"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 654381	NM_024426.6(WT1):c.658C>A (p.Gln220Lys)	LOC107982234, WT1 (Q220K)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +8 more	GUncertain significance
Select item 961780	NM_024426.6(WT1):c.653G>A (p.Arg218His)	LOC107982234, WT1 (R218H)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GUncertain significance
Select item 406691	NM_024426.6(WT1):c.653G>T (p.Arg218Leu)	LOC107982234, WT1 (R218L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 3073170	NM_024426.6(WT1):c.651T>C (p.Ile217=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 1039612	NM_024426.6(WT1):c.650T>G (p.Ile217Ser)	LOC107982234, WT1 (I217S)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1009159	NM_024426.6(WT1):c.649A>C (p.Ile217Leu)	LOC107982234, WT1 (I217L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 577219	NM_024426.6(WT1):c.641A>C (p.Gln214Pro)	LOC107982234, WT1 (Q214P)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 721318	NM_024426.6(WT1):c.627C>T (p.Ser209=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 414083	NM_024426.6(WT1):c.619C>T (p.Leu207=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 3073006	NM_024426.6(WT1):c.592G>T (p.Ala198Ser)	LOC107982234, WT1 (A125S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 940567	NM_024426.6(WT1):c.590A>G (p.Gln197Arg)	LOC107982234, WT1 (Q197R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 543154	NM_024426.6(WT1):c.585C>T (p.Ser195=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 406700	NM_024426.6(WT1):c.584C>G (p.Ser195Cys)	LOC107982234, WT1 (S195C)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1562460	NM_024426.6(WT1):c.579G>A (p.Ala193=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2932719	NM_024426.6(WT1):c.578C>T (p.Ala193Val)	LOC107982234, WT1 (A188V +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 806643	NM_024426.6(WT1):c.577G>A (p.Ala193Thr)	LOC107982234, WT1 (A193T)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 1000097	NM_024426.6(WT1):c.575A>G (p.Gln192Arg)	LOC107982234, WT1 (Q192R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 414074	NM_024426.6(WT1):c.564T>A (p.Pro188=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 1133055	NM_024426.6(WT1):c.549G>A (p.Gly183=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 934778	NM_024426.6(WT1):c.547G>C (p.Gly183Arg)	LOC107982234, WT1 (G183R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 241483	NM_024426.6(WT1):c.543C>T (p.Arg181=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +8 more	GBenign/Likely benign
Select item 3074982	NM_024426.6(WT1):c.522T>G (p.Thr174=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 1147854	NM_024426.6(WT1):c.510C>T (p.Ser170=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +3 more	GLikely benign
Select item 579939	NM_024426.6(WT1):c.480G>C (p.Gln160His)	LOC107982234, WT1 (Q160H)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GUncertain significance
Select item 543159	NM_024426.6(WT1):c.480G>A (p.Gln160=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 476706	NM_024426.6(WT1):c.475G>A (p.Glu159Lys)	LOC107982234, WT1 (E159K)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 1095994	NM_024426.6(WT1):c.471C>T (p.His157=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +3 more	GLikely benign
Select item 3071611	NM_024426.6(WT1):c.460G>A (p.Ala154Thr)	LOC107982234, WT1 (A149T +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 968290	NM_024426.6(WT1):c.448A>G (p.Ser150Gly)	LOC107982234, WT1 (S150G)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 3074259	NM_024426.6(WT1):c.440A>C (p.Gln147Pro)	LOC107982234, WT1 (Q142P +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 406695	NM_024426.6(WT1):c.439C>G (p.Gln147Glu)	LOC107982234, WT1 (Q147E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +9 more	GUncertain significance
Select item 3074353	NM_024426.6(WT1):c.436A>C (p.Lys146Gln)	LOC107982234, WT1 (K141Q +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 705924	NM_024426.6(WT1):c.432C>T (p.Phe144=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +3 more	GLikely benign
