ClinVar Miner

List of variants in gene WT1 studied for Nephrotic syndrome, type 4

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Total variants: 87
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HGVS dbSNP
NM_024426.6(WT1):c.*100A>G
NM_024426.6(WT1):c.*1021_*1022GT[14] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[15] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[18] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[19] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[20] rs58549495
NM_024426.6(WT1):c.*1049del rs568803808
NM_024426.6(WT1):c.*1058G>T rs886048211
NM_024426.6(WT1):c.*1066T>G
NM_024426.6(WT1):c.*1098C>T rs5030327
NM_024426.6(WT1):c.*110C>T rs757474299
NM_024426.6(WT1):c.*1132A>T rs5030328
NM_024426.6(WT1):c.*1167T>G rs771770230
NM_024426.6(WT1):c.*1209A>G rs5030329
NM_024426.6(WT1):c.*1225T>C rs886048210
NM_024426.6(WT1):c.*1239T>A rs534396876
NM_024426.6(WT1):c.*12C>T
NM_024426.6(WT1):c.*138G>A rs111351882
NM_024426.6(WT1):c.*159G>C rs746218880
NM_024426.6(WT1):c.*16G>T rs2234594
NM_024426.6(WT1):c.*224A>G rs5030316
NM_024426.6(WT1):c.*239G>A rs886048226
NM_024426.6(WT1):c.*267G>C rs5030317
NM_024426.6(WT1):c.*269G>T rs886048225
NM_024426.6(WT1):c.*345G>A rs5030318
NM_024426.6(WT1):c.*354G>T rs886048224
NM_024426.6(WT1):c.*366C>A rs886048223
NM_024426.6(WT1):c.*393G>T rs886048222
NM_024426.6(WT1):c.*460C>A rs886048221
NM_024426.6(WT1):c.*513C>T rs575602262
NM_024426.6(WT1):c.*534C>T rs868546165
NM_024426.6(WT1):c.*542G>A rs142726499
NM_024426.6(WT1):c.*574del rs5030319
NM_024426.6(WT1):c.*5T>C
NM_024426.6(WT1):c.*602A>G rs5030320
NM_024426.6(WT1):c.*611C>T rs886048220
NM_024426.6(WT1):c.*614A>C rs886048219
NM_024426.6(WT1):c.*629T>C
NM_024426.6(WT1):c.*666A>G rs374306749
NM_024426.6(WT1):c.*685G>T rs886048218
NM_024426.6(WT1):c.*707C>A rs886048217
NM_024426.6(WT1):c.*741G>T rs886048216
NM_024426.6(WT1):c.*768A>C rs886048215
NM_024426.6(WT1):c.*785C>A rs886048214
NM_024426.6(WT1):c.*820G>C rs1042347
NM_024426.6(WT1):c.*835A>G rs5030322
NM_024426.6(WT1):c.*841C>A rs886048213
NM_024426.6(WT1):c.*864T>A rs5030323
NM_024426.6(WT1):c.*864T>G rs5030323
NM_024426.6(WT1):c.*88A>G rs5030315
NM_024426.6(WT1):c.*897G>C rs5030324
NM_024426.6(WT1):c.*903G>A rs5030325
NM_024426.6(WT1):c.*978dup rs5030326
NM_024426.6(WT1):c.1017-15T>C rs374441355
NM_024426.6(WT1):c.1017-9T>C rs368486676
NM_024426.6(WT1):c.1020C>T (p.His340=)
NM_024426.6(WT1):c.1074A>G (p.Gln358=) rs2234590
NM_024426.6(WT1):c.1114-9T>C rs5030274
NM_024426.6(WT1):c.1122A>G (p.Arg374=) rs16754
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.1154G>A (p.Arg385Gln) rs147241955
NM_024426.6(WT1):c.1180C>T (p.Arg394Cys) rs1564972874
NM_024426.6(WT1):c.1182C>T (p.Arg394=) rs147939483
NM_024426.6(WT1):c.1198T>C (p.Tyr400His) rs746353651
NM_024426.6(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.6(WT1):c.1216A>G (p.Arg406Gly) rs1590338690
NM_024426.6(WT1):c.1259A>C (p.His420Pro) rs1554939785
NM_024426.6(WT1):c.1348C>T (p.His450Tyr) rs28942089
NM_024426.6(WT1):c.1366T>C (p.Phe456Leu) rs28941777
NM_024426.6(WT1):c.1388G>A (p.Arg463Gln) rs1037084691
NM_024426.6(WT1):c.1399C>T (p.Arg467Trp) rs121907900
NM_024426.6(WT1):c.1405G>A (p.Asp469Asn) rs28941778
NM_024426.6(WT1):c.1447+4C>T rs587776577
NM_024426.6(WT1):c.1447+5G>A rs587776576
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160
NM_024426.6(WT1):c.500T>A (p.Val167Asp)
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.760C>T (p.Pro254Ser) rs2234584
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738
NM_024426.6(WT1):c.813G>C (p.Pro271=)
NM_024426.6(WT1):c.887+4G>A rs778673400
NM_024426.6(WT1):c.973G>A (p.Ala325Thr)
NM_024426.6(WT1):c.977G>C (p.Gly326Ala) rs766054482
NM_024426.6:c.250C>T
NM_024426.6:c.278G>C

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