View genomic variant #0000022882

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136219295A>G
Published as -
GERP -
Segregation -
DB-ID SURF1_000020
MSCV MSCV_0022882
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01369 View details
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 0000022882 ./. - - c.424+6T>C p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022882 ./. - - c.751+6T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000128343; RCV000427963; RCV001080444;
Chromosome 9:136219295..136219295
Allele frequencies from ESP 0.01369
Allele frequencies from ExAC 0.00568
Allele frequencies from TGP 0.01138
ClinVar Allele ID 143079
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.136219295A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA293833
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 41296099
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