PIK3CA c.168C>G ;(p.Y56*)

Variant ID: 3-178916781-C-G

NM_006218.2(PIK3CA):c.168C>G;(p.Y56*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


An unusual case of Cowden syndrome associated with ganglioneuromatous polyposis.

Hereditary Cancer In Clinical Practice
Pistorius, Steffen S; Klink, Barbara B; Pablik, Jessica J; Rump, Andreas A; Aust, Daniela D; Garzarolli, Marlene M; Schröck, Evelin E; Schackert, Hans K HK
Publication Date: 2016

Variant appearance in text: PIK3CA: Tyr56*
PubMed Link: 27168869
Variant Present in the following documents:
  • Main text
  • 13053_2016_Article_51.pdf
View BVdb publication page