ClinVar for MedGen (Select 64512) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3244691	NC_000011.9:g.(?_32410601)_(32414311_?)dup	WT1	Duplication	Drash syndrome +3 more	GUncertain significance
Select item 3244690	NC_000011.9:g.(?_32456236)_(32460464_?)dup	WT1, WT1-AS	Duplication	Drash syndrome +3 more	GUncertain significance
Select item 3244689	NC_000011.9:g.(?_32410601)_(32421600_?)del	WT1	Deletion	Drash syndrome +3 more	GPathogenic
Select item 3244688	NC_000011.9:g.(?_32421474)_(32439220_?)del	WT1	Deletion	Drash syndrome +3 more	GPathogenic
Select item 3244687	NC_000011.9:g.(?_32449492)_(32450175_?)del	WT1	Deletion	Drash syndrome +3 more	GPathogenic
Select item 3244686	NC_000011.9:g.(?_32438026)_(32460464_?)del	WT1, WT1-AS	Deletion	Drash syndrome +3 more	GPathogenic
Select item 3244685	NC_000011.9:g.(?_32438026)_(32438096_?)del	WT1	Deletion	Drash syndrome +3 more	GUncertain significance
Select item 2954056	NM_024426.6(WT1):c.965+2T>C	WT1	Single nucleotide variant (non-coding transcript variant +1 more)	Frasier syndrome +3 more	GLikely pathogenic
Select item 2953840	NM_024426.6(WT1):c.422C>T (p.Pro141Leu)	LOC107982234, WT1 (P136L +1 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +3 more	GUncertain significance
Select item 2953812	NM_024426.6(WT1):c.447G>A (p.Pro149=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +3 more	GLikely benign
Select item 2953624	NM_024426.6(WT1):c.370T>C (p.Leu124=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2953324	NM_024426.6(WT1):c.1374del (p.Gln457_Cys458insTer)	WT1	Deletion (nonsense +3 more)	Wilms tumor 1 +3 more	GPathogenic
Select item 2952581	NM_024426.6(WT1):c.1505A>G (p.Asp502Gly)	WT1 (D106G +14 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2952507	NM_024426.6(WT1):c.887+17C>T	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +3 more	GLikely benign
Select item 2952389	NM_024426.6(WT1):c.405_413dup (p.Pro141_His142insProProPro)	LOC107982234, WT1	Duplication (inframe_insertion +2 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2952267	NM_024426.6(WT1):c.705C>T (p.His235=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2952265	NM_024426.6(WT1):c.834del (p.Thr279fs)	WT1 (T279fs +3 more)	Deletion (frameshift variant +1 more)	Wilms tumor 1 +3 more	GPathogenic
Select item 2952202	NM_024426.6(WT1):c.356C>T (p.Ser119Leu)	LOC107982234, WT1 (S119L +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2952168	NM_024426.6(WT1):c.887+15_887+16delinsAA	WT1	Indel (intron variant)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2952161	NM_024426.6(WT1):c.1289T>G (p.Phe430Cys)	WT1 (F196C +10 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2951912	NM_024426.6(WT1):c.557G>A (p.Gly186Asp)	LOC107982234, WT1 (G186D +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
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 2951606	NM_024426.6(WT1):c.869T>G (p.Leu290Arg)	WT1 (L290R +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2951591	NM_024426.6(WT1):c.196del (p.Ala66fs)	LOC107982234, WT1 (A66fs)	Deletion (frameshift variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2951175	NM_024426.6(WT1):c.1173T>A (p.Ser391Arg)	WT1 (S333R +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950764	NM_024426.6(WT1):c.1518C>G (p.Arg506=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2950763	NM_024426.6(WT1):c.1519del (p.His507fs)	WT1 (H111fs +13 more)	Deletion (frameshift variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950552	NM_024426.6(WT1):c.598A>G (p.Met200Val)	LOC107982234, WT1 (M195V +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950385	NM_024426.6(WT1):c.117G>T (p.Arg39=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2950348	NM_024426.6(WT1):c.91C>G (p.Gln31Glu)	LOC107982234, WT1 (Q26E +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2950194	NM_024426.6(WT1):c.1049C>G (p.Thr350Arg)	WT1 (T116R +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950151	NM_024426.6(WT1):c.799T>G (p.Ser267Ala)	WT1 (S267A +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950081	NM_024426.6(WT1):c.1016A>G (p.Asn339Ser)	WT1 (N122S +4 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950079	NM_024426.6(WT1):c.1513G>A (p.Val505Ile)	WT1 (V474I +14 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2950018	NM_024426.6(WT1):c.758A>T (p.Asp253Val)	WT1 (D36V +2 more)	Single nucleotide variant (missense variant +3 more)	Drash syndrome +3 more	GUncertain significance
