CN033288[trait identifier] AND "Illumina Laboratory Services, Illumina - 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 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 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 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 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 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 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 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 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 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 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 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
Select item 877311	NM_024426.6(WT1):c.-87C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304437	NM_024426.6(WT1):c.-102C>A	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304438	NM_024426.6(WT1):c.-106C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +4 more	GConflicting classifications of pathogenicity
Select item 304439	NM_024426.6(WT1):c.-110C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 304440	NM_024426.6(WT1):c.-114T>A	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304441	NM_024426.6(WT1):c.-135G>A	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 304442	NM_024426.6(WT1):c.-140C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 9342	NM_000059.4(BRCA2):c.658_659del (p.Val220fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 41567	NM_000059.4(BRCA2):c.865A>C (p.Asn289His)	BRCA2 (N289H)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 9329	NM_000059.4(BRCA2):c.1114A>C (p.Asn372His)	BRCA2 (N372H)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 41541	NM_000059.4(BRCA2):c.1151C>T (p.Ser384Phe)	BRCA2 (S384F)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 37754	NM_000059.4(BRCA2):c.1755_1759del (p.Lys585fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 51192	NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	BRCA2 (D596H)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51230	NM_000059.4(BRCA2):c.1938C>T (p.Ser646=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 37770	NM_000059.4(BRCA2):c.1964C>G (p.Pro655Arg)	BRCA2 (P655R)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 96780	NM_000059.4(BRCA2):c.2186T>C (p.Ile729Thr)	BRCA2 (I729T)	Single nucleotide variant (missense variant)	Ovarian cancer +13 more	GConflicting classifications of pathogenicity
Select item 125979	NM_000059.4(BRCA2):c.2229T>C (p.His743=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51349	NM_000059.4(BRCA2):c.2803G>A (p.Asp935Asn)	BRCA2 (D935N)	Single nucleotide variant (missense variant)	Wilms tumor 1 +12 more	GBenign/Likely benign
Select item 41545	NM_000059.4(BRCA2):c.2971A>G (p.Asn991Asp)	BRCA2 (N991D)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51435	NM_000059.4(BRCA2):c.3264T>C (p.Pro1088=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51481	NM_000059.4(BRCA2):c.3516G>A (p.Ser1172=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 37950	NM_000059.4(BRCA2):c.5198C>T (p.Ser1733Phe)	BRCA2 (S1733F)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51813	NM_000059.4(BRCA2):c.5199C>T (p.Ser1733=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 132781	NM_000059.4(BRCA2):c.5418A>G (p.Glu1806=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 37997	NM_000059.4(BRCA2):c.5785A>G (p.Ile1929Val)	BRCA2 (I1929V)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign

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