Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.43051066_43057138del | CA2581463411 | BRCA1 | c.5191_5329del c.5194_5332del c.5068_5206del c.5188_5326del c.5116_5254del c.1882_2020del c.1744_1882del c.4306_4444del c.5071_5209del c.5260_5398del c.5053_5191del c.1756_1894del c.5257_5395del c.1581_1719del c.1768_1906del c.*4977_*5115del c.124_262del c.667_805del c.-98-6945_-98-873del (n.-98-6945_-98-873del) n.5330_5468del n.5371_5509del | |
17 | g.43052946_43059974del | CA1139665560 | BRCA1 | c.5191-2834_5275-1824del c.5194-2834_5278-1824del c.5068-2834_5152-1824del c.5188-2834_5272-1824del c.5116-2834_5200-1824del c.1882-2834_1966-1824del c.1744-2834_1828-1824del c.4306-2834_4390-1824del c.5071-2834_5155-1824del c.5260-2834_5344-1824del c.5053-2834_5137-1824del c.1756-2834_1840-1824del c.5257-2834_5341-1824del c.1581-2834_1665-1824del c.1768-2834_1852-1824del c.*4977-2834_*5061-1824del c.124-2834_208-1824del c.667-2834_751-1824del c.-98-9779_-98-2751del (n.-98-9779_-98-2751del) n.5330-2834_5414-1824del n.5371-2834_5455-1824del | ClinVar |
17 | g.43053415_43057588del | CA10602575 | BRCA1 | c.5191-452_5275-2297del c.5194-452_5278-2297del c.5068-452_5152-2297del c.5188-452_5272-2297del c.5116-452_5200-2297del c.1882-452_1966-2297del c.1744-452_1828-2297del c.4306-452_4390-2297del c.5071-452_5155-2297del c.5260-452_5344-2297del c.5053-452_5137-2297del c.1756-452_1840-2297del c.5257-452_5341-2297del c.1581-452_1665-2297del c.1768-452_1852-2297del c.*4977-452_*5061-2297del c.124-452_208-2297del c.667-452_751-2297del c.-98-7397_-98-3224del (n.-98-7397_-98-3224del) n.5330-452_5414-2297del n.5371-452_5455-2297del | ClinVar |
17 | g.43053428_43057600del | CA913191184 | BRCA1 | c.5191-453_5275-2299del c.5194-453_5278-2299del c.5068-453_5152-2299del c.5188-453_5272-2299del c.5116-453_5200-2299del c.1882-453_1966-2299del c.1744-453_1828-2299del c.4306-453_4390-2299del c.5071-453_5155-2299del c.5260-453_5344-2299del c.5053-453_5137-2299del c.1756-453_1840-2299del c.5257-453_5341-2299del c.1581-453_1665-2299del c.1768-453_1852-2299del c.*4977-453_*5061-2299del c.124-453_208-2299del c.667-453_751-2299del c.-98-7398_-98-3226del (n.-98-7398_-98-3226del) n.5330-453_5414-2299del n.5371-453_5455-2299del | ClinVar |
17 | g.43054853_43063000del | CA10602578 | BRCA1 | c.5190+340_5274+2206del c.5193+340_5277+2206del c.5067+340_5151+2206del c.5187+340_5271+2206del c.5115+340_5199+2206del c.1881+340_1965+2206del c.1743+340_1827+2206del c.4305+340_4389+2206del c.5070+340_5154+2206del c.5259+340_5343+2206del c.5052+340_5136+2206del c.1755+340_1839+2206del c.5256+340_5340+2206del c.1580+340_1664+2206del c.1767+340_1851+2206del c.*4976+340_*5060+2206del c.123+340_207+2206del c.666+340_750+2206del c.-98-12803_-98-4656del (n.-98-12803_-98-4656del) n.5329+340_5413+2206del n.5370+340_5454+2206del | ClinVar |
17 | g.43056382_43060705del | CA16043345 | BRCA1 | c.5190+2628_5274+670del c.5193+2628_5277+670del c.5067+2628_5151+670del c.5187+2628_5271+670del c.5115+2628_5199+670del c.1881+2628_1965+670del c.1743+2628_1827+670del c.4305+2628_4389+670del c.5070+2628_5154+670del c.5259+2628_5343+670del c.5052+2628_5136+670del c.1755+2628_1839+670del c.5256+2628_5340+670del c.1580+2628_1664+670del c.1767+2628_1851+670del c.*4976+2628_*5060+670del c.123+2628_207+670del c.666+2628_750+670del c.-98-10515_-98-6192del (n.-98-10515_-98-6192del) n.5329+2628_5413+670del n.5370+2628_5454+670del | ClinVar |
17 | g.43057049_43057254del | CA2499224363 | BRCA1 | c.5191-119_5274+3del c.5194-119_5277+3del c.5068-119_5151+3del c.5188-119_5271+3del c.5116-119_5199+3del c.1882-119_1965+3del c.1744-119_1827+3del c.4306-119_4389+3del c.5071-119_5154+3del c.5260-119_5343+3del c.5053-119_5136+3del c.1756-119_1839+3del c.5257-119_5340+3del c.1581-119_1664+3del c.1768-119_1851+3del c.*4977-119_*5060+3del c.124-119_207+3del c.667-119_750+3del c.-98-7064_-98-6859del (n.-98-7064_-98-6859del) n.5330-119_5413+3del n.5371-119_5454+3del | ClinVar dbSNP |
