"Illumina Laboratory Services, Illumina"[submitter] AND "WT1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 304370	NM_024426.6(WT1):c.*1239T>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304371	NM_024426.6(WT1):c.*1225T>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304372	NM_024426.6(WT1):c.*1209A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304373	NM_024426.6(WT1):c.*1167T>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304374	NM_024426.6(WT1):c.*1132A>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304375	NM_024426.6(WT1):c.*1098C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 879412	NM_024426.6(WT1):c.*1066T>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 304376	NM_024426.6(WT1):c.*1058G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304380	NM_024426.6(WT1):c.*1021GT[18]	WT1	Microsatellite (3 prime UTR variant +1 more)	Nephroblastoma +3 more	GUncertain significance
Select item 304378	NM_024426.6(WT1):c.*1021GT[20]	WT1	Microsatellite (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304377	NM_024426.6(WT1):c.*1021GT[19]	WT1	Microsatellite (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304381	NM_024426.6(WT1):c.*1021GT[14]	WT1	Microsatellite (3 prime UTR variant +1 more)	Nephroblastoma +3 more	GUncertain significance
Select item 304379	NM_024426.6(WT1):c.*1021GT[15]	WT1	Microsatellite (3 prime UTR variant +1 more)	Meacham syndrome +3 more	GUncertain significance
Select item 304382	NM_024426.6(WT1):c.*1049del	WT1	Deletion (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign
Select item 304383	NM_024426.6(WT1):c.*978dup	WT1	Duplication (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign
Select item 304384	NM_024426.6(WT1):c.*903G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304385	NM_024426.6(WT1):c.*897G>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephroblastoma +3 more	GLikely benign
Select item 304387	NM_024426.6(WT1):c.*864T>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304386	NM_024426.6(WT1):c.*864T>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304388	NM_024426.6(WT1):c.*841C>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304389	NM_024426.6(WT1):c.*835A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign/Likely benign
Select item 304390	NM_024426.6(WT1):c.*820G>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GBenign
Select item 304391	NM_024426.6(WT1):c.*785C>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304392	NM_024426.6(WT1):c.*768A>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304393	NM_024426.6(WT1):c.*741G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304394	NM_024426.6(WT1):c.*707C>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +3 more	GUncertain significance
Select item 304395	NM_024426.6(WT1):c.*685G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +3 more	GUncertain significance
Select item 304396	NM_024426.6(WT1):c.*666A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 878010	NM_024426.6(WT1):c.*629T>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304397	NM_024426.6(WT1):c.*614A>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304398	NM_024426.6(WT1):c.*611C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GUncertain significance
Select item 304399	NM_024426.6(WT1):c.*602A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GBenign
Select item 304400	NM_024426.6(WT1):c.*574del	WT1	Deletion (3 prime UTR variant +1 more)	Meacham syndrome +3 more	GUncertain significance
Select item 304401	NM_024426.6(WT1):c.*542G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephroblastoma +3 more	GLikely benign
Select item 304402	NM_024426.6(WT1):c.*534C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +3 more	GConflicting classifications of pathogenicity
Select item 304403	NM_024426.6(WT1):c.*513C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 304404	NM_024426.6(WT1):c.*460C>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GUncertain significance
Select item 304405	NM_024426.6(WT1):c.*393G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +3 more	GUncertain significance
Select item 304406	NM_024426.6(WT1):c.*366C>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304407	NM_024426.6(WT1):c.*354G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304408	NM_024426.6(WT1):c.*345G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GBenign/Likely benign
Select item 304409	NM_024426.6(WT1):c.*269G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304410	NM_024426.6(WT1):c.*267G>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +5 more	GBenign
Select item 304411	NM_024426.6(WT1):c.*239G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304412	NM_024426.6(WT1):c.*224A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +5 more	GBenign
Select item 304413	NM_024426.6(WT1):c.*159G>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GUncertain significance
Select item 304414	NM_024426.6(WT1):c.*138G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephroblastoma +3 more	GLikely benign
Select item 304415	NM_024426.6(WT1):c.*110C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 879521	NM_024426.6(WT1):c.*100A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 304416	NM_024426.6(WT1):c.*88A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +5 more	GBenign
Select item 304417	NM_024426.6(WT1):c.*16G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +5 more	GBenign/Likely benign
Select item 877954	NM_024426.6(WT1):c.*12C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GConflicting classifications of pathogenicity
Select item 877955	NM_024426.6(WT1):c.*5T>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	WT1-related condition +3 more	GConflicting classifications of pathogenicity
Select item 515922	NM_024426.6(WT1):c.1568G>A (p.Ter523=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +8 more	GConflicting classifications of pathogenicity
Select item 304418	NM_024426.6(WT1):c.1200C>T (p.Tyr400=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Meacham syndrome +6 more	GConflicting classifications of pathogenicity
Select item 304419	NM_024426.6(WT1):c.1198T>C (p.Tyr400His)	WT1 (Y183H +9 more)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +6 more	GConflicting classifications of pathogenicity
Select item 414080	NM_024426.6(WT1):c.1182C>T (p.Arg394=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Drash syndrome +7 more	GConflicting classifications of pathogenicity
