EGFR c.265_267delinsATG ;(p.V89M)

Variant ID: 7-55211022-GTC-ATG

NM_005228.3(EGFR):c.265_267delinsATG;(p.V89M)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas.

Cell Reports
Way, Gregory P GP; Sanchez-Vega, Francisco F; La, Konnor K; Armenia, Joshua J; Chatila, Walid K WK; Luna, Augustin A; Sander, Chris C; Cherniack, Andrew D AD; Mina, Marco M; Ciriello, Giovanni G; Schultz, Nikolaus N; , ; Sanchez, Yolanda Y; Greene, Casey S CS
Publication Date: 2018-04-03

Variant appearance in text: EGFR: Val89Met
PubMed Link: 29617658
Variant Present in the following documents:
  • NIHMS958974-supplement-6.xlsx, sheet 1
View BVdb publication page



An In Silico Evaluation of Deleterious Nonsynonymous Single Nucleotide Polymorphisms in the ErbB3 Oncogene.

Bioresearch Open Access
Raghav, Dhwani D; Sharma, Vinay V
Publication Date: 2013-06

Variant appearance in text: EGFR: V89M
PubMed Link: 23741632
Variant Present in the following documents:
  • Main text
View BVdb publication page



Slitrks as emerging candidate genes involved in neuropsychiatric disorders.

Trends In Neurosciences
Proenca, Catia C CC; Gao, Kate P KP; Shmelkov, Sergey V SV; Rafii, Shahin S; Lee, Francis S FS
Publication Date: 2011-03

Variant appearance in text: EGFR: V89M
PubMed Link: 21315458
Variant Present in the following documents:
  • Main text
View BVdb publication page