ClinVar Miner

Submissions for variant NM_005076.5(CNTN2):c.418C>T (p.Arg140Ter)

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
Labcorp Genetics (formerly Invitae), Labcorp RCV002667041 SCV002973393 pathogenic Epilepsy, familial adult myoclonic, 5 2022-11-15 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with CNTN2-related conditions. This variant is present in population databases (rs779892361, gnomAD 0.0009%). This sequence change creates a premature translational stop signal (p.Arg140*) in the CNTN2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in CNTN2 are known to be pathogenic (PMID: 11178983, 23518707).
Revvity Omics, Revvity RCV002667041 SCV003831075 uncertain significance Epilepsy, familial adult myoclonic, 5 2019-07-08 criteria provided, single submitter clinical testing

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.