EGFR c.2933A>T ;(p.Y978F)

Variant ID: 7-55268093-A-T

NM_005228.3(EGFR):c.2933A>T;(p.Y978F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Integrated genomic approaches identify upregulation of SCRN1 as a novel mechanism associated with acquired resistance to erlotinib in PC9 cells harboring oncogenic EGFR mutation.

Oncotarget
Kim, Nayoung N; Cho, Ahye A; Watanabe, Hideo H; Choi, Yoon-La YL; Aziz, Meraj M; Kassner, Michelle M; Joung, Je-Gun JG; Park, Angela Kyung-Joo AK; Francis, Joshua M JM; Bae, Joon Seol JS; Ahn, Soo-Min SM; Kim, Kyoung-Mee KM; Park, Joon Oh JO; Park, Woong-Yang WY; Ahn, Myung-Ju MJ; Park, Keunchil K; Koo, Jaehyung J; Yin, Hongwei Holly HH; Cho, Jeonghee J
Publication Date: 2016-03-22

Variant appearance in text: EGFR: Y978F
PubMed Link: 26883194
Variant Present in the following documents:
  • Main text
  • oncotarget-07-13797.pdf
View BVdb publication page