List of variants reported as likely pathogenic for Hereditary cancer-predisposing syndrome by Genomic Center, National Cancer Institute

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1508del (p.Lys503fs)	rs886038066
NM_000059.4(BRCA2):c.3956del (p.Asn1319fs)	rs2137501511
NM_000059.4(BRCA2):c.4904del (p.Phe1634_Leu1635insTer)	rs80359471
NM_000059.4(BRCA2):c.7340del (p.Asn2447fs)	rs786204281
NM_000059.4(BRCA2):c.7654del (p.Ile2552fs)	rs879255463
NM_000059.4(BRCA2):c.937del (p.Ser313fs)	rs2137466022
NM_007294.4(BRCA1):c.2857del (p.Cys953fs)	rs397509019
NM_007294.4(BRCA1):c.4526del (p.Tyr1509fs)	rs2154020080

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