ClinVar Miner

List of variants in gene BRCA2 reported as likely pathogenic for Breast and/or ovarian cancer

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Total variants: 12
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HGVS dbSNP
NM_000059.3(BRCA2):c.3G>T (p.Met1Ile) rs80358650
NM_000059.3(BRCA2):c.4003G>T (p.Glu1335Ter) rs747070579
NM_000059.3(BRCA2):c.4258G>T (p.Asp1420Tyr) rs28897727
NM_000059.3(BRCA2):c.6938-2A>G rs81002863
NM_000059.3(BRCA2):c.7008-1G>A rs786204280
NM_000059.3(BRCA2):c.7471del (p.Gln2491fs) rs886038170
NM_000059.3(BRCA2):c.7843_7844del (p.Ile2615fs) rs886040867
NM_000059.3(BRCA2):c.7958T>C (p.Leu2653Pro) rs80359022
NM_000059.3(BRCA2):c.8084C>T (p.Ser2695Leu) rs80359048
NM_000059.3(BRCA2):c.9064delinsGG (p.Arg3022fs) rs1566253262
NM_000059.3(BRCA2):c.9281C>G (p.Ser3094Ter) rs786204283
NM_000059.3(BRCA2):c.9925G>T (p.Glu3309Ter) rs80359251

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