EGFR c.886C>T ;(p.P296S)

Variant ID: 7-55221842-C-T

NM_005228.3(EGFR):c.886C>T;(p.P296S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Characterization of Molecular Targets in Korean Patients with Gastrointestinal Stromal Tumors.

Journal Of Gastric Cancer
Park, Joonhong J; Yoo, Han Mo HM; Sul, Hae Jung HJ; Shin, Soyoung S; Lee, Seung Woo SW; Kim, Jeong Goo JG
Publication Date: 2020-03

Variant appearance in text: EGFR: 886C>T; Pro296Ser
PubMed Link: 32269842
Variant Present in the following documents:
  • Main text
  • jgc-20-29.pdf
View BVdb publication page



Kinome-wide decoding of network-attacking mutations rewiring cancer signaling.

Cell
Creixell, Pau P; Schoof, Erwin M EM; Simpson, Craig D CD; Longden, James J; Miller, Chad J CJ; Lou, Hua Jane HJ; Perryman, Lara L; Cox, Thomas R TR; Zivanovic, Nevena N; Palmeri, Antonio A; Wesolowska-Andersen, Agata A; Helmer-Citterich, Manuela M; Ferkinghoff-Borg, Jesper J; Itamochi, Hiroaki H; Bodenmiller, Bernd B; Erler, Janine T JT; Turk, Benjamin E BE; Linding, Rune R
Publication Date: 2015-09-24

Variant appearance in text: EGFR: P296S
PubMed Link: 26388441
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
View BVdb publication page