ClinVar Miner

List of variants in gene WT1 studied for not specified

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Total variants: 25
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HGVS dbSNP gnomAD frequency
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.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.1131T>C (p.Pro377=) rs151034312 0.00047
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg) rs142059681 0.00044
NM_024426.6(WT1):c.662-6C>A rs372418954 0.00034
NM_024426.6(WT1):c.1182C>T (p.Arg394=) rs147939483 0.00027
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584 0.00022
NM_024426.6(WT1):c.696C>T (p.Ser232=) rs9332974 0.00006
NM_024426.6(WT1):c.813G>C (p.Pro271=) rs1341857958 0.00004
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955 0.00003
NM_024426.6(WT1):c.1092C>A (p.His364Gln) rs587778756 0.00002
NM_024426.6(WT1):c.1304G>A (p.Arg435Gln) rs144788858 0.00002
NM_024426.6(WT1):c.977G>C (p.Gly326Ala) rs766054482 0.00001
NM_024426.6(WT1):c.1174G>A (p.Glu392Lys) rs1851970123
NM_024426.6(WT1):c.1349A>G (p.His450Arg) rs1851851609
NM_024426.6(WT1):c.1354+5G>A rs2132919246
NM_024426.6(WT1):c.1354+9G>A rs765187288
NM_024426.6(WT1):c.784+6C>T rs1455790542
NM_024426.6(WT1):c.840C>A (p.Asp280Glu) rs1554945044
NM_024426.6(WT1):c.900C>T (p.Tyr300=) rs190440703

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