A (p.Pro1596=) c.1112T>A c.1299T>A (p.Pro433=) c.*4508T>A (n.*4508T>A) c.1038T>A (p.Pro346=) c.5-7238T>A (n.5-7238T>A) c.198T>A (p.Pro66=) c.-98-20999T>A (n.-98-20999T>A) n.4861T>A n.4902T>A | |
17 | g.43071189_43071190delinsAG | CA2260772998 | BRCA1 | c.4721_4722delinsCT (p.Pro1574=) c.4724_4725delinsCT (p.Pro1575=) c.4598_4599delinsCT (p.Pro1533=) c.4718_4719delinsCT (p.Pro1573=) c.4646_4647delinsCT (p.Pro1549=) c.1412_1413delinsCT (p.Pro471=) c.1274_1275delinsCT (p.Pro425=) c.3836_3837delinsCT (p.Pro1279=) c.4601_4602delinsCT (p.Pro1534=) c.4790_4791delinsCT (p.Pro1597=) c.4583_4584delinsCT (p.Pro1528=) c.1286_1287delinsCT (p.Pro429=) c.1331_1332delinsCT (p.Pro444=) c.4787_4788delinsCT (p.Pro1596=) c.1111_1112delinsCT c.1298_1299delinsCT (p.Pro433=) c.*4507_*4508delinsCT (n.*4507_*4508delinsCT) c.1037_1038delinsCT (p.Pro346=) c.5-7239_5-7238delinsCT (n.5-7239_5-7238delinsCT) c.197_198delinsCT (p.Pro66=) c.-98-21000_-98-20999delinsCT (n.-98-21000_-98-20999delinsCT) n.4860_4861delinsCT n.4901_4902delinsCT | |
17 | g.43071190G>A | CA10592057 | BRCA1 | c.4721C>T (p.Pro1574Leu) c.4724C>T (p.Pro1575Leu) c.4598C>T (p.Pro1533Leu) c.4718C>T (p.Pro1573Leu) c.4646C>T (p.Pro1549Leu) c.1412C>T (p.Pro471Leu) c.1274C>T (p.Pro425Leu) c.3836C>T (p.Pro1279Leu) c.4601C>T (p.Pro1534Leu) c.4790C>T (p.Pro1597Leu) c.4583C>T (p.Pro1528Leu) c.1286C>T (p.Pro429Leu) c.1331C>T (p.Pro444Leu) c.4787C>T (p.Pro1596Leu) c.1111C>T c.1298C>T (p.Pro433Leu) c.*4507C>T (n.*4507C>T) c.1037C>T (p.Pro346Leu) c.5-7239C>T (n.5-7239C>T) c.197C>T (p.Pro66Leu) c.-98-21000C>T (n.-98-21000C>T) n.4860C>T n.4901C>T | ClinVar dbSNP |
17 | g.43071190G>C | CA10592058 | BRCA1 | c.4721C>G (p.Pro1574Arg) c.4724C>G (p.Pro1575Arg) c.4598C>G (p.Pro1533Arg) c.4718C>G (p.Pro1573Arg) c.4646C>G (p.Pro1549Arg) c.1412C>G (p.Pro471Arg) c.1274C>G (p.Pro425Arg) c.3836C>G (p.Pro1279Arg) c.4601C>G (p.Pro1534Arg) c.4790C>G (p.Pro1597Arg) c.4583C>G (p.Pro1528Arg) c.1286C>G (p.Pro429Arg) c.1331C>G (p.Pro444Arg) c.4787C>G (p.Pro1596Arg) c.1111C>G c.1298C>G (p.Pro433Arg) c.*4507C>G (n.*4507C>G) c.1037C>G (p.Pro346Arg) c.5-7239C>G (n.5-7239C>G) c.197C>G (p.Pro66Arg) c.-98-21000C>G (n.-98-21000C>G) n.4860C>G n.4901C>G | dbSNP gnomAD v4 |
17 | g.43071190G= | CA2260773000 | BRCA1 | c.4721C= (p.Pro1574=) c.4724C= (p.Pro1575=) c.4598C= (p.Pro1533=) c.4718C= (p.Pro1573=) c.4646C= (p.Pro1549=) c.1412C= (p.Pro471=) c.1274C= (p.Pro425=) c.3836C= (p.Pro1279=) c.4601C= (p.Pro1534=) c.4790C= (p.Pro1597=) c.4583C= (p.Pro1528=) c.1286C= (p.Pro429=) c.1331C= (p.Pro444=) c.4787C= (p.Pro1596=) c.1111C= c.1298C= (p.Pro433=) c.*4507C= (n.*4507C=) c.1037C= (p.Pro346=) c.5-7239C= (n.5-7239C=) c.197C= (p.Pro66=) c.-98-21000C= (n.-98-21000C=) n.4860C= n.4901C= | |
17 | g.43071190G>T | CA002992 | BRCA1 | c.4721C>A (p.Pro1574His) c.4724C>A (p.Pro1575His) c.4598C>A (p.Pro1533His) c.4718C>A (p.Pro1573His) c.4646C>A (p.Pro1549His) c.1412C>A (p.Pro471His) c.1274C>A (p.Pro425His) c.3836C>A (p.Pro1279His) c.4601C>A (p.Pro1534His) c.4790C>A (p.Pro1597His) c.4583C>A (p.Pro1528His) c.1286C>A (p.Pro429His) c.1331C>A (p.Pro444His) c.4787C>A (p.Pro1596His) c.1111C>A c.1298C>A (p.Pro433His) c.*4507C>A (n.*4507C>A) c.1037C>A (p.Pro346His) c.5-7239C>A (n.5-7239C>A) c.197C>A (p.Pro66His) c.-98-21000C>A (n.-98-21000C>A) n.4860C>A n.4901C>A | ClinVar dbSNP |
17 | g.43071192del | CA002993 | BRCA1 | c.4721del (p.Pro1574LeufsTer26) c.4724del (p.Pro1575LeufsTer26) c.4598del (p.Pro1533LeufsTer26) c.4718del (p.Pro1573LeufsTer26) c.4646del (p.Pro1549LeufsTer26) c.1412del (p.Pro471LeufsTer26) c.1274del (p.Pro425LeufsTer26) c.3836del (p.Pro1279LeufsTer26) c.4601del (p.Pro1534LeufsTer26) c.4790del (p.Pro1597LeufsTer26) c.4583del (p.Pro1528LeufsTer26) c.1286del (p.Pro429LeufsTer26) c.1331del (p.Pro444LeufsTer26) c.4787del (p.Pro1596LeufsTer26) c.1111del c.1298del (p.Pro433LeufsTer26) c.*4507del (n.*4507del) c.1037del (p.Pro346LeufsTer26) c.5-7239del (n.5-7239del) c.197del (p.Pro66LeufsTer26) c.-98-21000del (n.-98-21000del) n.4860del n.4901del | ClinVar dbSNP |
17 | g.43071191G>A | CA10592059 | BRCA1 | c.4720C>T (p.Pro1574Ser) c.4723C>T (p.Pro1575Ser) c.4597C>T (p.Pro1533Ser) c.4717C>T (p.Pro1573Ser) c.4645C>T (p.Pro1549Ser) c.1411C>T (p.Pro471Ser) c.1273C>T (p.Pro425Ser) c.3835C>T (p.Pro1279Ser) c.4600C>T (p.Pro1534Ser) c.4789C>T (p.Pro1597Ser) c.4582C>T (p.Pro1528Ser) c.1285C>T (p.Pro429Ser) c.1330C>T (p.Pro444Ser) c.4786C>T (p.Pro1596Ser) c.1110C>T c.1297C>T (p.Pro433Ser) c.*4506C>T (n.*4506C>T) c.1036C>T (p.Pro346Ser) c.5-7240C>T (n.5-7240C>T) c.196C>T (p.Pro66Ser) c.-98-21001C>T (n.-98-21001C>T) n.4859C>T n.4900C>T | dbSNP |
17 | g.43071191G>C | CA10592060 | BRCA1 | c.4720C>G (p.Pro1574Ala) c.4723C>G (p.Pro1575Ala) c.4597C>G (p.Pro1533Ala) c.4717C>G (p.Pro1573Ala) c.4645C>G (p.Pro1549Ala) c.1411C>G (p.Pro471Ala) c.1273C>G (p.Pro425Ala) c.3835C>G (p.Pro1279Ala) c.4600C>G (p.Pro1534Ala) c.4789C>G (p.Pro1597Ala) c.4582C>G (p.Pro1528Ala) c.1285C>G (p.Pro429Ala) c.1330C>G (p.Pro444Ala) c.4786C>G (p.Pro1596Ala) c.1110C>G c.1297C>G (p.Pro433Ala) c.*4506C>G (n.*4506C>G) c.1036C>G (p.Pro346Ala) c.5-7240C>G (n.5-7240C>G) c.196C>G (p.Pro66Ala) c.-98-21001C>G (n.-98-21001C>G) n.4859C>G n.4900C>G | |
17 | g.43071191G= | CA2260773001 | BRCA1 | c.4720C= (p.Pro1574=) c.4723C= (p.Pro1575=) c.4597C= (p.Pro1533=) c.4717C= (p.Pro1573=) c.4645C= (p.Pro1549=) c.1411C= (p.Pro471=) c.1273C= (p.Pro425=) c.3835C= (p.Pro1279=) c.4600C= (p.Pro1534=) c.4789C= (p.Pro1597=) c.4582C= (p.Pro1528=) c.1285C= (p.Pro429=) c.1330C= (p.Pro444=) c.4786C= (p.Pro1596=) c.1110C= c.1297C= (p.Pro433=) c.*4506C= (n.*4506C=) c.1036C= (p.Pro346=) c.5-7240C= (n.5-7240C=) c.196C= (p.Pro66=) c.-98-21001C= (n.-98-21001C=) n.4859C= n.4900C= | |
