ClinVar Miner

Submissions for variant NM_001382.4(DPAGT1):c.398C>G (p.Ser133Ter)

dbSNP: rs1315559074
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000792938 SCV000932267 pathogenic DPAGT1-congenital disorder of glycosylation; Congenital myasthenic syndrome 13 2018-09-18 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in DPAGT1 are known to be pathogenic (PMID: 22742743). This variant has not been reported in the literature in individuals with DPAGT1-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Ser133*) in the DPAGT1 gene. It is expected to result in an absent or disrupted protein product.

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.