View genomic variant #0000022881

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.136219000_136219001insT
Published as -
GERP -
Segregation -
DB-ID SURF1_000019
MSCV MSCV_0022881
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 0000022881 ./. - - c.425-4_425-3insA p.? - - - -
SURF1 00000318 NM_003172.3 0000022881 ./. - - c.752-4_752-3insA p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000631406;
Chromosome 9:136219000..136219001
ClinVar Allele ID 524241
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.136219001dup
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA658797340
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 1159512660
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002179786;
Chromosome 9:136219001..136219001
ClinVar Allele ID 1522987
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.136219001T>G
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 1458022944
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