View genomic variant #0000018266

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.13977769G>A
Published as -
GERP -
Segregation -
DB-ID COX10_000043
MSCV MSCV_0018266
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
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     
COX10 00000076 NM_001303.3 0000018266 ./. - - c.173G>A p.(Arg58His) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000315497; RCV000351189; RCV001859908; RCV002495013; RCV003243077;
Chromosome 17:13977769..13977769
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 343332
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0033635, MedGen:C5436682, OMIM:619046|MedGen:CN517202|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name Inborn genetic diseases|Mitochondrial complex 4 deficiency, nuclear type 3|not provided|Leigh syndrome|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000017.10:g.13977769G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8402250
Gene symbol:Gene id. COX10:1352
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 772223730
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None