View genomic variant #0000016305

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.101489418C>T
Published as -
GERP -
Segregation -
DB-ID COX15_000025
MSCV MSCV_0016305
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

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 0000016305 ./. - - c.164G>A p.(Arg55Lys) - - - -
COX15 00000084 NM_078470.4 0000016305 ./. - - c.164G>A p.(Arg55Lys) - - - -
COX15 00000082 XM_005269539.1 0000016305 ./. - - c.164G>A p.(Arg55Lys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000197287; RCV000291406; RCV002515389; RCV002517204;
Chromosome 10:101489418..101489418
Allele frequencies from ExAC 0.00005
ClinVar Allele ID 211476
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:CN517202|MedGen:CN169374|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Inborn genetic diseases|not provided|not specified|Leigh syndrome
HGVS variant names NC 000010.10:g.101489418C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(3)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA321735
Gene symbol:Gene id. COX15:1355
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 777532861
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