ClinVar Miner

List of variants reported as likely benign for Drash syndrome; Frasier syndrome; Wilms tumor 1; Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome by Invitae

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Total variants: 61
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HGVS dbSNP
NM_024426.6(WT1):c.1035G>A (p.Glu345=) rs757962229
NM_024426.6(WT1):c.1038C>T (p.Ser346=) rs750018485
NM_024426.6(WT1):c.1059C>T (p.Ile353=) rs527655625
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg) rs142059681
NM_024426.6(WT1):c.1116T>C (p.Asp372=) rs901264376
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312
NM_024426.6(WT1):c.1140C>A (p.Ala380=) rs147126640
NM_024426.6(WT1):c.1143G>A (p.Pro381=) rs1554939849
NM_024426.6(WT1):c.1146T>A (p.Thr382=) rs371168589
NM_024426.6(WT1):c.1182C>T (p.Arg394=) rs147939483
NM_024426.6(WT1):c.1227G>A (p.Lys409=) rs1554939791
NM_024426.6(WT1):c.1260C>T (p.His420=) rs1554939784
NM_024426.6(WT1):c.1265-4C>T rs918343735
NM_024426.6(WT1):c.1269G>A (p.Glu423=) rs767850636
NM_024426.6(WT1):c.1341A>G (p.Gln447=) rs772822466
NM_024426.6(WT1):c.1354+9G>A rs765187288
NM_024426.6(WT1):c.1404C>T (p.Ser468=) rs374799820
NM_024426.6(WT1):c.1422C>T (p.His474=) rs1554939066
NM_024426.6(WT1):c.1479T>C (p.Ser493=) rs1334930117
NM_024426.6(WT1):c.150C>T (p.Ala50=) rs1554946724
NM_024426.6(WT1):c.1515C>A (p.Val505=) rs1338629886
NM_024426.6(WT1):c.1563G>A (p.Ala521=) rs202118284
NM_024426.6(WT1):c.159C>T (p.Ala53=) rs1021307133
NM_024426.6(WT1):c.204G>A (p.Gly68=) rs1554946680
NM_024426.6(WT1):c.315G>A (p.Ala105=) rs1554946607
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406
NM_024426.6(WT1):c.381C>T (p.Pro127=) rs771681406
NM_024426.6(WT1):c.393G>T (p.Pro131=) rs1229890218
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.450C>T (p.Ser150=) rs1213710686
NM_024426.6(WT1):c.468G>T (p.Pro156=) rs961309280
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.522T>C (p.Thr174=) rs747958111
NM_024426.6(WT1):c.531C>T (p.Ala177=) rs1354094843
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.585C>T (p.Ser195=) rs1332888095
NM_024426.6(WT1):c.619C>T (p.Leu207=) rs1060504180
NM_024426.6(WT1):c.633C>T (p.Leu211=) rs576677344
NM_024426.6(WT1):c.662-10G>T rs1554945255
NM_024426.6(WT1):c.662-5C>T rs780259089
NM_024426.6(WT1):c.662-6C>A rs372418954
NM_024426.6(WT1):c.672G>A (p.Thr224=) rs756695525
NM_024426.6(WT1):c.687G>C (p.Gly229=) rs760001898
NM_024426.6(WT1):c.708G>A (p.Thr236=) rs768828897
NM_024426.6(WT1):c.714G>T (p.Ser238=) rs772409488
NM_024426.6(WT1):c.726G>T (p.Ala242=) rs1473494675
NM_024426.6(WT1):c.75C>T (p.Ser25=) rs1417997475
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584
NM_024426.6(WT1):c.780G>C (p.Ser260=) rs1403311573
NM_024426.6(WT1):c.784+10C>A rs1554945172
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738
NM_024426.6(WT1):c.789G>A (p.Glu263=) rs878855087
NM_024426.6(WT1):c.804G>A (p.Val268=) rs1060504179
NM_024426.6(WT1):c.849C>T (p.Thr283=) rs145425799
NM_024426.6(WT1):c.865C>T (p.Leu289=) rs1554945037
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770
NM_024426.6(WT1):c.882C>T (p.Tyr294=) rs1554945031
NM_024426.6(WT1):c.945C>T (p.Asn315=) rs775085343
NM_024426.6(WT1):c.966-4del rs1438888966

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