Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.209626856del | CA528652714 | LAMB3 | c.1597+13del (n.1597+13del) c.1405+13del (n.1405+13del) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626856T>A | CA2739275552 | LAMB3 | c.1597+11A>T (n.1597+11A>T) c.1405+11A>T (n.1405+11A>T) | ClinVar |
1 | g.209626857G>C | CA1375536 | LAMB3 | c.1597+10C>G (n.1597+10C>G) c.1405+10C>G (n.1405+10C>G) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
1 | g.209626857G= | CA1143474897 | LAMB3 | c.1597+10C= (n.1597+10C=) c.1405+10C= (n.1405+10C=) | |
1 | g.209626857G>T | CA2650322164 | LAMB3 | c.1597+10C>A (n.1597+10C>A) c.1405+10C>A (n.1405+10C>A) | gnomAD v4 |
1 | g.209626859G>T | CA2650322165 | LAMB3 | c.1597+8C>A (n.1597+8C>A) c.1405+8C>A (n.1405+8C>A) | gnomAD v4 |
1 | g.209626860C= | CA2484299659 | LAMB3 | c.1597+7G= (n.1597+7G=) c.1405+7G= (n.1405+7G=) | |
1 | g.209626860C>T | CA730829278 | LAMB3 | c.1597+7G>A (n.1597+7G>A) c.1405+7G>A (n.1405+7G>A) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626861A= | CA2484299660 | LAMB3 | c.1597+6T= (n.1597+6T=) c.1405+6T= (n.1405+6T=) | |
1 | g.209626861A>G | CA1375537 | LAMB3 | c.1597+6T>C (n.1597+6T>C) c.1405+6T>C (n.1405+6T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209626862T>C | CA2544921050 | LAMB3 | c.1597+5A>G (n.1597+5A>G) c.1405+5A>G (n.1405+5A>G) | gnomAD v4 |
1 | g.209626863G>A | CA2650322166 | LAMB3 | c.1597+4C>T (n.1597+4C>T) c.1405+4C>T (n.1405+4C>T) | gnomAD v4 |
1 | g.209626863G>T | CA2650322167 | LAMB3 | c.1597+4C>A (n.1597+4C>A) c.1405+4C>A (n.1405+4C>A) | gnomAD v4 |
1 | g.209626864C>A | CA2484299662 | LAMB3 | c.1597+3G>T (n.1597+3G>T) c.1405+3G>T (n.1405+3G>T) | dbSNP gnomAD v4 |
1 | g.209626864C= | CA2484299661 | LAMB3 | c.1597+3G= (n.1597+3G=) c.1405+3G= (n.1405+3G=) | |
1 | g.209626864C>T | CA2484299663 | LAMB3 | c.1597+3G>A (n.1597+3G>A) c.1405+3G>A (n.1405+3G>A) | dbSNP |
1 | g.209626865A= | CA2484299664 | LAMB3 | c.1597+2T= (n.1597+2T=) c.1405+2T= (n.1405+2T=) | |
1 | g.209626865A>C | CA344590043 | LAMB3 | c.1597+2T>G (n.1597+2T>G) c.1405+2T>G (n.1405+2T>G) | dbSNP |
1 | g.209626865A>G | CA344590044 | LAMB3 | c.1597+2T>C (n.1597+2T>C) c.1405+2T>C (n.1405+2T>C) | |
1 | g.209626865A>T | CA344590045 | LAMB3 | c.1597+2T>A (n.1597+2T>A) c.1405+2T>A (n.1405+2T>A) | |
1 | g.209626866C>A | CA344590046 | LAMB3 | c.1597+1G>T (n.1597+1G>T) c.1405+1G>T (n.1405+1G>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626866C= | CA2484299665 | LAMB3 | c.1597+1G= (n.1597+1G=) c.1405+1G= (n.1405+1G=) | |
1 | g.209626866C>G | CA344590047 | LAMB3 | c.1597+1G>C (n.1597+1G>C) c.1405+1G>C (n.1405+1G>C) | |
1 | g.209626866C>T | CA344590048 | LAMB3 | c.1597+1G>A (n.1597+1G>A) c.1405+1G>A (n.1405+1G>A) | ClinVar dbSNP |
1 | g.209626867C>A | CA344590049 | LAMB3 | c.1597G>T (p.Ala533Ser) c.1405G>T (p.Ala469Ser) | |
1 | g.209626867C>G | CA344590050 | LAMB3 | c.1597G>C (p.Ala533Pro) c.1405G>C (p.Ala469Pro) | |
1 | g.209626867C>T | CA344590051 | LAMB3 | c.1597G>A (p.Ala533Thr) c.1405G>A (p.Ala469Thr) | |
1 | g.209626868T>A | CA423031189 | LAMB3 | c.1596A>T (p.Arg532=) c.1404A>T (p.Arg468=) | |
1 | g.209626868T>C | CA423031188 | LAMB3 | c.1596A>G (p.Arg532=) c.1404A>G (p.Arg468=) | |
1 | g.209626868T>G | CA423031187 | LAMB3 | c.1596A>C (p.Arg532=) c.1404A>C (p.Arg468=) | |
1 | g.209626869C>A | CA344590053 | LAMB3 | c.1595G>T (p.Arg532Leu) c.1403G>T (p.Arg468Leu) | gnomAD v4 |
1 | g.209626869C= | CA1149043432 | LAMB3 | c.1595G= (p.Arg532=) c.1403G= (p.Arg468=) | |
1 | g.209626869C>G | CA344590052 | LAMB3 | c.1595G>C (p.Arg532Pro) c.1403G>C (p.Arg468Pro) | |
1 | g.209626869C>T | CA1375538 | LAMB3 | c.1595G>A (p.Arg532Gln) c.1403G>A (p.Arg468Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626870G>A | CA36756919 | LAMB3 | c.1594C>T (p.Arg532Ter) c.1402C>T (p.Arg468Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626870G>C | CA344590054 | LAMB3 | c.1594C>G (p.Arg532Gly) c.1402C>G (p.Arg468Gly) | gnomAD v4 |
1 | g.209626870G= | CA2484299666 | LAMB3 | c.1594C= (p.Arg532=) c.1402C= (p.Arg468=) | |
1 | g.209626870G>T | CA423031191 | LAMB3 | c.1594C>A (p.Arg532=) c.1402C>A (p.Arg468=) | gnomAD v4 |
1 | g.209626871G>A | CA423031192 | LAMB3 | c.1593C>T (p.Cys531=) c.1401C>T (p.Cys467=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626871G>C | CA344590055 | LAMB3 | c.1593C>G (p.Cys531Trp) c.1401C>G (p.Cys467Trp) | |
1 | g.209626871G= | CA2484299667 | LAMB3 | c.1593C= (p.Cys531=) c.1401C= (p.Cys467=) | |
