ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by Laboratory of Molecular Diagnosis of Cancer,West China Hospital, Sichuan University

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Total variants: 47
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HGVS dbSNP
NM_000059.3(BRCA2):c.10150C>G (p.Arg3384Gly) rs397507568
NM_000059.3(BRCA2):c.1211A>G (p.Asn404Ser) rs80358414
NM_000059.3(BRCA2):c.1462A>G (p.Ile488Val) rs864622352
NM_000059.3(BRCA2):c.1511C>G (p.Ser504Cys) rs886037807
NM_000059.3(BRCA2):c.1568A>G (p.His523Arg) rs80358443
NM_000059.3(BRCA2):c.1591A>G (p.Lys531Glu) rs876659050
NM_000059.3(BRCA2):c.171C>T (p.Tyr57=) rs201523522
NM_000059.3(BRCA2):c.1786G>A (p.Asp596Asn) rs56328701
NM_000059.3(BRCA2):c.2127G>C (p.Leu709=) rs554040246
NM_000059.3(BRCA2):c.2136G>T (p.Leu712=) rs886037813
NM_000059.3(BRCA2):c.2186T>C (p.Ile729Thr) rs431825296
NM_000059.3(BRCA2):c.3052A>C (p.Lys1018Gln) rs886037810
NM_000059.3(BRCA2):c.3256A>G (p.Ile1086Val) rs80358571
NM_000059.3(BRCA2):c.3473A>G (p.Glu1158Gly) rs886037808
NM_000059.3(BRCA2):c.3475T>G (p.Cys1159Gly) rs886037814
NM_000059.3(BRCA2):c.352C>T (p.Arg118Cys) rs375125172
NM_000059.3(BRCA2):c.4376A>G (p.Asn1459Ser) rs117187202
NM_000059.3(BRCA2):c.4548C>G (p.Ile1516Met) rs886037815
NM_000059.3(BRCA2):c.454A>G (p.Thr152Ala) rs886037806
NM_000059.3(BRCA2):c.4578A>G (p.Thr1526=) rs202022822
NM_000059.3(BRCA2):c.461A>G (p.Gln154Arg) rs756335278
NM_000059.3(BRCA2):c.4906A>G (p.Lys1636Glu) rs398122788
NM_000059.3(BRCA2):c.4915G>A (p.Val1639Ile) rs80358716
NM_000059.3(BRCA2):c.5345A>G (p.Gln1782Arg) rs758959174
NM_000059.3(BRCA2):c.5487G>T (p.Leu1829Phe) rs779967765
NM_000059.3(BRCA2):c.5590G>A (p.Asp1864Asn) rs587781536
NM_000059.3(BRCA2):c.5683G>A (p.Glu1895Lys) rs146351301
NM_000059.3(BRCA2):c.6148G>A (p.Val2050Ile) rs80358854
NM_000059.3(BRCA2):c.6235G>T (p.Val2079Leu) rs886037812
NM_000059.3(BRCA2):c.6256A>G (p.Ile2086Val) rs886037811
NM_000059.3(BRCA2):c.6325G>A (p.Val2109Ile) rs79456940
NM_000059.3(BRCA2):c.641_643AAG[1] (p.Glu215del) rs80359588
NM_000059.3(BRCA2):c.6598T>C (p.Phe2200Leu) rs886037809
NM_000059.3(BRCA2):c.7188G>A (p.Leu2396=) rs587780871
NM_000059.3(BRCA2):c.7509C>T (p.Val2503=) rs766080516
NM_000059.3(BRCA2):c.7521A>G (p.Pro2507=) rs759383358
NM_000059.3(BRCA2):c.7522G>A (p.Gly2508Ser) rs80358978
NM_000059.3(BRCA2):c.7545A>G (p.Thr2515=) rs767555621
NM_000059.3(BRCA2):c.7672G>C (p.Glu2558Gln) rs886037816
NM_000059.3(BRCA2):c.7772A>G (p.Asn2591Ser) rs80359006
NM_000059.3(BRCA2):c.7967T>C (p.Leu2656Pro) rs886037817
NM_000059.3(BRCA2):c.8329A>G (p.Lys2777Glu) rs886037818
NM_000059.3(BRCA2):c.8500A>G (p.Thr2834Ala) rs886037819
NM_000059.3(BRCA2):c.9014G>C (p.Arg3005Thr) rs886037821
NM_000059.3(BRCA2):c.9020G>A (p.Arg3007Lys) rs886037820
NM_000059.3(BRCA2):c.9285C>T (p.Asp3095=) rs80359198
NM_000059.3(BRCA2):c.92G>T (p.Trp31Leu) rs397508045

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