ClinVar Miner

List of variants reported as benign for BAP1-related tumor predisposition syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_000059.3(BRCA2):c.10095delCins11 (p.?)
NM_004656.4(BAP1):c.*45C>G rs56898787
NM_004656.4(BAP1):c.1413T>G (p.Ala471=) rs34736117
NM_004656.4(BAP1):c.1786A>G (p.Ser596Gly) rs79014342
NM_004656.4(BAP1):c.2057-4G>T rs149499021

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.