View genomic variant #0000022893

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.136219563G>A
Published as -
GERP -
Segregation -
DB-ID SURF1_000030
MSCV MSCV_0022893
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 0000022893 ./. - - c.247C>T p.(Arg83Trp) - - - -
SURF1 00000318 NM_003172.3 0000022893 ./. - - c.574C>T p.(Arg192Trp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000199387; RCV000202523; RCV000631410; RCV002492907; RCV003314575;
Chromosome 9:136219563..136219563
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 211361
Disease database name and identifier MONDO:MONDO:0014733, MedGen:C4225246, OMIM:616684, Orphanet:391351|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MedGen:C3661900|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380
ClinVar preferred disease name Charcot-Marie-Tooth disease type 4K|Cytochrome-c oxidase deficiency disease|Leigh syndrome|not provided|Mitochondrial disease
HGVS variant names NC 000009.11:g.136219563G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA215067|OMIM:185620.0017|UniProtKB:Q15526#VAR 076315
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 782190413
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