ClinVar Miner

List of variants in gene WT1 reported as uncertain significance for Wilms tumor 1

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Total variants: 30
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HGVS dbSNP
NM_024426.6(WT1):c.*100A>G
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.*159G>C rs746218880
NM_024426.6(WT1):c.*239G>A rs886048226
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.*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.*785C>A rs886048214
NM_024426.6(WT1):c.1017-15T>C rs374441355
NM_024426.6(WT1):c.1020C>T (p.His340=)
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg) rs142059681
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.1478G>A (p.Ser493Asn) rs763551837
NM_024426.6(WT1):c.1541A>G (p.Asn514Ser) rs1554938531
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160
NM_024426.6(WT1):c.662G>A (p.Gly221Asp) rs369444006
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)

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