View genomic variant #0000022876

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.136218956_136218957del
Published as -
GERP -
Segregation -
DB-ID SURF1_000014
MSCV MSCV_0022876
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 0000022876 ./. - - c.465_466del p.(Arg155Serfs*27) - - - -
SURF1 00000318 NM_003172.3 0000022876 ./. - - c.792_793del p.(Arg264Serfs*27) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000198901; RCV000534608; RCV001813769; RCV002517264; RCV000013605;
Chromosome 9:136218956..136218957
ClinVar Allele ID 211358
Disease database name and identifier MONDO:MONDO:0014733, MedGen:C4225246, OMIM:616684, Orphanet:391351|MedGen:C3661900|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Charcot-Marie-Tooth disease type 4K|not provided|Cytochrome-c oxidase deficiency disease|Leigh syndrome|Inborn genetic diseases
HGVS variant names NC 000009.11:g.136218956CT[1]
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type Microsatellite
Sequence Ontology for variant type SO:0000289
Variant clinical sources reported ClinGen:CA323428|OMIM:185620.0011
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001589|frameshift variant
Allele origin
dbSNP ID 782490558
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