View genomic variant #0000018261

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.13972924T>C
Published as -
GERP -
Segregation -
DB-ID COX10_000052
MSCV MSCV_0018261
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 0000018261 ./. - - c.2T>C p.? - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000007962;
Chromosome 17:13972924..13972924
ClinVar Allele ID 22566
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.13972924T>C
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:CA118864|OMIM:602125.0006
Gene symbol:Gene id. COX10:1352|LOC130060303:130060303
Molecular consequence SO:0001582|initiator codon variant, SO:0001583|missense variant
Allele origin germline
dbSNP ID 387906383
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