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

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg)	rs142059681	0.00044
NM_024426.6(WT1):c.124G>A (p.Gly42Ser)	rs762288656	0.00019
NM_024426.6(WT1):c.314C>G (p.Ala105Gly)	rs948061247	0.00008
NM_024426.6(WT1):c.162C>G (p.Ser54Arg)	rs776954184	0.00006
NM_024426.6(WT1):c.404C>T (p.Pro135Leu)	rs769642496	0.00001
NM_024426.6(WT1):c.662G>A (p.Gly221Asp)	rs369444006	0.00001
NM_024426.6(WT1):c.1478G>A (p.Ser493Asn)	rs763551837
NM_024426.6(WT1):c.1541A>G (p.Asn514Ser)	rs1554938531
NM_024426.6(WT1):c.205T>A (p.Ser69Thr)	rs1565002158
NM_024426.6(WT1):c.29C>A (p.Ala10Asp)	rs997104313
NM_024426.6(WT1):c.314C>A (p.Ala105Glu)	rs948061247
NM_024426.6(WT1):c.391C>T (p.Pro131Ser)	rs564706633
NM_024426.6(WT1):c.471C>A (p.His157Gln)	rs753238865
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)	rs9332973
NM_024426.6(WT1):c.649A>G (p.Ile217Val)	rs1384974578

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