EGFR c.1907G>T ;(p.C636F)

Variant ID: 7-55238894-G-T

NM_005228.3(EGFR):c.1907G>T;(p.C636F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Resolving the phylogenetic origin of glioblastoma via multifocal genomic analysis of pre-treatment and treatment-resistant autopsy specimens.

Npj Precision Oncology
Brastianos, Priscilla K PK; Nayyar, Naema N; Rosebrock, Daniel D; Leshchiner, Ignaty I; Gill, Corey M CM; Livitz, Dimitri D; Bertalan, Mia S MS; D'Andrea, Megan M; Hoang, Kaitlin K; Aquilanti, Elisa E; Chukwueke, Ugonma N UN; Kaneb, Andrew A; Chi, Andrew A; Plotkin, Scott S; Gerstner, Elizabeth R ER; Frosch, Mathew P MP; Suva, Mario L ML; Cahill, Daniel P DP; Getz, Gad G; Batchelor, Tracy T TT
Publication Date: 2017

Variant appearance in text: EGFR: C636F
PubMed Link: 29872714
Variant Present in the following documents:
  • Main text
  • 41698_2017_Article_35.pdf
  • 41698_2017_35_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page