ClinVar Miner

List of variants reported as pathogenic for Wilms tumor type 1

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NC_000011.10:g.(?_32389058)_(32435345_?)del
NC_000011.10:g.(?_32396251)_(32417660_?)del
NC_000023.10:g.(?_132795738)_(133119496_?)del
NC_000023.10:g.(?_132795758)_(132888203_?)del
NM_000059.3(BRCA2):c.100G>T (p.Glu34Ter) rs80358391
NM_000059.3(BRCA2):c.1399A>T (p.Lys467Ter) rs80358427
NM_000059.3(BRCA2):c.145G>T (p.Glu49Ter) rs80358435
NM_000059.3(BRCA2):c.3109C>T (p.Gln1037Ter) rs80358557
NM_000059.3(BRCA2):c.4243G>T (p.Glu1415Ter) rs397507327
NM_000059.3(BRCA2):c.4965C>G (p.Tyr1655Ter) rs80358721
NM_000059.3(BRCA2):c.5645C>G (p.Ser1882Ter) rs80358785
NM_000059.3(BRCA2):c.5682C>G (p.Tyr1894Ter) rs41293497
NM_000059.3(BRCA2):c.5791C>T (p.Gln1931Ter) rs80358807
NM_000059.3(BRCA2):c.5857G>T (p.Glu1953Ter) rs80358814
NM_000059.3(BRCA2):c.658_659delGT (p.Val220Ilefs) rs80359604
NM_000059.3(BRCA2):c.6656C>G (p.Ser2219Ter) rs80358893
NM_000059.3(BRCA2):c.6952C>T (p.Arg2318Ter) rs80358920
NM_000059.3(BRCA2):c.7480C>T (p.Arg2494Ter) rs80358972
NM_000059.3(BRCA2):c.7879A>T (p.Ile2627Phe) rs80359014
NM_000059.3(BRCA2):c.7988A>T (p.Glu2663Val) rs80359031
NM_000059.3(BRCA2):c.8167G>C (p.Asp2723His) rs41293511
NM_000059.3(BRCA2):c.8488-1G>A rs397507404
NM_000059.3(BRCA2):c.9117G>A (p.Pro3039=) rs28897756
NM_000059.3(BRCA2):c.9294C>G (p.Tyr3098Ter) rs80359200
NM_000059.3(BRCA2):c.92G>A (p.Trp31Ter) rs397508045
NM_000059.3(BRCA2):c.9382C>T (p.Arg3128Ter) rs80359212
NM_001198551.1(WT1):c.229_231delTAC (p.Tyr77del) rs1554945033
NM_004484.3(GPC3):c.1159C>T (p.Arg387Ter) rs122453121
NM_004484.3(GPC3):c.1307delC (p.Ala436Glufs)
NM_004484.3(GPC3):c.1471G>T (p.Glu491Ter)
NM_004484.3(GPC3):c.1574-?_*379+?del
NM_004484.3(GPC3):c.1705G>A (p.Ala569Thr) rs122453120
NM_004484.3(GPC3):c.361C>T (p.His121Tyr) rs122453119
NM_004484.3(GPC3):c.595C>T (p.Arg199Ter) rs104894855
NM_004484.3(GPC3):c.629_654del26insCTTGCA (p.Asn210Thrfs) rs1556297749
NM_024426.4(WT1):c.1079delG (p.Gly360Valfs) rs587776574
NM_024426.4(WT1):c.1288C>T (p.Arg430Ter) rs121907906
NM_024426.4(WT1):c.1372C>T (p.Arg458Ter) rs121907909
NM_024426.4(WT1):c.1384C>T (p.Arg462Trp) rs121907900
NM_024426.4(WT1):c.319delG (p.Asp107Thrfs) rs1554946600
NM_024426.4(WT1):c.531C>A (p.Tyr177Ter) rs121907911
NM_024426.4(WT1):c.576delG (p.Ala193Profs) rs1131690795
NM_024426.4(WT1):c.667dup (p.Asp223Glyfs) rs1554945232
NM_024426.4(WT1):c.797delC (p.Pro266Argfs) rs1060501253
NM_024426.4(WT1):c.878_894del17 (p.Asn293Ilefs) rs587776573
NM_024426.5(WT1):c.1120C>T (p.Arg374Ter) rs1423753702
NM_024426.5(WT1):c.1149del (p.Val384Tyrfs) rs1554939839
NM_024426.5(WT1):c.1447+5G>A rs587776576
NM_024426.5(WT1):c.472G>T (p.Glu158Ter)
NM_024426.5(WT1):c.478C>T (p.Gln160Ter) rs1554946500
NM_024426.5(WT1):c.653del (p.Arg218Profs)

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