CDH1 c.1195A>G ;(p.T399A)

Variant ID: 16-68847273-A-G

NM_004360.3(CDH1):c.1195A>G;(p.T399A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Amplicon-Based NGS Panels for Actionable Cancer Target Identification in Follicular Cell-Derived Thyroid Neoplasia.

Frontiers In Endocrinology
Madsen, Majbritt Busk MB; Kiss, Katalin K; Cilius Nielsen, Finn F; Bennedbæk, Finn Noe FN; Rossing, Maria M
Publication Date: 2020

Variant appearance in text: CDH1: 1195A>G; T399A
PubMed Link: 32265839
Variant Present in the following documents:
  • Table_1.pdf
View BVdb publication page



Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.

Nature Genetics
Dulak, Austin M AM; Stojanov, Petar P; Peng, Shouyong S; Lawrence, Michael S MS; Fox, Cameron C; Stewart, Chip C; Bandla, Santhoshi S; Imamura, Yu Y; Schumacher, Steven E SE; Shefler, Erica E; McKenna, Aaron A; Carter, Scott L SL; Cibulskis, Kristian K; Sivachenko, Andrey A; Saksena, Gordon G; Voet, Douglas D; Ramos, Alex H AH; Auclair, Daniel D; Thompson, Kristin K; Sougnez, Carrie C; Onofrio, Robert C RC; Guiducci, Candace C; Beroukhim, Rameen R; Zhou, Zhongren Z; Lin, Lin L; Lin, Jules J; Reddy, Rishindra R; Chang, Andrew A; Landrenau, Rodney R; Pennathur, Arjun A; Ogino, Shuji S; Luketich, James D JD; Golub, Todd R TR; Gabriel, Stacey B SB; Lander, Eric S ES; Beer, David G DG; Godfrey, Tony E TE; Getz, Gad G; Bass, Adam J AJ
Publication Date: 2013-05

Variant appearance in text: CDH1: T399A
PubMed Link: 23525077
Variant Present in the following documents:
  • NIHMS474888-supplement-1.pdf
View BVdb publication page