ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as likely benign for Wilms tumor

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661
NM_024426.6(WT1):c.150C>T (p.Ala50=) rs1554946724
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.204G>A (p.Gly68=) rs1554946680
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427
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.513C>A (p.Gly171=) rs536728682
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.609C>T (p.Asn203=) rs2234583
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.75C>T (p.Ser25=) rs1417997475
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770

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