ClinVar Miner

List of variants in gene WT1 reported as likely benign for Wilms tumor type 1

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP
NM_024426.6(WT1):c.*12C>T
NM_024426.6(WT1):c.1008G>A (p.Gly336=) rs1369099437
NM_024426.6(WT1):c.1017-4G>C rs1043846933
NM_024426.6(WT1):c.1017-9T>C rs368486676
NM_024426.6(WT1):c.1032C>T (p.Tyr344=) rs1338914258
NM_024426.6(WT1):c.1035G>A (p.Glu345=) rs757962229
NM_024426.6(WT1):c.1038C>T (p.Ser346=) rs750018485
NM_024426.6(WT1):c.1053G>A (p.Thr351=) rs1260693060
NM_024426.6(WT1):c.1059C>T (p.Ile353=) rs527655625
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg) rs142059681
NM_024426.6(WT1):c.1116T>C (p.Asp372=) rs901264376
NM_024426.6(WT1):c.1124G>A (p.Arg375His) rs554416372
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312
NM_024426.6(WT1):c.1140C>A (p.Ala380=) rs147126640
NM_024426.6(WT1):c.1143G>A (p.Pro381=) rs1554939849
NM_024426.6(WT1):c.1146T>A (p.Thr382=) rs371168589
NM_024426.6(WT1):c.1146T>C (p.Thr382=) rs371168589
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955
NM_024426.6(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.6(WT1):c.1227G>A (p.Lys409=) rs1554939791
NM_024426.6(WT1):c.1260C>T (p.His420=) rs1554939784
NM_024426.6(WT1):c.1265-4C>T rs918343735
NM_024426.6(WT1):c.1269G>A (p.Glu423=) rs767850636
NM_024426.6(WT1):c.1278C>T (p.Tyr426=) rs759955361
NM_024426.6(WT1):c.1281G>A (p.Gln427=) rs774650640
NM_024426.6(WT1):c.1341A>G (p.Gln447=) rs772822466
NM_024426.6(WT1):c.1354+9G>A rs765187288
NM_024426.6(WT1):c.1404C>T (p.Ser468=) rs374799820
NM_024426.6(WT1):c.1422C>T (p.His474=) rs1554939066
NM_024426.6(WT1):c.1434T>C (p.His478=) rs761414130
NM_024426.6(WT1):c.1448-10G>T rs185744719
NM_024426.6(WT1):c.1448-9T>C rs1590326385
NM_024426.6(WT1):c.1479T>C (p.Ser493=) rs1334930117
NM_024426.6(WT1):c.1515C>A (p.Val505=) rs1338629886
NM_024426.6(WT1):c.1563G>A (p.Ala521=) rs202118284
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160
NM_024426.6(WT1):c.662-10G>T rs1554945255
NM_024426.6(WT1):c.662-5C>T rs780259089
NM_024426.6(WT1):c.662-6C>A rs372418954
NM_024426.6(WT1):c.666C>T (p.Tyr222=) rs1590396134
NM_024426.6(WT1):c.672G>A (p.Thr224=) rs756695525
NM_024426.6(WT1):c.675C>T (p.Val225=) rs1172028723
NM_024426.6(WT1):c.687G>C (p.Gly229=) rs760001898
NM_024426.6(WT1):c.695G>C (p.Ser232Thr) rs761913397
NM_024426.6(WT1):c.696C>T (p.Ser232=) rs9332974
NM_024426.6(WT1):c.708G>A (p.Thr236=) rs768828897
NM_024426.6(WT1):c.711C>T (p.Pro237=) rs183263057
NM_024426.6(WT1):c.714G>T (p.Ser238=) rs772409488
NM_024426.6(WT1):c.726G>T (p.Ala242=) rs1473494675
NM_024426.6(WT1):c.741C>T (p.His247=) rs1050903370
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584
NM_024426.6(WT1):c.764T>A (p.Met255Lys) rs377573993
NM_024426.6(WT1):c.784+10C>A rs1554945172
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738
NM_024426.6(WT1):c.804G>A (p.Val268=) rs1060504179
NM_024426.6(WT1):c.810C>A (p.Pro270=) rs1357760274
NM_024426.6(WT1):c.849C>T (p.Thr283=) rs145425799
NM_024426.6(WT1):c.855C>T (p.Ser285=) rs1320428764
NM_024426.6(WT1):c.945C>T (p.Asn315=) rs775085343
NM_024426.6(WT1):c.965+7T>G rs1590375400
NM_024426.6(WT1):c.966-15CTT[2] rs1316773733
NM_024426.6(WT1):c.966-4del rs1438888966

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