View genomic variant #0000018235

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.12915101T>C
Published as -
GERP -
Segregation -
DB-ID ELAC2_000013
MSCV MSCV_0018235
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00231 View details
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 0000018235 ./. - - c.560-1113A>G p.(=) - - - -
ELAC2 00001871 NM_018127.6 0000018235 ./. - - c.560-2A>G p.? - - - -
ELAC2 00001870 NM_173717.1 0000018235 ./. - - c.560-2A>G p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000224217; RCV001088164;
Chromosome 17:12915101..12915101
Allele frequencies from ESP 0.00231
Allele frequencies from ExAC 0.00083
Allele frequencies from TGP 0.00300
ClinVar Allele ID 237324
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913
ClinVar preferred disease name not provided|Combined oxidative phosphorylation defect type 17
HGVS variant names NC 000017.10:g.12915101T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8401584
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001574|splice acceptor variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 149733287
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