ClinVar for OMIM (Select 194070) - 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 3075351	NM_024426.6(WT1):c.1096G>A (p.Val366Ile)	WT1 (V112I +11 more)	Single nucleotide variant (missense variant +2 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 3074944	NM_024426.6(WT1):c.1419C>G (p.Thr473=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	GLikely benign
Select item 3074942	NM_024426.6(WT1):c.*2G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3074927	NM_024426.6(WT1):c.795G>C (p.Gln265His)	WT1 (Q11H +5 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3074617	NM_024426.6(WT1):c.966-9C>G	WT1	Single nucleotide variant (intron variant)	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 3074219	NM_024426.6(WT1):c.803T>C (p.Val268Ala)	WT1 (V14A +5 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3074174	NM_024426.6(WT1):c.662-14C>T	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1	GLikely benign
Select item 3074169	NM_024426.6(WT1):c.675C>A (p.Val225=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Wilms tumor 1	GLikely benign
Select item 3074163	NM_024426.6(WT1):c.966-11T>C	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1	GLikely benign
Select item 3074162	NM_024426.6(WT1):c.1026A>C (p.Thr342=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	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	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 3073451	NM_024426.6(WT1):c.801G>C (p.Ser267=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
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 3072850	NM_024426.6(WT1):c.777C>G (p.Gly259=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	GLikely benign
Select item 3072694	NM_024426.6(WT1):c.1345A>G (p.Arg449Gly)	WT1 (R195G +12 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3072683	NM_024426.6(WT1):c.*3G>A	WT1	Single nucleotide variant (3 prime UTR 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 3072297	NM_024426.6(WT1):c.737A>G (p.Asn246Ser)	WT1 (N173S +3 more)	Single nucleotide variant (missense variant +3 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 3072226	NM_024426.6(WT1):c.832C>T (p.Pro278Ser)	WT1 (P205S +5 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 3072067	NM_024426.6(WT1):c.792G>A (p.Gln264=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1	GLikely benign
Select item 3071936	NM_024426.6(WT1):c.991G>A (p.Val331Met)	WT1 (V114M +5 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3071858	NM_024426.6(WT1):c.671C>A (p.Thr224Lys)	WT1 (T151K +3 more)	Single nucleotide variant (missense variant +3 more)	Wilms tumor 1	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 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 3071539	NM_024426.6(WT1):c.1086C>A (p.His362Gln)	WT1 (H108Q +11 more)	Single nucleotide variant (missense variant +2 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 3071239	NM_024426.6(WT1):c.887+5del	WT1	Deletion (intron variant)	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 3071216	NM_024426.6(WT1):c.941T>C (p.Met314Thr)	WT1 (M241T +5 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 3069983	NM_024426.6(WT1):c.723G>A (p.Ala241=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Wilms tumor 1	GLikely benign
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 3069639	NM_024426.6(WT1):c.1031A>T (p.Tyr344Phe)	WT1 (Y110F +11 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	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 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 3069301	NM_024426.6(WT1):c.796T>C (p.Tyr266His)	WT1 (Y12H +5 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3024046	NM_004484.4(GPC3):c.257G>T (p.Arg86Leu)	GPC3 (R86L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3017013	NM_004484.4(GPC3):c.1735G>A (p.Val579Met)	GPC3 (V525M +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 3016463	NM_004484.4(GPC3):c.1236T>C (p.His412=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1	GBenign
Select item 3015056	NM_004484.4(GPC3):c.382G>A (p.Ala128Thr)	GPC3 (A112T +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 3011320	NM_004484.4(GPC3):c.1679C>T (p.Ser560Phe)	GPC3 (S560F +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 3007290	NM_004484.4(GPC3):c.175+7A>C	GPC3	Single nucleotide variant (intron variant)	Wilms tumor 1	GLikely benign
Select item 3005131	NM_004484.4(GPC3):c.1488A>G (p.Gly496=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1	GLikely benign
Select item 3001238	NM_004484.4(GPC3):c.504T>C (p.Asn168=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1	GLikely benign
Select item 2999702	NM_004484.4(GPC3):c.752A>T (p.Asp251Val)	GPC3 (D235V +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 2994303	NM_004484.4(GPC3):c.1293A>G (p.Arg431=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1	GUncertain significance
Select item 2989977	NM_004484.4(GPC3):c.652C>A (p.Gln218Lys)	GPC3 (Q164K +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 2989250	NM_004484.4(GPC3):c.1292+17G>T	GPC3	Single nucleotide variant (intron variant)	Wilms tumor 1	GLikely benign
Select item 2988110	NM_004484.4(GPC3):c.1401G>A (p.Lys467=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1	GLikely benign
Select item 2975308	NM_004484.4(GPC3):c.937A>G (p.Ile313Val)	GPC3 (I313V +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 2975233	NM_004484.4(GPC3):c.116G>T (p.Arg39Leu)	GPC3 (R39L)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 2971581	NM_004484.4(GPC3):c.790T>A (p.Tyr264Asn)	GPC3 (Y248N +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 2963861	NM_004484.4(GPC3):c.281A>G (p.Gln94Arg)	GPC3 (Q94R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 2960833	NM_004484.4(GPC3):c.1573+5C>T	GPC3	Single nucleotide variant (intron variant)	Wilms tumor 1	GUncertain significance
Select item 2956497	NM_004484.4(GPC3):c.290G>A (p.Ser97Asn)	GPC3 (S97N)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 2954056	NM_024426.6(WT1):c.965+2T>C	WT1	Single nucleotide variant (non-coding transcript variant +1 more)	Drash 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)	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 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)	11p partial monosomy syndrome +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)	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 2951175	NM_024426.6(WT1):c.1173T>A (p.Ser391Arg)	WT1 (S333R +9 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2950764	NM_024426.6(WT1):c.1518C>G (p.Arg506=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +3 more	GLikely benign
Select item 2950763	NM_024426.6(WT1):c.1519del (p.His507fs)	WT1 (H111fs +13 more)	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)	11p partial monosomy syndrome +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)	Wilms tumor 1 +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)	Wilms tumor 1 +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)	Wilms tumor 1 +3 more	GUncertain significance

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