17 | g.43071191G>T | CA10592061 | BRCA1 | c.4720C>A (p.Pro1574Thr) c.4723C>A (p.Pro1575Thr) c.4597C>A (p.Pro1533Thr) c.4717C>A (p.Pro1573Thr) c.4645C>A (p.Pro1549Thr) c.1411C>A (p.Pro471Thr) c.1273C>A (p.Pro425Thr) c.3835C>A (p.Pro1279Thr) c.4600C>A (p.Pro1534Thr) c.4789C>A (p.Pro1597Thr) c.4582C>A (p.Pro1528Thr) c.1285C>A (p.Pro429Thr) c.1330C>A (p.Pro444Thr) c.4786C>A (p.Pro1596Thr) c.1110C>A c.1297C>A (p.Pro433Thr) c.*4506C>A (n.*4506C>A) c.1036C>A (p.Pro346Thr) c.5-7240C>A (n.5-7240C>A) c.196C>A (p.Pro66Thr) c.-98-21001C>A (n.-98-21001C>A) n.4859C>A n.4900C>A | ClinVar dbSNP |
17 | g.43071192G>A | CA500231880 | BRCA1 | c.4719C>T (p.Asp1573=) c.4722C>T (p.Asp1574=) c.4596C>T (p.Asp1532=) c.4716C>T (p.Asp1572=) c.4644C>T (p.Asp1548=) c.1410C>T (p.Asp470=) c.1272C>T (p.Asp424=) c.3834C>T (p.Asp1278=) c.4599C>T (p.Asp1533=) c.4788C>T (p.Asp1596=) c.4581C>T (p.Asp1527=) c.1284C>T (p.Asp428=) c.1329C>T (p.Asp443=) c.4785C>T (p.Asp1595=) c.1109C>T c.1296C>T (p.Asp432=) c.*4505C>T (n.*4505C>T) c.1035C>T (p.Asp345=) c.5-7241C>T (n.5-7241C>T) c.195C>T (p.Asp65=) c.-98-21002C>T (n.-98-21002C>T) n.4858C>T n.4899C>T | ClinVar dbSNP gnomAD v4 |
17 | g.43071192G>C | CA10592062 | BRCA1 | c.4719C>G (p.Asp1573Glu) c.4722C>G (p.Asp1574Glu) c.4596C>G (p.Asp1532Glu) c.4716C>G (p.Asp1572Glu) c.4644C>G (p.Asp1548Glu) c.1410C>G (p.Asp470Glu) c.1272C>G (p.Asp424Glu) c.3834C>G (p.Asp1278Glu) c.4599C>G (p.Asp1533Glu) c.4788C>G (p.Asp1596Glu) c.4581C>G (p.Asp1527Glu) c.1284C>G (p.Asp428Glu) c.1329C>G (p.Asp443Glu) c.4785C>G (p.Asp1595Glu) c.1109C>G c.1296C>G (p.Asp432Glu) c.*4505C>G (n.*4505C>G) c.1035C>G (p.Asp345Glu) c.5-7241C>G (n.5-7241C>G) c.195C>G (p.Asp65Glu) c.-98-21002C>G (n.-98-21002C>G) n.4858C>G n.4899C>G | dbSNP |
17 | g.43071192G>T | CA10592063 | BRCA1 | c.4719C>A (p.Asp1573Glu) c.4722C>A (p.Asp1574Glu) c.4596C>A (p.Asp1532Glu) c.4716C>A (p.Asp1572Glu) c.4644C>A (p.Asp1548Glu) c.1410C>A (p.Asp470Glu) c.1272C>A (p.Asp424Glu) c.3834C>A (p.Asp1278Glu) c.4599C>A (p.Asp1533Glu) c.4788C>A (p.Asp1596Glu) c.4581C>A (p.Asp1527Glu) c.1284C>A (p.Asp428Glu) c.1329C>A (p.Asp443Glu) c.4785C>A (p.Asp1595Glu) c.1109C>A c.1296C>A (p.Asp432Glu) c.*4505C>A (n.*4505C>A) c.1035C>A (p.Asp345Glu) c.5-7241C>A (n.5-7241C>A) c.195C>A (p.Asp65Glu) c.-98-21002C>A (n.-98-21002C>A) n.4858C>A n.4899C>A | dbSNP |
17 | g.43071193del | CA2638062624 | BRCA1 | c.4718del (p.Asp1573AlafsTer27) c.4721del (p.Asp1574AlafsTer27) c.4595del (p.Asp1532AlafsTer27) c.4715del (p.Asp1572AlafsTer27) c.4643del (p.Asp1548AlafsTer27) c.1409del (p.Asp470AlafsTer27) c.1271del (p.Asp424AlafsTer27) c.3833del (p.Asp1278AlafsTer27) c.4598del (p.Asp1533AlafsTer27) c.4787del (p.Asp1596AlafsTer27) c.4580del (p.Asp1527AlafsTer27) c.1283del (p.Asp428AlafsTer27) c.1328del (p.Asp443AlafsTer27) c.4784del (p.Asp1595AlafsTer27) c.1108del c.1295del (p.Asp432AlafsTer27) c.*4504del (n.*4504del) c.1034del (p.Asp345AlafsTer27) c.5-7242del (n.5-7242del) c.194del (p.Asp65AlafsTer27) c.-98-21003del (n.-98-21003del) n.4857del n.4898del | gnomAD v4 |
17 | g.43071193T>A | CA10592064 | BRCA1 | c.4718A>T (p.Asp1573Val) c.4721A>T (p.Asp1574Val) c.4595A>T (p.Asp1532Val) c.4715A>T (p.Asp1572Val) c.4643A>T (p.Asp1548Val) c.1409A>T (p.Asp470Val) c.1271A>T (p.Asp424Val) c.3833A>T (p.Asp1278Val) c.4598A>T (p.Asp1533Val) c.4787A>T (p.Asp1596Val) c.4580A>T (p.Asp1527Val) c.1283A>T (p.Asp428Val) c.1328A>T (p.Asp443Val) c.4784A>T (p.Asp1595Val) c.1108A>T c.1295A>T (p.Asp432Val) c.*4504A>T (n.*4504A>T) c.1034A>T (p.Asp345Val) c.5-7242A>T (n.5-7242A>T) c.194A>T (p.Asp65Val) c.-98-21003A>T (n.-98-21003A>T) n.4857A>T n.4898A>T | dbSNP |
17 | g.43071193T>C | CA10592065 | BRCA1 | c.4718A>G (p.Asp1573Gly) c.4721A>G (p.Asp1574Gly) c.4595A>G (p.Asp1532Gly) c.4715A>G (p.Asp1572Gly) c.4643A>G (p.Asp1548Gly) c.1409A>G (p.Asp470Gly) c.1271A>G (p.Asp424Gly) c.3833A>G (p.Asp1278Gly) c.4598A>G (p.Asp1533Gly) c.4787A>G (p.Asp1596Gly) c.4580A>G (p.Asp1527Gly) c.1283A>G (p.Asp428Gly) c.1328A>G (p.Asp443Gly) c.4784A>G (p.Asp1595Gly) c.1108A>G c.1295A>G (p.Asp432Gly) c.*4504A>G (n.*4504A>G) c.1034A>G (p.Asp345Gly) c.5-7242A>G (n.5-7242A>G) c.194A>G (p.Asp65Gly) c.-98-21003A>G (n.-98-21003A>G) n.4857A>G n.4898A>G | dbSNP |
17 | g.43071193T>G | CA10592066 | BRCA1 | c.4718A>C (p.Asp1573Ala) c.4721A>C (p.Asp1574Ala) c.4595A>C (p.Asp1532Ala) c.4715A>C (p.Asp1572Ala) c.4643A>C (p.Asp1548Ala) c.1409A>C (p.Asp470Ala) c.1271A>C (p.Asp424Ala) c.3833A>C (p.Asp1278Ala) c.4598A>C (p.Asp1533Ala) c.4787A>C (p.Asp1596Ala) c.4580A>C (p.Asp1527Ala) c.1283A>C (p.Asp428Ala) c.1328A>C (p.Asp443Ala) c.4784A>C (p.Asp1595Ala) c.1108A>C c.1295A>C (p.Asp432Ala) c.*4504A>C (n.*4504A>C) c.1034A>C (p.Asp345Ala) c.5-7242A>C (n.5-7242A>C) c.194A>C (p.Asp65Ala) c.-98-21003A>C (n.-98-21003A>C) n.4857A>C n.4898A>C | dbSNP |
17 | g.43071194C>A | CA10592067 | BRCA1 | c.4717G>T (p.Asp1573Tyr) c.4720G>T (p.Asp1574Tyr) c.4594G>T (p.Asp1532Tyr) c.4714G>T (p.Asp1572Tyr) c.4642G>T (p.Asp1548Tyr) c.1408G>T (p.Asp470Tyr) c.1270G>T (p.Asp424Tyr) c.3832G>T (p.Asp1278Tyr) c.4597G>T (p.Asp1533Tyr) c.4786G>T (p.Asp1596Tyr) c.4579G>T (p.Asp1527Tyr) c.1282G>T (p.Asp428Tyr) c.1327G>T (p.Asp443Tyr) c.4783G>T (p.Asp1595Tyr) c.1107G>T c.1294G>T (p.Asp432Tyr) c.*4503G>T (n.*4503G>T) c.1033G>T (p.Asp345Tyr) c.5-7243G>T (n.5-7243G>T) c.193G>T (p.Asp65Tyr) c.-98-21004G>T (n.-98-21004G>T) n.4856G>T n.4897G>T | ClinVar dbSNP |
17 | g.43071194C= | CA2260773002 | BRCA1 | c.4717G= (p.Asp1573=) c.4720G= (p.Asp1574=) c.4594G= (p.Asp1532=) c.4714G= (p.Asp1572=) c.4642G= (p.Asp1548=) c.1408G= (p.Asp470=) c.1270G= (p.Asp424=) c.3832G= (p.Asp1278=) c.4597G= (p.Asp1533=) c.4786G= (p.Asp1596=) c.4579G= (p.Asp1527=) c.1282G= (p.Asp428=) c.1327G= (p.Asp443=) c.4783G= (p.Asp1595=) c.1107G= c.1294G= (p.Asp432=) c.*4503G= (n.*4503G=) c.1033G= (p.Asp345=) c.5-7243G= (n.5-7243G=) c.193G= (p.Asp65=) c.-98-21004G= (n.-98-21004G=) n.4856G= n.4897G= | |
