ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.532del (p.His178fs) (rs786202525)

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
Ambry Genetics RCV000215848 SCV000273318 pathogenic Hereditary cancer-predisposing syndrome 2016-01-20 criteria provided, single submitter clinical testing
OMIM RCV000013176 SCV000033423 pathogenic Li-Fraumeni syndrome 1 1998-04-01 no assertion criteria provided literature only
German Consortium for Hereditary Breast and Ovarian Cancer Center Cologne,University Hospital Cologne RCV000785474 SCV000924046 pathogenic Ovarian Neoplasms 2018-12-01 no assertion criteria provided research

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.