ClinVar Miner

List of variants in gene BRCA1 reported as likely pathogenic by Sharing Clinical Reports Project (SCRP)

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Total variants: 25
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HGVS dbSNP
NM_007294.3(BRCA1):c.134+5G>A rs80358038
NM_007294.3(BRCA1):c.134+5G>C rs80358038
NM_007294.3(BRCA1):c.134+5G>T rs80358038
NM_007294.3(BRCA1):c.302-3C>G rs80358051
NM_007294.3(BRCA1):c.4096+3A>G rs80358015
NM_007294.3(BRCA1):c.442C>T (p.Gln148Ter) rs876659614
NM_007294.3(BRCA1):c.4675G>C (p.Glu1559Gln) rs80356988
NM_007294.3(BRCA1):c.5074+1G>T rs80358053
NM_007294.3(BRCA1):c.5074G>A (p.Asp1692Asn) rs80187739
NM_007294.3(BRCA1):c.5075-3C>G rs398122690
NM_007294.3(BRCA1):c.5096G>A (p.Arg1699Gln) rs41293459
NM_007294.3(BRCA1):c.5117G>A (p.Gly1706Glu) rs80356860
NM_007294.3(BRCA1):c.5152+2dupT rs397509231
NM_007294.3(BRCA1):c.5152+5G>A rs80358165
NM_007294.3(BRCA1):c.5153-1G>C rs80358137
NM_007294.3(BRCA1):c.5194-12G>A rs80358079
NM_007294.3(BRCA1):c.5213G>A (p.Gly1738Glu) rs80357450
NM_007294.3(BRCA1):c.5324T>A (p.Met1775Lys) rs41293463
NM_007294.3(BRCA1):c.5333-2A>T rs397509264
NM_007294.3(BRCA1):c.53T>C (p.Met18Thr) rs80356929
NM_007294.3(BRCA1):c.5468-2A>G rs398122699
NM_007294.3(BRCA1):c.5509T>C (p.Trp1837Arg) rs80356959
NM_007299.4(BRCA1):c.*92dup rs397507254
NM_007299.4(BRCA1):c.1895T>C (p.Val632Ala) rs45553935
NP_009225.1(BRCA1):p.Trp1837Arg

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