17 | g.43057049_43057971del | CA2499224364 | BRCA1 | c.5191-836_5274+3del c.5194-836_5277+3del c.5068-836_5151+3del c.5188-836_5271+3del c.5116-836_5199+3del c.1882-836_1965+3del c.1744-836_1827+3del c.4306-836_4389+3del c.5071-836_5154+3del c.5260-836_5343+3del c.5053-836_5136+3del c.1756-836_1839+3del c.5257-836_5340+3del c.1581-836_1664+3del c.1768-836_1851+3del c.*4977-836_*5060+3del c.124-836_207+3del c.667-836_750+3del c.-98-7781_-98-6859del (n.-98-7781_-98-6859del) n.5330-836_5413+3del n.5371-836_5454+3del | ClinVar dbSNP |
17 | g.43057050_43057136del | CA2499224366 | BRCA1 | c.5191-1_5274+2del c.5194-1_5277+2del c.5068-1_5151+2del c.5188-1_5271+2del c.5116-1_5199+2del c.1882-1_1965+2del c.1744-1_1827+2del c.4306-1_4389+2del c.5071-1_5154+2del c.5260-1_5343+2del c.5053-1_5136+2del c.1756-1_1839+2del c.5257-1_5340+2del c.1581-1_1664+2del c.1768-1_1851+2del c.*4977-1_*5060+2del c.124-1_207+2del c.667-1_750+2del c.-98-6946_-98-6860del (n.-98-6946_-98-6860del) n.5330-1_5413+2del n.5371-1_5454+2del | ClinVar dbSNP |
17 | g.43057051_43057178del | CA2499224365 | BRCA1 | c.5191-42_5274+2del c.5194-42_5277+2del c.5068-42_5151+2del c.5188-42_5271+2del c.5116-42_5199+2del c.1882-42_1965+2del c.1744-42_1827+2del c.4306-42_4389+2del c.5071-42_5154+2del c.5260-42_5343+2del c.5053-42_5136+2del c.1756-42_1839+2del c.5257-42_5340+2del c.1581-42_1664+2del c.1768-42_1851+2del c.*4977-42_*5060+2del c.124-42_207+2del c.667-42_750+2del c.-98-6987_-98-6860del (n.-98-6987_-98-6860del) n.5330-42_5413+2del n.5371-42_5454+2del | ClinVar dbSNP |
17 | g.43057052_43063333del | CA913189458 | BRCA1 | c.5190+1_5274+1del c.5193+1_5277+1del c.5067+1_5151+1del c.5187+1_5271+1del c.5115+1_5199+1del c.1881+1_1965+1del c.1743+1_1827+1del c.4305+1_4389+1del c.5070+1_5154+1del c.5259+1_5343+1del c.5052+1_5136+1del c.1755+1_1839+1del c.5256+1_5340+1del c.1580+1_1664+1del c.1767+1_1851+1del c.*4976+1_*5060+1del c.123+1_207+1del c.666+1_750+1del c.-98-13142_-98-6861del (n.-98-13142_-98-6861del) n.5329+1_5413+1del n.5370+1_5454+1del | ClinVar |
17 | g.43057054_43063375del | CA658655493 | BRCA1 | c.5151_5274+1del c.5154_5277+1del c.5028_5151+1del c.5148_5271+1del c.5076_5199+1del c.1842_1965+1del c.1704_1827+1del c.4266_4389+1del c.5031_5154+1del c.5220_5343+1del c.5013_5136+1del c.1716_1839+1del c.5217_5340+1del c.1541_1664+1del c.1728_1851+1del c.*4937_*5060+1del c.84_207+1del c.627_750+1del c.-98-13182_-98-6861del (n.-98-13182_-98-6861del) n.5290_5413+1del n.5331_5454+1del | |
17 | g.43057054_43057137del | CA915940681 | BRCA1 | c.5191_5274del c.5194_5277del c.5068_5151del c.5188_5271del c.5116_5199del c.1882_1965del c.1744_1827del c.4306_4389del c.5071_5154del c.5260_5343del c.5053_5136del c.1756_1839del c.5257_5340del c.1581_1664del c.1768_1851del c.*4977_*5060del c.124_207del c.667_750del c.-98-6945_-98-6862del (n.-98-6945_-98-6862del) n.5330_5413del n.5371_5454del | |
17 | g.43057080_43057120delinsTTTGGACCTTGGTGGTTTCTTCCATTGACCACATCTCCTCT | CA2260766396 | BRCA1 | c.5206_5246delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1736=) c.5209_5249delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1737=) c.5083_5123delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1695=) c.5203_5243delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1735=) c.5131_5171delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1711=) c.1897_1937delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg633=) c.1759_1799delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg587=) c.4321_4361delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1441=) c.5086_5126delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1696=) c.5275_5315delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1759=) c.5068_5108delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1690=) c.1771_1811delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg591=) c.5272_5312delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg1758=) c.1596_1636delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA c.1783_1823delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg595=) c.