ClinVar Miner

List of variants reported as likely benign for Denys-Drash syndrome

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 119
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HGVS dbSNP
NM_024426.6(WT1):c.*1098C>T rs5030327
NM_024426.6(WT1):c.*1132A>T rs5030328
NM_024426.6(WT1):c.*1209A>G rs5030329
NM_024426.6(WT1):c.*1239T>A rs534396876
NM_024426.6(WT1):c.*138G>A rs111351882
NM_024426.6(WT1):c.*16G>T rs2234594
NM_024426.6(WT1):c.*345G>A rs5030318
NM_024426.6(WT1):c.*542G>A rs142726499
NM_024426.6(WT1):c.*835A>G rs5030322
NM_024426.6(WT1):c.*864T>A rs5030323
NM_024426.6(WT1):c.*864T>G rs5030323
NM_024426.6(WT1):c.*897G>C rs5030324
NM_024426.6(WT1):c.*903G>A rs5030325
NM_024426.6(WT1):c.1008G>A (p.Gly336=)
NM_024426.6(WT1):c.1017-19C>T
NM_024426.6(WT1):c.1017-4G>C
NM_024426.6(WT1):c.1032C>T (p.Tyr344=)
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.1053G>A (p.Thr351=)
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.1114-9T>C rs5030274
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.1146T>C (p.Thr382=)
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955
NM_024426.6(WT1):c.115C>A (p.Arg39=)
NM_024426.6(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.6(WT1):c.1227G>A (p.Lys409=) rs1554939791
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661
NM_024426.6(WT1):c.124G>A (p.Gly42Ser) rs762288656
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.1278C>T (p.Tyr426=)
NM_024426.6(WT1):c.1281G>A (p.Gln427=)
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.1434T>C (p.His478=)
NM_024426.6(WT1):c.1448-10G>T
NM_024426.6(WT1):c.1448-9T>C
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.153C>T (p.Ala51=)
NM_024426.6(WT1):c.1563G>A (p.Ala521=) rs202118284
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160
NM_024426.6(WT1):c.159C>T (p.Ala53=) rs1021307133
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581
NM_024426.6(WT1):c.195G>A (p.Gly65=)
NM_024426.6(WT1):c.201C>T (p.Ser67=)
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135
NM_024426.6(WT1):c.246C>T (p.Asn82=)
NM_024426.6(WT1):c.259G>A (p.Ala87Thr)
NM_024426.6(WT1):c.267C>T (p.Pro89=)
NM_024426.6(WT1):c.279C>T (p.Gly93=)
NM_024426.6(WT1):c.27G>A (p.Pro9=)
NM_024426.6(WT1):c.312G>A (p.Ala104=)
NM_024426.6(WT1):c.315G>A (p.Ala105=) rs1554946607
NM_024426.6(WT1):c.366G>A (p.Gly122=)
NM_024426.6(WT1):c.381C>A (p.Pro127=)
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.402G>A (p.Pro134=)
NM_024426.6(WT1):c.417G>A (p.Pro139=)
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.432C>T (p.Phe144=)
NM_024426.6(WT1):c.444G>A (p.Glu148=)
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.513C>A (p.Gly171=) rs536728682
NM_024426.6(WT1):c.51G>A (p.Pro17=)
NM_024426.6(WT1):c.522T>C (p.Thr174=) rs747958111
NM_024426.6(WT1):c.549G>T (p.Gly183=)
NM_024426.6(WT1):c.54G>A (p.Ala18=)
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=)
NM_024426.6(WT1):c.585C>T (p.Ser195=) rs1332888095
NM_024426.6(WT1):c.615C>G (p.Pro205=) rs769467940
NM_024426.6(WT1):c.619C>T (p.Leu207=) rs1060504180
NM_024426.6(WT1):c.627C>T (p.Ser209=)
NM_024426.6(WT1):c.633C>T (p.Leu211=) rs576677344
NM_024426.6(WT1):c.662-10G>T rs1554945255
NM_024426.6(WT1):c.662-2031G>A
NM_024426.6(WT1):c.662-5C>T rs780259089
NM_024426.6(WT1):c.662-6C>A rs372418954
NM_024426.6(WT1):c.666C>T (p.Tyr222=)
NM_024426.6(WT1):c.672G>A (p.Thr224=) rs756695525
NM_024426.6(WT1):c.675C>T (p.Val225=)
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.711C>T (p.Pro237=)
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.741C>T (p.His247=)
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.764T>A (p.Met255Lys) rs377573993
NM_024426.6(WT1):c.784+10C>A rs1554945172
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738
NM_024426.6(WT1):c.804G>A (p.Val268=) rs1060504179
NM_024426.6(WT1):c.810C>A (p.Pro270=)
NM_024426.6(WT1):c.849C>T (p.Thr283=) rs145425799
NM_024426.6(WT1):c.855C>T (p.Ser285=)
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770
NM_024426.6(WT1):c.945C>T (p.Asn315=) rs775085343
NM_024426.6(WT1):c.965+7T>G
NM_024426.6(WT1):c.966-15CTT[2]
NM_024426.6(WT1):c.966-4del rs1438888966

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