C1854465[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 365385	NM_000368.5(TSC1):c.*4826A>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 913083	NM_000368.5(TSC1):c.*4788A>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365386	NM_000368.5(TSC1):c.*4763T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 913084	NM_000368.5(TSC1):c.*4680G>T	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 914228	NM_000368.5(TSC1):c.*4538A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914229	NM_000368.5(TSC1):c.*4522C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365390	NM_000368.5(TSC1):c.*4515G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GUncertain significance
Select item 914230	NM_000368.5(TSC1):c.*4492T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365391	NM_000368.5(TSC1):c.*4447C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365392	NM_000368.5(TSC1):c.*4437G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365393	NM_000368.5(TSC1):c.*4385G>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365394	NM_000368.5(TSC1):c.*4356C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365395	NM_000368.5(TSC1):c.*4254G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365402	NM_000368.5(TSC1):c.*4128G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 912765	NM_000368.5(TSC1):c.*4119T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 912766	NM_000368.5(TSC1):c.*4105C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365404	NM_000368.5(TSC1):c.*4057G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365405	NM_000368.5(TSC1):c.*3997G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365406	NM_000368.5(TSC1):c.*3988G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 913127	NM_000368.5(TSC1):c.*3959T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365408	NM_000368.5(TSC1):c.*3952A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365410	NM_000368.5(TSC1):c.*3836G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365411	NM_000368.5(TSC1):c.*3830C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 365413	NM_000368.5(TSC1):c.*3729G>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 914772	NM_000368.5(TSC1):c.*3685G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365414	NM_000368.5(TSC1):c.*3679G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 912812	NM_000368.5(TSC1):c.*3648C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365416	NM_000368.5(TSC1):c.*3565C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GUncertain significance
Select item 365418	NM_000368.5(TSC1):c.*3538A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 912813	NM_000368.5(TSC1):c.*3484A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365420	NM_000368.5(TSC1):c.*3448C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 913173	NM_000368.5(TSC1):c.*3272A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365427	NM_000368.5(TSC1):c.*3238T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GUncertain significance
Select item 913174	NM_000368.5(TSC1):c.*3170G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 913175	NM_000368.5(TSC1):c.*3092T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365428	NM_000368.5(TSC1):c.*3063A>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914310	NM_000368.5(TSC1):c.*3045A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914311	NM_000368.5(TSC1):c.*3034T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914312	NM_000368.5(TSC1):c.*2924T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365431	NM_000368.5(TSC1):c.*2904G>T	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 914814	NM_000368.5(TSC1):c.*2890A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365434	NM_000368.5(TSC1):c.*2874G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365435	NM_000368.5(TSC1):c.*2872G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 912853	NM_000368.5(TSC1):c.*2854T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365436	NM_000368.5(TSC1):c.*2829A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GUncertain significance
Select item 365437	NM_000368.5(TSC1):c.*2733A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 912854	NM_000368.5(TSC1):c.*2724C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365438	NM_000368.5(TSC1):c.*2708G>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365442	NM_000368.5(TSC1):c.*2651G>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365443	NM_000368.5(TSC1):c.*2647C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GUncertain significance
Select item 365445	NM_000368.5(TSC1):c.*2638C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 365446	NM_000368.5(TSC1):c.*2637C>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914350	NM_000368.5(TSC1):c.*2628G>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365449	NM_000368.5(TSC1):c.*2576T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GUncertain significance
Select item 914843	NM_000368.5(TSC1):c.*2558A>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365450	NM_000368.5(TSC1):c.*2558A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 914844	NM_000368.5(TSC1):c.*2515T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365452	NM_000368.5(TSC1):c.*2461G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365453	NM_000368.5(TSC1):c.*2446A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365455	NM_000368.5(TSC1):c.*2418G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 912899	NM_000368.5(TSC1):c.*2354A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365459	NM_000368.5(TSC1):c.*2168C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365460	NM_000368.5(TSC1):c.*2142T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365461	NM_000368.5(TSC1):c.*2109C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 913270	NM_000368.5(TSC1):c.*2104A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365462	NM_000368.5(TSC1):c.*2094G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 913271	NM_000368.5(TSC1):c.*1972A>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365464	NM_000368.5(TSC1):c.*1970G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365466	NM_000368.5(TSC1):c.*1934A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 365467	NM_000368.5(TSC1):c.*1902T>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 365468	NM_000368.5(TSC1):c.*1861G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914897	NM_000368.5(TSC1):c.*1839G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365469	NM_000368.5(TSC1):c.*1785A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365470	NM_000368.5(TSC1):c.*1680G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365475	NM_000368.5(TSC1):c.*1508A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign/Likely benign
Select item 365476	NM_000368.5(TSC1):c.*1507G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 365477	NM_000368.5(TSC1):c.*1488C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 64737	NM_000368.5(TSC1):c.*1487C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 913307	NM_000368.5(TSC1):c.*1474G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 64739	NM_000368.5(TSC1):c.*1468C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 913308	NM_000368.5(TSC1):c.*1452A>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365478	NM_000368.5(TSC1):c.*1372T>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 914427	NM_000368.5(TSC1):c.*1355C>A	TSC1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 914428	NM_000368.5(TSC1):c.*1349G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365479	NM_000368.5(TSC1):c.*1322C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365480	NM_000368.5(TSC1):c.*1275T>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 914947	NM_000368.5(TSC1):c.*1251C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 912992	NM_000368.5(TSC1):c.*1239C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 912993	NM_000368.5(TSC1):c.*1215G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 912994	NM_000368.5(TSC1):c.*1127C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365481	NM_000368.5(TSC1):c.*1089G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365482	NM_000368.5(TSC1):c.*1052G>A	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365483	NM_000368.5(TSC1):c.*1050T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 913359	NM_000368.5(TSC1):c.*1036C>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365484	NM_000368.5(TSC1):c.*1000A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 365485	NM_000368.5(TSC1):c.*941A>G	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 914481	NM_000368.5(TSC1):c.*936T>C	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance
Select item 64772	NM_000368.5(TSC1):c.*913C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Tuberous sclerosis 1 +1 more	GBenign
Select item 365488	NM_000368.5(TSC1):c.*841C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GBenign
Select item 365489	NM_000368.5(TSC1):c.*824C>T	TSC1	Single nucleotide variant (3 prime UTR variant)	Isolated focal cortical dysplasia type II +1 more	GUncertain significance

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