17 | g.43071194C>G | CA10592068 | BRCA1 | c.4717G>C (p.Asp1573His) c.4720G>C (p.Asp1574His) c.4594G>C (p.Asp1532His) c.4714G>C (p.Asp1572His) c.4642G>C (p.Asp1548His) c.1408G>C (p.Asp470His) c.1270G>C (p.Asp424His) c.3832G>C (p.Asp1278His) c.4597G>C (p.Asp1533His) c.4786G>C (p.Asp1596His) c.4579G>C (p.Asp1527His) c.1282G>C (p.Asp428His) c.1327G>C (p.Asp443His) c.4783G>C (p.Asp1595His) c.1107G>C c.1294G>C (p.Asp432His) c.*4503G>C (n.*4503G>C) c.1033G>C (p.Asp345His) c.5-7243G>C (n.5-7243G>C) c.193G>C (p.Asp65His) c.-98-21004G>C (n.-98-21004G>C) n.4856G>C n.4897G>C | dbSNP |
17 | g.43071194C>T | CA10592069 | BRCA1 | c.4717G>A (p.Asp1573Asn) c.4720G>A (p.Asp1574Asn) c.4594G>A (p.Asp1532Asn) c.4714G>A (p.Asp1572Asn) c.4642G>A (p.Asp1548Asn) c.1408G>A (p.Asp470Asn) c.1270G>A (p.Asp424Asn) c.3832G>A (p.Asp1278Asn) c.4597G>A (p.Asp1533Asn) c.4786G>A (p.Asp1596Asn) c.4579G>A (p.Asp1527Asn) c.1282G>A (p.Asp428Asn) c.1327G>A (p.Asp443Asn) c.4783G>A (p.Asp1595Asn) c.1107G>A c.1294G>A (p.Asp432Asn) c.*4503G>A (n.*4503G>A) c.1033G>A (p.Asp345Asn) c.5-7243G>A (n.5-7243G>A) c.193G>A (p.Asp65Asn) c.-98-21004G>A (n.-98-21004G>A) n.4856G>A n.4897G>A | dbSNP |
17 | g.43071195A= | CA2260773003 | BRCA1 | c.4716T= (p.Asp1572=) c.4719T= (p.Asp1573=) c.4593T= (p.Asp1531=) c.4713T= (p.Asp1571=) c.4641T= (p.Asp1547=) c.1407T= (p.Asp469=) c.1269T= (p.Asp423=) c.3831T= (p.Asp1277=) c.4596T= (p.Asp1532=) c.4785T= (p.Asp1595=) c.4578T= (p.Asp1526=) c.1281T= (p.Asp427=) c.1326T= (p.Asp442=) c.4782T= (p.Asp1594=) c.1106T= c.1293T= (p.Asp431=) c.*4502T= (n.*4502T=) c.1032T= (p.Asp344=) c.5-7244T= (n.5-7244T=) c.192T= (p.Asp64=) c.-98-21005T= (n.-98-21005T=) n.4855T= n.4896T= | |
17 | g.43071195A>C | CA10592070 | BRCA1 | c.4716T>G (p.Asp1572Glu) c.4719T>G (p.Asp1573Glu) c.4593T>G (p.Asp1531Glu) c.4713T>G (p.Asp1571Glu) c.4641T>G (p.Asp1547Glu) c.1407T>G (p.Asp469Glu) c.1269T>G (p.Asp423Glu) c.3831T>G (p.Asp1277Glu) c.4596T>G (p.Asp1532Glu) c.4785T>G (p.Asp1595Glu) c.4578T>G (p.Asp1526Glu) c.1281T>G (p.Asp427Glu) c.1326T>G (p.Asp442Glu) c.4782T>G (p.Asp1594Glu) c.1106T>G c.1293T>G (p.Asp431Glu) c.*4502T>G (n.*4502T>G) c.1032T>G (p.Asp344Glu) c.5-7244T>G (n.5-7244T>G) c.192T>G (p.Asp64Glu) c.-98-21005T>G (n.-98-21005T>G) n.4855T>G n.4896T>G | |
17 | g.43071195A>G | CA16607259 | BRCA1 | c.4716T>C (p.Asp1572=) c.4719T>C (p.Asp1573=) c.4593T>C (p.Asp1531=) c.4713T>C (p.Asp1571=) c.4641T>C (p.Asp1547=) c.1407T>C (p.Asp469=) c.1269T>C (p.Asp423=) c.3831T>C (p.Asp1277=) c.4596T>C (p.Asp1532=) c.4785T>C (p.Asp1595=) c.4578T>C (p.Asp1526=) c.1281T>C (p.Asp427=) c.1326T>C (p.Asp442=) c.4782T>C (p.Asp1594=) c.1106T>C c.1293T>C (p.Asp431=) c.*4502T>C (n.*4502T>C) c.1032T>C (p.Asp344=) c.5-7244T>C (n.5-7244T>C) c.192T>C (p.Asp64=) c.-98-21005T>C (n.-98-21005T>C) n.4855T>C n.4896T>C | ClinVar dbSNP |
17 | g.43071195A>T | CA10592071 | BRCA1 | c.4716T>A (p.Asp1572Glu) c.4719T>A (p.Asp1573Glu) c.4593T>A (p.Asp1531Glu) c.4713T>A (p.Asp1571Glu) c.4641T>A (p.Asp1547Glu) c.1407T>A (p.Asp469Glu) c.1269T>A (p.Asp423Glu) c.3831T>A (p.Asp1277Glu) c.4596T>A (p.Asp1532Glu) c.4785T>A (p.Asp1595Glu) c.4578T>A (p.Asp1526Glu) c.1281T>A (p.Asp427Glu) c.1326T>A (p.Asp442Glu) c.4782T>A (p.Asp1594Glu) c.1106T>A c.1293T>A (p.Asp431Glu) c.*4502T>A (n.*4502T>A) c.1032T>A (p.Asp344Glu) c.5-7244T>A (n.5-7244T>A) c.192T>A (p.Asp64Glu) c.-98-21005T>A (n.-98-21005T>A) n.4855T>A n.4896T>A | dbSNP |
17 | g.43071196T>A | CA10592072 | BRCA1 | c.4715A>T (p.Asp1572Val) c.4718A>T (p.Asp1573Val) c.4592A>T (p.Asp1531Val) c.4712A>T (p.Asp1571Val) c.4640A>T (p.Asp1547Val) c.1406A>T (p.Asp469Val) c.1268A>T (p.Asp423Val) c.3830A>T (p.Asp1277Val) c.4595A>T (p.Asp1532Val) c.4784A>T (p.Asp1595Val) c.4577A>T (p.Asp1526Val) c.1280A>T (p.Asp427Val) c.1325A>T (p.Asp442Val) c.4781A>T (p.Asp1594Val) c.1105A>T c.1292A>T (p.Asp431Val) c.*4501A>T (n.*4501A>T) c.1031A>T (p.Asp344Val) c.5-7245A>T (n.5-7245A>T) c.191A>T (p.Asp64Val) c.-98-21006A>T (n.-98-21006A>T) n.4854A>T n.4895A>T | dbSNP |
17 | g.43071196T>C | CA10592073 | BRCA1 | c.4715A>G (p.Asp1572Gly) c.4718A>G (p.Asp1573Gly) c.4592A>G (p.Asp1531Gly) c.4712A>G (p.Asp1571Gly) c.4640A>G (p.Asp1547Gly) c.1406A>G (p.Asp469Gly) c.1268A>G (p.Asp423Gly) c.3830A>G (p.Asp1277Gly) c.4595A>G (p.Asp1532Gly) c.4784A>G (p.Asp1595Gly) c.4577A>G (p.Asp1526Gly) c.1280A>G (p.Asp427Gly) c.1325A>G (p.Asp442Gly) c.4781A>G (p.Asp1594Gly) c.1105A>G c.1292A>G (p.Asp431Gly) c.*4501A>G (n.*4501A>G) c.1031A>G (p.Asp344Gly) c.5-7245A>G (n.5-7245A>G) c.191A>G (p.Asp64Gly) c.-98-21006A>G (n.-98-21006A>G) n.4854A>G n.4895A>G | dbSNP |
17 | g.43071196T>G | CA10592074 | BRCA1 | c.4715A>C (p.Asp1572Ala) c.4718A>C (p.Asp1573Ala) c.4592A>C (p.Asp1531Ala) c.4712A>C (p.Asp1571Ala) c.4640A>C (p.Asp1547Ala) c.1406A>C (p.Asp469Ala) c.1268A>C (p.Asp423Ala) c.3830A>C (p.Asp1277Ala) c.4595A>C (p.Asp1532Ala) c.4784A>C (p.Asp1595Ala) c.4577A>C (p.Asp1526Ala) c.1280A>C (p.Asp427Ala) c.1325A>C (p.Asp442Ala) c.4781A>C (p.Asp1594Ala) c.1105A>C c.1292A>C (p.Asp431Ala) c.*4501A>C (n.*4501A>C) c.1031A>C (p.Asp344Ala) c.5-7245A>C (n.5-7245A>C) c.191A>C (p.Asp64Ala) c.-98-21006A>C (n.-98-21006A>C) n.4854A>C n.4895A>C | |
17 | g.43071196_43071197delinsTC | CA2260773004 | BRCA1 | c.4714_4715delinsGA (p.Asp1572=) c.4717_4718delinsGA (p.Asp1573=) c.4591_4592delinsGA (p.Asp1531=) c.4711_4712delinsGA (p.Asp1571=) c.4639_4640delinsGA (p.Asp1547=) c.1405_1406delinsGA (p.Asp469=) c.1267_1268delinsGA (p.Asp423=) c.3829_3830delinsGA (p.Asp1277=) c.4594_4595delinsGA (p.Asp1532=) c.4783_4784delinsGA (p.Asp1595=) c.4576_4577delinsGA (p.Asp1526=) c.1279_1280delinsGA (p.Asp427=) c.1324_1325delinsGA (p.Asp442=) c.4780_4781delinsGA (p.Asp1594=) c.1104_1105delinsGA c.1291_1292delinsGA (p.Asp431=) c.*4500_*4501delinsGA (n.*4500_*4501delinsGA) c.1030_1031delinsGA (p.Asp344=) c.5-7246_5-7245delinsGA (n.5-7246_5-7245delinsGA) c.190_191delinsGA (p.Asp64=) c.-98-21007_-98-21006delinsGA (n.-98-21007_-98-21006delinsGA) n.4853_4854delinsGA n.4894_4895delinsGA | |
