ClinVar Miner

List of variants reported as uncertain significance for Wilms tumor type 1 by Mendelics

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg) rs142059681
NM_024426.6(WT1):c.124G>A (p.Gly42Ser) rs762288656
NM_024426.6(WT1):c.1478G>A (p.Ser493Asn)
NM_024426.6(WT1):c.1541A>G (p.Asn514Ser) rs1554938531
NM_024426.6(WT1):c.162C>G (p.Ser54Arg) rs776954184
NM_024426.6(WT1):c.205T>A (p.Ser69Thr) rs1565002158
NM_024426.6(WT1):c.29C>A (p.Ala10Asp)
NM_024426.6(WT1):c.314C>A (p.Ala105Glu)
NM_024426.6(WT1):c.314C>G (p.Ala105Gly) rs948061247
NM_024426.6(WT1):c.391C>T (p.Pro131Ser)
NM_024426.6(WT1):c.404C>T (p.Pro135Leu) rs769642496
NM_024426.6(WT1):c.471C>A (p.His157Gln)
NM_024426.6(WT1):c.541C>A (p.Arg181Ser) rs1565001278
NM_024426.6(WT1):c.562C>T (p.Pro188Ser) rs1565001232
NM_024426.6(WT1):c.610G>T (p.Ala204Ser)
NM_024426.6(WT1):c.649A>G (p.Ile217Val) rs1384974578
NM_024426.6(WT1):c.662G>A (p.Gly221Asp)

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