View genomic variant #0000018306

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.14111606T>C
Published as -
GERP -
Segregation -
DB-ID COX10_000030
MSCV MSCV_0018306
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 0000018306 ./. - - c.*1076T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000266831; RCV000361388; RCV001613030;
Chromosome 17:14111606..14111606
Allele frequencies from TGP 0.21326
ClinVar Allele ID 344924
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905|MedGen:C3661900
ClinVar preferred disease name Leigh syndrome|Cytochrome-c oxidase deficiency disease|not provided
HGVS variant names NC 000017.10:g.14111606T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10649512
Gene symbol:Gene id. COX10:1352
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 1050216
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