View genomic variant #0000022911

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136223291_136223292insGCCCGCA
Published as -
GERP -
Segregation -
DB-ID SURF1_000005
MSCV MSCV_0022911
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 0000022911 ./. - - c.-238_-237insTGCGGGC p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022911 ./. - - c.38_39insTGCGGGC p.(Leu16Glyfs*46) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000198640; RCV001853202;
Chromosome 9:136223290..136223290
ClinVar Allele ID 211369
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.136223290C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA323176
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 863224224
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000543189;
Chromosome 9:136223291..136223292
ClinVar Allele ID 459618
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.136223296 136223302dup
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA658657935
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001589|frameshift variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 1410388157
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