1 | g.209626871G>T | CA344590056 | LAMB3 | c.1593C>A (p.Cys531Ter) c.1401C>A (p.Cys467Ter) | ClinVar gnomAD v4 |
1 | g.209626872C>A | CA10608979 | LAMB3 | c.1592G>T (p.Cys531Phe) c.1400G>T (p.Cys467Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626872C= | CA2484299668 | LAMB3 | c.1592G= (p.Cys531=) c.1400G= (p.Cys467=) | |
1 | g.209626872C>G | CA344590057 | LAMB3 | c.1592G>C (p.Cys531Ser) c.1400G>C (p.Cys467Ser) | |
1 | g.209626872C>T | CA344590058 | LAMB3 | c.1592G>A (p.Cys531Tyr) c.1400G>A (p.Cys467Tyr) | |
1 | g.209626873A>C | CA344590059 | LAMB3 | c.1591T>G (p.Cys531Gly) c.1399T>G (p.Cys467Gly) | gnomAD v4 |
1 | g.209626873A>G | CA344590060 | LAMB3 | c.1591T>C (p.Cys531Arg) c.1399T>C (p.Cys467Arg) | |
1 | g.209626873A>T | CA344590061 | LAMB3 | c.1591T>A (p.Cys531Ser) c.1399T>A (p.Cys467Ser) | |
1 | g.209626874T>A | CA423031193 | LAMB3 | c.1590A>T (p.Gly530=) c.1398A>T (p.Gly466=) | |
1 | g.209626874T>C | CA423031195 | LAMB3 | c.1590A>G (p.Gly530=) c.1398A>G (p.Gly466=) | |
1 | g.209626874T>G | CA423031197 | LAMB3 | c.1590A>C (p.Gly530=) c.1398A>C (p.Gly466=) | |
1 | g.209626875C>A | CA344590062 | LAMB3 | c.1589G>T (p.Gly530Val) c.1397G>T (p.Gly466Val) | |
1 | g.209626875C>G | CA344590063 | LAMB3 | c.1589G>C (p.Gly530Ala) c.1397G>C (p.Gly466Ala) | |
1 | g.209626875C>T | CA344590064 | LAMB3 | c.1589G>A (p.Gly530Glu) c.1397G>A (p.Gly466Glu) | |
1 | g.209626876del | CA2586964560 | LAMB3 | c.1589del (p.Gly530AspfsTer30) c.1397del (p.Gly466AspfsTer30) | |
1 | g.209626875_209626877delinsCCT | CA2484299669 | LAMB3 | c.1587_1589delinsAGG (p.Thr529=) c.1395_1397delinsAGG (p.Thr465=) | |
1 | g.209626876C>A | CA344590067 | LAMB3 | c.1588G>T (p.Gly530Ter) c.1396G>T (p.Gly466Ter) | |
1 | g.209626876C= | CA2484299670 | LAMB3 | c.1588G= (p.Gly530=) c.1396G= (p.Gly466=) | |
1 | g.209626876C>G | CA344590066 | LAMB3 | c.1588G>C (p.Gly530Arg) c.1396G>C (p.Gly466Arg) | |
1 | g.209626876C>T | CA344590065 | LAMB3 | c.1588G>A (p.Gly530Arg) c.1396G>A (p.Gly466Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626876_209626877del | CA257283 | LAMB3 | c.1587_1588del (p.Gly530MetfsTer5) c.1395_1396del (p.Gly466MetfsTer5) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209626877T>A | CA423031199 | LAMB3 | c.1587A>T (p.Thr529=) c.1395A>T (p.Thr465=) | |
1 | g.209626877T>C | CA423031200 | LAMB3 | c.1587A>G (p.Thr529=) c.1395A>G (p.Thr465=) | ClinVar dbSNP |
1 | g.209626877T>G | CA423031201 | LAMB3 | c.1587A>C (p.Thr529=) c.1395A>C (p.Thr465=) | |
1 | g.209626878G>A | CA1375539 | LAMB3 | c.1586C>T (p.Thr529Ile) c.1394C>T (p.Thr465Ile) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
1 | g.209626878G>C | CA344590068 | LAMB3 | c.1586C>G (p.Thr529Arg) c.1394C>G (p.Thr465Arg) | |
1 | g.209626878G= | CA2484299671 | LAMB3 | c.1586C= (p.Thr529=) c.1394C= (p.Thr465=) | |
1 | g.209626878G>T | CA344590069 | LAMB3 | c.1586C>A (p.Thr529Lys) c.1394C>A (p.Thr465Lys) | |
1 | g.209626879T>A | CA344590070 | LAMB3 | c.1585A>T (p.Thr529Ser) c.1393A>T (p.Thr465Ser) | |
1 | g.209626879T>C | CA344590071 | LAMB3 | c.1585A>G (p.Thr529Ala) c.1393A>G (p.Thr465Ala) | gnomAD v4 |
1 | g.209626879T>G | CA344590072 | LAMB3 | c.1585A>C (p.Thr529Pro) c.1393A>C (p.Thr465Pro) | |
1 | g.209626880G>A | CA423031202 | LAMB3 | c.1584C>T (p.Ala528=) c.1392C>T (p.Ala464=) | |
1 | g.209626880G>C | CA423031203 | LAMB3 | c.1584C>G (p.Ala528=) c.1392C>G (p.Ala464=) | |
1 | g.209626880G>T | CA423031204 | LAMB3 | c.1584C>A (p.Ala528=) c.1392C>A (p.Ala464=) | |
1 | g.209626881G>A | CA344590073 | LAMB3 | c.1583C>T (p.Ala528Val) c.1391C>T (p.Ala464Val) | |
1 | g.209626881G>C | CA344590074 | LAMB3 | c.1583C>G (p.Ala528Gly) c.1391C>G (p.Ala464Gly) | |
1 | g.209626881G>T | CA344590075 | LAMB3 | c.1583C>A (p.Ala528Asp) c.1391C>A (p.Ala464Asp) | |
1 | g.209626882C>A | CA344590076 | LAMB3 | c.1582G>T (p.Ala528Ser) c.1390G>T (p.Ala464Ser) | COSMIC |
1 | g.209626882C= | CA2484299672 | LAMB3 | c.1582G= (p.Ala528=) c.1390G= (p.Ala464=) | |
1 | g.209626882C>G | CA344590077 | LAMB3 | c.1582G>C (p.Ala528Pro) c.1390G>C (p.Ala464Pro) | |
1 | g.209626882C>T | CA344590078 | LAMB3 | c.1582G>A (p.Ala528Thr) c.1390G>A (p.Ala464Thr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626883C>A | CA423031210 | LAMB3 | c.1581G>T (p.Val527=) c.1389G>T (p.Val463=) | |
1 | g.209626883C>G | CA423031214 | LAMB3 | c.1581G>C (p.Val527=) c.1389G>C (p.Val463=) | |
1 | g.209626883C>T | CA423031215 | LAMB3 | c.1581G>A (p.Val527=) c.1389G>A (p.Val463=) | |
