View genomic variant #0000026824

Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136219307T>C
Published as -
GERP -
Segregation -
DB-ID SURF1_000044
MSCV -
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 Lishuang Shen




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 0000026824 ./. - - c.418A>G p.(Asn140Asp) - - - -
SURF1 00000318 NM_003172.3 0000026824 ./. - - c.745A>G p.(Asn249Asp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000699472; RCV001699229;
Chromosome 9:136219307..136219307
Allele frequencies from ExAC 0.00030
Allele frequencies from TGP 0.00020
ClinVar Allele ID 211359
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Leigh syndrome
HGVS variant names NC 000009.11:g.136219307T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA322228
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 587669420
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