ClinVar Miner

Submissions for variant NM_000127.3(EXT1):c.912G>A (p.Trp304Ter)

dbSNP: rs1817868370
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 RCV001233740 SCV001406349 pathogenic Multiple congenital exostosis 2019-07-11 criteria provided, single submitter clinical testing This variant has been observed in individuals affected with multiple osteochondromas (PMID: 19810120, 26961984). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Trp304*) in the EXT1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in EXT1 are known to be pathogenic (PMID: 10679937, 11391482, 19810120). 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.