ClinVar Miner

List of variants in gene WT1 reported as uncertain significance for Wilms tumor

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP
NM_024426.4(WT1):c.*1049_*1054delGTGTGT rs58549495
NM_024426.4(WT1):c.*1051_*1054delGTGT rs58549495
NM_024426.4(WT1):c.*574delG rs5030319
NM_024426.4(WT1):c.1024G>A (p.Asp342Asn) rs267602851
NM_024426.4(WT1):c.1139G>A (p.Arg380Gln) rs147241955
NM_024426.5(WT1):c.*1049_*1054dup rs58549495
NM_024426.5(WT1):c.*1051_*1054dup rs58549495
NM_024426.5(WT1):c.*1053_*1054dup rs58549495
NM_024426.5(WT1):c.*1058G>T rs886048211
NM_024426.5(WT1):c.*110C>T rs757474299
NM_024426.5(WT1):c.*1167T>G rs771770230
NM_024426.5(WT1):c.*1225T>C rs886048210
NM_024426.5(WT1):c.*159G>C rs746218880
NM_024426.5(WT1):c.*239G>A rs886048226
NM_024426.5(WT1):c.*269G>T rs886048225
NM_024426.5(WT1):c.*354G>T rs886048224
NM_024426.5(WT1):c.*366C>A rs886048223
NM_024426.5(WT1):c.*393G>T rs886048222
NM_024426.5(WT1):c.*460C>A rs886048221
NM_024426.5(WT1):c.*513C>T rs575602262
NM_024426.5(WT1):c.*534C>T rs868546165
NM_024426.5(WT1):c.*611C>T rs886048220
NM_024426.5(WT1):c.*614A>C rs886048219
NM_024426.5(WT1):c.*666A>G rs374306749
NM_024426.5(WT1):c.*685G>T rs886048218
NM_024426.5(WT1):c.*707C>A rs886048217
NM_024426.5(WT1):c.*741G>T rs886048216
NM_024426.5(WT1):c.*768A>C rs886048215
NM_024426.5(WT1):c.*785C>A rs886048214
NM_024426.5(WT1):c.*841C>A rs886048213
NM_024426.5(WT1):c.1017-15T>C rs374441355
NM_024426.5(WT1):c.1017-3C>T rs1554940545
NM_024426.5(WT1):c.1020_1021delCAinsAC (p.His340_Ser341delinsGlnArg)
NM_024426.5(WT1):c.1029G>T (p.Gly343=)
NM_024426.5(WT1):c.1057A>G (p.Ile353Val) rs1554940527
NM_024426.5(WT1):c.1063T>C (p.Cys355Arg) rs142059681
NM_024426.5(WT1):c.1067G>A (p.Gly356Glu) rs760654956
NM_024426.5(WT1):c.1073A>G (p.Gln358Arg) rs1554940518
NM_024426.5(WT1):c.1086C>G (p.His362Gln)
NM_024426.5(WT1):c.1094G>A (p.Gly365Asp) rs769934402
NM_024426.5(WT1):c.1100T>G (p.Phe367Cys) rs150194429
NM_024426.5(WT1):c.1113+5G>A rs930795675
NM_024426.5(WT1):c.1117G>A (p.Val373Met) rs747377024
NM_024426.5(WT1):c.1121G>A (p.Arg374Gln) rs772590420
NM_024426.5(WT1):c.1124G>A (p.Arg375His) rs554416372
NM_024426.5(WT1):c.1124G>C (p.Arg375Pro)
NM_024426.5(WT1):c.1135G>A (p.Val379Ile) rs755936509
NM_024426.5(WT1):c.1142C>T (p.Pro381Leu) rs1014605516
NM_024426.5(WT1):c.1158G>A (p.Ser386=) rs377446096
NM_024426.5(WT1):c.1198T>C (p.Tyr400His) rs746353651
NM_024426.5(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.5(WT1):c.1202C>T (p.Pro401Leu) rs1060501258
NM_024426.5(WT1):c.1211A>C (p.Asn404Thr) rs748864758
NM_024426.5(WT1):c.1218A>C (p.Arg406Ser) rs1554939793
NM_024426.5(WT1):c.1304G>A (p.Arg435Gln) rs144788858
NM_024426.5(WT1):c.1408C>T (p.His470Tyr) rs1554939072
NM_024426.5(WT1):c.1463G>A (p.Ser488Asn) rs267602849
NM_024426.5(WT1):c.1468C>T (p.Arg490Trp) rs1315549918
NM_024426.5(WT1):c.1469G>A (p.Arg490Gln) rs139893274
NM_024426.5(WT1):c.1474C>T (p.Pro492Ser) rs761360324
NM_024426.5(WT1):c.1478G>A (p.Ser493Asn)
NM_024426.5(WT1):c.1524C>A (p.His508Gln) rs1451629862
NM_024426.5(WT1):c.1528A>G (p.Met510Val) rs1554938534
NM_024426.5(WT1):c.1538G>C (p.Arg513Thr) rs1363144688
NM_024426.5(WT1):c.1541A>G (p.Asn514Ser)
NM_024426.5(WT1):c.1541A>T (p.Asn514Ile) rs1554938531
NM_024426.5(WT1):c.662G>A (p.Gly221Asp)
NM_024426.5(WT1):c.670A>T (p.Thr224Ser) rs1554945246
NM_024426.5(WT1):c.680T>C (p.Phe227Ser) rs1554945235
NM_024426.5(WT1):c.682G>A (p.Asp228Asn)
NM_024426.5(WT1):c.685G>A (p.Gly229Arg)
NM_024426.5(WT1):c.689C>T (p.Thr230Met)
NM_024426.5(WT1):c.695G>C (p.Ser232Thr) rs761913397
NM_024426.5(WT1):c.700G>C (p.Gly234Arg) rs1307992683
NM_024426.5(WT1):c.736A>G (p.Asn246Asp)
NM_024426.5(WT1):c.746T>G (p.Phe249Cys) rs777119782
NM_024426.5(WT1):c.747C>G (p.Phe249Leu) rs1060501259
NM_024426.5(WT1):c.752A>T (p.His251Leu) rs914029023
NM_024426.5(WT1):c.763A>G (p.Met255Val) rs142653301
NM_024426.5(WT1):c.765G>T (p.Met255Ile) rs1060501255
NM_024426.5(WT1):c.767G>T (p.Gly256Val) rs1554945190
NM_024426.5(WT1):c.779C>T (p.Ser260Leu) rs1444869026
NM_024426.5(WT1):c.806C>G (p.Pro269Arg) rs756078681
NM_024426.5(WT1):c.806C>T (p.Pro269Leu)
NM_024426.5(WT1):c.832C>G (p.Pro278Ala)
NM_024426.5(WT1):c.887+4G>A rs778673400
NM_024426.5(WT1):c.892A>G (p.Asn298Asp) rs1554943492
NM_024426.5(WT1):c.925A>G (p.Met309Val) rs754336808
NM_024426.5(WT1):c.977G>C (p.Gly326Ala) rs766054482

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