View genomic variant #0000022874

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136218929A>C
Published as -
GERP -
Segregation -
DB-ID SURF1_000002 See all 2 reported entries
MSCV MSCV_0003429
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

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SURF1 00000317 NM_001280787.1 0000022874 ./. - - c.493T>G p.(Tyr165Asp) - - - -
SURF1 00000318 NM_003172.3 0000022874 ./. - - c.820T>G p.(Tyr274Asp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000013603;
Chromosome 9:136218929..136218929
ClinVar Allele ID 27805
Disease database name and identifier MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000009.11:g.136218929A>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:CA122695|OMIM:185620.0010|UniProtKB:Q15526#VAR 015259
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121918658
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