ClinVar Miner

List of variants in gene BRCA2 reported as pathogenic for not specified

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Total variants: 20
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HGVS dbSNP
NM_000059.3(BRCA2):c.1329del (p.Asn444fs) rs869320781
NM_000059.3(BRCA2):c.2099_2102TATT[1] (p.Phe701fs) rs80359324
NM_000059.3(BRCA2):c.3103G>T (p.Glu1035Ter) rs80358556
NM_000059.3(BRCA2):c.4211_4215del (p.Thr1403_Ser1404insTer) rs786203340
NM_000059.3(BRCA2):c.4462_4463CA[1] (p.His1488fs) rs397507720
NM_000059.3(BRCA2):c.4474_4477AAAG[1] (p.Glu1493fs) rs80359454
NM_000059.3(BRCA2):c.4689G>A (p.Trp1563Ter) rs886038108
NM_000059.3(BRCA2):c.4965C>G (p.Tyr1655Ter) rs80358721
NM_000059.3(BRCA2):c.5217_5223del (p.Thr1738_Tyr1739insTer) rs80359496
NM_000059.3(BRCA2):c.572_573AT[1] (p.Met192fs) rs80359533
NM_000059.3(BRCA2):c.5864C>A (p.Ser1955Ter) rs80358815
NM_000059.3(BRCA2):c.6037A>T (p.Lys2013Ter) rs80358840
NM_000059.3(BRCA2):c.6644_6647del (p.Tyr2215fs) rs80359616
NM_000059.3(BRCA2):c.7558C>T (p.Arg2520Ter) rs80358981
NM_000059.3(BRCA2):c.7681C>T (p.Gln2561Ter) rs80358994
NM_000059.3(BRCA2):c.7977-1G>C rs81002874
NM_000059.3(BRCA2):c.8167G>C (p.Asp2723His) rs41293511
NM_000059.3(BRCA2):c.8695C>T (p.Gln2899Ter) rs397507411
NM_000059.3(BRCA2):c.8837T>A (p.Leu2946Ter) rs431825371
NM_000059.3(BRCA2):c.9235del (p.Val3079fs) rs397507422

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