ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.291A>C (p.Thr97=)

dbSNP: rs1131692085
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
Invitae RCV001452479 SCV001656146 likely benign Hereditary breast ovarian cancer syndrome 2018-03-14 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002259048 SCV002538163 likely benign Hereditary cancer-predisposing syndrome 2020-10-18 criteria provided, single submitter curation
Brotman Baty Institute, University of Washington RCV001073096 SCV001238592 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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.