View genomic variant #0000022904

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.136221708C>G
Published as -
GERP -
Segregation -
DB-ID SURF1_000039
MSCV MSCV_0022904
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00092 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 0000022904 ./. - - c.-117G>C p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022904 ./. - - c.211G>C p.(Val71Leu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001399689; RCV002552716; RCV003120601;
Chromosome 9:136221708..136221708
ClinVar Allele ID 1076174
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MeSH:D030342, MedGen:C0950123|MedGen:CN169374
ClinVar preferred disease name Leigh syndrome|Inborn genetic diseases|not specified
HGVS variant names NC 000009.11:g.136221708C>A
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
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 147993882
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000264670; RCV000507001; RCV001354540; RCV003168574;
Chromosome 9:136221708..136221708
Allele frequencies from ESP 0.00092
Allele frequencies from TGP 0.00140
ClinVar Allele ID 311526
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MedGen:CN169374|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Inborn genetic diseases|not provided|not specified|Leigh syndrome
HGVS variant names NC 000009.11:g.136221708C>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(3)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10629377
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 147993882
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