List of variants in gene BRCA1 reported as pathogenic by Genomic Center, National Cancer Institute

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.1378del (p.Ile460fs)
NM_007294.4(BRCA1):c.1439del (p.Asn480fs)
NM_007294.4(BRCA1):c.1728del (p.Glu577fs)	rs397507192
NM_007294.4(BRCA1):c.3101del (p.Asn1034fs)	rs2154342570
NM_007294.4(BRCA1):c.922del (p.Ser308fs)	rs2154485304

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