ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as uncertain significance for Wilms tumor 1

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Total variants: 33
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HGVS dbSNP
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.124G>A (p.Gly42Ser) rs762288656
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.205T>A (p.Ser69Thr) rs1565002158
NM_024426.6(WT1):c.298C>G (p.Pro100Ala)
NM_024426.6(WT1):c.29C>A (p.Ala10Asp) rs997104313
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.313G>T (p.Ala105Ser)
NM_024426.6(WT1):c.314C>A (p.Ala105Glu) rs948061247
NM_024426.6(WT1):c.314C>G (p.Ala105Gly) rs948061247
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.391C>T (p.Pro131Ser) rs564706633
NM_024426.6(WT1):c.402G>A (p.Pro134=) rs777527675
NM_024426.6(WT1):c.404C>T (p.Pro135Leu) rs769642496
NM_024426.6(WT1):c.471C>A (p.His157Gln) rs753238865
NM_024426.6(WT1):c.541C>A (p.Arg181Ser) rs1565001278
NM_024426.6(WT1):c.562C>T (p.Pro188Ser) rs1565001232
NM_024426.6(WT1):c.587G>A (p.Gly196Asp) rs753112302
NM_024426.6(WT1):c.610G>T (p.Ala204Ser) rs9332973
NM_024426.6(WT1):c.620T>G (p.Leu207Arg)
NM_024426.6(WT1):c.649A>G (p.Ile217Val) rs1384974578
NM_024426.6(WT1):c.83G>A (p.Gly28Glu) rs751641518

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