ClinVar Miner

Submissions for variant NM_080632.3(UPF3B):c.1060C>T (p.Arg354Ter)

dbSNP: rs2056119926
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
Diagnostic Laboratory, Strasbourg University Hospital RCV001260817 SCV001437913 likely pathogenic Intellectual disability 2020-09-10 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003485700 SCV004238790 likely pathogenic Syndromic X-linked intellectual disability 14 2023-03-30 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.