Select item 1091048	NM_024426.6(WT1):c.429C>T (p.Ser143=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 776098	NM_024426.6(WT1):c.429C>G (p.Ser143=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 3072227	NM_024426.6(WT1):c.412C>A (p.Pro138Thr)	LOC107982234, WT1 (P133T +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 836130	NM_024426.6(WT1):c.409C>G (p.Pro137Ala)	LOC107982234, WT1 (P137A)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +4 more	GUncertain significance
Select item 2923014	NM_024426.6(WT1):c.408C>T (p.Pro136=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 1983004	NM_024426.6(WT1):c.406C>T (p.Pro136Ser)	LOC107982234, WT1 (P131S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +4 more	GUncertain significance
Select item 406681	NM_024426.6(WT1):c.404C>T (p.Pro135Leu)	LOC107982234, WT1 (P135L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 3075104	NM_024426.6(WT1):c.401C>A (p.Pro134Gln)	LOC107982234, WT1 (P129Q +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 566443	NM_024426.6(WT1):c.397C>A (p.Pro133Thr)	LOC107982234, WT1 (P133T)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 584764	NM_024426.6(WT1):c.391C>T (p.Pro131Ser)	LOC107982234, WT1 (P131S)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 864016	NM_024426.6(WT1):c.382G>A (p.Ala128Thr)	LOC107982234, WT1 (A128T)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +3 more	GUncertain significance
Select item 658496	NM_024426.6(WT1):c.380C>G (p.Pro127Arg)	LOC107982234, WT1 (P127R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1981784	NM_024426.6(WT1):c.376G>C (p.Gly126Arg)	LOC107982234, WT1 (G121R +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2406757	NM_024426.6(WT1):c.367T>G (p.Ser123Ala)	LOC107982234, WT1 (S118A +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +1 more	GUncertain significance
Select item 700587	NM_024426.6(WT1):c.366G>A (p.Gly122=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +3 more	GLikely benign
Select item 1481650	NM_024426.6(WT1):c.363C>T (p.Tyr121=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 651615	NM_024426.6(WT1):c.358G>A (p.Ala120Thr)	LOC107982234, WT1 (A120T)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +4 more	GUncertain significance
Select item 836770	NM_024426.6(WT1):c.352G>C (p.Ala118Pro)	LOC107982234, WT1 (A118P)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1024394	NM_024426.6(WT1):c.350G>A (p.Gly117Asp)	LOC107982234, WT1 (G117D)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 304425	NM_024426.6(WT1):c.347C>T (p.Pro116Leu)	LOC107982234, WT1 (P116L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +6 more	GUncertain significance
Select item 570963	NM_024426.6(WT1):c.344C>A (p.Pro115His)	LOC107982234, WT1 (P115H)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 406698	NM_024426.6(WT1):c.343C>T (p.Pro115Ser)	LOC107982234, WT1 (P115S)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 3071774	NM_024426.6(WT1):c.328G>T (p.Val110Leu)	LOC107982234, WT1 (V105L +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3069980	NM_024426.6(WT1):c.327G>A (p.Pro109=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 1159790	NM_024426.6(WT1):c.327G>C (p.Pro109=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 662247	NM_024426.6(WT1):c.320G>T (p.Trp107Leu)	LOC107982234, WT1 (W107L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 3070834	NM_024426.6(WT1):c.318G>A (p.Gln106=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 759049	NM_024426.6(WT1):c.312G>A (p.Ala104=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 543132	NM_024426.6(WT1):c.307G>T (p.Gly103Cys)	LOC107982234, WT1 (G103C)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 839568	NM_024426.6(WT1):c.305G>A (p.Ser102Asn)	LOC107982234, WT1 (S102N)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1448032	NM_024426.6(WT1):c.277GGC[5] (p.Gly96dup)	LOC107982234, WT1	Microsatellite (inframe_insertion +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 3072223	NM_024426.6(WT1):c.288C>G (p.Gly96=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 3069445	NM_024426.6(WT1):c.287_288insGGA (p.Gly96_Cys97insAsp)	LOC107982234, WT1	Insertion (inframe_insertion +2 more)	Wilms tumor 1	GUncertain significance
Select item 406682	NM_024426.6(WT1):c.286G>A (p.Gly96Ser)	LOC107982234, WT1 (G96S)	Single nucleotide variant (missense variant +1 more)	WT1-related disorder +4 more	GUncertain significance
