ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.1977G>A (p.Trp659Ter) (rs1600182107)

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 RCV000823654 SCV000964521 pathogenic Alagille syndrome 1 2019-01-15 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Trp659*) in the JAG1 gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). Variants resulting in this protein change have been observed to be de novo in individuals affected with Alagille syndrome (PMID: 29783821, 12497640). Loss-of-function variants in JAG1 are known to be pathogenic (PMID: 11180599). For these reasons, this variant has been classified as 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.