ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.1870+2387_1870+4243del

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000801961 SCV000941767 likely pathogenic Familial focal epilepsy with variable foci 2019-06-28 criteria provided, single submitter clinical testing This variant is a deletion of the genomic region encompassing part of exon 23 and all of exon 24 (c.1981_2104+678del) of the DEPDC5 gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with DEPDC5-related disease. While this particular variant has not been reported in the literature, truncating variants in DEPDC5 are known to be pathogenic (PMID: 26505888). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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.