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

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 26

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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.1068A>G (p.Gln356=)	rs372212269
NM_004484.3(GPC3):c.1114G>A (p.Val372Ile)	rs140756498
NM_004484.3(GPC3):c.1131T>C (p.His377=)	rs367679653
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.1275A>G (p.Gly425=)	rs749258552
NM_004484.3(GPC3):c.1293-5T>C	rs766154973
NM_004484.3(GPC3):c.1296C>T (p.Tyr432=)	rs946461494
NM_004484.3(GPC3):c.1398G>A (p.Leu466=)	rs745968470
NM_004484.3(GPC3):c.1494C>T (p.Cys498=)	rs753210097
NM_004484.3(GPC3):c.1573+10T>A	rs878854706
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.171G>A (p.Val57=)	rs398124166
NM_004484.3(GPC3):c.1737G>A (p.Val579=)	rs1556111517
NM_004484.3(GPC3):c.175+9G>A	rs776234359
NM_004484.3(GPC3):c.249A>G (p.Leu83=)	rs755510528
NM_004484.3(GPC3):c.337+8C>G	rs1556359306
NM_004484.3(GPC3):c.338-4A>T	rs1490568896
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

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