List of variants reported as pathogenic for Familial cancer of breast by Genomic Center, National Cancer Institute

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.10248del (p.Lys3416fs)	rs776212316
NM_000059.4(BRCA2):c.1053del (p.Lys351fs)	rs886040342
NM_000059.4(BRCA2):c.1561del (p.Ser521fs)	rs886040374
NM_000059.4(BRCA2):c.2588del (p.Asn863fs)	rs80359335
NM_000059.4(BRCA2):c.4284del (p.Gln1429fs)	rs80359439
NM_000059.4(BRCA2):c.5297del (p.Asn1766fs)	rs1555284157
NM_000059.4(BRCA2):c.5362del (p.Ser1788fs)	rs587781849
NM_000059.4(BRCA2):c.5566_5567inv (p.His1856Cys)
NM_000059.4(BRCA2):c.5934del (p.Phe1978fs)	rs80359548
NM_000059.4(BRCA2):c.691_692delinsGA (p.Ser231Asp)	rs2072384735
NM_000059.4(BRCA2):c.7177del (p.Lys2392_Met2393insTer)	rs397507899
NM_000059.4(BRCA2):c.728del (p.Asn243fs)	rs886040697
NM_000059.4(BRCA2):c.7667del (p.Asn2556fs)	rs878853303
NM_000059.4(BRCA2):c.9163del (p.Leu3055fs)	rs2072913259
NM_007294.4(BRCA1):c.1728del (p.Glu577fs)	rs397507192
NM_007294.4(BRCA1):c.3982del (p.Ser1328fs)	rs2053490037

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