1 | g.209626884A= | CA2484299673 | LAMB3 | c.1580T= (p.Val527=) c.1388T= (p.Val463=) | |
1 | g.209626884A>C | CA344590081 | LAMB3 | c.1580T>G (p.Val527Gly) c.1388T>G (p.Val463Gly) | |
1 | g.209626884A>G | CA344590080 | LAMB3 | c.1580T>C (p.Val527Ala) c.1388T>C (p.Val463Ala) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626884A>T | CA344590079 | LAMB3 | c.1580T>A (p.Val527Glu) c.1388T>A (p.Val463Glu) | |
1 | g.209626885C>A | CA344590083 | LAMB3 | c.1579G>T (p.Val527Leu) c.1387G>T (p.Val463Leu) | |
1 | g.209626885C= | CA1139912089 | LAMB3 | c.1579G= (p.Val527=) c.1387G= (p.Val463=) | |
1 | g.209626885C>G | CA344590082 | LAMB3 | c.1579G>C (p.Val527Leu) c.1387G>C (p.Val463Leu) | |
1 | g.209626885C>T | CA1375540 | LAMB3 | c.1579G>A (p.Val527Met) c.1387G>A (p.Val463Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626886G>A | CA1375541 | LAMB3 | c.1578C>T (p.Asp526=) c.1386C>T (p.Asp462=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626886G>C | CA344590084 | LAMB3 | c.1578C>G (p.Asp526Glu) c.1386C>G (p.Asp462Glu) | gnomAD v4 |
1 | g.209626886G= | CA1147275104 | LAMB3 | c.1578C= (p.Asp526=) c.1386C= (p.Asp462=) | |
1 | g.209626886G>T | CA36756929 | LAMB3 | c.1578C>A (p.Asp526Glu) c.1386C>A (p.Asp462Glu) | dbSNP |
1 | g.209626887T>A | CA344590087 | LAMB3 | c.1577A>T (p.Asp526Val) c.1385A>T (p.Asp462Val) | |
1 | g.209626887T>C | CA344590086 | LAMB3 | c.1577A>G (p.Asp526Gly) c.1385A>G (p.Asp462Gly) | |
1 | g.209626887T>G | CA344590085 | LAMB3 | c.1577A>C (p.Asp526Ala) c.1385A>C (p.Asp462Ala) | |
1 | g.209626888C>A | CA344590088 | LAMB3 | c.1576G>T (p.Asp526Tyr) c.1384G>T (p.Asp462Tyr) | |
1 | g.209626888C>G | CA344590089 | LAMB3 | c.1576G>C (p.Asp526His) c.1384G>C (p.Asp462His) | |
1 | g.209626888C>T | CA344590090 | LAMB3 | c.1576G>A (p.Asp526Asn) c.1384G>A (p.Asp462Asn) | dbSNP gnomAD v4 |
1 | g.209626889T>A | CA423031219 | LAMB3 | c.1575A>T (p.Gly525=) c.1383A>T (p.Gly461=) | |
1 | g.209626889T>C | CA423031218 | LAMB3 | c.1575A>G (p.Gly525=) c.1383A>G (p.Gly461=) | |
1 | g.209626889T>G | CA423031217 | LAMB3 | c.1575A>C (p.Gly525=) c.1383A>C (p.Gly461=) | |
1 | g.209626890C>A | CA344590091 | LAMB3 | c.1574G>T (p.Gly525Val) c.1382G>T (p.Gly461Val) | |
1 | g.209626890C= | CA2484299674 | LAMB3 | c.1574G= (p.Gly525=) c.1382G= (p.Gly461=) | |
1 | g.209626890C>G | CA1375542 | LAMB3 | c.1574G>C (p.Gly525Ala) c.1382G>C (p.Gly461Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626890C>T | CA344590092 | LAMB3 | c.1574G>A (p.Gly525Glu) c.1382G>A (p.Gly461Glu) | |
1 | g.209626890_209626902delinsCCATAGGTCCGGT | CA2484299675 | LAMB3 | c.1562_1574delinsACCGGACCTATGG (p.Asp521=) c.1370_1382delinsACCGGACCTATGG (p.Asp457=) | |
1 | g.209626891C>A | CA344590093 | LAMB3 | c.1573G>T (p.Gly525Ter) c.1381G>T (p.Gly461Ter) | |
1 | g.209626891C>G | CA344590095 | LAMB3 | c.1573G>C (p.Gly525Arg) c.1381G>C (p.Gly461Arg) | |
1 | g.209626891C>T | CA344590094 | LAMB3 | c.1573G>A (p.Gly525Arg) c.1381G>A (p.Gly461Arg) | gnomAD v4 |
1 | g.209626892_209626903del | CA730829405 | LAMB3 | c.1562_1573del (p.Asp521_Tyr524del) c.1370_1381del (p.Asp457_Tyr460del) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626892A>C | CA344590096 | LAMB3 | c.1572T>G (p.Tyr524Ter) c.1380T>G (p.Tyr460Ter) | |
1 | g.209626892A>G | CA423031220 | LAMB3 | c.1572T>C (p.Tyr524=) c.1380T>C (p.Tyr460=) | ClinVar dbSNP gnomAD v4 |
1 | g.209626892A>T | CA344590097 | LAMB3 | c.1572T>A (p.Tyr524Ter) c.1380T>A (p.Tyr460Ter) | |
1 | g.209626893T>A | CA344590098 | LAMB3 | c.1571A>T (p.Tyr524Phe) c.1379A>T (p.Tyr460Phe) | |
1 | g.209626893T>C | CA1375543 | LAMB3 | c.1571A>G (p.Tyr524Cys) c.1379A>G (p.Tyr460Cys) | dbSNP ExAC gnomAD v4 |
1 | g.209626893T>G | CA344590099 | LAMB3 | c.1571A>C (p.Tyr524Ser) c.1379A>C (p.Tyr460Ser) | |
1 | g.209626893T= | CA2484299676 | LAMB3 | c.1571A= (p.Tyr524=) c.1379A= (p.Tyr460=) | |
1 | g.209626894A= | CA2484299677 | LAMB3 | c.1570T= (p.Tyr524=) c.1378T= (p.Tyr460=) | |
1 | g.209626894A>C | CA344590100 | LAMB3 | c.1570T>G (p.Tyr524Asp) c.1378T>G (p.Tyr460Asp) | |
1 | g.209626894A>G | CA344590101 | LAMB3 | c.1570T>C (p.Tyr524His) c.1378T>C (p.Tyr460His) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626894A>T | CA344590102 | LAMB3 | c.1570T>A (p.Tyr524Asn) c.1378T>A (p.Tyr460Asn) | |
1 | g.209626895G>A | CA423031224 | LAMB3 | c.1569C>T (p.Thr523=) c.1377C>T (p.Thr459=) | |
1 | g.209626895G>C | CA423031226 | LAMB3 | c.1569C>G (p.Thr523=) c.1377C>G (p.Thr459=) | |
