ClinVar Miner

List of variants in gene BRCA1 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

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Total variants: 26
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HGVS dbSNP
NM_007294.3(BRCA1):c.1704T>G (p.Pro568=) rs587780795
NM_007294.3(BRCA1):c.1843_1845TCT[1] (p.Ser616del) rs80358329
NM_007294.3(BRCA1):c.199G>T (p.Asp67Tyr) rs80357102
NM_007294.3(BRCA1):c.212+21G>A rs80358147
NM_007294.3(BRCA1):c.2207A>C (p.Glu736Ala) rs397507196
NM_007294.3(BRCA1):c.243A>G (p.Gln81=) rs863224418
NM_007294.3(BRCA1):c.2669G>T (p.Gly890Val) rs80356874
NM_007294.3(BRCA1):c.3597T>A (p.Ala1199=) rs1555587434
NM_007294.3(BRCA1):c.4096+30C>T rs369055904
NM_007294.3(BRCA1):c.4113G>A (p.Gly1371=) rs147448807
NM_007294.3(BRCA1):c.4185+24A>G rs763074389
NM_007294.3(BRCA1):c.4185+30G>A rs80358139
NM_007294.3(BRCA1):c.425C>A (p.Pro142His) rs55971303
NM_007294.3(BRCA1):c.4327C>G (p.Arg1443Gly) rs41293455
NM_007294.3(BRCA1):c.4635C>T (p.His1545=) rs373686790
NM_007294.3(BRCA1):c.5025T>C (p.Thr1675=) rs876658226
NM_007294.3(BRCA1):c.5382G>C (p.Glu1794Asp) rs397509275
NM_007294.3(BRCA1):c.5456A>G (p.Asn1819Ser) rs80357286
NM_007294.3(BRCA1):c.548-18T>G rs397507251
NM_007294.3(BRCA1):c.570C>T (p.Thr190=) rs201536070
NM_007294.3(BRCA1):c.593+3G>A rs80358013
NM_007294.3(BRCA1):c.670+26C>G rs368134697
NM_007294.3(BRCA1):c.739A>G (p.Asn247Asp) rs767720128
NM_007294.3(BRCA1):c.765G>A (p.Glu255=) rs62625299
NM_007294.3(BRCA1):c.81-13C>A rs56328013
NM_007294.3(BRCA1):c.987T>C (p.Asn329=) rs774849810

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