17 | g.43071197del | CA916080200 | BRCA1 | c.4714del (p.Asp1572MetfsTer28) c.4717del (p.Asp1573MetfsTer28) c.4591del (p.Asp1531MetfsTer28) c.4711del (p.Asp1571MetfsTer28) c.4639del (p.Asp1547MetfsTer28) c.1405del (p.Asp469MetfsTer28) c.1267del (p.Asp423MetfsTer28) c.3829del (p.Asp1277MetfsTer28) c.4594del (p.Asp1532MetfsTer28) c.4783del (p.Asp1595MetfsTer28) c.4576del (p.Asp1526MetfsTer28) c.1279del (p.Asp427MetfsTer28) c.1324del (p.Asp442MetfsTer28) c.4780del (p.Asp1594MetfsTer28) c.1104del c.1291del (p.Asp431MetfsTer28) c.*4500del (n.*4500del) c.1030del (p.Asp344MetfsTer28) c.5-7246del (n.5-7246del) c.190del (p.Asp64MetfsTer28) c.-98-21007del (n.-98-21007del) n.4853del n.4894del | ClinVar dbSNP |
17 | g.43071197C>A | CA10592075 | BRCA1 | c.4714G>T (p.Asp1572Tyr) c.4717G>T (p.Asp1573Tyr) c.4591G>T (p.Asp1531Tyr) c.4711G>T (p.Asp1571Tyr) c.4639G>T (p.Asp1547Tyr) c.1405G>T (p.Asp469Tyr) c.1267G>T (p.Asp423Tyr) c.3829G>T (p.Asp1277Tyr) c.4594G>T (p.Asp1532Tyr) c.4783G>T (p.Asp1595Tyr) c.4576G>T (p.Asp1526Tyr) c.1279G>T (p.Asp427Tyr) c.1324G>T (p.Asp442Tyr) c.4780G>T (p.Asp1594Tyr) c.1104G>T c.1291G>T (p.Asp431Tyr) c.*4500G>T (n.*4500G>T) c.1030G>T (p.Asp344Tyr) c.5-7246G>T (n.5-7246G>T) c.190G>T (p.Asp64Tyr) c.-98-21007G>T (n.-98-21007G>T) n.4853G>T n.4894G>T | dbSNP |
17 | g.43071197C= | CA2260773005 | BRCA1 | c.4714G= (p.Asp1572=) c.4717G= (p.Asp1573=) c.4591G= (p.Asp1531=) c.4711G= (p.Asp1571=) c.4639G= (p.Asp1547=) c.1405G= (p.Asp469=) c.1267G= (p.Asp423=) c.3829G= (p.Asp1277=) c.4594G= (p.Asp1532=) c.4783G= (p.Asp1595=) c.4576G= (p.Asp1526=) c.1279G= (p.Asp427=) c.1324G= (p.Asp442=) c.4780G= (p.Asp1594=) c.1104G= c.1291G= (p.Asp431=) c.*4500G= (n.*4500G=) c.1030G= (p.Asp344=) c.5-7246G= (n.5-7246G=) c.190G= (p.Asp64=) c.-98-21007G= (n.-98-21007G=) n.4853G= n.4894G= | |
17 | g.43071197C>G | CA10592076 | BRCA1 | c.4714G>C (p.Asp1572His) c.4717G>C (p.Asp1573His) c.4591G>C (p.Asp1531His) c.4711G>C (p.Asp1571His) c.4639G>C (p.Asp1547His) c.1405G>C (p.Asp469His) c.1267G>C (p.Asp423His) c.3829G>C (p.Asp1277His) c.4594G>C (p.Asp1532His) c.4783G>C (p.Asp1595His) c.4576G>C (p.Asp1526His) c.1279G>C (p.Asp427His) c.1324G>C (p.Asp442His) c.4780G>C (p.Asp1594His) c.1104G>C c.1291G>C (p.Asp431His) c.*4500G>C (n.*4500G>C) c.1030G>C (p.Asp344His) c.5-7246G>C (n.5-7246G>C) c.190G>C (p.Asp64His) c.-98-21007G>C (n.-98-21007G>C) n.4853G>C n.4894G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.43071197C>T | CA10592077 | BRCA1 | c.4714G>A (p.Asp1572Asn) c.4717G>A (p.Asp1573Asn) c.4591G>A (p.Asp1531Asn) c.4711G>A (p.Asp1571Asn) c.4639G>A (p.Asp1547Asn) c.1405G>A (p.Asp469Asn) c.1267G>A (p.Asp423Asn) c.3829G>A (p.Asp1277Asn) c.4594G>A (p.Asp1532Asn) c.4783G>A (p.Asp1595Asn) c.4576G>A (p.Asp1526Asn) c.1279G>A (p.Asp427Asn) c.1324G>A (p.Asp442Asn) c.4780G>A (p.Asp1594Asn) c.1104G>A c.1291G>A (p.Asp431Asn) c.*4500G>A (n.*4500G>A) c.1030G>A (p.Asp344Asn) c.5-7246G>A (n.5-7246G>A) c.190G>A (p.Asp64Asn) c.-98-21007G>A (n.-98-21007G>A) n.4853G>A n.4894G>A | dbSNP gnomAD v4 |
17 | g.43071197_43071202delinsCAGAGA | CA2260773006 | BRCA1 | c.4709_4714delinsTCTCTG (p.Phe1570=) c.4712_4717delinsTCTCTG (p.Phe1571=) c.4586_4591delinsTCTCTG (p.Phe1529=) c.4706_4711delinsTCTCTG (p.Phe1569=) c.4634_4639delinsTCTCTG (p.Phe1545=) c.1400_1405delinsTCTCTG (p.Phe467=) c.1262_1267delinsTCTCTG (p.Phe421=) c.3824_3829delinsTCTCTG (p.Phe1275=) c.4589_4594delinsTCTCTG (p.Phe1530=) c.4778_4783delinsTCTCTG (p.Phe1593=) c.4571_4576delinsTCTCTG (p.Phe1524=) c.1274_1279delinsTCTCTG (p.Phe425=) c.1319_1324delinsTCTCTG (p.Phe440=) c.4775_4780delinsTCTCTG (p.Phe1592=) c.1099_1104delinsTCTCTG c.1286_1291delinsTCTCTG (p.Phe429=) c.*4495_*4500delinsTCTCTG (n.*4495_*4500delinsTCTCTG) c.1025_1030delinsTCTCTG (p.Phe342=) c.5-7251_5-7246delinsTCTCTG (n.5-7251_5-7246delinsTCTCTG) c.185_190delinsTCTCTG (p.Phe62=) c.-98-21012_-98-21007delinsTCTCTG (n.-98-21012_-98-21007delinsTCTCTG) n.4848_4853delinsTCTCTG n.4889_4894delinsTCTCTG | |
17 | g.43071198_43074416dup | CA658653641 | BRCA1 | c.4588_4714dup c.4591_4717dup c.4465_4591dup c.4585_4711dup c.4513_4639dup c.1279_1405dup c.1141_1267dup c.3703_3829dup c.4468_4594dup c.4657_4783dup c.4450_4576dup c.1153_1279dup c.1198_1324dup c.4654_4780dup c.978_1104dup c.1165_1291dup c.*4374_*4500dup c.904_1030dup c.5-10464_5-7246dup (n.5-10464_5-7246dup) c.64_190dup c.-98-24225_-98-21007dup (n.-98-24225_-98-21007dup) n.4727_4853dup n.4768_4894dup | |
17 | g.43071198del | CA2733916232 | BRCA1 | c.4713del (p.Asp1572MetfsTer28) c.4716del (p.Asp1573MetfsTer28) c.4590del (p.Asp1531MetfsTer28) c.4710del (p.Asp1571MetfsTer28) c.4638del (p.Asp1547MetfsTer28) c.1404del (p.Asp469MetfsTer28) c.1266del (p.Asp423MetfsTer28) c.3828del (p.Asp1277MetfsTer28) c.4593del (p.Asp1532MetfsTer28) c.4782del (p.Asp1595MetfsTer28) c.4575del (p.Asp1526MetfsTer28) c.1278del (p.Asp427MetfsTer28) c.1323del (p.Asp442MetfsTer28) c.4779del (p.Asp1594MetfsTer28) c.1103del c.1290del (p.Asp431MetfsTer28) c.*4499del (n.*4499del) c.1029del (p.Asp344MetfsTer28) c.5-7247del (n.5-7247del) c.189del (p.Asp64MetfsTer28) c.-98-21008del (n.-98-21008del) n.4852del n.4893del | dbSNP |
17 | g.43071198A= | CA2260773007 | BRCA1 | c.4713T= (p.Ser1571=) c.4716T= (p.Ser1572=) c.4590T= (p.Ser1530=) c.4710T= (p.Ser1570=) c.4638T= (p.Ser1546=) c.1404T= (p.Ser468=) c.1266T= (p.Ser422=) c.3828T= (p.Ser1276=) c.4593T= (p.Ser1531=) c.4782T= (p.Ser1594=) c.4575T= (p.Ser1525=) c.1278T= (p.Ser426=) c.1323T= (p.Ser441=) c.4779T= (p.Ser1593=) c.1103T= c.1290T= (p.Ser430=) c.*4499T= (n.*4499T=) c.1029T= (p.Ser343=) c.5-7247T= (n.5-7247T=) c.189T= (p.Ser63=) c.-98-21008T= (n.-98-21008T=) n.4852T= n.4893T= | |
