ClinVar Miner

List of variants in gene WT1 reported as uncertain significance for Nephrotic syndrome, type 4

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Total variants: 51
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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.*1058G>T rs886048211
NM_024426.6(WT1):c.*1066T>G
NM_024426.6(WT1):c.*110C>T rs757474299
NM_024426.6(WT1):c.*1167T>G rs771770230
NM_024426.6(WT1):c.*1225T>C rs886048210
NM_024426.6(WT1):c.*12C>T
NM_024426.6(WT1):c.*159G>C rs746218880
NM_024426.6(WT1):c.*239G>A rs886048226
NM_024426.6(WT1):c.*269G>T rs886048225
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.*574del rs5030319
NM_024426.6(WT1):c.*5T>C
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.*841C>A rs886048213
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.1124G>A (p.Arg375His) rs554416372
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312
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.1568G>A (p.Ter523=) rs148856160
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.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

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