View genomic variant #0000018274

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.14005547C>A
Published as -
GERP -
Segregation -
DB-ID COX10_000002 See all 2 reported entries
MSCV MSCV_0000714
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 0000018274 ./. - - c.612C>A p.(Asn204Lys) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000007956;
Chromosome 17:14005547..14005547
ClinVar Allele ID 22561
Disease database name and identifier MONDO:MONDO:0033635, MedGen:C5436682, OMIM:619046
ClinVar preferred disease name Mitochondrial complex 4 deficiency, nuclear type 3
HGVS variant names NC 000017.10:g.14005547C>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA118859|OMIM:602125.0001|UniProtKB:Q12887#VAR 026563
Gene symbol:Gene id. COX10:1352
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 104894560
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