*4992_*5032delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (n.*4992_*5032delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA) c.139_179delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg47=) c.682_722delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (p.Arg228=) c.-98-6930_-98-6890delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA (n.-98-6930_-98-6890delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA) n.5345_5385delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA n.5386_5426delinsAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAAA | |
17 | g.43057081_43057120delinsGA | CA003359 | BRCA1 | c.5206_5245delinsTC (p.Arg1736SerfsTer?) c.5209_5248delinsTC (p.Arg1737SerfsTer?) c.5083_5122delinsTC (p.Arg1695SerfsTer?) c.5203_5242delinsTC (p.Arg1735SerfsTer?) c.5131_5170delinsTC (p.Arg1711SerfsTer?) c.1897_1936delinsTC (p.Arg633SerfsTer?) c.1759_1798delinsTC (p.Arg587SerfsTer?) c.4321_4360delinsTC (p.Arg1441SerfsTer?) c.5086_5125delinsTC (p.Arg1696SerfsTer?) c.5275_5314delinsTC (p.Arg1759SerfsTer?) c.5068_5107delinsTC (p.Arg1690SerfsTer?) c.1771_1810delinsTC (p.Arg591SerfsTer?) c.5272_5311delinsTC (p.Arg1758SerfsTer?) c.1596_1635delinsTC c.1783_1822delinsTC (p.Arg595SerfsTer?) c.*4992_*5031delinsTC (n.*4992_*5031delinsTC) c.139_178delinsTC (p.Arg47SerfsTer?) c.682_721delinsTC (p.Arg228SerfsTer?) c.-98-6930_-98-6891delinsTC (n.-98-6930_-98-6891delinsTC) n.5345_5384delinsTC n.5386_5425delinsTC | ClinVar dbSNP |
17 | g.43057081_43057121delinsTTGGACCTTGGTGGTTTCTTCCATTGACCACATCTCCTCTG | CA2260766399 | BRCA1 | c.5205_5245delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1735=) c.5208_5248delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1736=) c.5082_5122delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1694=) c.5202_5242delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1734=) c.5130_5170delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1710=) c.1896_1936delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val632=) c.1758_1798delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val586=) c.4320_4360delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1440=) c.5085_5125delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1695=) c.5274_5314delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1758=) c.5067_5107delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1689=) c.1770_1810delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val590=) c.5271_5311delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val1757=) c.1595_1635delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA c.1782_1822delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val594=) c.*4991_*5031delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (n.*4991_*5031delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA) c.138_178delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val46=) c.681_721delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (p.Val227=) c.-98-6931_-98-6891delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA (n.-98-6931_-98-6891delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA) n.5344_5384delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA n.5385_5425delinsCAGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA | |
