ClinVar Miner

List of variants studied for Combined oxidative phosphorylation defect type 17 by Service de Génétique Médicale, Centre Hospitalier Universitaire de Nice-Université Côte d'Azur

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018127.7(ELAC2):c.2249T>C (p.Met750Thr) rs769686385 0.00005
NM_018127.7(ELAC2):c.1943C>T (p.Ala648Val)
NM_018127.7(ELAC2):c.591G>A (p.Trp197Ter) rs1359575116

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.