ClinVar Miner

List of variants reported as likely pathogenic for Wilms tumor

Included ClinVar conditions (16):
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ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.7878G>C (p.Trp2626Cys) rs80359013 0.00001
NM_024426.6(WT1):c.965+1G>A rs771527206 0.00001
NC_000023.10:g.(?_132887489)_(132888223_?)dup
NC_000023.10:g.(?_132887499)_(132888213_?)dup
NM_000059.4(BRCA2):c.15del (p.Glu7fs) rs1064795072
NM_000059.4(BRCA2):c.1889del (p.Thr630fs) rs80359315
NM_000059.4(BRCA2):c.574_575del (p.Met192fs) rs80359533
NM_000612.6(IGF2):c.100G>T (p.Gly34Cys) rs1858937359
NM_004484.4(GPC3):c.1292+2T>A rs2071072322
NM_004484.4(GPC3):c.1413+2T>A rs2124401750
NM_004484.4(GPC3):c.1666G>C (p.Gly556Arg) rs267606850
NM_004484.4(GPC3):c.337+2T>A
NM_024426.6(WT1):c.1016+1G>A rs2133032244
NM_024426.6(WT1):c.1016+2T>G rs1852674417
NM_024426.6(WT1):c.1114-1G>T rs1851976798
NM_024426.6(WT1):c.1142del (p.Pro381fs) rs1564972993
NM_024426.6(WT1):c.1207T>G (p.Cys403Gly)
NM_024426.6(WT1):c.1245dup (p.His416fs) rs2132939399
NM_024426.6(WT1):c.1297T>G (p.Cys433Gly) rs121907905
NM_024426.6(WT1):c.1355G>A (p.Gly452Asp)
NM_024426.6(WT1):c.1406A>G (p.Asp469Gly) rs121907902
NM_024426.6(WT1):c.1447+2T>C rs1851829439
NM_024426.6(WT1):c.410del (p.Pro137fs)
NM_024426.6(WT1):c.455del (p.Gly152fs) rs2133103216
NM_024426.6(WT1):c.512G>T (p.Gly171Val) rs1554946480
NM_024426.6(WT1):c.649A>G (p.Ile217Val) rs1384974578
NM_024426.6(WT1):c.965+2T>C
NM_152383.5(DIS3L2):c.2381_2382del (p.Arg794fs) rs1553551874

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