View genomic variant #0000024028

Chromosome 10
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.101483814G>A
Published as -
GERP -
Segregation -
DB-ID COX15_000001 See all 2 reported entries
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
Owner Lishuang Shen




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
COX15 00000083 NM_004376.5 0000024028 ./. - - c.649C>T p.(Arg217Trp) - - - -
COX15 00000084 NM_078470.4 0000024028 ./. - - c.649C>T p.(Arg217Trp) - - - -
COX15 00000082 XM_005269539.1 0000024028 ./. - - c.649C>T p.(Arg217Trp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006551; RCV001553427; RCV002512834;
Chromosome 10:101483814..101483814
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 21214
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:CN517202|MONDO:MONDO:0014051, MedGen:C3554534, OMIM:615119, Orphanet:1561
ClinVar preferred disease name Inborn genetic diseases|not provided|Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
HGVS variant names NC 000010.10:g.101483814G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA118046|OMIM:603646.0001|UniProtKB:Q7KZN9#VAR 019596
Gene symbol:Gene id. COX15:1355
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 28939711
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