ClinVar Miner

Submissions for variant NM_006012.4(CLPP):c.440G>C (p.Cys147Ser)

dbSNP: rs398123034
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000049283 SCV000077541 pathogenic Perrault syndrome 3 2013-04-04 no assertion criteria provided literature only
Department of Molecular and Human Genetics, Baylor College of Medicine RCV000049283 SCV000249612 pathogenic Perrault syndrome 3 2013-06-17 no assertion criteria provided research
GeneReviews RCV002513676 SCV003525968 not provided Perrault syndrome no assertion provided literature only

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.