View genomic variant #0000001454

Chromosome M
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.10158T>C
Published as -
GERP -10.100
Segregation -
DB-ID chrM_000071 See all 2 reported entries
MSCV MSCV_0001454
dbSNP ID rs199476117
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 16023078;14684687;15576045;14705112;15372108
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MT-ND3 00001340 MT-ND3-201 0000001454 +/+ - . c.100T>C p.S34P - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000854624;
Chromosome M:10158..10158
ClinVar Allele ID 680157
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leigh syndrome
HGVS variant names NC 012920.1:m.10158T>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ND3:4537
Allele origin germline
dbSNP ID 199476117
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000010360; RCV000144009; RCV000224598; RCV001796716;
Chromosome M:10158..10158
ClinVar Allele ID 24753
Disease database name and identifier MONDO:MONDO:0027068, MedGen:C4746992, OMIM:500014|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex 1 deficiency, mitochondrial type 1|Mitochondrial disease|not provided|Leigh syndrome
HGVS variant names NC 012920.1:m.10158T>C
ClinVar review status reviewed by expert panel
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120639|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516002.0003
Gene symbol:Gene id. MT-ND3:4537
Allele origin germline
dbSNP ID 199476117
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND3Leigh DiseaseT10158CS-P++CfrmCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None