17 | g.43057082_43057121delinsGA | CA10589604 | BRCA1 | c.5205_5244delinsTC (p.Arg1736GlnfsTer?) c.5208_5247delinsTC (p.Arg1737GlnfsTer?) c.5082_5121delinsTC (p.Arg1695GlnfsTer?) c.5202_5241delinsTC (p.Arg1735GlnfsTer?) c.5130_5169delinsTC (p.Arg1711GlnfsTer?) c.1896_1935delinsTC (p.Arg633GlnfsTer?) c.1758_1797delinsTC (p.Arg587GlnfsTer?) c.4320_4359delinsTC (p.Arg1441GlnfsTer?) c.5085_5124delinsTC (p.Arg1696GlnfsTer?) c.5274_5313delinsTC (p.Arg1759GlnfsTer?) c.5067_5106delinsTC (p.Arg1690GlnfsTer?) c.1770_1809delinsTC (p.Arg591GlnfsTer?) c.5271_5310delinsTC (p.Arg1758GlnfsTer?) c.1595_1634delinsTC c.1782_1821delinsTC (p.Arg595GlnfsTer?) c.*4991_*5030delinsTC (n.*4991_*5030delinsTC) c.138_177delinsTC (p.Arg47GlnfsTer?) c.681_720delinsTC (p.Arg228GlnfsTer?) c.-98-6931_-98-6892delinsTC (n.-98-6931_-98-6892delinsTC) n.5344_5383delinsTC n.5385_5424delinsTC | ClinVar dbSNP |
17 | g.43057086_43057120del | CA2740089957 | BRCA1 | c.5206_5240del (p.Arg1736SerfsTer?) c.5209_5243del (p.Arg1737SerfsTer?) c.5083_5117del (p.Arg1695SerfsTer?) c.5203_5237del (p.Arg1735SerfsTer?) c.5131_5165del (p.Arg1711SerfsTer?) c.1897_1931del (p.Arg633SerfsTer?) c.1759_1793del (p.Arg587SerfsTer?) c.4321_4355del (p.Arg1441SerfsTer?) c.5086_5120del (p.Arg1696SerfsTer?) c.5275_5309del (p.Arg1759SerfsTer?) c.5068_5102del (p.Arg1690SerfsTer?) c.1771_1805del (p.Arg591SerfsTer?) c.5272_5306del (p.Arg1758SerfsTer?) c.1596_1630del c.1783_1817del (p.Arg595SerfsTer?) c.*4992_*5026del (n.*4992_*5026del) c.139_173del (p.Arg47SerfsTer?) c.682_716del (p.Arg228SerfsTer?) c.-98-6930_-98-6896del (n.-98-6930_-98-6896del) n.5345_5379del n.5386_5420del | |
17 | g.43057093_43057145dup | CA658684094 | BRCA1 | c.5191-10_5233dup c.5194-10_5236dup c.5068-10_5110dup c.5188-10_5230dup c.5116-10_5158dup c.1882-10_1924dup c.1744-10_1786dup c.4306-10_4348dup c.5071-10_5113dup c.5260-10_5302dup c.5053-10_5095dup c.1756-10_1798dup c.5257-10_5299dup c.1581-10_1623dup c.1768-10_1810dup c.*4977-10_*5019dup c.124-10_166dup c.667-10_709dup c.-98-6955_-98-6903dup (n.-98-6955_-98-6903dup) n.5330-10_5372dup n.5371-10_5413dup | ClinVar dbSNP |
17 | g.43057117_43057119del | CA003364 | BRCA1 | c.5210_5212del (p.Gly1737del) c.5213_5215del (p.Gly1738del) c.5087_5089del (p.Gly1696del) c.5207_5209del (p.Gly1736del) c.5135_5137del (p.Gly1712del) c.1901_1903del (p.Gly634del) c.1763_1765del (p.Gly588del) c.4325_4327del (p.Gly1442del) c.5090_5092del (p.Gly1697del) c.5279_5281del (p.Gly1760del) c.5072_5074del (p.Gly1691del) c.1775_1777del (p.Gly592del) c.5276_5278del (p.Gly1759del) c.1600_1602del c.1787_1789del (p.Gly596del) c.*4996_*4998del (n.*4996_*4998del) c.143_145del (p.Gly48del) c.686_688del (p.Gly229del) c.-98-6926_-98-6924del (n.-98-6926_-98-6924del) n.5349_5351del n.5390_5392del | ClinVar dbSNP |
17 | g.43057119_43057120del | CA658798061 | BRCA1 | c.5208_5209del (p.Gly1737ArgfsTer?) c.5211_5212del (p.Gly1738ArgfsTer?) c.5085_5086del (p.Gly1696ArgfsTer?) c.5205_5206del (p.Gly1736ArgfsTer?) c.5133_5134del (p.Gly1712ArgfsTer?) c.1899_1900del (p.Gly634ArgfsTer?) c.1761_1762del (p.Gly588ArgfsTer?) c.4323_4324del (p.Gly1442ArgfsTer?) c.5088_5089del (p.Gly1697ArgfsTer?) c.5277_5278del (p.Gly1760ArgfsTer?) c.5070_5071del (p.Gly1691ArgfsTer?) c.1773_1774del (p.Gly592ArgfsTer?) c.5274_5275del (p.Gly1759ArgfsTer?) c.1598_1599del c.1785_1786del (p.Gly596ArgfsTer?) c.*4994_*4995del (n.*4994_*4995del) c.141_142del (p.Gly48ArgfsTer?) c.684_685del (p.Gly229ArgfsTer?) c.-98-6928_-98-6927del (n.-98-6928_-98-6927del) n.5347_5348del n.5388_5389del | ClinVar dbSNP |
17 | g.43057119C>A | CA10591117 | BRCA1 | c.5207G>T (p.Arg1736Ile) c.5210G>T (p.Arg1737Ile) c.5084G>T (p.Arg1695Ile) c.5204G>T (p.Arg1735Ile) c.5132G>T (p.Arg1711Ile) c.1898G>T (p.Arg633Ile) c.1760G>T (p.Arg587Ile) c.4322G>T (p.Arg1441Ile) c.5087G>T (p.Arg1696Ile) c.5276G>T (p.Arg1759Ile) c.5069G>T (p.Arg1690Ile) c.1772G>T (p.Arg591Ile) c.5273G>T (p.Arg1758Ile) c.1597G>T c.1784G>T (p.Arg595Ile) c.*4993G>T (n.*4993G>T) c.140G>T (p.Arg47Ile) c.683G>T (p.Arg228Ile) c.-98-6929G>T (n.-98-6929G>T) n.5346G>T n.5387G>T | ClinVar dbSNP |