17 | g.43071198A>C | CA500231883 | BRCA1 | c.4713T>G (p.Ser1571=) c.4716T>G (p.Ser1572=) c.4590T>G (p.Ser1530=) c.4710T>G (p.Ser1570=) c.4638T>G (p.Ser1546=) c.1404T>G (p.Ser468=) c.1266T>G (p.Ser422=) c.3828T>G (p.Ser1276=) c.4593T>G (p.Ser1531=) c.4782T>G (p.Ser1594=) c.4575T>G (p.Ser1525=) c.1278T>G (p.Ser426=) c.1323T>G (p.Ser441=) c.4779T>G (p.Ser1593=) c.1103T>G c.1290T>G (p.Ser430=) c.*4499T>G (n.*4499T>G) c.1029T>G (p.Ser343=) c.5-7247T>G (n.5-7247T>G) c.189T>G (p.Ser63=) c.-98-21008T>G (n.-98-21008T>G) n.4852T>G n.4893T>G | ClinVar dbSNP |
17 | g.43071198A>G | CA500231881 | BRCA1 | c.4713T>C (p.Ser1571=) c.4716T>C (p.Ser1572=) c.4590T>C (p.Ser1530=) c.4710T>C (p.Ser1570=) c.4638T>C (p.Ser1546=) c.1404T>C (p.Ser468=) c.1266T>C (p.Ser422=) c.3828T>C (p.Ser1276=) c.4593T>C (p.Ser1531=) c.4782T>C (p.Ser1594=) c.4575T>C (p.Ser1525=) c.1278T>C (p.Ser426=) c.1323T>C (p.Ser441=) c.4779T>C (p.Ser1593=) c.1103T>C c.1290T>C (p.Ser430=) c.*4499T>C (n.*4499T>C) c.1029T>C (p.Ser343=) c.5-7247T>C (n.5-7247T>C) c.189T>C (p.Ser63=) c.-98-21008T>C (n.-98-21008T>C) n.4852T>C n.4893T>C | |
17 | g.43071198A>T | CA500231882 | BRCA1 | c.4713T>A (p.Ser1571=) c.4716T>A (p.Ser1572=) c.4590T>A (p.Ser1530=) c.4710T>A (p.Ser1570=) c.4638T>A (p.Ser1546=) c.1404T>A (p.Ser468=) c.1266T>A (p.Ser422=) c.3828T>A (p.Ser1276=) c.4593T>A (p.Ser1531=) c.4782T>A (p.Ser1594=) c.4575T>A (p.Ser1525=) c.1278T>A (p.Ser426=) c.1323T>A (p.Ser441=) c.4779T>A (p.Ser1593=) c.1103T>A c.1290T>A (p.Ser430=) c.*4499T>A (n.*4499T>A) c.1029T>A (p.Ser343=) c.5-7247T>A (n.5-7247T>A) c.189T>A (p.Ser63=) c.-98-21008T>A (n.-98-21008T>A) n.4852T>A n.4893T>A | dbSNP |
17 | g.43071201_43071202del | CA2580612628 | BRCA1 | c.4712_4713del (p.Ser1571Ter) c.4715_4716del (p.Ser1572Ter) c.4589_4590del (p.Ser1530Ter) c.4709_4710del (p.Ser1570Ter) c.4637_4638del (p.Ser1546Ter) c.1403_1404del (p.Ser468Ter) c.1265_1266del (p.Ser422Ter) c.3827_3828del (p.Ser1276Ter) c.4592_4593del (p.Ser1531Ter) c.4781_4782del (p.Ser1594Ter) c.4574_4575del (p.Ser1525Ter) c.1277_1278del (p.Ser426Ter) c.1322_1323del (p.Ser441Ter) c.4778_4779del (p.Ser1593Ter) c.1102_1103del c.1289_1290del (p.Ser430Ter) c.*4498_*4499del (n.*4498_*4499del) c.1028_1029del (p.Ser343Ter) c.5-7248_5-7247del (n.5-7248_5-7247del) c.188_189del (p.Ser63Ter) c.-98-21009_-98-21008del (n.-98-21009_-98-21008del) n.4851_4852del n.4892_4893del | ClinVar dbSNP |
17 | g.43071202_43071206del | CA002990 | BRCA1 | c.4709_4713del (p.Phe1570Ter) c.4712_4716del (p.Phe1571Ter) c.4586_4590del (p.Phe1529Ter) c.4706_4710del (p.Phe1569Ter) c.4634_4638del (p.Phe1545Ter) c.1400_1404del (p.Phe467Ter) c.1262_1266del (p.Phe421Ter) c.3824_3828del (p.Phe1275Ter) c.4589_4593del (p.Phe1530Ter) c.4778_4782del (p.Phe1593Ter) c.4571_4575del (p.Phe1524Ter) c.1274_1278del (p.Phe425Ter) c.1319_1323del (p.Phe440Ter) c.4775_4779del (p.Phe1592Ter) c.1099_1103del c.1286_1290del (p.Phe429Ter) c.*4495_*4499del (n.*4495_*4499del) c.1025_1029del (p.Phe342Ter) c.5-7251_5-7247del (n.5-7251_5-7247del) c.185_189del (p.Phe62Ter) c.-98-21012_-98-21008del (n.-98-21012_-98-21008del) n.4848_4852del n.4889_4893del | ClinVar dbSNP |
17 | g.43071199G>A | CA10592078 | BRCA1 | c.4712C>T (p.Ser1571Phe) c.4715C>T (p.Ser1572Phe) c.4589C>T (p.Ser1530Phe) c.4709C>T (p.Ser1570Phe) c.4637C>T (p.Ser1546Phe) c.1403C>T (p.Ser468Phe) c.1265C>T (p.Ser422Phe) c.3827C>T (p.Ser1276Phe) c.4592C>T (p.Ser1531Phe) c.4781C>T (p.Ser1594Phe) c.4574C>T (p.Ser1525Phe) c.1277C>T (p.Ser426Phe) c.1322C>T (p.Ser441Phe) c.4778C>T (p.Ser1593Phe) c.1102C>T c.1289C>T (p.Ser430Phe) c.*4498C>T (n.*4498C>T) c.1028C>T (p.Ser343Phe) c.5-7248C>T (n.5-7248C>T) c.188C>T (p.Ser63Phe) c.-98-21009C>T (n.-98-21009C>T) n.4851C>T n.4892C>T | ClinVar |
17 | g.43071199G>C | CA10592079 | BRCA1 | c.4712C>G (p.Ser1571Cys) c.4715C>G (p.Ser1572Cys) c.4589C>G (p.Ser1530Cys) c.4709C>G (p.Ser1570Cys) c.4637C>G (p.Ser1546Cys) c.1403C>G (p.Ser468Cys) c.1265C>G (p.Ser422Cys) c.3827C>G (p.Ser1276Cys) c.4592C>G (p.Ser1531Cys) c.4781C>G (p.Ser1594Cys) c.4574C>G (p.Ser1525Cys) c.1277C>G (p.Ser426Cys) c.1322C>G (p.Ser441Cys) c.4778C>G (p.Ser1593Cys) c.1102C>G c.1289C>G (p.Ser430Cys) c.*4498C>G (n.*4498C>G) c.1028C>G (p.Ser343Cys) c.5-7248C>G (n.5-7248C>G) c.188C>G (p.Ser63Cys) c.-98-21009C>G (n.-98-21009C>G) n.4851C>G n.4892C>G | ClinVar |
17 | g.43071199G>T | CA10592080 | BRCA1 | c.4712C>A (p.Ser1571Tyr) c.4715C>A (p.Ser1572Tyr) c.4589C>A (p.Ser1530Tyr) c.4709C>A (p.Ser1570Tyr) c.4637C>A (p.Ser1546Tyr) c.1403C>A (p.Ser468Tyr) c.1265C>A (p.Ser422Tyr) c.3827C>A (p.Ser1276Tyr) c.4592C>A (p.Ser1531Tyr) c.4781C>A (p.Ser1594Tyr) c.4574C>A (p.Ser1525Tyr) c.1277C>A (p.Ser426Tyr) c.1322C>A (p.Ser441Tyr) c.4778C>A (p.Ser1593Tyr) c.1102C>A c.1289C>A (p.Ser430Tyr) c.*4498C>A (n.*4498C>A) c.1028C>A (p.Ser343Tyr) c.5-7248C>A (n.5-7248C>A) c.188C>A (p.Ser63Tyr) c.-98-21009C>A (n.-98-21009C>A) n.4851C>A n.4892C>A | |
17 | g.43071200A>C | CA10592081 | BRCA1 | c.4711T>G (p.Ser1571Ala) c.4714T>G (p.Ser1572Ala) c.4588T>G (p.Ser1530Ala) c.4708T>G (p.Ser1570Ala) c.4636T>G (p.Ser1546Ala) c.1402T>G (p.Ser468Ala) c.1264T>G (p.Ser422Ala) c.3826T>G (p.Ser1276Ala) c.4591T>G (p.Ser1531Ala) c.4780T>G (p.Ser1594Ala) c.4573T>G (p.Ser1525Ala) c.1276T>G (p.Ser426Ala) c.1321T>G (p.Ser441Ala) c.4777T>G (p.Ser1593Ala) c.1101T>G c.1288T>G (p.Ser430Ala) c.*4497T>G (n.*4497T>G) c.1027T>G (p.Ser343Ala) c.5-7249T>G (n.5-7249T>G) c.187T>G (p.Ser63Ala) c.-98-21010T>G (n.-98-21010T>G) n.4850T>G n.4891T>G | |
17 | g.43071200A>G | CA10592082 | BRCA1 | c.4711T>C (p.Ser1571Pro) c.4714T>C (p.Ser1572Pro) c.4588T>C (p.Ser1530Pro) c.4708T>C (p.Ser1570Pro) c.4636T>C (p.Ser1546Pro) c.1402T>C (p.Ser468Pro) c.1264T>C (p.Ser422Pro) c.3826T>C (p.Ser1276Pro) c.4591T>C (p.Ser1531Pro) c.4780T>C (p.Ser1594Pro) c.4573T>C (p.Ser1525Pro) c.1276T>C (p.Ser426Pro) c.1321T>C (p.Ser441Pro) c.4777T>C (p.Ser1593Pro) c.1101T>C c.1288T>C (p.Ser430Pro) c.*4497T>C (n.*4497T>C) c.1027T>C (p.Ser343Pro) c.5-7249T>C (n.5-7249T>C) c.187T>C (p.Ser63Pro) c.-98-21010T>C (n.-98-21010T>C) n.4850T>C n.4891T>C | dbSNP |
