EGFR c.2318_2319insACC ;(p.H773delinsQP)

Variant ID: 7-55249020-A-AACC

NM_005228.3(EGFR):c.2318_2319insACC;(p.H773delinsQP)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Next generation sequencing and molecular imaging identify EGFR mutation and amplification in a glioblastoma multiforme patient treated with an EGFR inhibitor: a case report.

Oncotarget
Zhou, Ke K; Yao, Hui H; Zhang, Xuewen X; Liu, Jiangang J; Qi, Zhenyu Z; Xie, Xueshun X; Xu, Xiaoting X; Zhou, Youxin Y; Yu, Zhengquan Z; Wang, Zhong Z; Che, Yanjun Y; Huang, Yulun Y
Publication Date: 2017-07-25

Variant appearance in text: EGFR: 2318_2319insACC
PubMed Link: 28611289
Variant Present in the following documents:
  • Main text
View BVdb publication page