17 | g.43057119C= | CA2260766456 | BRCA1 | c.5207G= (p.Arg1736=) c.5210G= (p.Arg1737=) c.5084G= (p.Arg1695=) c.5204G= (p.Arg1735=) c.5132G= (p.Arg1711=) c.1898G= (p.Arg633=) c.1760G= (p.Arg587=) c.4322G= (p.Arg1441=) c.5087G= (p.Arg1696=) c.5276G= (p.Arg1759=) c.5069G= (p.Arg1690=) c.1772G= (p.Arg591=) c.5273G= (p.Arg1758=) c.1597G= c.1784G= (p.Arg595=) c.*4993G= (n.*4993G=) c.140G= (p.Arg47=) c.683G= (p.Arg228=) c.-98-6929G= (n.-98-6929G=) n.5346G= n.5387G= | |
17 | g.43057119C>G | CA10591118 | BRCA1 | c.5207G>C (p.Arg1736Thr) c.5210G>C (p.Arg1737Thr) c.5084G>C (p.Arg1695Thr) c.5204G>C (p.Arg1735Thr) c.5132G>C (p.Arg1711Thr) c.1898G>C (p.Arg633Thr) c.1760G>C (p.Arg587Thr) c.4322G>C (p.Arg1441Thr) c.5087G>C (p.Arg1696Thr) c.5276G>C (p.Arg1759Thr) c.5069G>C (p.Arg1690Thr) c.1772G>C (p.Arg591Thr) c.5273G>C (p.Arg1758Thr) c.1597G>C c.1784G>C (p.Arg595Thr) c.*4993G>C (n.*4993G>C) c.140G>C (p.Arg47Thr) c.683G>C (p.Arg228Thr) c.-98-6929G>C (n.-98-6929G>C) n.5346G>C n.5387G>C | ClinVar dbSNP |
17 | g.43057119C>T | CA10591119 | BRCA1 | c.5207G>A (p.Arg1736Lys) c.5210G>A (p.Arg1737Lys) c.5084G>A (p.Arg1695Lys) c.5204G>A (p.Arg1735Lys) c.5132G>A (p.Arg1711Lys) c.1898G>A (p.Arg633Lys) c.1760G>A (p.Arg587Lys) c.4322G>A (p.Arg1441Lys) c.5087G>A (p.Arg1696Lys) c.5276G>A (p.Arg1759Lys) c.5069G>A (p.Arg1690Lys) c.1772G>A (p.Arg591Lys) c.5273G>A (p.Arg1758Lys) c.1597G>A c.1784G>A (p.Arg595Lys) c.*4993G>A (n.*4993G>A) c.140G>A (p.Arg47Lys) c.683G>A (p.Arg228Lys) c.-98-6929G>A (n.-98-6929G>A) n.5346G>A n.5387G>A | ClinVar dbSNP |
17 | g.43057119_43057120insG | CA645373153 | BRCA1 | c.5206_5207insC (p.Arg1736ThrfsTer?) c.5209_5210insC (p.Arg1737ThrfsTer?) c.5083_5084insC (p.Arg1695ThrfsTer?) c.5203_5204insC (p.Arg1735ThrfsTer?) c.5131_5132insC (p.Arg1711ThrfsTer?) c.1897_1898insC (p.Arg633ThrfsTer?) c.1759_1760insC (p.Arg587ThrfsTer?) c.4321_4322insC (p.Arg1441ThrfsTer?) c.5086_5087insC (p.Arg1696ThrfsTer?) c.5275_5276insC (p.Arg1759ThrfsTer?) c.5068_5069insC (p.Arg1690ThrfsTer?) c.1771_1772insC (p.Arg591ThrfsTer?) c.5272_5273insC (p.Arg1758ThrfsTer?) c.1596_1597insC c.1783_1784insC (p.Arg595ThrfsTer?) c.*4992_*4993insC (n.*4992_*4993insC) c.139_140insC (p.Arg47ThrfsTer?) c.682_683insC (p.Arg228ThrfsTer?) c.-98-6930_-98-6929insC (n.-98-6930_-98-6929insC) n.5345_5346insC n.5386_5387insC | ClinVar dbSNP |
17 | g.43057120T>A | CA003361 | BRCA1 | c.5206A>T (p.Arg1736Ter) c.5209A>T (p.Arg1737Ter) c.5083A>T (p.Arg1695Ter) c.5203A>T (p.Arg1735Ter) c.5131A>T (p.Arg1711Ter) c.1897A>T (p.Arg633Ter) c.1759A>T (p.Arg587Ter) c.4321A>T (p.Arg1441Ter) c.5086A>T (p.Arg1696Ter) c.5275A>T (p.Arg1759Ter) c.5068A>T (p.Arg1690Ter) c.1771A>T (p.Arg591Ter) c.5272A>T (p.Arg1758Ter) c.1596A>T c.1783A>T (p.Arg595Ter) c.*4992A>T (n.*4992A>T) c.139A>T (p.Arg47Ter) c.682A>T (p.Arg228Ter) c.-98-6930A>T (n.-98-6930A>T) n.5345A>T n.5386A>T | ClinVar dbSNP |
17 | g.43057120T>C | CA10591120 | BRCA1 | c.5206A>G (p.Arg1736Gly) c.5209A>G (p.Arg1737Gly) c.5083A>G (p.Arg1695Gly) c.5203A>G (p.Arg1735Gly) c.5131A>G (p.Arg1711Gly) c.1897A>G (p.Arg633Gly) c.1759A>G (p.Arg587Gly) c.4321A>G (p.Arg1441Gly) c.5086A>G (p.Arg1696Gly) c.5275A>G (p.Arg1759Gly) c.5068A>G (p.Arg1690Gly) c.1771A>G (p.Arg591Gly) c.5272A>G (p.Arg1758Gly) c.1596A>G c.1783A>G (p.Arg595Gly) c.*4992A>G (n.*4992A>G) c.139A>G (p.Arg47Gly) c.682A>G (p.Arg228Gly) c.-98-6930A>G (n.-98-6930A>G) n.5345A>G n.5386A>G | ClinVar dbSNP |
17 | g.43057120T>G | CA500144837 | BRCA1 | c.5206A>C (p.Arg1736=) c.5209A>C (p.Arg1737=) c.5083A>C (p.Arg1695=) c.5203A>C (p.Arg1735=) c.5131A>C (p.Arg1711=) c.1897A>C (p.Arg633=) c.1759A>C (p.Arg587=) c.4321A>C (p.Arg1441=) c.5086A>C (p.Arg1696=) c.5275A>C (p.Arg1759=) c.5068A>C (p.Arg1690=) c.1771A>C (p.Arg591=) c.5272A>C (p.Arg1758=) c.1596A>C c.1783A>C (p.Arg595=) c.*4992A>C (n.*4992A>C) c.139A>C (p.Arg47=) c.682A>C (p.Arg228=) c.-98-6930A>C (n.-98-6930A>C) n.5345A>C n.5386A>C | ClinVar dbSNP |
