ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.3343G>A (p.Val1115Met) (rs201603222)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000472962 SCV000546538 benign Familial focal epilepsy with variable foci 2019-11-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV000720811 SCV000851695 likely benign Seizures 2017-05-25 criteria provided, single submitter clinical testing In silico models in agreement (benign);Subpopulation frequency in support of benign classification

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.