Select item 1359817	NM_024426.6(WT1):c.284G>T (p.Gly95Val)	LOC107982234, WT1 (G95V)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 3071613	NM_024426.6(WT1):c.275G>A (p.Gly92Asp)	LOC107982234, WT1 (G19D +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 949425	NM_024426.6(WT1):c.273G>A (p.Leu91=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 700917	NM_024426.6(WT1):c.267C>T (p.Pro89=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +3 more	GLikely benign
Select item 3070218	NM_024426.6(WT1):c.266C>G (p.Pro89Arg)	LOC107982234, WT1 (P16R +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 2928187	NM_024426.6(WT1):c.266C>T (p.Pro89Leu)	LOC107982234, WT1 (P84L +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1502337	NM_024426.6(WT1):c.262G>A (p.Val88Ile)	LOC107982234, WT1 (V88I)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2140947	NM_024426.6(WT1):c.261C>G (p.Ala87=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 715223	NM_024426.6(WT1):c.259G>A (p.Ala87Thr)	LOC107982234, WT1 (A87T)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2951766	NM_024426.6(WT1):c.254T>C (p.Leu85Pro)	LOC107982234, WT1 (L85P +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 476697	NM_024426.6(WT1):c.247G>C (p.Ala83Pro)	LOC107982234, WT1 (A83P)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1448791	NM_024426.6(WT1):c.240C>G (p.Asp80Glu)	LOC107982234, WT1 (D80E)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 3071291	NM_024426.6(WT1):c.239A>G (p.Asp80Gly)	LOC107982234, WT1 (D75G +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 2934745	NM_024426.6(WT1):c.237G>A (p.Arg79=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 3070741	NM_024426.6(WT1):c.228C>G (p.Ser76=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 3070809	NM_024426.6(WT1):c.220A>G (p.Met74Val)	LOC107982234, WT1 (M1V +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 476693	NM_024426.6(WT1):c.204G>A (p.Gly68=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 1155282	NM_024426.6(WT1):c.198G>T (p.Ala66=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2166037	NM_024426.6(WT1):c.197C>T (p.Ala66Val)	LOC107982234, WT1 (A61V +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 1044731	NM_024426.6(WT1):c.197C>A (p.Ala66Glu)	LOC107982234, WT1 (A66E)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +4 more	GUncertain significance
Select item 3072645	NM_024426.6(WT1):c.191G>T (p.Arg64Leu)	LOC107982234, WT1 (R59L +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 1057186	NM_024426.6(WT1):c.189C>A (p.Ser63Arg)	LOC107982234, WT1 (S63R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 733569	NM_024426.6(WT1):c.186G>A (p.Arg62=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 3073912	NM_024426.6(WT1):c.181C>G (p.Arg61Gly)	LOC107982234, WT1 (R56G +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +1 more	GUncertain significance
Select item 933960	NM_024426.6(WT1):c.170G>T (p.Arg57Leu)	LOC107982234, WT1 (R57L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1937697	NM_024426.6(WT1):c.163G>T (p.Ala55Ser)	LOC107982234, WT1 (A55S +1 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +3 more	GUncertain significance
Select item 304429	NM_024426.6(WT1):c.162C>G (p.Ser54Arg)	LOC107982234, WT1 (S54R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +6 more	GUncertain significance
Select item 543150	NM_024426.6(WT1):c.159C>T (p.Ala53=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 3072501	NM_024426.6(WT1):c.152C>A (p.Ala51Asp)	LOC107982234, WT1 (A46D +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 1008839	NM_024426.6(WT1):c.151G>A (p.Ala51Thr)	LOC107982234, WT1 (A51T)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 3069615	NM_024426.6(WT1):c.145G>A (p.Gly49Ser)	LOC107982234, WT1 (G44S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 571850	NM_024426.6(WT1):c.143T>C (p.Leu48Ser)	LOC107982234, WT1 (L48S)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 834611	NM_024426.6(WT1):c.133T>G (p.Trp45Gly)	LOC107982234, WT1 (W45G)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance

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