1 | g.209626895G>T | CA423031225 | LAMB3 | c.1569C>A (p.Thr523=) c.1377C>A (p.Thr459=) | |
1 | g.209626896G>A | CA344590103 | LAMB3 | c.1568C>T (p.Thr523Ile) c.1376C>T (p.Thr459Ile) | |
1 | g.209626896G>C | CA344590104 | LAMB3 | c.1568C>G (p.Thr523Ser) c.1376C>G (p.Thr459Ser) | |
1 | g.209626896G>T | CA344590105 | LAMB3 | c.1568C>A (p.Thr523Asn) c.1376C>A (p.Thr459Asn) | |
1 | g.209626897T>A | CA344590107 | LAMB3 | c.1567A>T (p.Thr523Ser) c.1375A>T (p.Thr459Ser) | |
1 | g.209626897T>C | CA344590108 | LAMB3 | c.1567A>G (p.Thr523Ala) c.1375A>G (p.Thr459Ala) | |
1 | g.209626897T>G | CA344590106 | LAMB3 | c.1567A>C (p.Thr523Pro) c.1375A>C (p.Thr459Pro) | |
1 | g.209626898C>A | CA423031231 | LAMB3 | c.1566G>T (p.Arg522=) c.1374G>T (p.Arg458=) | |
1 | g.209626898C= | CA1148287490 | LAMB3 | c.1566G= (p.Arg522=) c.1374G= (p.Arg458=) | |
1 | g.209626898C>G | CA1375544 | LAMB3 | c.1566G>C (p.Arg522=) c.1374G>C (p.Arg458=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626898C>T | CA423031233 | LAMB3 | c.1566G>A (p.Arg522=) c.1374G>A (p.Arg458=) | |
1 | g.209626899C>A | CA344590110 | LAMB3 | c.1565G>T (p.Arg522Leu) c.1373G>T (p.Arg458Leu) | |
1 | g.209626899C= | CA1141980260 | LAMB3 | c.1565G= (p.Arg522=) c.1373G= (p.Arg458=) | |
1 | g.209626899C>G | CA344590109 | LAMB3 | c.1565G>C (p.Arg522Pro) c.1373G>C (p.Arg458Pro) | |
1 | g.209626899C>T | CA1375545 | LAMB3 | c.1565G>A (p.Arg522Gln) c.1373G>A (p.Arg458Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626900G>A | CA1375546 | LAMB3 | c.1564C>T (p.Arg522Trp) c.1372C>T (p.Arg458Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.209626900G>C | CA344590111 | LAMB3 | c.1564C>G (p.Arg522Gly) c.1372C>G (p.Arg458Gly) | |
1 | g.209626900G= | CA2484299678 | LAMB3 | c.1564C= (p.Arg522=) c.1372C= (p.Arg458=) | |
1 | g.209626900G>T | CA423031235 | LAMB3 | c.1564C>A (p.Arg522=) c.1372C>A (p.Arg458=) | |
1 | g.209626901G>A | CA423031237 | LAMB3 | c.1563C>T (p.Asp521=) c.1371C>T (p.Asp457=) | |
1 | g.209626901G>C | CA344590112 | LAMB3 | c.1563C>G (p.Asp521Glu) c.1371C>G (p.Asp457Glu) | |
1 | g.209626901G= | CA2484299679 | LAMB3 | c.1563C= (p.Asp521=) c.1371C= (p.Asp457=) | |
1 | g.209626901G>T | CA344590113 | LAMB3 | c.1563C>A (p.Asp521Glu) c.1371C>A (p.Asp457Glu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626902T>A | CA344590114 | LAMB3 | c.1562A>T (p.Asp521Val) c.1370A>T (p.Asp457Val) | |
1 | g.209626902T>C | CA344590115 | LAMB3 | c.1562A>G (p.Asp521Gly) c.1370A>G (p.Asp457Gly) | dbSNP |
1 | g.209626902T>G | CA344590116 | LAMB3 | c.1562A>C (p.Asp521Ala) c.1370A>C (p.Asp457Ala) | |
1 | g.209626902T= | CA2484299680 | LAMB3 | c.1562A= (p.Asp521=) c.1370A= (p.Asp457=) | |
1 | g.209626903C>A | CA1375547 | LAMB3 | c.1561G>T (p.Asp521Tyr) c.1369G>T (p.Asp457Tyr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626903C= | CA1142328974 | LAMB3 | c.1561G= (p.Asp521=) c.1369G= (p.Asp457=) | |
1 | g.209626903C>G | CA344590117 | LAMB3 | c.1561G>C (p.Asp521His) c.1369G>C (p.Asp457His) | |
1 | g.209626903C>T | CA344590118 | LAMB3 | c.1561G>A (p.Asp521Asn) c.1369G>A (p.Asp457Asn) | dbSNP |
1 | g.209626904T>A | CA423031241 | LAMB3 | c.1560A>T (p.Pro520=) c.1368A>T (p.Pro456=) | ClinVar gnomAD v4 |
1 | g.209626904T>C | CA36756935 | LAMB3 | c.1560A>G (p.Pro520=) c.1368A>G (p.Pro456=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626904T>G | CA423031242 | LAMB3 | c.1560A>C (p.Pro520=) c.1368A>C (p.Pro456=) | |
1 | g.209626904T= | CA2484299681 | LAMB3 | c.1560A= (p.Pro520=) c.1368A= (p.Pro456=) | |
1 | g.209626905G>A | CA344590121 | LAMB3 | c.1559C>T (p.Pro520Leu) c.1367C>T (p.Pro456Leu) | |
1 | g.209626905G>C | CA344590119 | LAMB3 | c.1559C>G (p.Pro520Arg) c.1367C>G (p.Pro456Arg) | |
1 | g.209626905G>T | CA344590120 | LAMB3 | c.1559C>A (p.Pro520Gln) c.1367C>A (p.Pro456Gln) | |
1 | g.209626906G>A | CA1375548 | LAMB3 | c.1558C>T (p.Pro520Ser) c.1366C>T (p.Pro456Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209626906G>C | CA344590122 | LAMB3 | c.1558C>G (p.Pro520Ala) c.1366C>G (p.Pro456Ala) | |
1 | g.209626906G= | CA2484299682 | LAMB3 | c.1558C= (p.Pro520=) c.1366C= (p.Pro456=) | |
1 | g.209626906G>T | CA344590123 | LAMB3 | c.1558C>A (p.Pro520Thr) c.1366C>A (p.Pro456Thr) | gnomAD v4 |
1 | g.209626907A>C | CA344590124 | LAMB3 | c.1557T>G (p.Cys519Trp) c.1365T>G (p.Cys455Trp) | |
1 | g.209626907A>G | CA423031247 | LAMB3 | c.1557T>C (p.Cys519=) c.1365T>C (p.Cys455=) | |
