ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as likely benign for Drash syndrome; Frasier syndrome; Wilms tumor 1; Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome

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Gene type:
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Total variants: 97
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HGVS dbSNP
NM_024426.6(WT1):c.108G>A (p.Gln36=)
NM_024426.6(WT1):c.115C>A (p.Arg39=) rs763147828
NM_024426.6(WT1):c.117G>A (p.Arg39=)
NM_024426.6(WT1):c.120C>T (p.Asp40=)
NM_024426.6(WT1):c.123G>A (p.Pro41=)
NM_024426.6(WT1):c.124G>A (p.Gly42Ser) rs762288656
NM_024426.6(WT1):c.150C>T (p.Ala50=) rs1554946724
NM_024426.6(WT1):c.153C>T (p.Ala51=) rs1590411186
NM_024426.6(WT1):c.159C>T (p.Ala53=) rs1021307133
NM_024426.6(WT1):c.174C>G (p.Leu58=) rs886048232
NM_024426.6(WT1):c.186G>A (p.Arg62=) rs1294714508
NM_024426.6(WT1):c.189C>T (p.Ser63=) rs1215127008
NM_024426.6(WT1):c.195G>A (p.Gly65=) rs1439699290
NM_024426.6(WT1):c.198G>T (p.Ala66=)
NM_024426.6(WT1):c.201C>T (p.Ser67=) rs771769393
NM_024426.6(WT1):c.204G>A (p.Gly68=) rs1554946680
NM_024426.6(WT1):c.225C>A (p.Gly75=) rs1590410808
NM_024426.6(WT1):c.231C>T (p.Asp77=)
NM_024426.6(WT1):c.237G>C (p.Arg79=) rs1590410776
NM_024426.6(WT1):c.241C>T (p.Leu81=)
NM_024426.6(WT1):c.246C>T (p.Asn82=) rs1205117425
NM_024426.6(WT1):c.249G>A (p.Ala83=)
NM_024426.6(WT1):c.258C>T (p.Pro86=) rs1389359790
NM_024426.6(WT1):c.259G>A (p.Ala87Thr) rs752686863
NM_024426.6(WT1):c.261C>T (p.Ala87=)
NM_024426.6(WT1):c.267C>T (p.Pro89=) rs1172336462
NM_024426.6(WT1):c.279C>T (p.Gly93=) rs1590410564
NM_024426.6(WT1):c.27G>A (p.Pro9=) rs556835183
NM_024426.6(WT1):c.291T>C (p.Cys97=)
NM_024426.6(WT1):c.294C>T (p.Ala98=)
NM_024426.6(WT1):c.297G>A (p.Leu99=)
NM_024426.6(WT1):c.312G>A (p.Ala104=) rs1590410376
NM_024426.6(WT1):c.315G>A (p.Ala105=) rs1554946607
NM_024426.6(WT1):c.324G>A (p.Ala108=) rs1229643010
NM_024426.6(WT1):c.327G>C (p.Pro109=)
NM_024426.6(WT1):c.331C>T (p.Leu111=)
NM_024426.6(WT1):c.336C>T (p.Asp112=)
NM_024426.6(WT1):c.339T>C (p.Phe113=)
NM_024426.6(WT1):c.342G>C (p.Ala114=)
NM_024426.6(WT1):c.366G>A (p.Gly122=) rs1362739411
NM_024426.6(WT1):c.369G>A (p.Ser123=)
NM_024426.6(WT1):c.369G>T (p.Ser123=)
NM_024426.6(WT1):c.36G>T (p.Thr12=) rs1313371480
NM_024426.6(WT1):c.381C>A (p.Pro127=) rs771681406
NM_024426.6(WT1):c.381C>T (p.Pro127=) rs771681406
NM_024426.6(WT1):c.387G>T (p.Pro129=) rs1590410053
NM_024426.6(WT1):c.390A>G (p.Pro130=) rs886048228
NM_024426.6(WT1):c.393G>C (p.Pro131=)
NM_024426.6(WT1):c.393G>T (p.Pro131=) rs1229890218
NM_024426.6(WT1):c.402G>A (p.Pro134=) rs777527675
NM_024426.6(WT1):c.417G>A (p.Pro139=) rs758361767
NM_024426.6(WT1):c.417G>T (p.Pro139=)
NM_024426.6(WT1):c.429C>G (p.Ser143=) rs531076591
NM_024426.6(WT1):c.429C>T (p.Ser143=)
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.432C>T (p.Phe144=) rs754173303
NM_024426.6(WT1):c.444G>A (p.Glu148=) rs761166030
NM_024426.6(WT1):c.450C>T (p.Ser150=) rs1213710686
NM_024426.6(WT1):c.462G>A (p.Ala154=)
NM_024426.6(WT1):c.465G>A (p.Glu155=) rs1590409614
NM_024426.6(WT1):c.468G>T (p.Pro156=) rs961309280
NM_024426.6(WT1):c.471C>T (p.His157=)
NM_024426.6(WT1):c.474G>A (p.Glu158=)
NM_024426.6(WT1):c.480G>A (p.Gln160=) rs758900425
NM_024426.6(WT1):c.498T>C (p.Thr166=) rs1554946487
NM_024426.6(WT1):c.510C>T (p.Ser170=)
NM_024426.6(WT1):c.51G>A (p.Pro17=) rs1590411695
NM_024426.6(WT1):c.51G>C (p.Pro17=)
NM_024426.6(WT1):c.522T>C (p.Thr174=) rs747958111
NM_024426.6(WT1):c.531C>G (p.Ala177=) rs1354094843
NM_024426.6(WT1):c.531C>T (p.Ala177=) rs1354094843
NM_024426.6(WT1):c.549G>A (p.Gly183=)
NM_024426.6(WT1):c.549G>T (p.Gly183=) rs1199167878
NM_024426.6(WT1):c.54G>A (p.Ala18=) rs1409626312
NM_024426.6(WT1):c.555C>T (p.Phe185=) rs1554946465
NM_024426.6(WT1):c.564T>A (p.Pro188=) rs1060504178
NM_024426.6(WT1):c.567G>T (p.Pro189=) rs141135091
NM_024426.6(WT1):c.582A>C (p.Ser194=)
NM_024426.6(WT1):c.582A>T (p.Ser194=)
NM_024426.6(WT1):c.585C>T (p.Ser195=) rs1332888095
NM_024426.6(WT1):c.588C>A (p.Gly196=)
NM_024426.6(WT1):c.597G>A (p.Arg199=)
NM_024426.6(WT1):c.612G>T (p.Ala204=)
NM_024426.6(WT1):c.615C>G (p.Pro205=) rs769467940
NM_024426.6(WT1):c.618C>T (p.Tyr206=)
NM_024426.6(WT1):c.619C>T (p.Leu207=) rs1060504180
NM_024426.6(WT1):c.627C>T (p.Ser209=) rs761530541
NM_024426.6(WT1):c.630C>T (p.Cys210=) rs1590408912
NM_024426.6(WT1):c.633C>G (p.Leu211=)
NM_024426.6(WT1):c.633C>T (p.Leu211=) rs576677344
NM_024426.6(WT1):c.645C>G (p.Pro215=) rs749405227
NM_024426.6(WT1):c.661+9G>A
NM_024426.6(WT1):c.75C>G (p.Ser25=)
NM_024426.6(WT1):c.75C>T (p.Ser25=) rs1417997475
NM_024426.6(WT1):c.78G>A (p.Gly26=) rs1240715155
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770
NM_024426.6(WT1):c.99A>G (p.Pro33=)

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