Select item 2949881	NM_024426.6(WT1):c.661+17G>T	LOC107982234, WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2949798	NM_024426.6(WT1):c.506T>C (p.Phe169Ser)	LOC107982234, WT1 (F164S +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2949440	NM_024426.6(WT1):c.1029del (p.Tyr344fs)	WT1 (Y110fs +7 more)	Deletion (frameshift variant +2 more)	Drash syndrome +3 more	GPathogenic
Select item 2949114	NM_024426.6(WT1):c.1016+15C>A	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2949086	NM_024426.6(WT1):c.1428G>A (p.Arg476=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Drash syndrome +3 more	GLikely benign
Select item 2948604	NM_024426.6(WT1):c.965+20A>G	WT1	Single nucleotide variant (non-coding transcript variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2948439	NM_024426.6(WT1):c.338T>C (p.Phe113Ser)	LOC107982234, WT1 (F108S +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2948393	NM_024426.6(WT1):c.23A>T (p.Asp8Val)	LOC107982234, WT1 (D8V +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2948348	NM_024426.6(WT1):c.836C>T (p.Thr279Ile)	WT1 (T274I +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2948304	NM_024426.6(WT1):c.648_654dup (p.Asn219fs)	LOC107982234, WT1 (N219fs)	Duplication (frameshift variant +1 more)	Drash syndrome +3 more	GPathogenic
Select item 2948258	NM_024426.6(WT1):c.661+11C>A	LOC107982234, WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2948230	NM_024426.6(WT1):c.964G>A (p.Gly322Arg)	WT1 (G105R +8 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2948028	NM_024426.6(WT1):c.1113+10C>T	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2947926	NM_024426.6(WT1):c.325C>T (p.Pro109Ser)	LOC107982234, WT1 (P104S +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2947909	NM_024426.6(WT1):c.49C>T (p.Pro17Ser)	LOC107982234, WT1 (P17S +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2947859	NM_024426.6(WT1):c.1016+7G>A	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2947644	NM_024426.6(WT1):c.389C>T (p.Pro130Leu)	LOC107982234, WT1 (P130L +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2947403	NM_024426.6(WT1):c.729G>A (p.Gln243=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Drash syndrome +3 more	GLikely benign
Select item 2947139	NM_024426.6(WT1):c.1126G>A (p.Val376Met)	WT1 (V142M +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2947117	NM_024426.6(WT1):c.939G>A (p.Gln313=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2946974	NM_024426.6(WT1):c.941T>G (p.Met314Arg)	WT1 (M309R +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2946654	NM_024426.6(WT1):c.908C>T (p.Thr303Ile)	WT1 (T303I +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2946545	NM_024426.6(WT1):c.812C>A (p.Pro271Gln)	WT1 (P230Q +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2946394	NM_024426.6(WT1):c.246C>G (p.Asn82Lys)	LOC107982234, WT1 (N77K +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2946326	NM_024426.6(WT1):c.332T>C (p.Leu111Pro)	LOC107982234, WT1 (L106P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 2946069	NM_024426.6(WT1):c.546C>T (p.Tyr182=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2945965	NM_024426.6(WT1):c.1163C>G (p.Ser388Cys)	WT1 (S154C +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2945795	NM_024426.6(WT1):c.98C>A (p.Pro33Gln)	LOC107982234, WT1 (P33Q +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2945688	NM_024426.6(WT1):c.383C>A (p.Ala128Glu)	LOC107982234, WT1 (A128E +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2945282	NM_024426.6(WT1):c.570C>T (p.Pro190=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2945253	NM_024426.6(WT1):c.1017-20dup	WT1	Duplication (intron variant)	Drash syndrome +3 more	GBenign
Select item 2944949	NM_024426.6(WT1):c.275dup (p.Gly93fs)	LOC107982234, WT1 (G93fs)	Duplication (frameshift variant +1 more)	Drash syndrome +3 more	GPathogenic