1 | g.209626907A>T | CA344590125 | LAMB3 | c.1557T>A (p.Cys519Ter) c.1365T>A (p.Cys455Ter) | |
1 | g.209626908C>A | CA344590126 | LAMB3 | c.1556G>T (p.Cys519Phe) c.1364G>T (p.Cys455Phe) | |
1 | g.209626908C= | CA2484299683 | LAMB3 | c.1556G= (p.Cys519=) c.1364G= (p.Cys455=) | |
1 | g.209626908C>G | CA344590127 | LAMB3 | c.1556G>C (p.Cys519Ser) c.1364G>C (p.Cys455Ser) | |
1 | g.209626908C>T | CA344590128 | LAMB3 | c.1556G>A (p.Cys519Tyr) c.1364G>A (p.Cys455Tyr) | dbSNP gnomAD v2 |
1 | g.209626909A= | CA2484299684 | LAMB3 | c.1555T= (p.Cys519=) c.1363T= (p.Cys455=) | |
1 | g.209626909A>C | CA344590129 | LAMB3 | c.1555T>G (p.Cys519Gly) c.1363T>G (p.Cys455Gly) | |
1 | g.209626909A>G | CA344590130 | LAMB3 | c.1555T>C (p.Cys519Arg) c.1363T>C (p.Cys455Arg) | |
1 | g.209626909A>T | CA1375549 | LAMB3 | c.1555T>A (p.Cys519Ser) c.1363T>A (p.Cys455Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626910C>A | CA344590132 | LAMB3 | c.1554G>T (p.Gln518His) c.1362G>T (p.Gln454His) | |
1 | g.209626910C= | CA2484299685 | LAMB3 | c.1554G= (p.Gln518=) c.1362G= (p.Gln454=) | |
1 | g.209626910C>G | CA344590131 | LAMB3 | c.1554G>C (p.Gln518His) c.1362G>C (p.Gln454His) | |
1 | g.209626910C>T | CA423031249 | LAMB3 | c.1554G>A (p.Gln518=) c.1362G>A (p.Gln454=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626911T>A | CA344590133 | LAMB3 | c.1553A>T (p.Gln518Leu) c.1361A>T (p.Gln454Leu) | |
1 | g.209626911T>C | CA344590134 | LAMB3 | c.1553A>G (p.Gln518Arg) c.1361A>G (p.Gln454Arg) | |
1 | g.209626911T>G | CA344590135 | LAMB3 | c.1553A>C (p.Gln518Pro) c.1361A>C (p.Gln454Pro) | |
1 | g.209626912G>A | CA344590136 | LAMB3 | c.1552C>T (p.Gln518Ter) c.1360C>T (p.Gln454Ter) | ClinVar gnomAD v4 |
1 | g.209626912G>C | CA344590137 | LAMB3 | c.1552C>G (p.Gln518Glu) c.1360C>G (p.Gln454Glu) | |
1 | g.209626912G>T | CA344590138 | LAMB3 | c.1552C>A (p.Gln518Lys) c.1360C>A (p.Gln454Lys) | |
1 | g.209626913G>A | CA423031250 | LAMB3 | c.1551C>T (p.Arg517=) c.1359C>T (p.Arg453=) | |
1 | g.209626913G>C | CA423031251 | LAMB3 | c.1551C>G (p.Arg517=) c.1359C>G (p.Arg453=) | |
1 | g.209626913G>T | CA423031252 | LAMB3 | c.1551C>A (p.Arg517=) c.1359C>A (p.Arg453=) | |
1 | g.209626914C>A | CA36756937 | LAMB3 | c.1550G>T (p.Arg517Leu) c.1358G>T (p.Arg453Leu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626914C= | CA2484299686 | LAMB3 | c.1550G= (p.Arg517=) c.1358G= (p.Arg453=) | |
1 | g.209626914C>G | CA344590139 | LAMB3 | c.1550G>C (p.Arg517Pro) c.1358G>C (p.Arg453Pro) | |
1 | g.209626914C>T | CA344590140 | LAMB3 | c.1550G>A (p.Arg517His) c.1358G>A (p.Arg453His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.209626915G>A | CA1375550 | LAMB3 | c.1549C>T (p.Arg517Cys) c.1357C>T (p.Arg453Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626915G>C | CA344590141 | LAMB3 | c.1549C>G (p.Arg517Gly) c.1357C>G (p.Arg453Gly) | |
1 | g.209626915G= | CA1141110836 | LAMB3 | c.1549C= (p.Arg517=) c.1357C= (p.Arg453=) | |
1 | g.209626915G>T | CA344590142 | LAMB3 | c.1549C>A (p.Arg517Ser) c.1357C>A (p.Arg453Ser) | |
1 | g.209626916G>A | CA423031257 | LAMB3 | c.1548C>T (p.Ile516=) c.1356C>T (p.Ile452=) | ClinVar |
1 | g.209626916G>C | CA344590143 | LAMB3 | c.1548C>G (p.Ile516Met) c.1356C>G (p.Ile452Met) | gnomAD v4 |
1 | g.209626916G>T | CA423031258 | LAMB3 | c.1548C>A (p.Ile516=) c.1356C>A (p.Ile452=) | gnomAD v4 |
1 | g.209626917A>C | CA344590146 | LAMB3 | c.1547T>G (p.Ile516Ser) c.1355T>G (p.Ile452Ser) | |
1 | g.209626917A>G | CA344590144 | LAMB3 | c.1547T>C (p.Ile516Thr) c.1355T>C (p.Ile452Thr) | |
1 | g.209626917A>T | CA344590145 | LAMB3 | c.1547T>A (p.Ile516Asn) c.1355T>A (p.Ile452Asn) | |
1 | g.209626918T>A | CA344590147 | LAMB3 | c.1546A>T (p.Ile516Phe) c.1354A>T (p.Ile452Phe) | |
1 | g.209626918T>C | CA1375551 | LAMB3 | c.1546A>G (p.Ile516Val) c.1354A>G (p.Ile452Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626918T>G | CA344590148 | LAMB3 | c.1546A>C (p.Ile516Leu) c.1354A>C (p.Ile452Leu) | |
1 | g.209626918T= | CA1142275416 | LAMB3 | c.1546A= (p.Ile516=) c.1354A= (p.Ile452=) | |
1 | g.209626919G>A | CA423031259 | LAMB3 | c.1545C>T (p.Ala515=) c.1353C>T (p.Ala451=) | |
1 | g.209626919G>C | CA423031260 | LAMB3 | c.1545C>G (p.Ala515=) c.1353C>G (p.Ala451=) | |
1 | g.209626919G>T | CA423031261 | LAMB3 | c.1545C>A (p.Ala515=) c.1353C>A (p.Ala451=) | |
1 | g.209626920G>A | CA344590149 | LAMB3 | c.1544C>T (p.Ala515Val) c.1352C>T (p.Ala451Val) | |
