View genomic variant #0000026822

Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136218934_136218935insGATGCTC
Published as -
GERP -
Segregation -
DB-ID SURF1_000051
MSCV -
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 Lishuang Shen




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 0000026822 ./. - - c.487_488insGAGCATC p.(Leu163Argfs*22) - - - -
SURF1 00000318 NM_003172.3 0000026822 ./. - - c.814_815insGAGCATC p.(Leu272Argfs*22) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000662036; RCV000662037; RCV001090695;
Chromosome 9:136218934..136218935
ClinVar Allele ID 539019
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0014733, MedGen:C4225246, OMIM:616684, Orphanet:391351|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Charcot-Marie-Tooth disease type 4K|Leigh syndrome
HGVS variant names NC 000009.11:g.136218936 136218942dup
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(1)|Uncertain significance(2)
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001589|frameshift variant
Allele origin
dbSNP ID 1554768224
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002833045;
Chromosome 9:136218934..136218934
ClinVar Allele ID 2061954
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.136218934A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant
Allele origin germline
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