ClinVar Miner

List of variants reported as uncertain significance for not specified by Department of Pathology and Molecular Medicine,Queen's University

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Total variants: 24
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HGVS dbSNP
NM_000059.3(BRCA2):c.1834G>A (p.Glu612Lys) rs1135401938
NM_000059.3(BRCA2):c.1909+22del rs276174816
NM_000059.3(BRCA2):c.2287C>G (p.His763Asp) rs863224585
NM_000059.3(BRCA2):c.2389A>G (p.Lys797Glu) rs587782737
NM_000059.3(BRCA2):c.3073A>G (p.Lys1025Glu) rs80358550
NM_000059.3(BRCA2):c.3861_3863TAA[1] (p.Asn1288del) rs276174837
NM_000059.3(BRCA2):c.4648G>C (p.Glu1550Gln) rs80358695
NM_000059.3(BRCA2):c.467A>G (p.Asp156Gly) rs68071147
NM_000059.3(BRCA2):c.4957A>G (p.Thr1653Ala) rs587782186
NM_000059.3(BRCA2):c.68-7del rs276174878
NM_000059.3(BRCA2):c.6841+80_6841+83del rs11571661
NM_000059.3(BRCA2):c.7448G>A (p.Ser2483Asn) rs80358967
NM_000059.3(BRCA2):c.8524C>T (p.Arg2842Cys) rs80359104
NM_000059.3(BRCA2):c.9019A>G (p.Arg3007Gly) rs397507417
NM_000059.3(BRCA2):c.956A>G (p.Asn319Ser) rs55939572
NM_007294.3(BRCA1):c.1397G>A (p.Arg466Gln) rs199540030
NM_007294.3(BRCA1):c.19C>T (p.Arg7Cys) rs80356994
NM_007294.3(BRCA1):c.2050C>T (p.Pro684Ser) rs397508934
NM_007294.3(BRCA1):c.3155A>G (p.Asn1052Ser) rs398122672
NM_007294.3(BRCA1):c.3220A>G (p.Arg1074Gly) rs80357263
NM_007294.3(BRCA1):c.3454G>A (p.Asp1152Asn) rs80357175
NM_007294.3(BRCA1):c.3708T>G (p.Asn1236Lys) rs28897687
NM_007294.3(BRCA1):c.4073A>G (p.Glu1358Gly) rs397507225
NM_007294.3(BRCA1):c.547G>C (p.Gly183Arg) rs1135401931

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