ClinVar Miner

List of variants reported as uncertain significance for malignant mixed neoplasm by All of Us Research Program, National Institutes of Health

Included ClinVar conditions (20):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 139
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.343C>T (p.Pro115Ser) rs916583720 0.00011
NM_024426.6(WT1):c.162C>G (p.Ser54Arg) rs776954184 0.00006
NM_024426.6(WT1):c.689C>T (p.Thr230Met) rs777166391 0.00006
NM_024426.6(WT1):c.925A>G (p.Met309Val) rs754336808 0.00004
NM_024426.6(WT1):c.1123C>T (p.Arg375Cys) rs1172760612 0.00003
NM_024426.6(WT1):c.1142C>T (p.Pro381Leu) rs1014605516 0.00003
NM_024426.6(WT1):c.397C>A (p.Pro133Thr) rs1202603651 0.00003
NM_024426.6(WT1):c.475G>A (p.Glu159Lys) rs768165877 0.00003
NM_024426.6(WT1):c.1121G>A (p.Arg374Gln) rs772590420 0.00002
NM_024426.6(WT1):c.1304G>A (p.Arg435Gln) rs144788858 0.00002
NM_024426.6(WT1):c.806C>G (p.Pro269Arg) rs756078681 0.00002
NM_024426.6(WT1):c.830C>T (p.Thr277Ile) rs138073760 0.00002
NM_024426.6(WT1):c.887+4G>A rs778673400 0.00002
NM_024426.6(WT1):c.1094G>A (p.Gly365Asp) rs769934402 0.00001
NM_024426.6(WT1):c.1100T>G (p.Phe367Cys) rs150194429 0.00001
NM_024426.6(WT1):c.1113+5G>A rs930795675 0.00001
NM_024426.6(WT1):c.1117G>A (p.Val373Met) rs747377024 0.00001
NM_024426.6(WT1):c.1210A>C (p.Asn404His) rs774976881 0.00001
NM_024426.6(WT1):c.133T>C (p.Trp45Arg) rs1186470250 0.00001
NM_024426.6(WT1):c.1385A>T (p.Gln462Leu) rs533043871 0.00001
NM_024426.6(WT1):c.1487A>G (p.Lys496Arg) rs760370132 0.00001
NM_024426.6(WT1):c.1513G>C (p.Val505Leu) rs1399910889 0.00001
NM_024426.6(WT1):c.1555C>T (p.Gln519Ter) rs866837692 0.00001
NM_024426.6(WT1):c.1562C>T (p.Ala521Val) rs749266841 0.00001
NM_024426.6(WT1):c.262G>A (p.Val88Ile) rs1410971862 0.00001
NM_024426.6(WT1):c.284G>T (p.Gly95Val) rs1454795891 0.00001
NM_024426.6(WT1):c.286G>A (p.Gly96Ser) rs1060501254 0.00001
NM_024426.6(WT1):c.350G>A (p.Gly117Asp) rs939385459 0.00001
NM_024426.6(WT1):c.352G>C (p.Ala118Pro) rs1253163678 0.00001
NM_024426.6(WT1):c.380C>G (p.Pro127Arg) rs1387576357 0.00001
NM_024426.6(WT1):c.404C>T (p.Pro135Leu) rs769642496 0.00001
NM_024426.6(WT1):c.439C>G (p.Gln147Glu) rs953087575 0.00001
NM_024426.6(WT1):c.584C>G (p.Ser195Cys) rs778194188 0.00001
NM_024426.6(WT1):c.641A>C (p.Gln214Pro) rs771024882 0.00001
NM_024426.6(WT1):c.650T>G (p.Ile217Ser) rs1853431800 0.00001