1 | g.209626920G>C | CA344590150 | LAMB3 | c.1544C>G (p.Ala515Gly) c.1352C>G (p.Ala451Gly) | |
1 | g.209626920G>T | CA344590151 | LAMB3 | c.1544C>A (p.Ala515Asp) c.1352C>A (p.Ala451Asp) | |
1 | g.209626921C>A | CA344590152 | LAMB3 | c.1543G>T (p.Ala515Ser) c.1351G>T (p.Ala451Ser) | |
1 | g.209626921C= | CA2484299687 | LAMB3 | c.1543G= (p.Ala515=) c.1351G= (p.Ala451=) | |
1 | g.209626921C>G | CA344590153 | LAMB3 | c.1543G>C (p.Ala515Pro) c.1351G>C (p.Ala451Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626921C>T | CA344590154 | LAMB3 | c.1543G>A (p.Ala515Thr) c.1351G>A (p.Ala451Thr) | |
1 | g.209626922T>A | CA423031264 | LAMB3 | c.1542A>T (p.Ala514=) c.1350A>T (p.Ala450=) | |
1 | g.209626922T>C | CA423031268 | LAMB3 | c.1542A>G (p.Ala514=) c.1350A>G (p.Ala450=) | |
1 | g.209626922T>G | CA423031269 | LAMB3 | c.1542A>C (p.Ala514=) c.1350A>C (p.Ala450=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626922T= | CA2484299688 | LAMB3 | c.1542A= (p.Ala514=) c.1350A= (p.Ala450=) | |
1 | g.209626923G>A | CA344590155 | LAMB3 | c.1541C>T (p.Ala514Val) c.1349C>T (p.Ala450Val) | |
1 | g.209626923G>C | CA344590156 | LAMB3 | c.1541C>G (p.Ala514Gly) c.1349C>G (p.Ala450Gly) | |
1 | g.209626923G= | CA2484299689 | LAMB3 | c.1541C= (p.Ala514=) c.1349C= (p.Ala450=) | |
1 | g.209626923G>T | CA1375552 | LAMB3 | c.1541C>A (p.Ala514Glu) c.1349C>A (p.Ala450Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209626924C>A | CA344590158 | LAMB3 | c.1540G>T (p.Ala514Ser) c.1348G>T (p.Ala450Ser) | |
1 | g.209626924C= | CA2484299690 | LAMB3 | c.1540G= (p.Ala514=) c.1348G= (p.Ala450=) | |
1 | g.209626924C>G | CA344590159 | LAMB3 | c.1540G>C (p.Ala514Pro) c.1348G>C (p.Ala450Pro) | |
1 | g.209626924C>T | CA344590157 | LAMB3 | c.1540G>A (p.Ala514Thr) c.1348G>A (p.Ala450Thr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626925A>C | CA423031272 | LAMB3 | c.1539T>G (p.Ala513=) c.1347T>G (p.Ala449=) | |
1 | g.209626925A>G | CA423031274 | LAMB3 | c.1539T>C (p.Ala513=) c.1347T>C (p.Ala449=) | gnomAD v4 |
1 | g.209626925A>T | CA423031275 | LAMB3 | c.1539T>A (p.Ala513=) c.1347T>A (p.Ala449=) | |
1 | g.209626926G>A | CA344590161 | LAMB3 | c.1538C>T (p.Ala513Val) c.1346C>T (p.Ala449Val) | dbSNP |
1 | g.209626926G>C | CA344590160 | LAMB3 | c.1538C>G (p.Ala513Gly) c.1346C>G (p.Ala449Gly) | |
1 | g.209626926G= | CA2484299691 | LAMB3 | c.1538C= (p.Ala513=) c.1346C= (p.Ala449=) | |
1 | g.209626926G>T | CA344590162 | LAMB3 | c.1538C>A (p.Ala513Asp) c.1346C>A (p.Ala449Asp) | |
1 | g.209626927C>A | CA344590163 | LAMB3 | c.1537G>T (p.Ala513Ser) c.1345G>T (p.Ala449Ser) | gnomAD v4 |
1 | g.209626927C= | CA2484299692 | LAMB3 | c.1537G= (p.Ala513=) c.1345G= (p.Ala449=) | |
1 | g.209626927C>G | CA344590165 | LAMB3 | c.1537G>C (p.Ala513Pro) c.1345G>C (p.Ala449Pro) | dbSNP gnomAD v2 |
1 | g.209626927C>T | CA344590164 | LAMB3 | c.1537G>A (p.Ala513Thr) c.1345G>A (p.Ala449Thr) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626928G>A | CA1375553 | LAMB3 | c.1536C>T (p.Ser512=) c.1344C>T (p.Ser448=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626928G>C | CA344590166 | LAMB3 | c.1536C>G (p.Ser512Arg) c.1344C>G (p.Ser448Arg) | |
1 | g.209626928G= | CA1144048421 | LAMB3 | c.1536C= (p.Ser512=) c.1344C= (p.Ser448=) | |
1 | g.209626928G>T | CA36756955 | LAMB3 | c.1536C>A (p.Ser512Arg) c.1344C>A (p.Ser448Arg) | ClinVar dbSNP gnomAD v4 |
1 | g.209626929C>A | CA344590167 | LAMB3 | c.1535G>T (p.Ser512Ile) c.1343G>T (p.Ser448Ile) | |
1 | g.209626929C>G | CA344590168 | LAMB3 | c.1535G>C (p.Ser512Thr) c.1343G>C (p.Ser448Thr) | |
1 | g.209626929C>T | CA344590169 | LAMB3 | c.1535G>A (p.Ser512Asn) c.1343G>A (p.Ser448Asn) | |
1 | g.209626930T>A | CA344590170 | LAMB3 | c.1534A>T (p.Ser512Cys) c.1342A>T (p.Ser448Cys) | |
1 | g.209626930T>C | CA344590171 | LAMB3 | c.1534A>G (p.Ser512Gly) c.1342A>G (p.Ser448Gly) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626930T>G | CA344590172 | LAMB3 | c.1534A>C (p.Ser512Arg) c.1342A>C (p.Ser448Arg) | |
1 | g.209626930T= | CA2484299693 | LAMB3 | c.1534A= (p.Ser512=) c.1342A= (p.Ser448=) | |
1 | g.209626931G>A | CA423031286 | LAMB3 | c.1533C>T (p.Cys511=) c.1341C>T (p.Cys447=) | dbSNP |
1 | g.209626931G>C | CA344590173 | LAMB3 | c.1533C>G (p.Cys511Trp) c.1341C>G (p.Cys447Trp) | |
1 | g.209626931G= | CA2484299694 | LAMB3 | c.1533C= (p.Cys511=) c.1341C= (p.Cys447=) | |
1 | g.209626931G>T | CA344590174 | LAMB3 | c.1533C>A (p.Cys511Ter) c.1341C>A (p.Cys447Ter) | |