17 | g.43057120T= | CA2260766457 | BRCA1 | c.5206A= (p.Arg1736=) c.5209A= (p.Arg1737=) c.5083A= (p.Arg1695=) c.5203A= (p.Arg1735=) c.5131A= (p.Arg1711=) c.1897A= (p.Arg633=) c.1759A= (p.Arg587=) c.4321A= (p.Arg1441=) c.5086A= (p.Arg1696=) c.5275A= (p.Arg1759=) c.5068A= (p.Arg1690=) c.1771A= (p.Arg591=) c.5272A= (p.Arg1758=) c.1596A= c.1783A= (p.Arg595=) c.*4992A= (n.*4992A=) c.139A= (p.Arg47=) c.682A= (p.Arg228=) c.-98-6930A= (n.-98-6930A=) n.5345A= n.5386A= | |
17 | g.43057120dup | CA10589611 | BRCA1 | c.5206dup (p.Arg1736LysfsTer?) c.5209dup (p.Arg1737LysfsTer?) c.5083dup (p.Arg1695LysfsTer?) c.5203dup (p.Arg1735LysfsTer?) c.5131dup (p.Arg1711LysfsTer?) c.1897dup (p.Arg633LysfsTer?) c.1759dup (p.Arg587LysfsTer?) c.4321dup (p.Arg1441LysfsTer?) c.5086dup (p.Arg1696LysfsTer?) c.5275dup (p.Arg1759LysfsTer?) c.5068dup (p.Arg1690LysfsTer?) c.1771dup (p.Arg591LysfsTer?) c.5272dup (p.Arg1758LysfsTer?) c.1596dup c.1783dup (p.Arg595LysfsTer?) c.*4992dup (n.*4992dup) c.139dup (p.Arg47LysfsTer?) c.682dup (p.Arg228LysfsTer?) c.-98-6930dup (n.-98-6930dup) n.5345dup n.5386dup | ClinVar dbSNP |
17 | g.43057121G>A | CA500144845 | BRCA1 | c.5205C>T (p.Val1735=) c.5208C>T (p.Val1736=) c.5082C>T (p.Val1694=) c.5202C>T (p.Val1734=) c.5130C>T (p.Val1710=) c.1896C>T (p.Val632=) c.1758C>T (p.Val586=) c.4320C>T (p.Val1440=) c.5085C>T (p.Val1695=) c.5274C>T (p.Val1758=) c.5067C>T (p.Val1689=) c.1770C>T (p.Val590=) c.5271C>T (p.Val1757=) c.1595C>T c.1782C>T (p.Val594=) c.*4991C>T (n.*4991C>T) c.138C>T (p.Val46=) c.681C>T (p.Val227=) c.-98-6931C>T (n.-98-6931C>T) n.5344C>T n.5385C>T | ClinVar dbSNP |
17 | g.43057121G>C | CA500144840 | BRCA1 | c.5205C>G (p.Val1735=) c.5208C>G (p.Val1736=) c.5082C>G (p.Val1694=) c.5202C>G (p.Val1734=) c.5130C>G (p.Val1710=) c.1896C>G (p.Val632=) c.1758C>G (p.Val586=) c.4320C>G (p.Val1440=) c.5085C>G (p.Val1695=) c.5274C>G (p.Val1758=) c.5067C>G (p.Val1689=) c.1770C>G (p.Val590=) c.5271C>G (p.Val1757=) c.1595C>G c.1782C>G (p.Val594=) c.*4991C>G (n.*4991C>G) c.138C>G (p.Val46=) c.681C>G (p.Val227=) c.-98-6931C>G (n.-98-6931C>G) n.5344C>G n.5385C>G | ClinVar dbSNP |
17 | g.43057121G= | CA2260766459 | BRCA1 | c.5205C= (p.Val1735=) c.5208C= (p.Val1736=) c.5082C= (p.Val1694=) c.5202C= (p.Val1734=) c.5130C= (p.Val1710=) c.1896C= (p.Val632=) c.1758C= (p.Val586=) c.4320C= (p.Val1440=) c.5085C= (p.Val1695=) c.5274C= (p.Val1758=) c.5067C= (p.Val1689=) c.1770C= (p.Val590=) c.5271C= (p.Val1757=) c.1595C= c.1782C= (p.Val594=) c.*4991C= (n.*4991C=) c.138C= (p.Val46=) c.681C= (p.Val227=) c.-98-6931C= (n.-98-6931C=) n.5344C= n.5385C= | |
17 | g.43057121G>T | CA500144843 | BRCA1 | c.5205C>A (p.Val1735=) c.5208C>A (p.Val1736=) c.5082C>A (p.Val1694=) c.5202C>A (p.Val1734=) c.5130C>A (p.Val1710=) c.1896C>A (p.Val632=) c.1758C>A (p.Val586=) c.4320C>A (p.Val1440=) c.5085C>A (p.Val1695=) c.5274C>A (p.Val1758=) c.5067C>A (p.Val1689=) c.1770C>A (p.Val590=) c.5271C>A (p.Val1757=) c.1595C>A c.1782C>A (p.Val594=) c.*4991C>A (n.*4991C>A) c.138C>A (p.Val46=) c.681C>A (p.Val227=) c.-98-6931C>A (n.-98-6931C>A) n.5344C>A n.5385C>A | ClinVar dbSNP |
17 | g.43057121_43057122delinsGA | CA2260766458 | BRCA1 | c.5204_5205delinsTC (p.Val1735=) c.5207_5208delinsTC (p.Val1736=) c.5081_5082delinsTC (p.Val1694=) c.5201_5202delinsTC (p.Val1734=) c.5129_5130delinsTC (p.Val1710=) c.1895_1896delinsTC (p.Val632=) c.1757_1758delinsTC (p.Val586=) c.4319_4320delinsTC (p.Val1440=) c.5084_5085delinsTC (p.Val1695=) c.5273_5274delinsTC (p.Val1758=) c.5066_5067delinsTC (p.Val1689=) c.1769_1770delinsTC (p.Val590=) c.5270_5271delinsTC (p.Val1757=) c.1594_1595delinsTC c.1781_1782delinsTC (p.Val594=) c.*4990_*4991delinsTC (n.*4990_*4991delinsTC) c.137_138delinsTC (p.Val46=) c.680_681delinsTC (p.Val227=) c.-98-6932_-98-6931delinsTC (n.-98-6932_-98-6931delinsTC) n.5343_5344delinsTC n.5384_5385delinsTC | |