NM_024426.6(WT1):c.658C>A (p.Gln220Lys) rs373935628 0.00001
NM_024426.6(WT1):c.86G>A (p.Cys29Tyr) rs992227366 0.00001
NM_024426.6(WT1):c.973G>A (p.Ala325Thr) rs1712081462 0.00001
NM_024426.6(WT1):c.977G>C (p.Gly326Ala) rs766054482 0.00001
NM_024426.6(WT1):c.*2G>A
NM_024426.6(WT1):c.*3G>A
NM_024426.6(WT1):c.*5T>C rs765743928
NM_024426.6(WT1):c.1031A>T (p.Tyr344Phe)
NM_024426.6(WT1):c.1038C>G (p.Ser346Arg) rs750018485
NM_024426.6(WT1):c.1057A>G (p.Ile353Val) rs1554940527
NM_024426.6(WT1):c.1086C>A (p.His362Gln)
NM_024426.6(WT1):c.1093G>A (p.Gly365Ser)
NM_024426.6(WT1):c.1096G>A (p.Val366Ile)
NM_024426.6(WT1):c.1162T>C (p.Ser388Pro) rs992930804
NM_024426.6(WT1):c.1168A>G (p.Thr390Ala)
NM_024426.6(WT1):c.1196C>G (p.Ala399Gly) rs1590338798
NM_024426.6(WT1):c.1265-16_1265-15del rs1447574915
NM_024426.6(WT1):c.1280A>C (p.Gln427Pro) rs1358408901
NM_024426.6(WT1):c.133T>G (p.Trp45Gly) rs1186470250
NM_024426.6(WT1):c.1345A>G (p.Arg449Gly)
NM_024426.6(WT1):c.143T>C (p.Leu48Ser) rs1565002394
NM_024426.6(WT1):c.1448-13A>G
NM_024426.6(WT1):c.145G>A (p.Gly49Ser)
NM_024426.6(WT1):c.1478G>A (p.Ser493Asn) rs763551837
NM_024426.6(WT1):c.151G>A (p.Ala51Thr) rs1853473868
NM_024426.6(WT1):c.152C>A (p.Ala51Asp)
NM_024426.6(WT1):c.163G>T (p.Ala55Ser)
NM_024426.6(WT1):c.170G>T (p.Arg57Leu) rs1011628259
NM_024426.6(WT1):c.181C>G (p.Arg61Gly)
NM_024426.6(WT1):c.189C>A (p.Ser63Arg) rs1215127008
NM_024426.6(WT1):c.191G>T (p.Arg64Leu)
NM_024426.6(WT1):c.197C>A (p.Ala66Glu) rs1341675324
NM_024426.6(WT1):c.197C>T (p.Ala66Val)
NM_024426.6(WT1):c.220A>G (p.Met74Val)
NM_024426.6(WT1):c.239A>G (p.Asp80Gly)
NM_024426.6(WT1):c.240C>G (p.Asp80Glu) rs2133105820
NM_024426.6(WT1):c.247G>C (p.Ala83Pro) rs886048231
NM_024426.6(WT1):c.254T>C (p.Leu85Pro)
NM_024426.6(WT1):c.25C>G (p.Pro9Ala)
NM_024426.6(WT1):c.266C>G (p.Pro89Arg)
NM_024426.6(WT1):c.266C>T (p.Pro89Leu)
NM_024426.6(WT1):c.275G>A (p.Gly92Asp)
NM_024426.6(WT1):c.277GGC[5] (p.Gly96dup) rs770519620
NM_024426.6(WT1):c.287_288insGGA (p.Gly96_Cys97insAsp)
NM_024426.6(WT1):c.28G>A (p.Ala10Thr)
NM_024426.6(WT1):c.305G>A (p.Ser102Asn) rs1210117032
NM_024426.6(WT1):c.307G>T (p.Gly103Cys) rs1348287926
NM_024426.6(WT1):c.320G>T (p.Trp107Leu) rs1009810769
NM_024426.6(WT1):c.328G>T (p.Val110Leu)
NM_024426.6(WT1):c.344C>A (p.Pro115His) rs1565001804
NM_024426.6(WT1):c.347C>T (p.Pro116Leu) rs886048229
NM_024426.6(WT1):c.358G>A (p.Ala120Thr) rs1590410151
