ClinVar Miner

List of variants in gene BRCA1 reported as likely benign by True Health Diagnostics

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Gene type:
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Total variants: 27
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HGVS dbSNP
NM_007294.3(BRCA1):c.4039A>G (p.Arg1347Gly) rs28897689
NM_007294.3(BRCA1):c.5406+8T>C rs55946644
NM_007299.4(BRCA1):c.114G>A (p.Lys38=) rs1800062
NM_007299.4(BRCA1):c.1223G>T (p.Ser408Ile) rs1800744
NM_007299.4(BRCA1):c.1370C>T (p.Thr457Ile) rs56158747
NM_007299.4(BRCA1):c.591C>T (p.Cys197=) rs1799965
NM_007299.4(BRCA1):c.736T>G (p.Leu246Val) rs28897675
NM_007299.4(BRCA1):c.787+1184A>G rs28897679
NM_007299.4(BRCA1):c.787+917T>G rs587780795
NM_007300.4(BRCA1):c.1137T>G (p.Ile379Met) rs56128296
NM_007300.4(BRCA1):c.1456T>C (p.Phe486Leu) rs55906931
NM_007300.4(BRCA1):c.1648A>C (p.Asn550His) rs56012641
NM_007300.4(BRCA1):c.19C>T (p.Arg7Cys) rs80356994
NM_007300.4(BRCA1):c.2167A>G (p.Asn723Asp) rs4986845
NM_007300.4(BRCA1):c.2447A>G (p.His816Arg) rs80357108
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.3063T>C (p.Ser1021=) rs1364539273
NM_007300.4(BRCA1):c.3153T>C (p.Thr1051=) rs1057521053
NM_007300.4(BRCA1):c.3394A>G (p.Asn1132Asp) rs530464947
NM_007300.4(BRCA1):c.4754T>C (p.Leu1585Pro) rs56119278
NM_007300.4(BRCA1):c.4828C>T (p.Arg1610Cys) rs80357002
NM_007300.4(BRCA1):c.4875A>G (p.Gln1625=) rs28897693
NM_007300.4(BRCA1):c.4946T>C (p.Met1649Thr) rs4986854
NM_007300.4(BRCA1):c.5018T>C (p.Met1673Thr) rs80356968
NM_007300.4(BRCA1):c.536A>G (p.Tyr179Cys) rs56187033
NM_007300.4(BRCA1):c.981A>G (p.Thr327=) rs1800063

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