ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.9307A>G (p.Ile3103Val) (rs80359203)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162720 SCV000213182 uncertain significance Hereditary cancer-predisposing syndrome 2014-09-02 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence,In silico models in agreement (benign),Rarity in general population databases (dbsnp, esp, 1000 genomes)
Counsyl RCV000077468 SCV000785126 uncertain significance Breast-ovarian cancer, familial 2 2017-05-01 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000077468 SCV000109266 uncertain significance Breast-ovarian cancer, familial 2 2010-05-26 no assertion criteria provided clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000077468 SCV000147607 uncertain significance Breast-ovarian cancer, familial 2 2011-10-19 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.