ClinVar Miner

List of variants reported as uncertain significance for Wilms tumor by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
NM_024426.6(WT1):c.*1021_*1022GT[14] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[15] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[18] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[19] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[20] rs58549495
NM_024426.6(WT1):c.*1058G>T rs886048211
NM_024426.6(WT1):c.*110C>T rs757474299
NM_024426.6(WT1):c.*1167T>G rs771770230
NM_024426.6(WT1):c.*1225T>C rs886048210
NM_024426.6(WT1):c.*159G>C rs746218880
NM_024426.6(WT1):c.*239G>A rs886048226
NM_024426.6(WT1):c.*269G>T rs886048225
NM_024426.6(WT1):c.*354G>T rs886048224
NM_024426.6(WT1):c.*366C>A rs886048223
NM_024426.6(WT1):c.*393G>T rs886048222
NM_024426.6(WT1):c.*460C>A rs886048221
NM_024426.6(WT1):c.*513C>T rs575602262
NM_024426.6(WT1):c.*534C>T rs868546165
NM_024426.6(WT1):c.*574del rs5030319
NM_024426.6(WT1):c.*611C>T rs886048220
NM_024426.6(WT1):c.*614A>C rs886048219
NM_024426.6(WT1):c.*666A>G rs374306749
NM_024426.6(WT1):c.*685G>T rs886048218
NM_024426.6(WT1):c.*707C>A rs886048217
NM_024426.6(WT1):c.*741G>T rs886048216
NM_024426.6(WT1):c.*768A>C rs886048215
NM_024426.6(WT1):c.*785C>A rs886048214
NM_024426.6(WT1):c.*841C>A rs886048213
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.-31G>T rs886048234
NM_024426.6(WT1):c.-76T>C rs886048235
NM_024426.6(WT1):c.-82A>C rs886048236
NM_024426.6(WT1):c.-86T>C rs886048237
NM_024426.6(WT1):c.-90T>C rs886048238
NM_024426.6(WT1):c.-94G>C rs886048239
NM_024426.6(WT1):c.1017-15T>C rs374441355
NM_024426.6(WT1):c.1198T>C (p.Tyr400His) rs746353651
NM_024426.6(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.6(WT1):c.136G>T (p.Ala46Ser) rs886048233
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.247G>T (p.Ala83Ser) rs886048231
NM_024426.6(WT1):c.285C>T (p.Gly95=) rs886048230
NM_024426.6(WT1):c.347C>T (p.Pro116Leu) rs886048229
NM_024426.6(WT1):c.375C>T (p.Gly125=) rs776209354
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.587G>A (p.Gly196Asp) rs753112302
NM_024426.6(WT1):c.695G>C (p.Ser232Thr) rs761913397
NM_024426.6(WT1):c.83G>A (p.Gly28Glu) rs751641518
NM_024426.6(WT1):c.887+4G>A rs778673400

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.