ClinVar Miner

List of variants reported as likely benign for Cowden syndrome 1 by Mendelics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_006218.4(PIK3CA):c.-138C>T rs149946088
NM_006218.4(PIK3CA):c.1060-9T>C rs750875731
NM_006218.4(PIK3CA):c.1146-30G>A rs8192676
NM_006218.4(PIK3CA):c.168C>T (p.Tyr56=) rs200868796
NM_006218.4(PIK3CA):c.1743C>T (p.Ala581=) rs370692448
NM_006218.4(PIK3CA):c.1747-9C>T rs201779641
NM_006218.4(PIK3CA):c.1767T>C (p.Asp589=) rs199540873
NM_006218.4(PIK3CA):c.2418T>C (p.Asp806=) rs199693043

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.