EGFR c.2074C>T ;(p.L692F)

Variant ID: 7-55241626-C-T

NM_005228.3(EGFR):c.2074C>T;(p.L692F)

This variant was identified in 3 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: L692F
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 3
View BVdb publication page



N-acetylgalactosaminyltransferases in cancer.

Oncotarget
Hussain, Muhammad Ramzan Manwar MR; Hoessli, Daniel C DC; Fang, Min M
Publication Date: 2016-08-16

Variant appearance in text: EGFR: L692F
PubMed Link: 27322213
Variant Present in the following documents:
  • oncotarget-07-54067.pdf
View BVdb publication page



Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC.

British Journal Of Cancer
Kalikaki, A A; Koutsopoulos, A A; Trypaki, M M; Souglakos, J J; Stathopoulos, E E; Georgoulias, V V; Mavroudis, D D; Voutsina, A A
Publication Date: 2008-09-16

Variant appearance in text: EGFR: L692F
PubMed Link: 19238633
Variant Present in the following documents:
  • Main text
  • 6604629a.pdf
View BVdb publication page