View genomic variant #0000024029

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.101486914G>C
Published as -
GERP -
Segregation -
DB-ID COX15_000057
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 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 0000024029 ./. - - c.396-3C>G p.? - - - -
COX15 00000084 NM_078470.4 0000024029 ./. - - c.396-3C>G p.? - - - -
COX15 00000082 XM_005269539.1 0000024029 ./. - - c.396-3C>G p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006553; RCV000266470; RCV002469094;
Chromosome 10:101486914..101486914
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00011
Allele frequencies from TGP 0.00040
ClinVar Allele ID 264384
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0014051, MedGen:C3554534, OMIM:615119, Orphanet:1561|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2|Leigh syndrome
HGVS variant names NC 000010.10:g.101486914G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(2)|Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA5642274|OMIM:603646.0002
Gene symbol:Gene id. COX15:1355
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 200910834
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