EGFR c.1677C>G ;(p.H559Q)

Variant ID: 7-55231471-C-G

NM_005228.3(EGFR):c.1677C>G;(p.H559Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Composite Clonal Analysis Reveals Transition of NSCLC Subtypes Through Accumulation of Gene Mutations: A Case Report.

Jto Clinical And Research Reports
Ando, Takahiro T; Kage, Hidenori H; Shinozaki-Ushiku, Aya A; Tatsuno, Kenji K; Tsutsumi, Shuichi S; Nagayama, Kazuhiro K; Nakajima, Jun J; Kohsaka, Shinji S; Miyagawa, Kiyoshi K; Aburatani, Hiroyuki H; Mano, Hiroyuki H; Nagase, Takahide T
Publication Date: 2022-02

Variant appearance in text: EGFR: 1677C>G
PubMed Link: 35199052
Variant Present in the following documents:
  • Main text
  • main.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: H559Q
PubMed Link: 26388441
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
View BVdb publication page