EGFR c.1386A>G ;(p.I462M)

Variant ID: 7-55227919-A-G

NM_005228.3(EGFR):c.1386A>G;(p.I462M)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022

Variant appearance in text: EGFR: I462M
PubMed Link: 36561320
Variant Present in the following documents:
  • Table3.xlsx, sheet 1
  • Table2.xlsx, sheet 4
View BVdb publication page



Preclinical assessment of combination therapy of EGFR tyrosine kinase inhibitors in a highly heterogeneous tumor model.

Oncogene
Ikeuchi, Hiroshi H; Hirose, Takeshi T; Ikegami, Masachika M; Takamochi, Kazuya K; Suzuki, Kenji K; Mano, Hiroyuki H; Kohsaka, Shinji S
Publication Date: 2022-04

Variant appearance in text: EGFR: I462M
PubMed Link: 35304574
Variant Present in the following documents:
  • 41388_2022_Article_2263.pdf
View BVdb publication page



Discordant Mutations in Paired Primary and Metastatic Endometrial Adenocarcinomas Identified by Semiconductor-Based Sequencing for Rapid Cancer Genotyping.

Reproductive Sciences (Thousand Oaks, Calif.)
Bergstrom, Colin P CP; Geest, Koen De K; O'Gara, Rebecca R; Corless, Christopher L CL; Morgan, Terry K TK
Publication Date: 2016-11

Variant appearance in text: EGFR: I462M
PubMed Link: 27170661
Variant Present in the following documents:
  • Main text
View BVdb publication page