View genomic variant #0000018260

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.13972899G>A
Published as -
GERP -
Segregation -
DB-ID COX10_000051
MSCV MSCV_0018260
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
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     
COX10 00000076 NM_001303.3 0000018260 ./. - - c.-24G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000279297; RCV000373740; RCV000827262;
Chromosome 17:13972899..13972899
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00010
Allele frequencies from TGP 0.00020
ClinVar Allele ID 344908
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name not provided|Leigh syndrome|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000017.10:g.13972899G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8402192
Gene symbol:Gene id. COX10:1352
Molecular consequence SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 201257809
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