ClinVar Miner

List of variants reported as uncertain significance for Wilms tumor 1 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 48
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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.-102C>A rs886048240
NM_024426.6(WT1):c.-106C>T rs867975105
NM_024426.6(WT1):c.-110C>T rs886048241
NM_024426.6(WT1):c.-114T>A rs886048242
NM_024426.6(WT1):c.-135G>A rs886048243
NM_024426.6(WT1):c.-140C>T rs886048244
NM_024426.6(WT1):c.-76T>C rs886048235
NM_024426.6(WT1):c.-87C>T
NM_024426.6(WT1):c.1017-15T>C rs374441355
NM_024426.6(WT1):c.1020C>T (p.His340=)
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.124G>A (p.Gly42Ser) rs762288656
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160
NM_024426.6(WT1):c.162C>G (p.Ser54Arg) rs776954184
NM_024426.6(WT1):c.174C>G (p.Leu58=) rs886048232
NM_024426.6(WT1):c.193G>A (p.Gly65Arg) rs374404615
NM_024426.6(WT1):c.298C>G (p.Pro100Ala)
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.313G>T (p.Ala105Ser)
NM_024426.6(WT1):c.347C>T (p.Pro116Leu) rs886048229
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406
NM_024426.6(WT1):c.390A>G (p.Pro130=) rs886048228
NM_024426.6(WT1):c.402G>A (p.Pro134=) rs777527675
NM_024426.6(WT1):c.587G>A (p.Gly196Asp) rs753112302
NM_024426.6(WT1):c.620T>G (p.Leu207Arg)
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738
NM_024426.6(WT1):c.813G>C (p.Pro271=)
NM_024426.6(WT1):c.83G>A (p.Gly28Glu) rs751641518
NM_024426.6(WT1):c.887+4G>A rs778673400
NM_024426.6(WT1):c.973G>A (p.Ala325Thr)

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