17 | g.43071200A>T | CA10592083 | BRCA1 | c.4711T>A (p.Ser1571Thr) c.4714T>A (p.Ser1572Thr) c.4588T>A (p.Ser1530Thr) c.4708T>A (p.Ser1570Thr) c.4636T>A (p.Ser1546Thr) c.1402T>A (p.Ser468Thr) c.1264T>A (p.Ser422Thr) c.3826T>A (p.Ser1276Thr) c.4591T>A (p.Ser1531Thr) c.4780T>A (p.Ser1594Thr) c.4573T>A (p.Ser1525Thr) c.1276T>A (p.Ser426Thr) c.1321T>A (p.Ser441Thr) c.4777T>A (p.Ser1593Thr) c.1101T>A c.1288T>A (p.Ser430Thr) c.*4497T>A (n.*4497T>A) c.1027T>A (p.Ser343Thr) c.5-7249T>A (n.5-7249T>A) c.187T>A (p.Ser63Thr) c.-98-21010T>A (n.-98-21010T>A) n.4850T>A n.4891T>A | |
17 | g.43071201G>A | CA500231884 | BRCA1 | c.4710C>T (p.Phe1570=) c.4713C>T (p.Phe1571=) c.4587C>T (p.Phe1529=) c.4707C>T (p.Phe1569=) c.4635C>T (p.Phe1545=) c.1401C>T (p.Phe467=) c.1263C>T (p.Phe421=) c.3825C>T (p.Phe1275=) c.4590C>T (p.Phe1530=) c.4779C>T (p.Phe1593=) c.4572C>T (p.Phe1524=) c.1275C>T (p.Phe425=) c.1320C>T (p.Phe440=) c.4776C>T (p.Phe1592=) c.1100C>T c.1287C>T (p.Phe429=) c.*4496C>T (n.*4496C>T) c.1026C>T (p.Phe342=) c.5-7250C>T (n.5-7250C>T) c.186C>T (p.Phe62=) c.-98-21011C>T (n.-98-21011C>T) n.4849C>T n.4890C>T | ClinVar dbSNP |
17 | g.43071201G>C | CA052816 | BRCA1 | c.4710C>G (p.Phe1570Leu) c.4713C>G (p.Phe1571Leu) c.4587C>G (p.Phe1529Leu) c.4707C>G (p.Phe1569Leu) c.4635C>G (p.Phe1545Leu) c.1401C>G (p.Phe467Leu) c.1263C>G (p.Phe421Leu) c.3825C>G (p.Phe1275Leu) c.4590C>G (p.Phe1530Leu) c.4779C>G (p.Phe1593Leu) c.4572C>G (p.Phe1524Leu) c.1275C>G (p.Phe425Leu) c.1320C>G (p.Phe440Leu) c.4776C>G (p.Phe1592Leu) c.1100C>G c.1287C>G (p.Phe429Leu) c.*4496C>G (n.*4496C>G) c.1026C>G (p.Phe342Leu) c.5-7250C>G (n.5-7250C>G) c.186C>G (p.Phe62Leu) c.-98-21011C>G (n.-98-21011C>G) n.4849C>G n.4890C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.43071201G= | CA2260773008 | BRCA1 | c.4710C= (p.Phe1570=) c.4713C= (p.Phe1571=) c.4587C= (p.Phe1529=) c.4707C= (p.Phe1569=) c.4635C= (p.Phe1545=) c.1401C= (p.Phe467=) c.1263C= (p.Phe421=) c.3825C= (p.Phe1275=) c.4590C= (p.Phe1530=) c.4779C= (p.Phe1593=) c.4572C= (p.Phe1524=) c.1275C= (p.Phe425=) c.1320C= (p.Phe440=) c.4776C= (p.Phe1592=) c.1100C= c.1287C= (p.Phe429=) c.*4496C= (n.*4496C=) c.1026C= (p.Phe342=) c.5-7250C= (n.5-7250C=) c.186C= (p.Phe62=) c.-98-21011C= (n.-98-21011C=) n.4849C= n.4890C= | |
17 | g.43071201G>T | CA10592084 | BRCA1 | c.4710C>A (p.Phe1570Leu) c.4713C>A (p.Phe1571Leu) c.4587C>A (p.Phe1529Leu) c.4707C>A (p.Phe1569Leu) c.4635C>A (p.Phe1545Leu) c.1401C>A (p.Phe467Leu) c.1263C>A (p.Phe421Leu) c.3825C>A (p.Phe1275Leu) c.4590C>A (p.Phe1530Leu) c.4779C>A (p.Phe1593Leu) c.4572C>A (p.Phe1524Leu) c.1275C>A (p.Phe425Leu) c.1320C>A (p.Phe440Leu) c.4776C>A (p.Phe1592Leu) c.1100C>A c.1287C>A (p.Phe429Leu) c.*4496C>A (n.*4496C>A) c.1026C>A (p.Phe342Leu) c.5-7250C>A (n.5-7250C>A) c.186C>A (p.Phe62Leu) c.-98-21011C>A (n.-98-21011C>A) n.4849C>A n.4890C>A | dbSNP |
17 | g.43071201_43071202delinsGA | CA2260773009 | BRCA1 | c.4709_4710delinsTC (p.Phe1570=) c.4712_4713delinsTC (p.Phe1571=) c.4586_4587delinsTC (p.Phe1529=) c.4706_4707delinsTC (p.Phe1569=) c.4634_4635delinsTC (p.Phe1545=) c.1400_1401delinsTC (p.Phe467=) c.1262_1263delinsTC (p.Phe421=) c.3824_3825delinsTC (p.Phe1275=) c.4589_4590delinsTC (p.Phe1530=) c.4778_4779delinsTC (p.Phe1593=) c.4571_4572delinsTC (p.Phe1524=) c.1274_1275delinsTC (p.Phe425=) c.1319_1320delinsTC (p.Phe440=) c.4775_4776delinsTC (p.Phe1592=) c.1099_1100delinsTC c.1286_1287delinsTC (p.Phe429=) c.*4495_*4496delinsTC (n.*4495_*4496delinsTC) c.1025_1026delinsTC (p.Phe342=) c.5-7251_5-7250delinsTC (n.5-7251_5-7250delinsTC) c.185_186delinsTC (p.Phe62=) c.-98-21012_-98-21011delinsTC (n.-98-21012_-98-21011delinsTC) n.4848_4849delinsTC n.4889_4890delinsTC | |
17 | g.43071202A= | CA2260773010 | BRCA1 | c.4709T= (p.Phe1570=) c.4712T= (p.Phe1571=) c.4586T= (p.Phe1529=) c.4706T= (p.Phe1569=) c.4634T= (p.Phe1545=) c.1400T= (p.Phe467=) c.1262T= (p.Phe421=) c.3824T= (p.Phe1275=) c.4589T= (p.Phe1530=) c.4778T= (p.Phe1593=) c.4571T= (p.Phe1524=) c.1274T= (p.Phe425=) c.1319T= (p.Phe440=) c.4775T= (p.Phe1592=) c.1099T= c.1286T= (p.Phe429=) c.*4495T= (n.*4495T=) c.1025T= (p.Phe342=) c.5-7251T= (n.5-7251T=) c.185T= (p.Phe62=) c.-98-21012T= (n.-98-21012T=) n.4848T= n.4889T= | |
17 | g.43071202A>C | CA10592085 | BRCA1 | c.4709T>G (p.Phe1570Cys) c.4712T>G (p.Phe1571Cys) c.4586T>G (p.Phe1529Cys) c.4706T>G (p.Phe1569Cys) c.4634T>G (p.Phe1545Cys) c.1400T>G (p.Phe467Cys) c.1262T>G (p.Phe421Cys) c.3824T>G (p.Phe1275Cys) c.4589T>G (p.Phe1530Cys) c.4778T>G (p.Phe1593Cys) c.4571T>G (p.Phe1524Cys) c.1274T>G (p.Phe425Cys) c.1319T>G (p.Phe440Cys) c.4775T>G (p.Phe1592Cys) c.1099T>G c.1286T>G (p.Phe429Cys) c.*4495T>G (n.*4495T>G) c.1025T>G (p.Phe342Cys) c.5-7251T>G (n.5-7251T>G) c.185T>G (p.Phe62Cys) c.-98-21012T>G (n.-98-21012T>G) n.4848T>G n.4889T>G | |
17 | g.43071202A>G | CA002991 | BRCA1 | c.4709T>C (p.Phe1570Ser) c.4712T>C (p.Phe1571Ser) c.4586T>C (p.Phe1529Ser) c.4706T>C (p.Phe1569Ser) c.4634T>C (p.Phe1545Ser) c.1400T>C (p.Phe467Ser) c.1262T>C (p.Phe421Ser) c.3824T>C (p.Phe1275Ser) c.4589T>C (p.Phe1530Ser) c.4778T>C (p.Phe1593Ser) c.4571T>C (p.Phe1524Ser) c.1274T>C (p.Phe425Ser) c.1319T>C (p.Phe440Ser) c.4775T>C (p.Phe1592Ser) c.1099T>C c.1286T>C (p.Phe429Ser) c.*4495T>C (n.*4495T>C) c.1025T>C (p.Phe342Ser) c.5-7251T>C (n.5-7251T>C) c.185T>C (p.Phe62Ser) c.-98-21012T>C (n.-98-21012T>C) n.4848T>C n.4889T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.43071202A>T | CA10592086 | BRCA1 | c.4709T>A (p.Phe1570Tyr) c.4712T>A (p.Phe1571Tyr) c.4586T>A (p.Phe1529Tyr) c.4706T>A (p.Phe1569Tyr) c.4634T>A (p.Phe1545Tyr) c.1400T>A (p.Phe467Tyr) c.1262T>A (p.Phe421Tyr) c.3824T>A (p.Phe1275Tyr) c.4589T>A (p.Phe1530Tyr) c.4778T>A (p.Phe1593Tyr) c.4571T>A (p.Phe1524Tyr) c.1274T>A (p.Phe425Tyr) c.1319T>A (p.Phe440Tyr) c.4775T>A (p.Phe1592Tyr) c.1099T>A c.1286T>A (p.Phe429Tyr) c.*4495T>A (n.*4495T>A) c.1025T>A (p.Phe342Tyr) c.5-7251T>A (n.5-7251T>A) c.185T>A (p.Phe62Tyr) c.-98-21012T>A (n.-98-21012T>A) n.4848T>A n.4889T>A | dbSNP |
