View genomic variant #0000022908

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136223254_136223267del
Published as -
GERP -
Segregation -
DB-ID SURF1_000010
MSCV MSCV_0022908
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 0000022908 ./. - - c.-222+9_-222+22del p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022908 ./. - - c.54+9_54+22del p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000483880; RCV000531800;
Chromosome 9:136223254..136223267
ClinVar Allele ID 407586
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not specified|Leigh syndrome
HGVS variant names NC 000009.11:g.136223256 136223269del
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely benign
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA16618783
Gene symbol:Gene id. SURF1:6834|LOC130002899:130002899
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 782659731
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000128345; RCV000383935;
Chromosome 9:136223267..136223267
Allele frequencies from TGP 0.00978
ClinVar Allele ID 143081
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not specified|Leigh syndrome
HGVS variant names NC 000009.11:g.136223267G>C
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:CA293837
Gene symbol:Gene id. SURF1:6834|LOC130002899:130002899
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 587675928
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