17 | g.43057122del | CA003356 | BRCA1 | c.5204del (p.Val1735AlafsTer29) c.5207del (p.Val1736AlafsTer29) c.5081del (p.Val1694AlafsTer29) c.5201del (p.Val1734AlafsTer29) c.5129del (p.Val1710AlafsTer29) c.1895del (p.Val632AlafsTer29) c.1757del (p.Val586AlafsTer29) c.4319del (p.Val1440AlafsTer29) c.5084del (p.Val1695AlafsTer29) c.5273del (p.Val1758AlafsTer29) c.5066del (p.Val1689AlafsTer29) c.1769del (p.Val590AlafsTer29) c.5270del (p.Val1757AlafsTer29) c.1594del c.1781del (p.Val594AlafsTer29) c.*4990del (n.*4990del) c.137del (p.Val46AlafsTer29) c.680del (p.Val227AlafsTer29) c.-98-6932del (n.-98-6932del) n.5343del n.5384del | ClinVar dbSNP |
17 | g.43057122A= | CA2260766460 | BRCA1 | c.5204T= (p.Val1735=) c.5207T= (p.Val1736=) c.5081T= (p.Val1694=) c.5201T= (p.Val1734=) c.5129T= (p.Val1710=) c.1895T= (p.Val632=) c.1757T= (p.Val586=) c.4319T= (p.Val1440=) c.5084T= (p.Val1695=) c.5273T= (p.Val1758=) c.5066T= (p.Val1689=) c.1769T= (p.Val590=) c.5270T= (p.Val1757=) c.1594T= c.1781T= (p.Val594=) c.*4990T= (n.*4990T=) c.137T= (p.Val46=) c.680T= (p.Val227=) c.-98-6932T= (n.-98-6932T=) n.5343T= n.5384T= | |
17 | g.43057122A>C | CA003358 | BRCA1 | c.5204T>G (p.Val1735Gly) c.5207T>G (p.Val1736Gly) c.5081T>G (p.Val1694Gly) c.5201T>G (p.Val1734Gly) c.5129T>G (p.Val1710Gly) c.1895T>G (p.Val632Gly) c.1757T>G (p.Val586Gly) c.4319T>G (p.Val1440Gly) c.5084T>G (p.Val1695Gly) c.5273T>G (p.Val1758Gly) c.5066T>G (p.Val1689Gly) c.1769T>G (p.Val590Gly) c.5270T>G (p.Val1757Gly) c.1594T>G c.1781T>G (p.Val594Gly) c.*4990T>G (n.*4990T>G) c.137T>G (p.Val46Gly) c.680T>G (p.Val227Gly) c.-98-6932T>G (n.-98-6932T>G) n.5343T>G n.5384T>G | ClinVar dbSNP |
17 | g.43057122A>G | CA003357 | BRCA1 | c.5204T>C (p.Val1735Ala) c.5207T>C (p.Val1736Ala) c.5081T>C (p.Val1694Ala) c.5201T>C (p.Val1734Ala) c.5129T>C (p.Val1710Ala) c.1895T>C (p.Val632Ala) c.1757T>C (p.Val586Ala) c.4319T>C (p.Val1440Ala) c.5084T>C (p.Val1695Ala) c.5273T>C (p.Val1758Ala) c.5066T>C (p.Val1689Ala) c.1769T>C (p.Val590Ala) c.5270T>C (p.Val1757Ala) c.1594T>C c.1781T>C (p.Val594Ala) c.*4990T>C (n.*4990T>C) c.137T>C (p.Val46Ala) c.680T>C (p.Val227Ala) c.-98-6932T>C (n.-98-6932T>C) n.5343T>C n.5384T>C | ClinVar dbSNP gnomAD v4 |
17 | g.43057122A>T | CA10591121 | BRCA1 | c.5204T>A (p.Val1735Asp) c.5207T>A (p.Val1736Asp) c.5081T>A (p.Val1694Asp) c.5201T>A (p.Val1734Asp) c.5129T>A (p.Val1710Asp) c.1895T>A (p.Val632Asp) c.1757T>A (p.Val586Asp) c.4319T>A (p.Val1440Asp) c.5084T>A (p.Val1695Asp) c.5273T>A (p.Val1758Asp) c.5066T>A (p.Val1689Asp) c.1769T>A (p.Val590Asp) c.5270T>A (p.Val1757Asp) c.1594T>A c.1781T>A (p.Val594Asp) c.*4990T>A (n.*4990T>A) c.137T>A (p.Val46Asp) c.680T>A (p.Val227Asp) c.-98-6932T>A (n.-98-6932T>A) n.5343T>A n.5384T>A | ClinVar dbSNP |
17 | g.43057123C>A | CA10591122 | BRCA1 | c.5203G>T (p.Val1735Phe) c.5206G>T (p.Val1736Phe) c.5080G>T (p.Val1694Phe) c.5200G>T (p.Val1734Phe) c.5128G>T (p.Val1710Phe) c.1894G>T (p.Val632Phe) c.1756G>T (p.Val586Phe) c.4318G>T (p.Val1440Phe) c.5083G>T (p.Val1695Phe) c.5272G>T (p.Val1758Phe) c.5065G>T (p.Val1689Phe) c.1768G>T (p.Val590Phe) c.5269G>T (p.Val1757Phe) c.1593G>T c.1780G>T (p.Val594Phe) c.*4989G>T (n.*4989G>T) c.136G>T (p.Val46Phe) c.679G>T (p.Val227Phe) c.-98-6933G>T (n.-98-6933G>T) n.5342G>T n.5383G>T | ClinVar dbSNP gnomAD v4 |
17 | g.43057123C= | CA2260766461 | BRCA1 | c.5203G= (p.Val1735=) c.5206G= (p.Val1736=) c.5080G= (p.Val1694=) c.5200G= (p.Val1734=) c.5128G= (p.Val1710=) c.1894G= (p.Val632=) c.1756G= (p.Val586=) c.4318G= (p.Val1440=) c.5083G= (p.Val1695=) c.5272G= (p.Val1758=) c.5065G= (p.Val1689=) c.1768G= (p.Val590=) c.5269G= (p.Val1757=) c.1593G= c.1780G= (p.Val594=) c.*4989G= (n.*4989G=) c.136G= (p.Val46=) c.679G= (p.Val227=) c.-98-6933G= (n.-98-6933G=) n.5342G= n.5383G= | |