NM_024426.6(WT1):c.367T>G (p.Ser123Ala)
NM_024426.6(WT1):c.376G>C (p.Gly126Arg)
NM_024426.6(WT1):c.382G>A (p.Ala128Thr) rs1853454136
NM_024426.6(WT1):c.391C>T (p.Pro131Ser) rs564706633
NM_024426.6(WT1):c.401C>A (p.Pro134Gln)
NM_024426.6(WT1):c.406C>T (p.Pro136Ser)
NM_024426.6(WT1):c.409C>G (p.Pro137Ala) rs1853451078
NM_024426.6(WT1):c.412C>A (p.Pro138Thr)
NM_024426.6(WT1):c.436A>C (p.Lys146Gln)
NM_024426.6(WT1):c.440A>C (p.Gln147Pro)
NM_024426.6(WT1):c.448A>G (p.Ser150Gly) rs1853447534
NM_024426.6(WT1):c.460G>A (p.Ala154Thr)
NM_024426.6(WT1):c.480G>C (p.Gln160His) rs758900425
NM_024426.6(WT1):c.49C>A (p.Pro17Thr)
NM_024426.6(WT1):c.50C>T (p.Pro17Leu) rs1853481697
NM_024426.6(WT1):c.547G>C (p.Gly183Arg) rs1462705405
NM_024426.6(WT1):c.575A>G (p.Gln192Arg) rs1853438394
NM_024426.6(WT1):c.577G>A (p.Ala193Thr) rs1590409175
NM_024426.6(WT1):c.578C>T (p.Ala193Val)
NM_024426.6(WT1):c.590A>G (p.Gln197Arg) rs1853436737
NM_024426.6(WT1):c.592G>T (p.Ala198Ser)
NM_024426.6(WT1):c.649A>C (p.Ile217Leu) rs1384974578
NM_024426.6(WT1):c.653G>A (p.Arg218His) rs756414084
NM_024426.6(WT1):c.653G>T (p.Arg218Leu) rs756414084
NM_024426.6(WT1):c.65C>A (p.Thr22Lys)
NM_024426.6(WT1):c.671C>A (p.Thr224Lys)
NM_024426.6(WT1):c.671C>T (p.Thr224Met) rs779451877
NM_024426.6(WT1):c.677C>T (p.Thr226Ile) rs556804456
NM_024426.6(WT1):c.680T>C (p.Phe227Ser) rs1554945235
NM_024426.6(WT1):c.69_70del (p.Arg24fs)
NM_024426.6(WT1):c.700G>C (p.Gly234Arg) rs1307992683
NM_024426.6(WT1):c.70C>G (p.Arg24Gly)
NM_024426.6(WT1):c.718C>T (p.His240Tyr) rs2133075605
NM_024426.6(WT1):c.737A>G (p.Asn246Ser)
NM_024426.6(WT1):c.752A>T (p.His251Leu) rs914029023
NM_024426.6(WT1):c.76_80del (p.Gly26fs)
NM_024426.6(WT1):c.785-14G>A rs375514482
NM_024426.6(WT1):c.785-7T>G rs758280375
NM_024426.6(WT1):c.795G>C (p.Gln265His)
NM_024426.6(WT1):c.796T>C (p.Tyr266His)
NM_024426.6(WT1):c.79C>T (p.Pro27Ser)
NM_024426.6(WT1):c.7T>G (p.Phe3Val)
NM_024426.6(WT1):c.803T>C (p.Val268Ala)
NM_024426.6(WT1):c.832C>T (p.Pro278Ser)
NM_024426.6(WT1):c.854G>C (p.Ser285Thr) rs779813097
NM_024426.6(WT1):c.887+5del
NM_024426.6(WT1):c.905T>A (p.Met302Lys) rs1208241960
NM_024426.6(WT1):c.91C>G (p.Gln31Glu)
NM_024426.6(WT1):c.941T>C (p.Met314Thr)
NM_024426.6(WT1):c.953C>G (p.Ala318Gly) rs1201042140
NM_024426.6(WT1):c.965G>A (p.Gly322Glu)
NM_024426.6(WT1):c.991G>A (p.Val331Met)

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