View genomic variant #0000022896

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.136220748C>T
Published as -
GERP -
Segregation -
DB-ID SURF1_000001 See all 2 reported entries
MSCV MSCV_0003431
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 0000022896 ./. - - c.44G>A p.(Gly15Glu) - - - -
SURF1 00000318 NM_003172.3 0000022896 ./. - - c.371G>A p.(Gly124Glu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000013606; RCV001851829;
Chromosome 9:136220748..136220748
ClinVar Allele ID 27807
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name Leigh syndrome|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000009.11:g.136220748C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA122697|OMIM:185620.0012|UniProtKB:Q15526#VAR 007450
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 28933402
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