ClinVar Miner

List of variants in gene LOC107982234, WT1 studied for Wilms tumor 1

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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.213G>T (p.Pro71=) rs2234582 0.31689
NM_024426.6(WT1):c.345C>T (p.Pro115=) rs1799925 0.15374
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583 0.13287
NM_024426.6(WT1):c.662-1928_662-1927del rs71873106 0.02282
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581 0.00270
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427 0.00197
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661 0.00188
NM_024426.6(WT1):c.-110C>T rs886048241 0.00048
NM_024426.6(WT1):c.375C>T (p.Gly125=) rs776209354 0.00039
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135 0.00036
NM_024426.6(WT1):c.-76T>C rs886048235 0.00032
NM_024426.6(WT1):c.-106C>T rs867975105 0.00021
NM_024426.6(WT1):c.124G>A (p.Gly42Ser) rs762288656 0.00019
NM_024426.6(WT1):c.193G>A (p.Gly65Arg) rs374404615 0.00019
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406 0.00009
NM_024426.6(WT1):c.314C>G (p.Ala105Gly) rs948061247 0.00008
NM_024426.6(WT1):c.-140C>T rs886048244 0.00006
NM_024426.6(WT1):c.162C>G (p.Ser54Arg) rs776954184 0.00006
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682 0.00004
NM_024426.6(WT1):c.70C>T (p.Arg24Cys) rs878855086 0.00004
NM_024426.6(WT1):c.587G>A (p.Gly196Asp) rs753112302 0.00002
NM_024426.6(WT1):c.628T>G (p.Cys210Gly) rs776426005 0.00002
NM_024426.6(WT1):c.154G>A (p.Glu52Lys) rs1212035248 0.00001
NM_024426.6(WT1):c.404C>T (p.Pro135Leu) rs769642496 0.00001
NM_024426.6(WT1):c.620T>G (p.Leu207Arg) rs1258754686 0.00001
NM_024426.6(WT1):c.83G>A (p.Gly28Glu) rs751641518 0.00001
NM_024426.6(WT1):c.-102C>A rs886048240
NM_024426.6(WT1):c.-114T>A rs886048242
NM_024426.6(WT1):c.-135G>A rs886048243
NM_024426.6(WT1):c.-87C>T rs1395440150
NM_024426.6(WT1):c.174C>G (p.Leu58=) rs886048232
NM_024426.6(WT1):c.205T>A (p.Ser69Thr) rs1565002158
NM_024426.6(WT1):c.298C>G (p.Pro100Ala) rs567200038
NM_024426.6(WT1):c.29C>A (p.Ala10Asp) rs997104313
NM_024426.6(WT1):c.313G>T (p.Ala105Ser) rs1236417259
NM_024426.6(WT1):c.314C>A (p.Ala105Glu) rs948061247
NM_024426.6(WT1):c.347C>T (p.Pro116Leu) rs886048229
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.410del (p.Pro137fs)
NM_024426.6(WT1):c.455del (p.Gly152fs) rs2133103216
NM_024426.6(WT1):c.471C>A (p.His157Gln) rs753238865
NM_024426.6(WT1):c.472G>T (p.Glu158Ter) rs1565001383
NM_024426.6(WT1):c.514del (p.Gln172fs) rs2133102575
NM_024426.6(WT1):c.52G>C (p.Ala18Pro) rs1590411684
NM_024426.6(WT1):c.541C>A (p.Arg181Ser) rs1565001278
NM_024426.6(WT1):c.546C>A (p.Tyr182Ter) rs121907911
NM_024426.6(WT1):c.562C>T (p.Pro188Ser) rs1565001232
NM_024426.6(WT1):c.592del (p.Ala198fs) rs1131690795
NM_024426.6(WT1):c.610G>T (p.Ala204Ser) rs9332973
NM_024426.6(WT1):c.649A>G (p.Ile217Val) rs1384974578
NM_024426.6(WT1):c.70C>G (p.Arg24Gly)

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