ClinVar Miner

List of variants in gene GPC3 reported as likely benign for Wilms tumor type 1

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP
NM_004484.3(GPC3):c.1002C>T (p.Val334=) rs747775536
NM_004484.3(GPC3):c.1029C>T (p.Thr343=) rs890143711
NM_004484.3(GPC3):c.1032+10_1032+11delinsTT rs1556297529
NM_004484.3(GPC3):c.1037G>T (p.Gly346Val) rs373916851
NM_004484.3(GPC3):c.1114G>A (p.Val372Ile) rs140756498
NM_004484.3(GPC3):c.1130A>G (p.His377Arg) rs1060502172
NM_004484.3(GPC3):c.1212T>C (p.Ala404=) rs1556263726
NM_004484.3(GPC3):c.1224C>T (p.Tyr408=) rs764743087
NM_004484.3(GPC3):c.1255G>A (p.Asp419Asn) rs755544588
NM_004484.3(GPC3):c.1263T>G (p.Leu421=) rs1474137107
NM_004484.3(GPC3):c.1293-5T>C rs766154973
NM_004484.3(GPC3):c.1296C>T (p.Tyr432=) rs946461494
NM_004484.3(GPC3):c.1494C>T (p.Cys498=) rs753210097
NM_004484.3(GPC3):c.1686G>C (p.Leu562=) rs1556111740
NM_004484.3(GPC3):c.1713G>A (p.Ser571=) rs149209315
NM_004484.3(GPC3):c.1724T>G (p.Phe575Cys) rs981077333
NM_004484.3(GPC3):c.1737G>A (p.Val579=) rs1556111517
NM_004484.3(GPC3):c.175+9G>A rs776234359
NM_004484.3(GPC3):c.326C>T (p.Ala109Val) rs761660909
NM_004484.3(GPC3):c.338-4A>T rs1490568896
NM_004484.3(GPC3):c.363T>A (p.His121Gln) rs754433681
NM_004484.3(GPC3):c.367A>G (p.Lys123Glu) rs755733724
NM_004484.3(GPC3):c.384C>A (p.Ala128=) rs761541528
NM_004484.3(GPC3):c.39G>T (p.Ala13=) rs1057522079
NM_004484.3(GPC3):c.414T>C (p.Thr138=) rs1048793393
NM_004484.3(GPC3):c.516C>T (p.Asp172=) rs369607601
NM_004484.3(GPC3):c.569C>T (p.Ser190Leu) rs780667597
NM_004484.3(GPC3):c.608G>A (p.Arg203His) rs375160737
NM_004484.3(GPC3):c.672A>G (p.Gln224=) rs373406834
NM_004484.3(GPC3):c.727A>G (p.Thr243Ala) rs1203561413
NM_004484.3(GPC3):c.761G>A (p.Arg254Gln) rs756844729
NM_004484.3(GPC3):c.761G>T (p.Arg254Leu) rs756844729
NM_004484.3(GPC3):c.802C>T (p.Leu268=) rs754903885
NM_004484.3(GPC3):c.805A>T (p.Met269Leu) rs1556297682
NM_004484.3(GPC3):c.826G>T (p.Gly276Cys) rs141100113
NM_004484.3(GPC3):c.93G>A (p.Pro31=) rs781232455
NM_004484.3(GPC3):c.983A>G (p.His328Arg) rs761141186
NM_004484.4(GPC3):c.1033-8T>A
NM_004484.4(GPC3):c.1033-9dup
NM_004484.4(GPC3):c.1414-7C>T
NM_004484.4(GPC3):c.1605G>A (p.Ala535=)
NM_004484.4(GPC3):c.1605G>T (p.Ala535=)
NM_004484.4(GPC3):c.1619A>G (p.Gln540Arg)
NM_004484.4(GPC3):c.1665C>T (p.Leu555=)
NM_004484.4(GPC3):c.1683G>A (p.Pro561=)
NM_004484.4(GPC3):c.1698C>T (p.Thr566=)
NM_004484.4(GPC3):c.259T>C (p.Leu87=)
NM_004484.4(GPC3):c.327G>A (p.Ala109=)
NM_004484.4(GPC3):c.415C>T (p.Pro139Ser)
NM_004484.4(GPC3):c.72G>A (p.Ala24=)
NM_004484.4(GPC3):c.762A>G (p.Arg254=)
NM_004484.4(GPC3):c.942T>C (p.Tyr314=)

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