List of variants reported as benign for Wilms tumor by Invitae

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 100

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HGVS	dbSNP	gnomAD frequency
NM_004484.4(GPC3):c.1292+9706A>G	rs2205704	0.35691
NM_024426.6(WT1):c.213G>T (p.Pro71=)	rs2234582	0.31689
NM_024426.6(WT1):c.887+16G>A	rs1799933	0.26810
NM_024426.6(WT1):c.1122A>G (p.Arg374=)	rs16754	0.16617
NR_120546.1(WT1-AS):n.1873G>A	rs6508	0.16158
NM_024426.6(WT1):c.345C>T (p.Pro115=)	rs1799925	0.15374
NM_024426.6(WT1):c.609C>T (p.Asn203=)	rs2234583	0.13287
NM_004484.4(GPC3):c.1500T>C (p.Asp500=)	rs2314298	0.06746
NM_004484.4(GPC3):c.1626A>G (p.Ala542=)	rs61754631	0.05751
NM_024426.6(WT1):c.1074A>G (p.Gln358=)	rs2234590	0.04693
NM_004484.4(GPC3):c.204G>A (p.Lys68=)	rs61754632	0.01163
NM_024426.6(WT1):c.785-20G>T	rs5030168	0.00663
NM_024426.6(WT1):c.1114-9T>C	rs5030274	0.00465
NM_004484.4(GPC3):c.1285G>A (p.Val429Met)	rs11539789	0.00333
NM_004484.4(GPC3):c.1167-8T>C	rs182950534	0.00303
NM_024426.6(WT1):c.181C>A (p.Arg61=)	rs2234581	0.00270
NM_024426.6(WT1):c.309C>A (p.Gly103=)	rs547333427	0.00197
NM_024426.6(WT1):c.123G>C (p.Pro41=)	rs555140661	0.00188
NM_004484.4(GPC3):c.826G>A (p.Gly276Ser)	rs141100113	0.00082
NM_004484.4(GPC3):c.1032+9C>T	rs200782847	0.00069
NM_004484.4(GPC3):c.995A>G (p.Gln332Arg)	rs78696048	0.00065
NM_004484.4(GPC3):c.359G>A (p.Arg120His)	rs148021273	0.00052
NM_024426.6(WT1):c.1161A>G (p.Ala387=)	rs141834493	0.00051
NM_004484.4(GPC3):c.660C>T (p.Ser220=)	rs138450923	0.00050
NM_024426.6(WT1):c.1131T>C (p.Pro377=)	rs151034312	0.00047
NM_024426.6(WT1):c.375C>T (p.Gly125=)	rs776209354	0.00039
NM_024426.6(WT1):c.216G>T (p.Gln72His)	rs5030135	0.00036
NM_004484.4(GPC3):c.1254C>T (p.Asn418=)	rs150766741	0.00032
NM_024426.6(WT1):c.1182C>T (p.Arg394=)	rs147939483	0.00027
NM_004484.4(GPC3):c.876T>C (p.Ile292=)	rs61754633	0.00024
NM_024426.6(WT1):c.760C>T (p.Pro254Ser)	rs2234584	0.00022
NM_004484.4(GPC3):c.889A>G (p.Arg297Gly)	rs148951753	0.00019
NM_004484.4(GPC3):c.172C>T (p.Pro58Ser)	rs147231796	0.00014
NM_004484.4(GPC3):c.676A>G (p.Thr226Ala)	rs145141525	0.00014
NM_004484.4(GPC3):c.1033-18T>C	rs368015595	0.00013
NM_004484.4(GPC3):c.1631C>T (p.Pro544Leu)	rs375606908	0.00011
NM_004484.4(GPC3):c.1232G>T (p.Ser411Ile)	rs139206747	0.00010
NM_024426.6(WT1):c.381C>G (p.Pro127=)	rs771681406	0.00009
NM_004484.4(GPC3):c.1680C>T (p.Ser560=)	rs748480657	0.00008
NM_004484.4(GPC3):c.1716G>C (p.Val572=)	rs779688123	0.00008
NM_024426.6(WT1):c.887+14G>A	rs757237600	0.00008
NM_004484.4(GPC3):c.1149C>T (p.Thr383=)	rs147245792	0.00007
NM_024426.6(WT1):c.1017-9T>C	rs368486676	0.00007
NM_004484.4(GPC3):c.1287G>A (p.Val429=)	rs756598026	0.00006
NM_004484.4(GPC3):c.358C>T (p.Arg120Cys)	rs587778392	0.00006
NM_004484.4(GPC3):c.825C>T (p.Gly275=)	rs753811089	0.00006
NM_024426.6(WT1):c.696C>T (p.Ser232=)	rs9332974	0.00006
NM_024426.6(WT1):c.785G>A (p.Gly262Asp)	rs372225738	0.00006