Select item 135455	NM_024426.6(WT1):c.1154G>A (p.Arg385Gln)	WT1 (R168Q +8 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +6 more	GConflicting classifications of pathogenicity
Select item 198590	NM_024426.6(WT1):c.1131T>C (p.Pro377=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Drash syndrome +8 more	GConflicting classifications of pathogenicity
Select item 406692	NM_024426.6(WT1):c.1124G>A (p.Arg375His)	WT1 (R158H +8 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4 +5 more	GConflicting classifications of pathogenicity
Select item 198591	NM_024426.6(WT1):c.1122A>G (p.Arg374=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Nephrotic syndrome, type 4 +8 more	GBenign
Select item 241475	NM_024426.6(WT1):c.1114-9T>C	WT1	Single nucleotide variant (intron variant)	Meacham syndrome +10 more	GBenign/Likely benign
Select item 261708	NM_024426.6(WT1):c.1074A>G (p.Gln358=)	WT1	Single nucleotide variant (synonymous variant +2 more)	not provided +9 more	GBenign
Select item 877125	NM_024426.6(WT1):c.1020C>T (p.His340=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 414075	NM_024426.6(WT1):c.1017-9T>C	WT1	Single nucleotide variant (intron variant)	Nephrotic syndrome, type 4 +5 more	GConflicting classifications of pathogenicity
Select item 304420	NM_024426.6(WT1):c.1017-15T>C	WT1	Single nucleotide variant (intron variant)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 878161	NM_024426.6(WT1):c.973G>A (p.Ala325Thr)	WT1 (A108T +4 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4 +5 more	GUncertain significance
Select item 304421	NM_024426.6(WT1):c.887+4G>A	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +5 more	GConflicting classifications of pathogenicity
Select item 879620	NM_024426.6(WT1):c.813G>C (p.Pro271=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Nephrotic syndrome, type 4 +6 more	GConflicting classifications of pathogenicity
Select item 406688	NM_024426.6(WT1):c.785G>A (p.Gly262Asp)	WT1 (G45D +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 135453	NM_024426.6(WT1):c.760C>T (p.Pro254Ser)	WT1 (P37S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +11 more	GConflicting classifications of pathogenicity
Select item 261714	NM_024426.6(WT1):c.696C>T (p.Ser232=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Frasier syndrome +7 more	GConflicting classifications of pathogenicity
Select item 304422	NM_024426.6(WT1):c.695G>C (p.Ser232Thr)	WT1 (S15T +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 842948	NM_024426.6(WT1):c.620T>G (p.Leu207Arg)	LOC107982234, WT1 (L207R)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +6 more	GUncertain significance
Select item 261713	NM_024426.6(WT1):c.609C>T (p.Asn203=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	WT1-related condition +9 more	GBenign
Select item 304423	NM_024426.6(WT1):c.587G>A (p.Gly196Asp)	LOC107982234, WT1 (G196D)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +6 more	GConflicting classifications of pathogenicity
Select item 261712	NM_024426.6(WT1):c.513C>A (p.Gly171=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign/Likely benign
Select item 721377	NM_024426.6(WT1):c.402G>A (p.Pro134=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +6 more	GConflicting classifications of pathogenicity
Select item 304424	NM_024426.6(WT1):c.390A>G (p.Pro130=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	11p partial monosomy syndrome +5 more	GConflicting classifications of pathogenicity
Select item 261711	NM_024426.6(WT1):c.381C>G (p.Pro127=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +8 more	GConflicting classifications of pathogenicity
Select item 241481	NM_024426.6(WT1):c.375C>T (p.Gly125=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +8 more	GConflicting classifications of pathogenicity
Select item 304425	NM_024426.6(WT1):c.347C>T (p.Pro116Leu)	LOC107982234, WT1 (P116L)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +6 more	GUncertain significance
Select item 193454	NM_024426.6(WT1):c.345C>T (p.Pro115=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +8 more	GBenign
Select item 840419	NM_024426.6(WT1):c.313G>T (p.Ala105Ser)	LOC107982234, WT1 (A105S)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +5 more	GUncertain significance
Select item 241480	NM_024426.6(WT1):c.309C>A (p.Gly103=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +7 more	GConflicting classifications of pathogenicity
Select item 877249	NM_024426.6(WT1):c.298C>G (p.Pro100Ala)	LOC107982234, WT1 (P100A)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304426	NM_024426.6(WT1):c.285C>T (p.Gly95=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304427	NM_024426.6(WT1):c.247G>T (p.Ala83Ser)	LOC107982234, WT1 (A83S)	Single nucleotide variant (missense variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 241479	NM_024426.6(WT1):c.216G>T (p.Gln72His)	LOC107982234, WT1 (Q72H)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +8 more	GBenign/Likely benign
Select item 261710	NM_024426.6(WT1):c.213G>T (p.Pro71=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign
Select item 241478	NM_024426.6(WT1):c.193G>A (p.Gly65Arg)	LOC107982234, WT1 (G65R)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +9 more	GConflicting classifications of pathogenicity
Select item 241476	NM_024426.6(WT1):c.181C>A (p.Arg61=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +9 more	GBenign/Likely benign
Select item 304428	NM_024426.6(WT1):c.174C>G (p.Leu58=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 304429	NM_024426.6(WT1):c.162C>G (p.Ser54Arg)	LOC107982234, WT1 (S54R)	Single nucleotide variant (missense variant +1 more)	11p partial monosomy syndrome +6 more	GUncertain significance
Select item 304430	NM_024426.6(WT1):c.136G>T (p.Ala46Ser)	LOC107982234, WT1 (A46S)	Single nucleotide variant (missense variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 543129	NM_024426.6(WT1):c.124G>A (p.Gly42Ser)	LOC107982234, WT1 (G42S)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +6 more	GConflicting classifications of pathogenicity
Select item 193453	NM_024426.6(WT1):c.123G>C (p.Pro41=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +9 more	GBenign/Likely benign
Select item 241487	NM_024426.6(WT1):c.83G>A (p.Gly28Glu)	LOC107982234, WT1 (G28E)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +5 more	GUncertain significance
Select item 304431	NM_024426.6(WT1):c.-31G>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304432	NM_024426.6(WT1):c.-76T>C	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GUncertain significance

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