EGFR c.2132A>G ;(p.E711G)

Variant ID: 7-55241684-A-G

NM_005228.3(EGFR):c.2132A>G;(p.E711G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Formalin fixation increases deamination mutation signature but should not lead to false positive mutations in clinical practice.

Plos One
Prentice, Leah M LM; Miller, Ruth R RR; Knaggs, Jeff J; Mazloomian, Alborz A; Aguirre Hernandez, Rosalia R; Franchini, Patrick P; Parsa, Kourosh K; Tessier-Cloutier, Basile B; Lapuk, Anna A; Huntsman, David D; Schaeffer, David F DF; Sheffield, Brandon S BS
Publication Date: 2018

Variant appearance in text: EGFR: E711G
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 2
  • pone.0196434.s001.xlsx, sheet 3
  • pone.0196434.s001.xlsx, sheet 1
View BVdb publication page



Prevalence of EGFR Mutations in Lung Cancer in Uruguayan Population.

Journal Of Cancer Epidemiology
Berois, Nora N; Touya, Diego D; Ubillos, Luis L; Bertoni, Bernardo B; Osinaga, Eduardo E; Varangot, Mario M
Publication Date: 2017

Variant appearance in text: EGFR: 2132A>G; E711G
PubMed Link: 28744312
Variant Present in the following documents:
  • Main text
  • JCE2017-6170290.pdf
View BVdb publication page