List of variants in gene BRCA1 reported as not provided for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 39

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3113A>G (p.Glu1038Gly)	rs16941	0.29115
NM_007294.4(BRCA1):c.2077G>A (p.Asp693Asn)	rs4986850	0.05782
NM_007294.4(BRCA1):c.1067A>G (p.Gln356Arg)	rs1799950	0.04695
NM_007294.4(BRCA1):c.4956G>A (p.Met1652Ile)	rs1799967	0.01348
NM_007294.4(BRCA1):c.3119G>A (p.Ser1040Asn)	rs4986852	0.01109
NM_007294.4(BRCA1):c.2458A>G (p.Lys820Glu)	rs56082113	0.00964
NM_007294.4(BRCA1):c.557C>A (p.Ser186Tyr)	rs55688530	0.00301
NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)	rs1800744	0.00240
NM_007294.4(BRCA1):c.1137T>G (p.Ile379Met)	rs56128296	0.00158
NM_007294.4(BRCA1):c.4600G>A (p.Val1534Met)	rs55815649	0.00145
NM_007294.4(BRCA1):c.2521C>T (p.Arg841Trp)	rs1800709	0.00137
NM_007294.4(BRCA1):c.3083G>A (p.Arg1028His)	rs80357459	0.00106
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr)	rs4986854	0.00098
NM_007294.4(BRCA1):c.3022A>G (p.Met1008Val)	rs56321129	0.00095
NM_007294.4(BRCA1):c.1427A>G (p.His476Arg)	rs55720177	0.00066
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.1487G>A (p.Arg496His)	rs28897677	0.00060
NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro)	rs56119278	0.00059
NM_007294.4(BRCA1):c.1456T>C (p.Phe486Leu)	rs55906931	0.00034
NM_007294.4(BRCA1):c.5411T>A (p.Val1804Asp)	rs80356920	0.00021
NM_007294.4(BRCA1):c.4410A>T (p.Glu1470Asp)	rs80357075	0.00016
NM_007294.4(BRCA1):c.1561G>A (p.Ala521Thr)	rs80357122	0.00014
NM_007294.4(BRCA1):c.2773A>C (p.Ile925Leu)	rs4986847	0.00013
NM_007294.4(BRCA1):c.2596C>T (p.Arg866Cys)	rs41286300	0.00011
NM_007294.4(BRCA1):c.2412G>C (p.Gln804His)	rs55746541	0.00006
NM_007294.4(BRCA1):c.1511G>A (p.Arg504His)	rs56272539	0.00004
NM_007294.4(BRCA1):c.1616C>T (p.Thr539Met)	rs80357374	0.00004
NM_007294.4(BRCA1):c.824G>A (p.Gly275Asp)	rs397509327	0.00002
NM_007294.4(BRCA1):c.2207A>C (p.Glu736Ala)	rs397507196	0.00001
NM_007294.4(BRCA1):c.397C>T (p.Arg133Cys)	rs80357457	0.00001
NM_007294.4(BRCA1):c.5504G>A (p.Arg1835Gln)	rs273902776	0.00001
NM_007294.4(BRCA1):c.1387A>G (p.Lys463Glu)	rs1135401844
NM_007294.4(BRCA1):c.2330A>G (p.Tyr777Cys)	rs587778116
NM_007294.4(BRCA1):c.2612C>T (p.Pro871Leu)	rs799917
NM_007294.4(BRCA1):c.290C>T (p.Thr97Ile)	rs431825393
NM_007294.4(BRCA1):c.466C>G (p.Leu156Val)	rs587778115
NM_007294.4(BRCA1):c.4837A>G (p.Ser1613Gly)	rs1799966
NM_007294.4(BRCA1):c.5306A>G (p.Tyr1769Cys)	rs397509257
NM_007294.4(BRCA1):c.787G>A (p.Gly263Ser)	rs397509318

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