Select item 2944909	NM_024426.6(WT1):c.225del (p.Ser76fs)	LOC107982234, WT1 (S76fs)	Deletion (frameshift variant +1 more)	Drash syndrome +3 more	GPathogenic
Select item 2944567	NM_024426.6(WT1):c.784G>T (p.Gly262Cys)	WT1 (G257C +3 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2944556	NM_024426.6(WT1):c.689C>A (p.Thr230Lys)	WT1 (T13K +2 more)	Single nucleotide variant (missense variant +3 more)	Drash syndrome +3 more	GUncertain significance
Select item 2944476	NM_024426.6(WT1):c.533G>A (p.Gly178Glu)	LOC107982234, WT1 (G178E +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2943881	NM_024426.6(WT1):c.1293G>A (p.Lys431=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Drash syndrome +3 more	GLikely benign
Select item 2943738	NM_024426.6(WT1):c.1354+20A>G	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2943604	NM_024426.6(WT1):c.1264+15T>C	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2943564	NM_024426.6(WT1):c.1563G>C (p.Ala521=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2943460	NM_024426.6(WT1):c.1448-13A>G	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +3 more	GConflicting classifications of pathogenicity
Select item 2943297	NM_024426.6(WT1):c.244A>G (p.Asn82Asp)	LOC107982234, WT1 (N77D +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2943129	NM_024426.6(WT1):c.723G>C (p.Ala241=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Drash syndrome +3 more	GLikely benign
Select item 2942867	NM_024426.6(WT1):c.698A>G (p.Tyr233Cys)	WT1 (Y16C +2 more)	Single nucleotide variant (missense variant +3 more)	not provided +4 more	GUncertain significance
Select item 2942720	NM_024426.6(WT1):c.338T>A (p.Phe113Tyr)	LOC107982234, WT1 (F113Y +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2942653	NM_024426.6(WT1):c.119A>C (p.Asp40Ala)	LOC107982234, WT1 (D35A +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2942338	NM_024426.6(WT1):c.930C>G (p.Thr310=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2942260	NM_024426.6(WT1):c.976G>C (p.Gly326Arg)	WT1 (G72R +4 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2942040	NM_024426.6(WT1):c.449G>T (p.Ser150Ile)	LOC107982234, WT1 (S150I +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2941960	NM_024426.6(WT1):c.357G>T (p.Ser119=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2941724	NM_024426.6(WT1):c.70C>A (p.Arg24Ser)	LOC107982234, WT1 (R19S +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2941479	NM_024426.6(WT1):c.143T>G (p.Leu48Ter)	LOC107982234, WT1 (L43* +1 more)	Single nucleotide variant (nonsense +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2941440	NM_024426.6(WT1):c.532G>A (p.Gly178Arg)	LOC107982234, WT1 (G173R +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2941308	NM_024426.6(WT1):c.1249A>G (p.Ser417Gly)	WT1 (S359G +10 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2941271	NM_024426.6(WT1):c.181_182delinsTA (p.Arg61Ter)	LOC107982234, WT1 (R56* +1 more)	Indel (nonsense +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2941224	NM_024426.6(WT1):c.624C>T (p.Pro208=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2941174	NM_024426.6(WT1):c.1016+20A>G	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2940962	NM_024426.6(WT1):c.539G>A (p.Cys180Tyr)	LOC107982234, WT1 (C180Y +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2940785	NM_024426.6(WT1):c.110G>A (p.Gly37Glu)	LOC107982234, WT1 (G32E +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2940696	NM_024426.6(WT1):c.1157C>T (p.Ser386Leu)	WT1 (S364L +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2940054	NM_024426.6(WT1):c.1448-19C>A	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2939977	NM_024426.6(WT1):c.423T>G (p.Pro141=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +3 more	GLikely benign
Select item 2939890	NM_024426.6(WT1):c.1355-10G>A	WT1	Single nucleotide variant (intron variant)	Drash syndrome +3 more	GLikely benign
Select item 2939595	NM_024426.6(WT1):c.553T>G (p.Phe185Val)	LOC107982234, WT1 (F185V +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2939570	NM_024426.6(WT1):c.1379C>T (p.Thr460Ile)	WT1 (T206I +11 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance

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