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 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	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)	Wilms tumor 1	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 (synonymous variant +1 more)	WT1-related condition	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)	Drash 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)	Drash 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)	Drash syndrome +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)	Wilms tumor 1 +3 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
Select item 2941224	NM_024426.6(WT1):c.624C>T (p.Pro208=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2939977	NM_024426.6(WT1):c.423T>G (p.Pro141=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2938948	NM_024426.6(WT1):c.511G>C (p.Gly171Arg)	LOC107982234, WT1 (G166R +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2938890	NM_024426.6(WT1):c.567G>A (p.Pro189=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2937904	NM_024426.6(WT1):c.654C>T (p.Arg218=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2937658	NM_024426.6(WT1):c.489C>G (p.Ser163Arg)	LOC107982234, WT1 (S158R +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2937351	NM_024426.6(WT1):c.398C>A (p.Pro133Gln)	LOC107982234, WT1 (P133Q +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2936526	NM_024426.6(WT1):c.53C>A (p.Ala18Glu)	LOC107982234, WT1 (A18E +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2935986	NM_024426.6(WT1):c.265C>A (p.Pro89Thr)	LOC107982234, WT1 (P84T +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2935870	NM_024426.6(WT1):c.36G>C (p.Thr12=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2935852	NM_024426.6(WT1):c.246C>A (p.Asn82Lys)	LOC107982234, WT1 (N77K +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2935563	NM_024426.6(WT1):c.247_248delinsCT (p.Ala83Leu)	LOC107982234, WT1 (A83L +1 more)	Indel (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2935406	NM_024426.6(WT1):c.28G>A (p.Ala10Thr)	LOC107982234, WT1 (A10T +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2935359	NM_024426.6(WT1):c.519C>A (p.Phe173Leu)	LOC107982234, WT1 (F173L +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2935211	NM_024426.6(WT1):c.640C>T (p.Gln214Ter)	LOC107982234, WT1 (Q209* +1 more)	Single nucleotide variant (nonsense +1 more)	Wilms tumor 1 +3 more	GPathogenic
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 2932914	NM_024426.6(WT1):c.347C>G (p.Pro116Arg)	LOC107982234, WT1 (P111R +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2932719	NM_024426.6(WT1):c.578C>T (p.Ala193Val)	LOC107982234, WT1 (A188V +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2932463	NM_024426.6(WT1):c.661+12G>C	LOC107982234, WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +3 more	GLikely benign
Select item 2931972	NM_024426.6(WT1):c.529G>T (p.Ala177Ser)	LOC107982234, WT1 (A172S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2931534	NM_024426.6(WT1):c.325C>G (p.Pro109Ala)	LOC107982234, WT1 (P104A +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2930851	NM_024426.6(WT1):c.395C>G (p.Ala132Gly)	LOC107982234, WT1 (A127G +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2930682	NM_024426.6(WT1):c.17T>C (p.Leu6Pro)	LOC107982234, WT1 (L6P +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2930681	NM_024426.6(WT1):c.126C>A (p.Gly42=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2930680	NM_024426.6(WT1):c.127G>A (p.Gly43Ser)	LOC107982234, WT1 (G38S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2930426	NM_024426.6(WT1):c.497C>G (p.Thr166Ser)	LOC107982234, WT1 (T166S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2930097	NM_024426.6(WT1):c.481T>G (p.Cys161Gly)	LOC107982234, WT1 (C156G +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance

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