List of variants in gene combination BRCA1, LOC126862571 reported as pathogenic for Breast and/or ovarian cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3607C>T (p.Arg1203Ter)	rs62625308	0.00001
NM_007294.4(BRCA1):c.4096+1G>A	rs80358178	0.00001
NM_007294.4(BRCA1):c.3228_3229del (p.Gly1077fs)	rs80357635
NM_007294.4(BRCA1):c.3279del (p.Tyr1094fs)	rs397509050
NM_007294.4(BRCA1):c.3331_3334del (p.Gln1111fs)	rs80357701
NM_007294.4(BRCA1):c.3342_3345del (p.Glu1114_Glu1115insTer)	rs397509058
NM_007294.4(BRCA1):c.3481_3491del (p.Glu1161fs)	rs80357877
NM_007294.4(BRCA1):c.3640G>T (p.Glu1214Ter)	rs80356923
NM_007294.4(BRCA1):c.3642_3643del (p.Asn1215fs)	rs80357805
NM_007294.4(BRCA1):c.3648dup (p.Ser1217fs)	rs80357902
NM_007294.4(BRCA1):c.3649_3650insA (p.Ser1217fs)	rs80357831
NM_007294.4(BRCA1):c.3661G>T (p.Glu1221Ter)	rs80357310
NM_007294.4(BRCA1):c.3668_3671dup (p.Cys1225fs)	rs80357797
NM_007294.4(BRCA1):c.3700_3704del (p.Val1234fs)	rs80357609
NM_007294.4(BRCA1):c.3756_3759del (p.Ser1253fs)	rs80357868
NM_007294.4(BRCA1):c.3764dup (p.Asn1255fs)	rs80357848
NM_007294.4(BRCA1):c.3868A>T (p.Lys1290Ter)	rs80357254
NM_007294.4(BRCA1):c.4035del (p.Glu1346fs)	rs80357711
NM_007294.4(BRCA1):c.4052T>A (p.Leu1351Ter)	rs397509132
NM_007294.4(BRCA1):c.4062_4068del (p.Asn1354fs)	rs397509134
NM_007294.4(BRCA1):c.4065_4068del (p.Asn1355fs)	rs80357508
NM_007294.4(BRCA1):c.4096+3A>G	rs80358015

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