EGFR c.382A>G ;(p.N128D)

Variant ID: 7-55211139-A-G

NM_005228.3(EGFR):c.382A>G;(p.N128D)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic polymorphisms as non-modifiable susceptibility factors to laryngeal cancer.

Bioscience Reports
Escalante, Paula P; Barría, Tamara T; Cancino, Miguel M; Rahal, Maritza M; Cerpa, Leslie L; Sandoval, Christopher C; Molina-Mellico, Sebastian S; Suárez, Marcelo M; Martínez, Matias M; Cáceres, Dante Daniel DD; Quiñones, Luis Abel LA; Varela, Nelson Miguel NM
Publication Date: 2020-05-29

Variant appearance in text: EGFR: 382A>G
PubMed Link: 32338278
Variant Present in the following documents:
  • Main text
  • bsr-40-bsr20191188.pdf
View BVdb publication page



Hellebrin and its aglycone form hellebrigenin display similar in vitro growth inhibitory effects in cancer cells and binding profiles to the alpha subunits of the Na+/K+-ATPase.

Molecular Cancer
Moreno Y Banuls, Laetitia L; Katz, Adriana A; Miklos, Walter W; Cimmino, Alessio A; Tal, Daniel M DM; Ainbinder, Elena E; Zehl, Martin M; Urban, Ernst E; Evidente, Antonio A; Kopp, Brigitte B; Berger, Walter W; Feron, Olivier O; Karlish, Steven S; Kiss, Robert R
Publication Date: 2013-04-26

Variant appearance in text: EGFR: N128D
PubMed Link: 23621895
Variant Present in the following documents:
  • 1476-4598-12-33.pdf
View BVdb publication page