EGFR c.567G>T ;(p.K189N)

Variant ID: 7-55218994-G-T

NM_005228.3(EGFR):c.567G>T;(p.K189N)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: K189N
PubMed Link: 26388441
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
View BVdb publication page



Red fluorescent protein with reversibly photoswitchable absorbance for photochromic FRET.

Chemistry & Biology
Subach, Fedor V FV; Zhang, Lijuan L; Gadella, Theodorus W J TW; Gurskaya, Nadya G NG; Lukyanov, Konstantin A KA; Verkhusha, Vladislav V VV
Publication Date: 2010-07-30

Variant appearance in text: EGFR: K189N
PubMed Link: 20659687
Variant Present in the following documents:
  • Main text
View BVdb publication page