View genomic variant #0000018199

Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.12896267_12896278del
Published as -
GERP -
Segregation -
DB-ID ELAC2_000025
MSCV MSCV_0018199
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

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ELAC2 00001869 NM_001165962.1 0000018199 ./. - - c.2218_2229del p.(Glu740_Glu743del) - - - -
ELAC2 00001871 NM_018127.6 0000018199 ./. - - c.2338_2349del p.(Glu780_Glu783del) - - - -
ELAC2 00001870 NM_173717.1 0000018199 ./. - - c.2335_2346del p.(Glu779_Glu782del) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000529336;
Chromosome 17:12896267..12896278
ClinVar Allele ID 467411
Disease database name and identifier MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913
ClinVar preferred disease name Combined oxidative phosphorylation defect type 17
HGVS variant names NC 000017.10:g.12896271 12896282del
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA625311401
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001822|inframe deletion
Allele origin germline
dbSNP ID 1395507635
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