1 | g.209626932C>A | CA344590175 | LAMB3 | c.1532G>T (p.Cys511Phe) c.1340G>T (p.Cys447Phe) | |
1 | g.209626932C>G | CA344590177 | LAMB3 | c.1532G>C (p.Cys511Ser) c.1340G>C (p.Cys447Ser) | |
1 | g.209626932C>T | CA344590176 | LAMB3 | c.1532G>A (p.Cys511Tyr) c.1340G>A (p.Cys447Tyr) | gnomAD v4 |
1 | g.209626933A>C | CA344590178 | LAMB3 | c.1531T>G (p.Cys511Gly) c.1339T>G (p.Cys447Gly) | |
1 | g.209626933A>G | CA344590179 | LAMB3 | c.1531T>C (p.Cys511Arg) c.1339T>C (p.Cys447Arg) | |
1 | g.209626933A>T | CA344590180 | LAMB3 | c.1531T>A (p.Cys511Ser) c.1339T>A (p.Cys447Ser) | |
1 | g.209626934C>A | CA344590181 | LAMB3 | c.1530G>T (p.Met510Ile) c.1338G>T (p.Met446Ile) | |
1 | g.209626934C>G | CA344590182 | LAMB3 | c.1530G>C (p.Met510Ile) c.1338G>C (p.Met446Ile) | |
1 | g.209626934C>T | CA344590183 | LAMB3 | c.1530G>A (p.Met510Ile) c.1338G>A (p.Met446Ile) | gnomAD v4 |
1 | g.209626935A= | CA2484299695 | LAMB3 | c.1529T= (p.Met510=) c.1337T= (p.Met446=) | |
1 | g.209626935A>C | CA344590184 | LAMB3 | c.1529T>G (p.Met510Arg) c.1337T>G (p.Met446Arg) | |
1 | g.209626935A>G | CA344590185 | LAMB3 | c.1529T>C (p.Met510Thr) c.1337T>C (p.Met446Thr) | |
1 | g.209626935A>T | CA344590186 | LAMB3 | c.1529T>A (p.Met510Lys) c.1337T>A (p.Met446Lys) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626936T>A | CA344590188 | LAMB3 | c.1528A>T (p.Met510Leu) c.1336A>T (p.Met446Leu) | |
1 | g.209626936T>C | CA344590189 | LAMB3 | c.1528A>G (p.Met510Val) c.1336A>G (p.Met446Val) | gnomAD v4 |
1 | g.209626936T>G | CA344590187 | LAMB3 | c.1528A>C (p.Met510Leu) c.1336A>C (p.Met446Leu) | |
1 | g.209626937C>A | CA423031303 | LAMB3 | c.1527G>T (p.Leu509=) c.1335G>T (p.Leu445=) | |
1 | g.209626937C>G | CA423031306 | LAMB3 | c.1527G>C (p.Leu509=) c.1335G>C (p.Leu445=) | ClinVar dbSNP |
1 | g.209626937C>T | CA423031305 | LAMB3 | c.1527G>A (p.Leu509=) c.1335G>A (p.Leu445=) | |
1 | g.209626938A= | CA1147528782 | LAMB3 | c.1526T= (p.Leu509=) c.1334T= (p.Leu445=) | |
1 | g.209626938A>C | CA344590190 | LAMB3 | c.1526T>G (p.Leu509Arg) c.1334T>G (p.Leu445Arg) | |
1 | g.209626938A>G | CA344590191 | LAMB3 | c.1526T>C (p.Leu509Pro) c.1334T>C (p.Leu445Pro) | |
1 | g.209626938A>T | CA1375554 | LAMB3 | c.1526T>A (p.Leu509Gln) c.1334T>A (p.Leu445Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626939G>A | CA423031310 | LAMB3 | c.1525C>T (p.Leu509=) c.1333C>T (p.Leu445=) | |
1 | g.209626939G>C | CA344590192 | LAMB3 | c.1525C>G (p.Leu509Val) c.1333C>G (p.Leu445Val) | |
1 | g.209626939G>T | CA344590193 | LAMB3 | c.1525C>A (p.Leu509Met) c.1333C>A (p.Leu445Met) | |
1 | g.209626940G>A | CA423031317 | LAMB3 | c.1524C>T (p.Gly508=) c.1332C>T (p.Gly444=) | gnomAD v4 |
1 | g.209626940G>C | CA423031315 | LAMB3 | c.1524C>G (p.Gly508=) c.1332C>G (p.Gly444=) | |
1 | g.209626940G>T | CA423031313 | LAMB3 | c.1524C>A (p.Gly508=) c.1332C>A (p.Gly444=) | |
1 | g.209626941C>A | CA344590194 | LAMB3 | c.1523G>T (p.Gly508Val) c.1331G>T (p.Gly444Val) | |
1 | g.209626941C= | CA2484299696 | LAMB3 | c.1523G= (p.Gly508=) c.1331G= (p.Gly444=) | |
1 | g.209626941C>G | CA344590195 | LAMB3 | c.1523G>C (p.Gly508Ala) c.1331G>C (p.Gly444Ala) | |
1 | g.209626941C>T | CA344590196 | LAMB3 | c.1523G>A (p.Gly508Asp) c.1331G>A (p.Gly444Asp) | dbSNP gnomAD v2 |
1 | g.209626942C>A | CA344590197 | LAMB3 | c.1522G>T (p.Gly508Cys) c.1330G>T (p.Gly444Cys) | |
1 | g.209626942C= | CA2484299697 | LAMB3 | c.1522G= (p.Gly508=) c.1330G= (p.Gly444=) | |
1 | g.209626942C>G | CA344590198 | LAMB3 | c.1522G>C (p.Gly508Arg) c.1330G>C (p.Gly444Arg) | gnomAD v4 |
1 | g.209626942C>T | CA1375555 | LAMB3 | c.1522G>A (p.Gly508Ser) c.1330G>A (p.Gly444Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.209626943A= | CA2484299698 | LAMB3 | c.1521T= (p.Gly507=) c.1329T= (p.Gly443=) | |
1 | g.209626943A>C | CA423031326 | LAMB3 | c.1521T>G (p.Gly507=) c.1329T>G (p.Gly443=) | |
1 | g.209626943A>G | CA423031329 | LAMB3 | c.1521T>C (p.Gly507=) c.1329T>C (p.Gly443=) | ClinVar dbSNP |
1 | g.209626943A>T | CA423031328 | LAMB3 | c.1521T>A (p.Gly507=) c.1329T>A (p.Gly443=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626944C>A | CA344590200 | LAMB3 | c.1520G>T (p.Gly507Val) c.1328G>T (p.Gly443Val) | |
1 | g.209626944C= | CA2484299699 | LAMB3 | c.1520G= (p.Gly507=) c.1328G= (p.Gly443=) | |
1 | g.209626944C>G | CA344590201 | LAMB3 | c.1520G>C (p.Gly507Ala) c.1328G>C (p.Gly443Ala) | |
1 | g.209626944C>T | CA344590199 | LAMB3 | c.1520G>A (p.Gly507Asp) c.1328G>A (p.Gly443Asp) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626945C>A | CA344590202 | LAMB3 | c.1519G>T (p.Gly507Cys) c.1327G>T (p.Gly443Cys) | dbSNP gnomAD v4 |
