ClinVar Miner

Submissions for variant NM_000313.4(PROS1):c.1518G>A (p.Trp506Ter)

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 RCV002651716 SCV003525267 pathogenic Thrombophilia due to protein S deficiency, autosomal recessive 2022-06-14 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant is also known as W465X. This premature translational stop signal has been observed in individual(s) with protein S deficiency (PMID: 9031443). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Trp506*) in the PROS1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PROS1 are known to be pathogenic (PMID: 9241758).

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.