17 | g.43071203del | CA10575941 | BRCA1 | c.4709del (p.Phe1570SerfsTer30) c.4712del (p.Phe1571SerfsTer30) c.4586del (p.Phe1529SerfsTer30) c.4706del (p.Phe1569SerfsTer30) c.4634del (p.Phe1545SerfsTer30) c.1400del (p.Phe467SerfsTer30) c.1262del (p.Phe421SerfsTer30) c.3824del (p.Phe1275SerfsTer30) c.4589del (p.Phe1530SerfsTer30) c.4778del (p.Phe1593SerfsTer30) c.4571del (p.Phe1524SerfsTer30) c.1274del (p.Phe425SerfsTer30) c.1319del (p.Phe440SerfsTer30) c.4775del (p.Phe1592SerfsTer30) c.1099del c.1286del (p.Phe429SerfsTer30) c.*4495del (n.*4495del) c.1025del (p.Phe342SerfsTer30) c.5-7251del (n.5-7251del) c.185del (p.Phe62SerfsTer30) c.-98-21012del (n.-98-21012del) n.4848del n.4889del | ClinVar dbSNP |
17 | g.43071203A= | CA2260773011 | BRCA1 | c.4708T= (p.Phe1570=) c.4711T= (p.Phe1571=) c.4585T= (p.Phe1529=) c.4705T= (p.Phe1569=) c.4633T= (p.Phe1545=) c.1399T= (p.Phe467=) c.1261T= (p.Phe421=) c.3823T= (p.Phe1275=) c.4588T= (p.Phe1530=) c.4777T= (p.Phe1593=) c.4570T= (p.Phe1524=) c.1273T= (p.Phe425=) c.1318T= (p.Phe440=) c.4774T= (p.Phe1592=) c.1098T= c.1285T= (p.Phe429=) c.*4494T= (n.*4494T=) c.1024T= (p.Phe342=) c.5-7252T= (n.5-7252T=) c.184T= (p.Phe62=) c.-98-21013T= (n.-98-21013T=) n.4847T= n.4888T= | |
17 | g.43071203A>C | CA10592087 | BRCA1 | c.4708T>G (p.Phe1570Val) c.4711T>G (p.Phe1571Val) c.4585T>G (p.Phe1529Val) c.4705T>G (p.Phe1569Val) c.4633T>G (p.Phe1545Val) c.1399T>G (p.Phe467Val) c.1261T>G (p.Phe421Val) c.3823T>G (p.Phe1275Val) c.4588T>G (p.Phe1530Val) c.4777T>G (p.Phe1593Val) c.4570T>G (p.Phe1524Val) c.1273T>G (p.Phe425Val) c.1318T>G (p.Phe440Val) c.4774T>G (p.Phe1592Val) c.1098T>G c.1285T>G (p.Phe429Val) c.*4494T>G (n.*4494T>G) c.1024T>G (p.Phe342Val) c.5-7252T>G (n.5-7252T>G) c.184T>G (p.Phe62Val) c.-98-21013T>G (n.-98-21013T>G) n.4847T>G n.4888T>G | |
17 | g.43071203A>G | CA10592088 | BRCA1 | c.4708T>C (p.Phe1570Leu) c.4711T>C (p.Phe1571Leu) c.4585T>C (p.Phe1529Leu) c.4705T>C (p.Phe1569Leu) c.4633T>C (p.Phe1545Leu) c.1399T>C (p.Phe467Leu) c.1261T>C (p.Phe421Leu) c.3823T>C (p.Phe1275Leu) c.4588T>C (p.Phe1530Leu) c.4777T>C (p.Phe1593Leu) c.4570T>C (p.Phe1524Leu) c.1273T>C (p.Phe425Leu) c.1318T>C (p.Phe440Leu) c.4774T>C (p.Phe1592Leu) c.1098T>C c.1285T>C (p.Phe429Leu) c.*4494T>C (n.*4494T>C) c.1024T>C (p.Phe342Leu) c.5-7252T>C (n.5-7252T>C) c.184T>C (p.Phe62Leu) c.-98-21013T>C (n.-98-21013T>C) n.4847T>C n.4888T>C | ClinVar dbSNP |
17 | g.43071203A>T | CA10592089 | BRCA1 | c.4708T>A (p.Phe1570Ile) c.4711T>A (p.Phe1571Ile) c.4585T>A (p.Phe1529Ile) c.4705T>A (p.Phe1569Ile) c.4633T>A (p.Phe1545Ile) c.1399T>A (p.Phe467Ile) c.1261T>A (p.Phe421Ile) c.3823T>A (p.Phe1275Ile) c.4588T>A (p.Phe1530Ile) c.4777T>A (p.Phe1593Ile) c.4570T>A (p.Phe1524Ile) c.1273T>A (p.Phe425Ile) c.1318T>A (p.Phe440Ile) c.4774T>A (p.Phe1592Ile) c.1098T>A c.1285T>A (p.Phe429Ile) c.*4494T>A (n.*4494T>A) c.1024T>A (p.Phe342Ile) c.5-7252T>A (n.5-7252T>A) c.184T>A (p.Phe62Ile) c.-98-21013T>A (n.-98-21013T>A) n.4847T>A n.4888T>A | ClinVar dbSNP |
17 | g.43071203_43071214delinsAGAGGCTGATTC | CA2260773012 | BRCA1 | c.4697_4708delinsGAATCAGCCTCT (p.Gly1566=) c.4700_4711delinsGAATCAGCCTCT (p.Gly1567=) c.4574_4585delinsGAATCAGCCTCT (p.Gly1525=) c.4694_4705delinsGAATCAGCCTCT (p.Gly1565=) c.4622_4633delinsGAATCAGCCTCT (p.Gly1541=) c.1388_1399delinsGAATCAGCCTCT (p.Gly463=) c.1250_1261delinsGAATCAGCCTCT (p.Gly417=) c.3812_3823delinsGAATCAGCCTCT (p.Gly1271=) c.4577_4588delinsGAATCAGCCTCT (p.Gly1526=) c.4766_4777delinsGAATCAGCCTCT (p.Gly1589=) c.4559_4570delinsGAATCAGCCTCT (p.Gly1520=) c.1262_1273delinsGAATCAGCCTCT (p.Gly421=) c.1307_1318delinsGAATCAGCCTCT (p.Gly436=) c.4763_4774delinsGAATCAGCCTCT (p.Gly1588=) c.1087_1098delinsGAATCAGCCTCT c.1274_1285delinsGAATCAGCCTCT (p.Gly425=) c.*4483_*4494delinsGAATCAGCCTCT (n.*4483_*4494delinsGAATCAGCCTCT) c.1013_1024delinsGAATCAGCCTCT (p.Gly338=) c.5-7263_5-7252delinsGAATCAGCCTCT (n.5-7263_5-7252delinsGAATCAGCCTCT) c.173_184delinsGAATCAGCCTCT (p.Gly58=) c.-98-21024_-98-21013delinsGAATCAGCCTCT (n.-98-21024_-98-21013delinsGAATCAGCCTCT) n.4836_4847delinsGAATCAGCCTCT n.4877_4888delinsGAATCAGCCTCT | |
17 | g.43071204G>A | CA002989 | BRCA1 | c.4707C>T (p.Leu1569=) c.4710C>T (p.Leu1570=) c.4584C>T (p.Leu1528=) c.4704C>T (p.Leu1568=) c.4632C>T (p.Leu1544=) c.1398C>T (p.Leu466=) c.1260C>T (p.Leu420=) c.3822C>T (p.Leu1274=) c.4587C>T (p.Leu1529=) c.4776C>T (p.Leu1592=) c.4569C>T (p.Leu1523=) c.1272C>T (p.Leu424=) c.1317C>T (p.Leu439=) c.4773C>T (p.Leu1591=) c.1097C>T c.1284C>T (p.Leu428=) c.*4493C>T (n.*4493C>T) c.1023C>T (p.Leu341=) c.5-7253C>T (n.5-7253C>T) c.183C>T (p.Leu61=) c.-98-21014C>T (n.-98-21014C>T) n.4846C>T n.4887C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.43071204G>C | CA500231885 | BRCA1 | c.4707C>G (p.Leu1569=) c.4710C>G (p.Leu1570=) c.4584C>G (p.Leu1528=) c.4704C>G (p.Leu1568=) c.4632C>G (p.Leu1544=) c.1398C>G (p.Leu466=) c.1260C>G (p.Leu420=) c.3822C>G (p.Leu1274=) c.4587C>G (p.Leu1529=) c.4776C>G (p.Leu1592=) c.4569C>G (p.Leu1523=) c.1272C>G (p.Leu424=) c.1317C>G (p.Leu439=) c.4773C>G (p.Leu1591=) c.1097C>G c.1284C>G (p.Leu428=) c.*4493C>G (n.*4493C>G) c.1023C>G (p.Leu341=) c.5-7253C>G (n.5-7253C>G) c.183C>G (p.Leu61=) c.-98-21014C>G (n.-98-21014C>G) n.4846C>G n.4887C>G | dbSNP |
