ALK c.3250C>G ;(p.R1084G)

Variant ID: 2-29446317-G-C

NM_004304.4(ALK):c.3250C>G;(p.R1084G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive genetic testing identifies targetable genomic alterations in most patients with non-small cell lung cancer, specifically adenocarcinoma, single institute investigation.

Oncotarget
Vigneswaran, Janani J; Tan, Yi-Hung Carol YH; Murgu, Septimiu D SD; Won, Brian M BM; Patton, Kathryn Alexa KA; Villaflor, Victoria M VM; Hoffman, Philip C PC; Hensing, Thomas T; Hogarth, D Kyle DK; Malik, Renuka R; MacMahon, Heber H; Mueller, Jeffrey J; Simon, Cassie A CA; Vigneswaran, Wickii T WT; Wigfield, Christopher H CH; Ferguson, Mark K MK; Husain, Aliya N AN; Vokes, Everett E EE; Salgia, Ravi R
Publication Date: 2016-04-05

Variant appearance in text: ALK: R1084G
PubMed Link: 26934441
Variant Present in the following documents:
  • Main text
  • oncotarget-07-18876.pdf
View BVdb publication page