View genomic variant #0000001502

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.14674T>G
Published as -
GERP -8.300
Segregation -
DB-ID chrM_000039 See all 2 reported entries
MSCV MSCV_0001502
dbSNP ID rs387906421
Frequency -
Sources ; clinvar; ensembl;
Reference 21931168;19720722;21194154
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.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MT-TE 00001349 MT-TE-201 0000001502 +/+ - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010243; RCV000224954; RCV000495655; RCV000851087;
Chromosome M:14674..14674
ClinVar Allele ID 24657
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550|MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864
ClinVar preferred disease name not provided|Mitochondrial disease|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
HGVS variant names NC 012920.1:m.14674T>C
ClinVar review status reviewed by expert panel
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120581|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591969|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:590025.0002
Gene symbol:Gene id. MT-TE:4556
Allele origin germline
dbSNP ID 387906421
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000022898;
Chromosome M:14674..14674
ClinVar Allele ID 38958
Disease database name and identifier MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864
ClinVar preferred disease name Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
HGVS variant names NC 012920.1:m.14674T>G
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA128830|OMIM:590025.0003
Gene symbol:Gene id. MT-TE:4556
Allele origin germline
dbSNP ID 387906421
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TEReversible COX deficiency myopathyT14674CtRNA Glu+-CfrmRNA
MT-TEReversible COX deficiency myopathyT14674GtRNA Glu+-ReportedRNA

Ensembl Variant Phenotype Information:

None