ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.2185A>G (p.Ile729Val) (rs431825295)

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 RCV000219501 SCV000277581 uncertain significance Hereditary cancer-predisposing syndrome 2015-08-04 criteria provided, single submitter clinical testing
Color RCV000219501 SCV000906035 uncertain significance Hereditary cancer-predisposing syndrome 2018-04-26 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000082900 SCV000114974 uncertain significance Breast-ovarian cancer, familial 2 2012-05-01 no assertion criteria provided clinical testing

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.