EGFR c.292_294delinsTGG ;(p.R98W)

Variant ID: 7-55211049-CGA-TGG

NM_005228.3(EGFR):c.292_294delinsTGG;(p.R98W)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.

Clinical Pharmacology And Therapeutics
Kalman, L V LV; Agúndez, Jag J; Appell, M Lindqvist ML; Black, J L JL; Bell, G C GC; Boukouvala, S S; Bruckner, C C; Bruford, E E; Caudle, K K; Coulthard, S A SA; Daly, A K AK; Del Tredici, Al A; den Dunnen, J T JT; Drozda, K K; Everts, R E RE; Flockhart, D D; Freimuth, R R RR; Gaedigk, A A; Hachad, H H; Hartshorne, T T; Ingelman-Sundberg, M M; Klein, T E TE; Lauschke, V M VM; Maglott, D R DR; McLeod, H L HL; McMillin, G A GA; Meyer, U A UA; Müller, D J DJ; Nickerson, D A DA; Oetting, W S WS; Pacanowski, M M; Pratt, V M VM; Relling, M V MV; Roberts, A A; Rubinstein, W S WS; Sangkuhl, K K; Schwab, M M; Scott, S A SA; Sim, S C SC; Thirumaran, R K RK; Toji, L H LH; Tyndale, R F RF; van Schaik, Rhn R; Whirl-Carrillo, M M; Yeo, Ktj K; Zanger, U M UM
Publication Date: 2016-02

Variant appearance in text: EGFR: R98W
PubMed Link: 26479518
Variant Present in the following documents:
  • Main text
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: R98W
PubMed Link: 26388441
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
View BVdb publication page