View genomic variant #0000022909

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136223266C>T
Published as -
GERP -
Segregation -
DB-ID SURF1_000011
MSCV MSCV_0022909
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 0000022909 ./. - - c.-222+10G>A p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022909 ./. - - c.54+10G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000128346; RCV000329138; RCV000676736;
Chromosome 9:136223266..136223266
Allele frequencies from ExAC 0.00807
Allele frequencies from TGP 0.00120
ClinVar Allele ID 143082
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not specified|not provided|Leigh syndrome
HGVS variant names NC 000009.11:g.136223266C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(2)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA293839
Gene symbol:Gene id. SURF1:6834|LOC130002899:130002899
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 587598397
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