ClinVar Miner

Submissions for variant NM_004656.3(BAP1):c.1962A>C (p.Val654=) (rs148624125)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000565610 SCV000672738 likely benign Hereditary cancer-predisposing syndrome 2015-07-03 criteria provided, single submitter clinical testing
Color RCV000565610 SCV000682605 likely benign Hereditary cancer-predisposing syndrome 2016-08-05 criteria provided, single submitter clinical testing
GeneDx RCV000443767 SCV000535767 likely benign not specified 2017-11-24 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Clinical Services Laboratory,Illumina RCV000227884 SCV000445461 likely benign Tumor susceptibility linked to germline BAP1 mutations 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000227884 SCV000288748 benign Tumor susceptibility linked to germline BAP1 mutations 2018-01-02 criteria provided, single submitter 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.