EGFR c.2299_2301del ;(p.A767del)

Variant ID: 7-55249001-GGCC-G

NM_005228.3(EGFR):c.2299_2301del;(p.A767del)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Successful treatment of a lung adenocarcinoma patient with a novel EGFR exon 20-ins mutation with afatinib: A case report.

Medicine
Cai, Yangyang Y; Wang, Xu X; Guo, Ye Y; Sun, Chao C; Xu, Yinghui Y; Qiu, Shi S; Ma, Kewei K
Publication Date: 2019-01

Variant appearance in text: EGFR: A767del
PubMed Link: 30608413
Variant Present in the following documents:
  • Main text
  • medi-98-e13890.pdf
View BVdb publication page



Impact of Concurrent Genomic Alterations Detected by Comprehensive Genomic Sequencing on Clinical Outcomes in East-Asian Patients with EGFR-Mutated Lung Adenocarcinoma.

Scientific Reports
Sato, Seijiro S; Nagahashi, Masayuki M; Koike, Terumoto T; Ichikawa, Hiroshi H; Shimada, Yoshifumi Y; Watanabe, Satoshi S; Kikuchi, Toshiaki T; Takada, Kazuki K; Nakanishi, Ryota R; Oki, Eiji E; Okamoto, Tatsuro T; Akazawa, Kouhei K; Lyle, Stephen S; Ling, Yiwei Y; Takabe, Kazuaki K; Okuda, Shujiro S; Wakai, Toshifumi T; Tsuchida, Masanori M
Publication Date: 2018-01-17

Variant appearance in text: EGFR: A767del
PubMed Link: 29343775
Variant Present in the following documents:
View BVdb publication page