EGFR c.2235_2252delinsTT ;(p.K745Nfs*16)

Variant ID: 7-55242465-GGAATTAAGAGAAGCAAC-TT

NM_005228.3(EGFR):c.2235_2252delinsTT;(p.K745Nfs*16)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Evolution and clinical impact of co-occurring genetic alterations in advanced-stage EGFR-mutant lung cancers.

Nature Genetics
Blakely, Collin M CM; Watkins, Thomas B K TBK; Wu, Wei W; Gini, Beatrice B; Chabon, Jacob J JJ; McCoach, Caroline E CE; McGranahan, Nicholas N; Wilson, Gareth A GA; Birkbak, Nicolai J NJ; Olivas, Victor R VR; Rotow, Julia J; Maynard, Ashley A; Wang, Victoria V; Gubens, Matthew A MA; Banks, Kimberly C KC; Lanman, Richard B RB; Caulin, Aleah F AF; St John, John J; Cordero, Anibal R AR; Giannikopoulos, Petros P; Simmons, Andrew D AD; Mack, Philip C PC; Gandara, David R DR; Husain, Hatim H; Doebele, Robert C RC; Riess, Jonathan W JW; Diehn, Maximilian M; Swanton, Charles C; Bivona, Trever G TG
Publication Date: 2017-12

Variant appearance in text: EGFR: 2233_2252delinsAATT
PubMed Link: 29106415
Variant Present in the following documents:
  • Main text
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