View genomic variant #0000018243

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.12920250_12920251delinsA
Published as -
GERP -
Segregation -
DB-ID ELAC2_000011
MSCV MSCV_0018243
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 0000018243 ./. - - c.297-2_297-1delinsT p.? - - - -
ELAC2 00001871 NM_018127.6 0000018243 ./. - - c.297-2_297-1delinsT p.? - - - -
ELAC2 00001870 NM_173717.1 0000018243 ./. - - c.297-2_297-1delinsT p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000472057; RCV000484886; RCV002525574;
Chromosome 17:12920250..12920251
ClinVar Allele ID 401547
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913|MedGen:CN517202
ClinVar preferred disease name Inborn genetic diseases|Combined oxidative phosphorylation defect type 17|not provided
HGVS variant names NC 000017.10:g.12920250 12920251delinsA
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type Indel
Sequence Ontology for variant type SO:1000032
Variant clinical sources reported ClinGen:CA16615102
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001574|splice acceptor variant
Allele origin germline
dbSNP ID 1060502161
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