ClinVar Miner

List of variants in gene WT1 studied for Drash syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.*267G>C rs5030317 0.44381
NM_024426.6(WT1):c.1448-49T>C rs1799937 0.34839
NM_024426.6(WT1):c.887+16G>A rs1799933 0.26810
NM_024426.6(WT1):c.1122A>G (p.Arg374=) rs16754 0.16617
NM_024426.6(WT1):c.*88A>G rs5030315 0.14706
NM_024426.6(WT1):c.*224A>G rs5030316 0.13669
NM_024426.6(WT1):c.1265-32C>A rs2234593 0.12726
NM_024426.6(WT1):c.1074A>G (p.Gln358=) rs2234590 0.04693
NM_024426.6(WT1):c.785-20G>T rs5030168 0.00663
NM_024426.6(WT1):c.1114-9T>C rs5030274 0.00465
NM_024426.6(WT1):c.*16G>T rs2234594 0.00421
NM_024426.6(WT1):c.662-6C>A rs372418954 0.00034
NM_024426.6(WT1):c.1150G>A (p.Val384Ile) rs977244044 0.00004
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955 0.00003
NM_024426.6(WT1):c.736A>G (p.Asn246Asp) rs1285224919 0.00002
NM_024426.6(WT1):c.1017-19C>T rs1398407708 0.00001
NM_024426.6(WT1):c.1100T>G (p.Phe367Cys) rs150194429 0.00001
NM_024426.6(WT1):c.1120C>T (p.Arg374Ter) rs1423753702 0.00001
NM_024426.6(WT1):c.1211A>C (p.Asn404Thr) rs748864758 0.00001
NM_024426.6(WT1):c.685G>A (p.Gly229Arg) rs767419243 0.00001
NM_024426.6(WT1):c.977G>C (p.Gly326Ala) rs766054482 0.00001
NM_024426.6(WT1):c.1081A>G (p.Ile361Val)
NM_024426.6(WT1):c.1127T>C (p.Val376Ala) rs1180529775
NM_024426.6(WT1):c.1208G>A (p.Cys403Tyr) rs121907904
NM_024426.6(WT1):c.1256A>G (p.Lys419Arg)
NM_024426.6(WT1):c.1265-52G>T rs869312745
NM_024426.6(WT1):c.1297T>G (p.Cys433Gly) rs121907905
NM_024426.6(WT1):c.1303C>T (p.Arg435Ter) rs121907906
NM_024426.6(WT1):c.1316G>A (p.Arg439His) rs121907901
NM_024426.6(WT1):c.1338C>G (p.His446Gln) rs121907907
NM_024426.6(WT1):c.1348C>T (p.His450Tyr) rs28942089
NM_024426.6(WT1):c.1354+4_1354+11del rs1590332435
NM_024426.6(WT1):c.1388G>A (p.Arg463Gln) rs1037084691
NM_024426.6(WT1):c.1399C>T (p.Arg467Trp) rs121907900
NM_024426.6(WT1):c.1400G>A (p.Arg467Gln) rs121907903
NM_024426.6(WT1):c.1400G>C (p.Arg467Pro) rs121907903
NM_024426.6(WT1):c.1405G>A (p.Asp469Asn) rs28941778
NM_024426.6(WT1):c.1406A>G (p.Asp469Gly) rs121907902
NM_024426.6(WT1):c.1421A>C (p.His474Pro) rs1564969626
NM_024426.6(WT1):c.1447+5G>A rs587776576
NM_024426.6(WT1):c.1499G>A (p.Arg500Gln) rs1590326226
NM_024426.6(WT1):c.1523A>G (p.His508Arg)
NM_024426.6(WT1):c.1541A>G (p.Asn514Ser) rs1554938531
NM_024426.6(WT1):c.667A>T (p.Ser223Cys)
NM_024426.6(WT1):c.700G>C (p.Gly234Arg) rs1307992683
NM_024426.6(WT1):c.769C>T (p.Gln257Ter)
NM_024426.6(WT1):c.785-14G>A rs375514482
NM_024426.6(WT1):c.892A>G (p.Asn298Asp) rs1554943492
NM_024426.6(WT1):c.992T>C (p.Val331Ala)

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.