1 | g.209626945C= | CA2484299700 | LAMB3 | c.1519G= (p.Gly507=) c.1327G= (p.Gly443=) | |
1 | g.209626945C>G | CA344590203 | LAMB3 | c.1519G>C (p.Gly507Arg) c.1327G>C (p.Gly443Arg) | |
1 | g.209626945C>T | CA344590204 | LAMB3 | c.1519G>A (p.Gly507Ser) c.1327G>A (p.Gly443Ser) | dbSNP gnomAD v4 |
1 | g.209626946A>C | CA344590205 | LAMB3 | c.1518T>G (p.Phe506Leu) c.1326T>G (p.Phe442Leu) | |
1 | g.209626946A>G | CA423031340 | LAMB3 | c.1518T>C (p.Phe506=) c.1326T>C (p.Phe442=) | ClinVar |
1 | g.209626946A>T | CA344590206 | LAMB3 | c.1518T>A (p.Phe506Leu) c.1326T>A (p.Phe442Leu) | |
1 | g.209626947A= | CA2484299701 | LAMB3 | c.1517T= (p.Phe506=) c.1325T= (p.Phe442=) | |
1 | g.209626947A>C | CA1375556 | LAMB3 | c.1517T>G (p.Phe506Cys) c.1325T>G (p.Phe442Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209626947A>G | CA344590207 | LAMB3 | c.1517T>C (p.Phe506Ser) c.1325T>C (p.Phe442Ser) | |
1 | g.209626947A>T | CA344590208 | LAMB3 | c.1517T>A (p.Phe506Tyr) c.1325T>A (p.Phe442Tyr) | |
1 | g.209626948A= | CA1142060841 | LAMB3 | c.1516T= (p.Phe506=) c.1324T= (p.Phe442=) | |
1 | g.209626948A>C | CA344590209 | LAMB3 | c.1516T>G (p.Phe506Val) c.1324T>G (p.Phe442Val) | |
1 | g.209626948A>G | CA344590210 | LAMB3 | c.1516T>C (p.Phe506Leu) c.1324T>C (p.Phe442Leu) | dbSNP |
1 | g.209626948A>T | CA1375557 | LAMB3 | c.1516T>A (p.Phe506Ile) c.1324T>A (p.Phe442Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209626949G>A | CA423031344 | LAMB3 | c.1515C>T (p.Gly505=) c.1323C>T (p.Gly441=) | |
1 | g.209626949G>C | CA423031345 | LAMB3 | c.1515C>G (p.Gly505=) c.1323C>G (p.Gly441=) | |
1 | g.209626949G= | CA2484299702 | LAMB3 | c.1515C= (p.Gly505=) c.1323C= (p.Gly441=) | |
1 | g.209626949G>T | CA423031346 | LAMB3 | c.1515C>A (p.Gly505=) c.1323C>A (p.Gly441=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.209626950C>A | CA344590211 | LAMB3 | c.1514G>T (p.Gly505Val) c.1322G>T (p.Gly441Val) | |
1 | g.209626950C= | CA2484299703 | LAMB3 | c.1514G= (p.Gly505=) c.1322G= (p.Gly441=) | |
1 | g.209626950C>G | CA344590212 | LAMB3 | c.1514G>C (p.Gly505Ala) c.1322G>C (p.Gly441Ala) | |
1 | g.209626950C>T | CA344590213 | LAMB3 | c.1514G>A (p.Gly505Asp) c.1322G>A (p.Gly441Asp) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209626951C>A | CA344590215 | LAMB3 | c.1513G>T (p.Gly505Cys) c.1321G>T (p.Gly441Cys) | |
1 | g.209626951C>G | CA344590216 | LAMB3 | c.1513G>C (p.Gly505Arg) c.1321G>C (p.Gly441Arg) | |
1 | g.209626951C>T | CA344590214 | LAMB3 | c.1513G>A (p.Gly505Ser) c.1321G>A (p.Gly441Ser) | |
1 | g.209626952T>A | CA344590217 | LAMB3 | c.1512A>T (p.Glu504Asp) c.1320A>T (p.Glu440Asp) | |
1 | g.209626952T>C | CA423031348 | LAMB3 | c.1512A>G (p.Glu504=) c.1320A>G (p.Glu440=) | |
1 | g.209626952T>G | CA36756987 | LAMB3 | c.1512A>C (p.Glu504Asp) c.1320A>C (p.Glu440Asp) | dbSNP gnomAD v4 |
1 | g.209626952T= | CA2484299704 | LAMB3 | c.1512A= (p.Glu504=) c.1320A= (p.Glu440=) | |
1 | g.209626953T>A | CA344590218 | LAMB3 | c.1511A>T (p.Glu504Val) c.1319A>T (p.Glu440Val) | |
1 | g.209626953T>C | CA344590219 | LAMB3 | c.1511A>G (p.Glu504Gly) c.1319A>G (p.Glu440Gly) | |
1 | g.209626953T>G | CA344590220 | LAMB3 | c.1511A>C (p.Glu504Ala) c.1319A>C (p.Glu440Ala) | |
1 | g.209626954C>A | CA344590221 | LAMB3 | c.1510G>T (p.Glu504Ter) c.1318G>T (p.Glu440Ter) | ClinVar dbSNP |
1 | g.209626954C= | CA2484299705 | LAMB3 | c.1510G= (p.Glu504=) c.1318G= (p.Glu440=) | |
1 | g.209626954C>G | CA344590222 | LAMB3 | c.1510G>C (p.Glu504Gln) c.1318G>C (p.Glu440Gln) | |
1 | g.209626954C>T | CA344590223 | LAMB3 | c.1510G>A (p.Glu504Lys) c.1318G>A (p.Glu440Lys) | |
1 | g.209626955C>A | CA423031362 | LAMB3 | c.1509G>T (p.Arg503=) c.1317G>T (p.Arg439=) | gnomAD v4 |
1 | g.209626955C>G | CA423031365 | LAMB3 | c.1509G>C (p.Arg503=) c.1317G>C (p.Arg439=) | |
1 | g.209626955C>T | CA423031368 | LAMB3 | c.1509G>A (p.Arg503=) c.1317G>A (p.Arg439=) | ClinVar dbSNP |
1 | g.209626956C>A | CA344590224 | LAMB3 | c.1508G>T (p.Arg503Leu) c.1316G>T (p.Arg439Leu) | dbSNP gnomAD v4 |
1 | g.209626956C= | CA1143525940 | LAMB3 | c.1508G= (p.Arg503=) c.1316G= (p.Arg439=) | |
1 | g.209626956C>G | CA344590225 | LAMB3 | c.1508G>C (p.Arg503Pro) c.1316G>C (p.Arg439Pro) | |
1 | g.209626956C>T | CA1375558 | LAMB3 | c.1508G>A (p.Arg503Gln) c.1316G>A (p.Arg439Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |