ClinVar Miner

List of variants in gene BRCA1 reported as benign by DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center

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Total variants: 35
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HGVS dbSNP
NM_007294.3(BRCA1):c.2077G>A (p.Asp693Asn) rs4986850
NM_007294.3(BRCA1):c.2412G>C (p.Gln804His) rs55746541
NM_007294.3(BRCA1):c.2612C>T (p.Pro871Leu) rs799917
NM_007294.3(BRCA1):c.3113A>G (p.Glu1038Gly) rs16941
NM_007294.3(BRCA1):c.3418A>G (p.Ser1140Gly) rs2227945
NM_007294.3(BRCA1):c.3548A>G (p.Lys1183Arg) rs16942
NM_007294.3(BRCA1):c.4039A>G (p.Arg1347Gly) rs28897689
NM_007294.3(BRCA1):c.4600G>A (p.Val1534Met) rs55815649
NM_007294.3(BRCA1):c.4837A>G (p.Ser1613Gly) rs1799966
NM_007294.3(BRCA1):c.5075-53C>T rs8176258
NM_007294.3(BRCA1):c.5117G>C (p.Gly1706Ala) rs80356860
NM_007294.3(BRCA1):c.5152+66G>A rs3092994
NM_007294.3(BRCA1):c.5152+85delT rs8176259
NM_007294.3(BRCA1):c.5158A>G (p.Thr1720Ala) rs56195342
NM_007294.3(BRCA1):c.5406+8T>C rs55946644
NM_007299.4(BRCA1):c.1223G>T (p.Ser408Ile) rs1800744
NM_007299.4(BRCA1):c.1324G>A (p.Asp442Asn) rs28897691
NM_007299.4(BRCA1):c.1644G>A (p.Met548Ile) rs1799967
NM_007299.4(BRCA1):c.787+1184A>G rs28897679
NM_007299.4(BRCA1):c.787+1295C>T rs1799949
NM_007299.4(BRCA1):c.787+1524T>C rs16940
NM_007299.4(BRCA1):c.787+1671A>G rs56082113
NM_007299.4(BRCA1):c.787+1779T>C rs80356892
NM_007299.4(BRCA1):c.787+1809C>T rs41286300
NM_007299.4(BRCA1):c.788-1380G>A rs4986852
NM_007299.4(BRCA1):c.999T>C (p.Ser333=) rs1060915
NM_007300.4(BRCA1):c.2315T>C (p.Val772Ala) rs80357467
NM_007300.4(BRCA1):c.2521C>T (p.Arg841Trp) rs1800709
NM_007300.4(BRCA1):c.2733A>G (p.Gly911=) rs1800740
NM_007300.4(BRCA1):c.3024G>A (p.Met1008Ile) rs1800704
NM_007300.4(BRCA1):c.3296C>T (p.Pro1099Leu) rs80357201
NM_007300.4(BRCA1):c.3748G>A (p.Glu1250Lys) rs28897686
NM_007300.4(BRCA1):c.3823A>G (p.Ile1275Val) rs80357280
NM_007300.4(BRCA1):c.4875A>G (p.Gln1625=) rs28897693
NM_007300.4(BRCA1):c.4946T>C (p.Met1649Thr) rs4986854

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