ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as likely benign for not provided

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Total variants: 21
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HGVS dbSNP
NM_024426.6(WT1):c.186G>A (p.Arg62=) rs1294714508
NM_024426.6(WT1):c.189C>T (p.Ser63=) rs1215127008
NM_024426.6(WT1):c.204G>A (p.Gly68=) rs1554946680
NM_024426.6(WT1):c.225C>A (p.Gly75=) rs1590410808
NM_024426.6(WT1):c.237G>C (p.Arg79=) rs1590410776
NM_024426.6(WT1):c.258C>T (p.Pro86=) rs1389359790
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.324G>A (p.Ala108=) rs1229643010
NM_024426.6(WT1):c.36G>T (p.Thr12=) rs1313371480
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.387G>T (p.Pro129=) rs1590410053
NM_024426.6(WT1):c.390A>G (p.Pro130=) rs886048228
NM_024426.6(WT1):c.429C>G (p.Ser143=) rs531076591
NM_024426.6(WT1):c.465G>A (p.Glu155=) rs1590409614
NM_024426.6(WT1):c.531C>G (p.Ala177=) rs1354094843
NM_024426.6(WT1):c.531C>T (p.Ala177=) rs1354094843
NM_024426.6(WT1):c.569C>T (p.Pro190Leu) rs757349907
NM_024426.6(WT1):c.630C>T (p.Cys210=) rs1590408912
NM_024426.6(WT1):c.645C>G (p.Pro215=) rs749405227
NM_024426.6(WT1):c.78G>A (p.Gly26=) rs1240715155

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