ClinVar 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 3470983	NM_024426.6(WT1):c.702T>C (p.Gly234=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Inborn genetic diseases	GLikely benign
Select item 3470982	NM_024426.6(WT1):c.812C>G (p.Pro271Arg)	WT1 (P198R +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3470980	NM_024426.6(WT1):c.785G>C (p.Gly262Ala)	WT1 (G189A +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3470979	NM_024426.6(WT1):c.971CTG[1] (p.Ala325del)	WT1 (A108del +5 more)	Microsatellite (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign
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 3391911	GRCh37/hg19 11p14.3-13(chr11:24192701-32455527)x1	ANO3, ARL14EP +23 more	Copy number loss	not provided	GPathogenic
Select item 3391910	GRCh37/hg19 11p14.3-12(chr11:22428384-37196643)x1	ABTB2, ANO3 +62 more	Copy number loss	not provided	GPathogenic
Select item 3391909	GRCh37/hg19 11p15.1-12(chr11:17120358-41424289)x1	ABCC8, ABTB2 +105 more	Copy number loss	not provided	GPathogenic
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 3390105	NM_024426.6(WT1):c.1295A>T (p.Asp432Val)	WT1 (D178V +11 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3389925	NM_024426.6(WT1):c.839_850del (p.Asp280_Thr283del)	WT1	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance
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 3386202	NM_024426.6(WT1):c.728A>C (p.Gln243Pro)	WT1 (Q170P +3 more)	Single nucleotide variant (missense variant +3 more)	Wilms tumor 1	GUncertain significance
Select item 3386201	NM_024426.6(WT1):c.785-4G>T	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1	GLikely benign
Select item 3386200	NM_024426.6(WT1):c.799T>C (p.Ser267Pro)	WT1 (S13P +5 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3386199	NM_024426.6(WT1):c.1024A>T (p.Thr342Ser)	WT1 (T108S +10 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3386198	NM_024426.6(WT1):c.1058T>A (p.Ile353Asn)	WT1 (I119N +10 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3386197	NM_024426.6(WT1):c.1080A>G (p.Arg360=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1	GLikely benign
Select item 3386196	NM_024426.6(WT1):c.1120_1122delinsTGG (p.Arg374Trp)	WT1 (R120W +10 more)	Indel (missense variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3386195	NM_024426.6(WT1):c.1123_1124del (p.Arg375fs)	WT1 (R121fs +9 more)	Deletion (frameshift variant +2 more)	Wilms tumor 1	GUncertain significance
Select item 3386194	NM_024426.6(WT1):c.1250G>A (p.Ser417Asn)	WT1 (S163N +11 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1	GUncertain significance
Select item 3386193	NM_024426.6(WT1):c.1355-6A>T	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1	GLikely benign
Select item 3377814	NM_024426.6(WT1):c.1426del (p.Arg476fs)	WT1 (R222fs +11 more)	Deletion (frameshift variant +2 more)	Wilms tumor 1	GLikely pathogenic
Select item 3377813	NC_000011.9:g.(?_32409321)_(32457085_?)del	WT1	Deletion	Wilms tumor 1	GPathogenic
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 3363871	NM_024426.6(WT1):c.1046A>C (p.His349Pro)	WT1 (H115P +10 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 3344917	NM_024426.6(WT1):c.1272_1273del (p.Lys424fs)	WT1 (K170fs +10 more)	Deletion (frameshift variant +2 more)	WT1-related disorder	GLikely pathogenic
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 3343604	NM_024426.6(WT1):c.1085A>G (p.His362Arg)	WT1 (H108R +10 more)	Single nucleotide variant (missense variant +2 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 3256922	NM_024426.6(WT1):c.1499G>T (p.Arg500Leu)	WT1 (R104L +13 more)	Single nucleotide variant (missense variant +1 more)	WT1-related disorder	GLikely pathogenic
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 3244690	NC_000011.9:g.(?_32456236)_(32460464_?)dup	WT1, WT1-AS	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 3244686	NC_000011.9:g.(?_32438026)_(32460464_?)del	WT1, WT1-AS	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 3235221	NM_024426.6(WT1):c.1403C>G (p.Ser468Cys)	WT1 (S214C +13 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4	GUncertain significance
Select item 3235191	NM_024426.6(WT1):c.1277A>G (p.Tyr426Cys)	WT1 (Y172C +12 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4	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 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 +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 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)	not provided +1 more	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

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