ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance for Neoplasm of the breast

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Total variants: 76
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HGVS dbSNP
NM_000059.3(BRCA2):c.10150C>G (p.Arg3384Gly) rs397507568
NM_000059.3(BRCA2):c.10234A>G (p.Ile3412Val) rs1801426
NM_000059.3(BRCA2):c.1151C>T (p.Ser384Phe) rs41293475
NM_000059.3(BRCA2):c.1166C>A (p.Pro389Gln) rs397507263
NM_000059.3(BRCA2):c.1211A>G (p.Asn404Ser) rs80358414
NM_000059.3(BRCA2):c.1324T>G (p.Ser442Ala) rs1057518641
NM_000059.3(BRCA2):c.1370A>G (p.Lys457Arg) rs771442299
NM_000059.3(BRCA2):c.1462A>G (p.Ile488Val) rs864622352
NM_000059.3(BRCA2):c.1483G>A (p.Ala495Thr) rs80358437
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.1763A>G (p.Asn588Ser) rs373400041
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.2138A>T (p.Gln713Leu) rs55816687
NM_000059.3(BRCA2):c.2186T>C (p.Ile729Thr) rs431825296
NM_000059.3(BRCA2):c.2350A>G (p.Met784Val) rs11571653
NM_000059.3(BRCA2):c.2482T>C (p.Tyr828His) rs1060502466
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.4312G>A (p.Val1438Ile) rs786202874
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.4599A>C (p.Lys1533Asn) rs80358694
NM_000059.3(BRCA2):c.461A>G (p.Gln154Arg) rs756335278
NM_000059.3(BRCA2):c.4639G>A (p.Asp1547Asn) rs1555283880
NM_000059.3(BRCA2):c.4681C>A (p.His1561Asn) rs2219594
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.5744C>T (p.Thr1915Met) rs4987117
NM_000059.3(BRCA2):c.5972C>T (p.Ala1991Val) rs80358829
NM_000059.3(BRCA2):c.6131G>T (p.Gly2044Val) rs56191579
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.63A>G (p.Lys21=) rs1280004443
NM_000059.3(BRCA2):c.6412G>T (p.Val2138Phe) rs11571659
NM_000059.3(BRCA2):c.641_643AAG[1] (p.Glu215del) rs80359588
NM_000059.3(BRCA2):c.6550C>T (p.Gln2184Ter) rs80358887
NM_000059.3(BRCA2):c.6598T>C (p.Phe2200Leu) rs886037809
NM_000059.3(BRCA2):c.6715G>A (p.Glu2239Lys) rs276174876
NM_000059.3(BRCA2):c.7188G>A (p.Leu2396=) rs587780871
NM_000059.3(BRCA2):c.742G>A (p.Ala248Thr) rs55854959
NM_000059.3(BRCA2):c.7469T>C (p.Ile2490Thr) rs11571707
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.8111C>T (p.Ser2704Phe) rs80359054
NM_000059.3(BRCA2):c.8329A>G (p.Lys2777Glu) rs886037818
NM_000059.3(BRCA2):c.8351G>A (p.Arg2784Gln) rs80359076
NM_000059.3(BRCA2):c.8500A>G (p.Thr2834Ala) rs886037819
NM_000059.3(BRCA2):c.8830A>T (p.Ile2944Phe) rs4987047
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.9085G>A (p.Ala3029Thr) rs56179254
NM_000059.3(BRCA2):c.9285C>T (p.Asp3095=) rs80359198
NM_000059.3(BRCA2):c.92G>T (p.Trp31Leu) rs397508045
NM_000059.3(BRCA2):c.9353T>C (p.Met3118Thr) rs56204128
NM_000059.3(BRCA2):c.964A>C (p.Lys322Gln) rs11571640

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