NM_004484.4(GPC3):c.168C>G (p.Pro56=)	rs188592483	0.00005
NM_004484.4(GPC3):c.459T>G (p.Ser153=)	rs775459305	0.00005
NM_004484.4(GPC3):c.1160G>A (p.Arg387Gln)	rs145280221	0.00004
NM_004484.4(GPC3):c.1632G>A (p.Pro544=)	rs766482434	0.00004
NM_004484.4(GPC3):c.394A>G (p.Asn132Asp)	rs143561452	0.00004
NM_004484.4(GPC3):c.648G>C (p.Met216Ile)	rs752516966	0.00004
NM_004484.4(GPC3):c.972T>C (p.Phe324=)	rs183678432	0.00004
NM_024426.6(WT1):c.513C>A (p.Gly171=)	rs536728682	0.00004
NM_024426.6(WT1):c.965+14T>C	rs369920807	0.00004
NM_004484.4(GPC3):c.1398G>A (p.Leu466=)	rs745968470	0.00003
NM_004484.4(GPC3):c.1426A>G (p.Met476Val)	rs200265913	0.00003
NM_004484.4(GPC3):c.1573+20C>T	rs368998078	0.00003
NM_004484.4(GPC3):c.1616G>C (p.Ser539Thr)	rs137858712	0.00003
NM_004484.4(GPC3):c.175+9G>A	rs776234359	0.00003
NM_004484.4(GPC3):c.365C>T (p.Ala122Val)	rs779679730	0.00003
NM_004484.4(GPC3):c.1002C>T (p.Val334=)	rs747775536	0.00002
NM_004484.4(GPC3):c.1068A>G (p.Gln356=)	rs372212269	0.00002
NM_004484.4(GPC3):c.1131T>C (p.His377=)	rs367679653	0.00002
NM_004484.4(GPC3):c.1332G>A (p.Gln444=)	rs771847990	0.00002
NM_004484.4(GPC3):c.485A>G (p.Asn162Ser)	rs780431445	0.00002
NM_004484.4(GPC3):c.693G>A (p.Gln231=)	rs768782219	0.00002
NM_004484.4(GPC3):c.897C>T (p.Tyr299=)	rs200421668	0.00002
NM_004484.4(GPC3):c.1063C>T (p.Arg355Cys)	rs745700691	0.00001
NM_004484.4(GPC3):c.1162A>G (p.Arg388Gly)	rs199812705	0.00001
NM_004484.4(GPC3):c.1248G>A (p.Ala416=)	rs201677091	0.00001
NM_004484.4(GPC3):c.1275A>G (p.Gly425=)	rs749258552	0.00001
NM_004484.4(GPC3):c.1318G>A (p.Gly440Arg)	rs1203009272	0.00001
NM_004484.4(GPC3):c.1641C>T (p.Asn547=)	rs772217919	0.00001
NM_004484.4(GPC3):c.1683G>A (p.Pro561=)	rs1302862383	0.00001
NM_004484.4(GPC3):c.171G>A (p.Val57=)	rs398124166	0.00001
NM_004484.4(GPC3):c.327G>A (p.Ala109=)	rs1466168469	0.00001
NM_004484.4(GPC3):c.384C>T (p.Ala128=)	rs761541528	0.00001
NM_004484.4(GPC3):c.392A>G (p.Lys131Arg)	rs751302717	0.00001
NM_004484.4(GPC3):c.584A>G (p.Asn195Ser)	rs745317547	0.00001
NM_004484.4(GPC3):c.844A>G (p.Met282Val)	rs151082475	0.00001
NM_004484.4(GPC3):c.924T>A (p.Asn308Lys)	rs368928269	0.00001
NM_004484.4(GPC3):c.1029C>T (p.Thr343=)	rs890143711
NM_004484.4(GPC3):c.1167-3del	rs2124430989
NM_004484.4(GPC3):c.1236T>C (p.His412=)
NM_004484.4(GPC3):c.1574-11T>C
NM_004484.4(GPC3):c.1574-7_1574-4del	rs751413609
NM_004484.4(GPC3):c.251C>T (p.Thr84Ile)	rs2076400566
NM_004484.4(GPC3):c.326C>T (p.Ala109Val)	rs761660909
NM_004484.4(GPC3):c.338-20dup	rs370737647
NM_004484.4(GPC3):c.338-5del	rs370737647
NM_004484.4(GPC3):c.79CCG[6] (p.Pro31dup)	rs749104500
NM_024426.6(WT1):c.1017-20dup
NM_024426.6(WT1):c.1122A>C (p.Arg374=)	rs16754
NM_024426.6(WT1):c.1448-10G>A	rs185744719
NM_024426.6(WT1):c.543C>T (p.Arg181=)	rs369870529
NM_024426.6(WT1):c.695G>C (p.Ser232Thr)	rs761913397
NM_024426.6(WT1):c.888-8dup

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