17 | g.43057123C>G | CA10591123 | BRCA1 | c.5203G>C (p.Val1735Leu) c.5206G>C (p.Val1736Leu) c.5080G>C (p.Val1694Leu) c.5200G>C (p.Val1734Leu) c.5128G>C (p.Val1710Leu) c.1894G>C (p.Val632Leu) c.1756G>C (p.Val586Leu) c.4318G>C (p.Val1440Leu) c.5083G>C (p.Val1695Leu) c.5272G>C (p.Val1758Leu) c.5065G>C (p.Val1689Leu) c.1768G>C (p.Val590Leu) c.5269G>C (p.Val1757Leu) c.1593G>C c.1780G>C (p.Val594Leu) c.*4989G>C (n.*4989G>C) c.136G>C (p.Val46Leu) c.679G>C (p.Val227Leu) c.-98-6933G>C (n.-98-6933G>C) n.5342G>C n.5383G>C | ClinVar dbSNP |
17 | g.43057123C>T | CA10591124 | BRCA1 | c.5203G>A (p.Val1735Ile) c.5206G>A (p.Val1736Ile) c.5080G>A (p.Val1694Ile) c.5200G>A (p.Val1734Ile) c.5128G>A (p.Val1710Ile) c.1894G>A (p.Val632Ile) c.1756G>A (p.Val586Ile) c.4318G>A (p.Val1440Ile) c.5083G>A (p.Val1695Ile) c.5272G>A (p.Val1758Ile) c.5065G>A (p.Val1689Ile) c.1768G>A (p.Val590Ile) c.5269G>A (p.Val1757Ile) c.1593G>A c.1780G>A (p.Val594Ile) c.*4989G>A (n.*4989G>A) c.136G>A (p.Val46Ile) c.679G>A (p.Val227Ile) c.-98-6933G>A (n.-98-6933G>A) n.5342G>A n.5383G>A | ClinVar dbSNP |
17 | g.43057123_43057124delinsCT | CA2260766462 | BRCA1 | c.5202_5203delinsAG (p.Glu1734=) c.5205_5206delinsAG (p.Glu1735=) c.5079_5080delinsAG (p.Glu1693=) c.5199_5200delinsAG (p.Glu1733=) c.5127_5128delinsAG (p.Glu1709=) c.1893_1894delinsAG (p.Glu631=) c.1755_1756delinsAG (p.Glu585=) c.4317_4318delinsAG (p.Glu1439=) c.5082_5083delinsAG (p.Glu1694=) c.5271_5272delinsAG (p.Glu1757=) c.5064_5065delinsAG (p.Glu1688=) c.1767_1768delinsAG (p.Glu589=) c.5268_5269delinsAG (p.Glu1756=) c.1592_1593delinsAG c.1779_1780delinsAG (p.Glu593=) c.*4988_*4989delinsAG (n.*4988_*4989delinsAG) c.135_136delinsAG (p.Glu45=) c.678_679delinsAG (p.Glu226=) c.-98-6934_-98-6933delinsAG (n.-98-6934_-98-6933delinsAG) n.5341_5342delinsAG n.5382_5383delinsAG | |
17 | g.43057124T>A | CA003354 | BRCA1 | c.5202A>T (p.Glu1734Asp) c.5205A>T (p.Glu1735Asp) c.5079A>T (p.Glu1693Asp) c.5199A>T (p.Glu1733Asp) c.5127A>T (p.Glu1709Asp) c.1893A>T (p.Glu631Asp) c.1755A>T (p.Glu585Asp) c.4317A>T (p.Glu1439Asp) c.5082A>T (p.Glu1694Asp) c.5271A>T (p.Glu1757Asp) c.5064A>T (p.Glu1688Asp) c.1767A>T (p.Glu589Asp) c.5268A>T (p.Glu1756Asp) c.1592A>T c.1779A>T (p.Glu593Asp) c.*4988A>T (n.*4988A>T) c.135A>T (p.Glu45Asp) c.678A>T (p.Glu226Asp) c.-98-6934A>T (n.-98-6934A>T) n.5341A>T n.5382A>T | ClinVar dbSNP |
17 | g.43057124T>C | CA500144860 | BRCA1 | c.5202A>G (p.Glu1734=) c.5205A>G (p.Glu1735=) c.5079A>G (p.Glu1693=) c.5199A>G (p.Glu1733=) c.5127A>G (p.Glu1709=) c.1893A>G (p.Glu631=) c.1755A>G (p.Glu585=) c.4317A>G (p.Glu1439=) c.5082A>G (p.Glu1694=) c.5271A>G (p.Glu1757=) c.5064A>G (p.Glu1688=) c.1767A>G (p.Glu589=) c.5268A>G (p.Glu1756=) c.1592A>G c.1779A>G (p.Glu593=) c.*4988A>G (n.*4988A>G) c.135A>G (p.Glu45=) c.678A>G (p.Glu226=) c.-98-6934A>G (n.-98-6934A>G) n.5341A>G n.5382A>G | ClinVar dbSNP |
17 | g.43057124T>G | CA10591125 | BRCA1 | c.5202A>C (p.Glu1734Asp) c.5205A>C (p.Glu1735Asp) c.5079A>C (p.Glu1693Asp) c.5199A>C (p.Glu1733Asp) c.5127A>C (p.Glu1709Asp) c.1893A>C (p.Glu631Asp) c.1755A>C (p.Glu585Asp) c.4317A>C (p.Glu1439Asp) c.5082A>C (p.Glu1694Asp) c.5271A>C (p.Glu1757Asp) c.5064A>C (p.Glu1688Asp) c.1767A>C (p.Glu589Asp) c.5268A>C (p.Glu1756Asp) c.1592A>C c.1779A>C (p.Glu593Asp) c.*4988A>C (n.*4988A>C) c.135A>C (p.Glu45Asp) c.678A>C (p.Glu226Asp) c.-98-6934A>C (n.-98-6934A>C) n.5341A>C n.5382A>C | ClinVar dbSNP |
17 | g.43057124T= | CA2260766463 | BRCA1 | c.5202A= (p.Glu1734=) c.5205A= (p.Glu1735=) c.5079A= (p.Glu1693=) c.5199A= (p.Glu1733=) c.5127A= (p.Glu1709=) c.1893A= (p.Glu631=) c.1755A= (p.Glu585=) c.4317A= (p.Glu1439=) c.5082A= (p.Glu1694=) c.5271A= (p.Glu1757=) c.5064A= (p.Glu1688=) c.1767A= (p.Glu589=) c.5268A= (p.Glu1756=) c.1592A= c.1779A= (p.Glu593=) c.*4988A= (n.*4988A=) c.135A= (p.Glu45=) c.678A= (p.Glu226=) c.-98-6934A= (n.-98-6934A=) n.5341A= n.5382A= |