View genomic variant #0000022907

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.136223123C>G
Published as -
GERP -
Segregation -
DB-ID SURF1_000009
MSCV MSCV_0022907
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 0000022907 ./. - - c.-222+153G>C p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022907 ./. - - c.106+1G>C p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000196131;
Chromosome 9:136223123..136223123
ClinVar Allele ID 213588
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leigh syndrome
HGVS variant names NC 000009.11:g.136223123C>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA278935
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001575|splice donor variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 863224926
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