Related gene-specific medical variations for Gene (Select 7490) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3470987	NM_024426.6(WT1):c.403C>T (p.Pro135Ser)	LOC107982234, WT1 (P135S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3470978	NM_024426.6(WT1):c.224G>A (p.Gly75Asp)	LOC107982234, WT1 (G2D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3390937	NM_024426.6(WT1):c.448_451del (p.Ser150fs)	LOC107982234, WT1 (S150fs +1 more)	Deletion (frameshift variant +1 more)	Leber congenital amaurosis 10	GPathogenic
Select item 3386212	NM_024426.6(WT1):c.13T>C (p.Leu5=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3386211	NM_024426.6(WT1):c.43C>T (p.Pro15Ser)	LOC107982234, WT1 (P10S +1 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3386210	NM_024426.6(WT1):c.165T>G (p.Ala55=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	GLikely benign
Select item 3386209	NM_024426.6(WT1):c.168A>G (p.Glu56=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	GLikely benign
Select item 3386208	NM_024426.6(WT1):c.287G>T (p.Gly96Val)	LOC107982234, WT1 (G23V +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3386207	NM_024426.6(WT1):c.344C>T (p.Pro115Leu)	LOC107982234, WT1 (P110L +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3386206	NM_024426.6(WT1):c.378C>T (p.Gly126=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 3386205	NM_024426.6(WT1):c.404C>G (p.Pro135Arg)	LOC107982234, WT1 (P130R +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3386204	NM_024426.6(WT1):c.410C>A (p.Pro137Gln)	LOC107982234, WT1 (P132Q +2 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3386203	NM_024426.6(WT1):c.591G>A (p.Gln197=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 3370888	NM_024426.6(WT1):c.373G>A (p.Gly125Ser)	LOC107982234, WT1 (G120S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3367494	NM_024426.6(WT1):c.190C>G (p.Arg64Gly)	LOC107982234, WT1 (R59G +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3359883	NM_024426.6(WT1):c.160A>C (p.Ser54Arg)	WT1 (S49R +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3343946	NM_024426.6(WT1):c.438A>T (p.Lys146Asn)	LOC107982234, WT1 (K141N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3343536	NM_024426.6(WT1):c.429C>A (p.Ser143=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 3255252	NM_024426.6(WT1):c.661+719G>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GBenign
Select item 3250365	NM_024426.6(WT1):c.662-1910G>T	LOC107982234, WT1	Single nucleotide variant (intron variant +1 more)	Nephrotic syndrome, type 4	GLikely benign
Select item 3248534	NM_024426.6(WT1):c.350del (p.Gly117fs)	LOC107982234, WT1 (G117fs)	Deletion (frameshift variant +1 more)	Wilms tumor 1	GPathogenic
Select item 3244691	NC_000011.9:g.(?_32410601)_(32414311_?)dup	WT1	Duplication	Wilms tumor 1 +3 more	GUncertain significance
Select item 3244689	NC_000011.9:g.(?_32410601)_(32421600_?)del	WT1	Deletion	Wilms tumor 1 +3 more	GPathogenic
Select item 3244688	NC_000011.9:g.(?_32421474)_(32439220_?)del	WT1	Deletion	Wilms tumor 1 +3 more	GPathogenic
Select item 3244687	NC_000011.9:g.(?_32449492)_(32450175_?)del	WT1	Deletion	Wilms tumor 1 +3 more	GPathogenic
Select item 3244685	NC_000011.9:g.(?_32438026)_(32438096_?)del	WT1	Deletion	Wilms tumor 1 +3 more	GUncertain significance
Select item 3240742	NM_024426.6(WT1):c.374G>A (p.Gly125Asp)	LOC107982234, WT1 (G120D +2 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome	GUncertain significance
Select item 3240741	NM_024426.6(WT1):c.1070C>T (p.Ala357Val)	WT1 (A103V +11 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome	GUncertain significance
Select item 3240740	NM_024426.6(WT1):c.779C>G (p.Ser260Trp)	WT1 (S187W +4 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome	GUncertain significance
Select item 3235157	NM_024426.6(WT1):c.434T>G (p.Ile145Ser)	LOC107982234, WT1 (I140S +2 more)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4	GUncertain significance
Select item 3075561	NM_024426.6(WT1):c.69_70del (p.Arg24fs)	LOC107982234, WT1 (R24fs)	Deletion (frameshift variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3075560	NM_024426.6(WT1):c.76_80del (p.Gly26fs)	LOC107982234, WT1 (G26fs)	Deletion (frameshift variant +1 more)	Wilms tumor 1	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 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 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 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 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 3073651	NM_024426.6(WT1):c.7T>G (p.Phe3Val)	LOC107982234, WT1 (F3V)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	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 3073049	NM_024426.6(WT1):c.65C>A (p.Thr22Lys)	LOC107982234, WT1 (T17K +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
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 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 3072554	NM_024426.6(WT1):c.79C>T (p.Pro27Ser)	LOC107982234, WT1 (P22S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
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 3072299	NM_024426.6(WT1):c.25C>G (p.Pro9Ala)	LOC107982234, WT1 (P4A +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
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 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 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 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 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 3071422	NM_024426.6(WT1):c.66G>C (p.Thr22=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
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 3071228	NM_024426.6(WT1):c.49C>A (p.Pro17Thr)	LOC107982234, WT1 (P12T +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	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 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 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 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 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 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 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 3042901	NM_024426.6(WT1):c.390A>C (p.Pro130=)	LOC107982234, WT1	Single nucleotide variant (non-coding transcript variant +1 more)	WT1-related disorder	GLikely benign
Select item 3026662	NM_024426.6(WT1):c.232G>T (p.Val78Leu)	LOC107982234, WT1 (V73L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2953840	NM_024426.6(WT1):c.422C>T (p.Pro141Leu)	LOC107982234, WT1 (P136L +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +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 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 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 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 2951591	NM_024426.6(WT1):c.196del (p.Ala66fs)	LOC107982234, WT1 (A66fs)	Deletion (frameshift variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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 2949881	NM_024426.6(WT1):c.661+17G>T	LOC107982234, WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2948439	NM_024426.6(WT1):c.338T>C (p.Phe113Ser)	LOC107982234, WT1 (F108S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2948304	NM_024426.6(WT1):c.648_654dup (p.Asn219fs)	LOC107982234, WT1 (N219fs)	Duplication (frameshift variant +1 more)	Wilms tumor 1 +3 more	GPathogenic
Select item 2948258	NM_024426.6(WT1):c.661+11C>A	LOC107982234, WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2947644	NM_024426.6(WT1):c.389C>T (p.Pro130Leu)	LOC107982234, WT1 (P130L +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GLikely benign
Select item 2945795	NM_024426.6(WT1):c.98C>A (p.Pro33Gln)	LOC107982234, WT1 (P33Q +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GLikely benign
Select item 2944949	NM_024426.6(WT1):c.275dup (p.Gly93fs)	LOC107982234, WT1 (G93fs)	Duplication (frameshift variant +1 more)	Wilms tumor 1 +3 more	GPathogenic
Select item 2944909	NM_024426.6(WT1):c.225del (p.Ser76fs)	LOC107982234, WT1 (S76fs)	Deletion (frameshift variant +1 more)	Wilms tumor 1 +3 more	GPathogenic
Select item 2944476	NM_024426.6(WT1):c.533G>A (p.Gly178Glu)	LOC107982234, WT1 (G178E +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2943297	NM_024426.6(WT1):c.244A>G (p.Asn82Asp)	LOC107982234, WT1 (N77D +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance

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