17 | g.43071204G= | CA2260773013 | BRCA1 | c.4707C= (p.Leu1569=) c.4710C= (p.Leu1570=) c.4584C= (p.Leu1528=) c.4704C= (p.Leu1568=) c.4632C= (p.Leu1544=) c.1398C= (p.Leu466=) c.1260C= (p.Leu420=) c.3822C= (p.Leu1274=) c.4587C= (p.Leu1529=) c.4776C= (p.Leu1592=) c.4569C= (p.Leu1523=) c.1272C= (p.Leu424=) c.1317C= (p.Leu439=) c.4773C= (p.Leu1591=) c.1097C= c.1284C= (p.Leu428=) c.*4493C= (n.*4493C=) c.1023C= (p.Leu341=) c.5-7253C= (n.5-7253C=) c.183C= (p.Leu61=) c.-98-21014C= (n.-98-21014C=) n.4846C= n.4887C= | |
17 | g.43071204G>T | CA500231886 | BRCA1 | c.4707C>A (p.Leu1569=) c.4710C>A (p.Leu1570=) c.4584C>A (p.Leu1528=) c.4704C>A (p.Leu1568=) c.4632C>A (p.Leu1544=) c.1398C>A (p.Leu466=) c.1260C>A (p.Leu420=) c.3822C>A (p.Leu1274=) c.4587C>A (p.Leu1529=) c.4776C>A (p.Leu1592=) c.4569C>A (p.Leu1523=) c.1272C>A (p.Leu424=) c.1317C>A (p.Leu439=) c.4773C>A (p.Leu1591=) c.1097C>A c.1284C>A (p.Leu428=) c.*4493C>A (n.*4493C>A) c.1023C>A (p.Leu341=) c.5-7253C>A (n.5-7253C>A) c.183C>A (p.Leu61=) c.-98-21014C>A (n.-98-21014C>A) n.4846C>A n.4887C>A | dbSNP |
17 | g.43071204_43071214delinsT | CA10589647 | BRCA1 | c.4697_4707delinsA (p.Gly1566AspfsTer?) c.4700_4710delinsA (p.Gly1567AspfsTer?) c.4574_4584delinsA (p.Gly1525AspfsTer?) c.4694_4704delinsA (p.Gly1565AspfsTer?) c.4622_4632delinsA (p.Gly1541AspfsTer?) c.1388_1398delinsA (p.Gly463AspfsTer?) c.1250_1260delinsA (p.Gly417AspfsTer?) c.3812_3822delinsA (p.Gly1271AspfsTer?) c.4577_4587delinsA (p.Gly1526AspfsTer?) c.4766_4776delinsA (p.Gly1589AspfsTer?) c.4559_4569delinsA (p.Gly1520AspfsTer?) c.1262_1272delinsA (p.Gly421AspfsTer?) c.1307_1317delinsA (p.Gly436AspfsTer?) c.4763_4773delinsA (p.Gly1588AspfsTer?) c.1087_1097delinsA c.1274_1284delinsA (p.Gly425AspfsTer?) c.*4483_*4493delinsA (n.*4483_*4493delinsA) c.1013_1023delinsA (p.Gly338AspfsTer?) c.5-7263_5-7253delinsA (n.5-7263_5-7253delinsA) c.173_183delinsA (p.Gly58AspfsTer?) c.-98-21024_-98-21014delinsA (n.-98-21024_-98-21014delinsA) n.4836_4846delinsA n.4877_4887delinsA | ClinVar dbSNP |
17 | g.43071205A= | CA2260773015 | BRCA1 | c.4706T= (p.Leu1569=) c.4709T= (p.Leu1570=) c.4583T= (p.Leu1528=) c.4703T= (p.Leu1568=) c.4631T= (p.Leu1544=) c.1397T= (p.Leu466=) c.1259T= (p.Leu420=) c.3821T= (p.Leu1274=) c.4586T= (p.Leu1529=) c.4775T= (p.Leu1592=) c.4568T= (p.Leu1523=) c.1271T= (p.Leu424=) c.1316T= (p.Leu439=) c.4772T= (p.Leu1591=) c.1096T= c.1283T= (p.Leu428=) c.*4492T= (n.*4492T=) c.1022T= (p.Leu341=) c.5-7254T= (n.5-7254T=) c.182T= (p.Leu61=) c.-98-21015T= (n.-98-21015T=) n.4845T= n.4886T= | |
17 | g.43071205A>C | CA10592090 | BRCA1 | c.4706T>G (p.Leu1569Arg) c.4709T>G (p.Leu1570Arg) c.4583T>G (p.Leu1528Arg) c.4703T>G (p.Leu1568Arg) c.4631T>G (p.Leu1544Arg) c.1397T>G (p.Leu466Arg) c.1259T>G (p.Leu420Arg) c.3821T>G (p.Leu1274Arg) c.4586T>G (p.Leu1529Arg) c.4775T>G (p.Leu1592Arg) c.4568T>G (p.Leu1523Arg) c.1271T>G (p.Leu424Arg) c.1316T>G (p.Leu439Arg) c.4772T>G (p.Leu1591Arg) c.1096T>G c.1283T>G (p.Leu428Arg) c.*4492T>G (n.*4492T>G) c.1022T>G (p.Leu341Arg) c.5-7254T>G (n.5-7254T>G) c.182T>G (p.Leu61Arg) c.-98-21015T>G (n.-98-21015T>G) n.4845T>G n.4886T>G | |
17 | g.43071205A>G | CA10592091 | BRCA1 | c.4706T>C (p.Leu1569Pro) c.4709T>C (p.Leu1570Pro) c.4583T>C (p.Leu1528Pro) c.4703T>C (p.Leu1568Pro) c.4631T>C (p.Leu1544Pro) c.1397T>C (p.Leu466Pro) c.1259T>C (p.Leu420Pro) c.3821T>C (p.Leu1274Pro) c.4586T>C (p.Leu1529Pro) c.4775T>C (p.Leu1592Pro) c.4568T>C (p.Leu1523Pro) c.1271T>C (p.Leu424Pro) c.1316T>C (p.Leu439Pro) c.4772T>C (p.Leu1591Pro) c.1096T>C c.1283T>C (p.Leu428Pro) c.*4492T>C (n.*4492T>C) c.1022T>C (p.Leu341Pro) c.5-7254T>C (n.5-7254T>C) c.182T>C (p.Leu61Pro) c.-98-21015T>C (n.-98-21015T>C) n.4845T>C n.4886T>C | ClinVar dbSNP COSMIC COSMIC |
17 | g.43071205A>T | CA10592092 | BRCA1 | c.4706T>A (p.Leu1569His) c.4709T>A (p.Leu1570His) c.4583T>A (p.Leu1528His) c.4703T>A (p.Leu1568His) c.4631T>A (p.Leu1544His) c.1397T>A (p.Leu466His) c.1259T>A (p.Leu420His) c.3821T>A (p.Leu1274His) c.4586T>A (p.Leu1529His) c.4775T>A (p.Leu1592His) c.4568T>A (p.Leu1523His) c.1271T>A (p.Leu424His) c.1316T>A (p.Leu439His) c.4772T>A (p.Leu1591His) c.1096T>A c.1283T>A (p.Leu428His) c.*4492T>A (n.*4492T>A) c.1022T>A (p.Leu341His) c.5-7254T>A (n.5-7254T>A) c.182T>A (p.Leu61His) c.-98-21015T>A (n.-98-21015T>A) n.4845T>A n.4886T>A | dbSNP |
17 | g.43071205dup | CA348034 | BRCA1 | c.4706dup (p.Phe1570LeufsTer3) c.4709dup (p.Phe1571LeufsTer3) c.4583dup (p.Phe1529LeufsTer3) c.4703dup (p.Phe1569LeufsTer3) c.4631dup (p.Phe1545LeufsTer3) c.1397dup (p.Phe467LeufsTer3) c.1259dup (p.Phe421LeufsTer3) c.3821dup (p.Phe1275LeufsTer3) c.4586dup (p.Phe1530LeufsTer3) c.4775dup (p.Phe1593LeufsTer3) c.4568dup (p.Phe1524LeufsTer3) c.1271dup (p.Phe425LeufsTer3) c.1316dup (p.Phe440LeufsTer3) c.4772dup (p.Phe1592LeufsTer3) c.1096dup c.1283dup (p.Phe429LeufsTer3) c.*4492dup (n.*4492dup) c.1022dup (p.Phe342LeufsTer3) c.5-7254dup (n.5-7254dup) c.182dup (p.Phe62LeufsTer3) c.-98-21015dup (n.-98-21015dup) n.4845dup n.4886dup | ClinVar dbSNP |
17 | g.43071205_43071215delinsAGGCTGATTCC | CA2260773014 | BRCA1 | c.4696_4706delinsGGAATCAGCCT (p.Gly1566=) c.4699_4709delinsGGAATCAGCCT (p.Gly1567=) c.4573_4583delinsGGAATCAGCCT (p.Gly1525=) c.4693_4703delinsGGAATCAGCCT (p.Gly1565=) c.4621_4631delinsGGAATCAGCCT (p.Gly1541=) c.1387_1397delinsGGAATCAGCCT (p.Gly463=) c.1249_1259delinsGGAATCAGCCT (p.Gly417=) c.3811_3821delinsGGAATCAGCCT (p.Gly1271=) c.4576_4586delinsGGAATCAGCCT (p.Gly1526=) c.4765_4775delinsGGAATCAGCCT (p.Gly1589=) c.4558_4568delinsGGAATCAGCCT (p.Gly1520=) c.1261_1271delinsGGAATCAGCCT (p.Gly421=) c.1306_1316delinsGGAATCAGCCT (p.Gly436=) c.4762_4772delinsGGAATCAGCCT (p.Gly1588=) c.1086_1096delinsGGAATCAGCCT c.1273_1283delinsGGAATCAGCCT (p.Gly425=) c.*4482_*4492delinsGGAATCAGCCT (n.*4482_*4492delinsGGAATCAGCCT) c.1012_1022delinsGGAATCAGCCT (p.Gly338=) c.5-7264_5-7254delinsGGAATCAGCCT (n.5-7264_5-7254delinsGGAATCAGCCT) c.172_182delinsGGAATCAGCCT (p.Gly58=) c.-98-21025_-98-21015delinsGGAATCAGCCT (n.-98-21025_-98-21015delinsGGAATCAGCCT) n.4835_4845delinsGGAATCAGCCT n.4876_4886delinsGGAATCAGCCT |