EGFR c.1495_1496insTGGCCAGCG ;(p.C499delinsLASG)

Variant ID: 7-55228028-T-TTGGCCAGCG

NM_005228.3(EGFR):c.1495_1496insTGGCCAGCG;(p.C499delinsLASG)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identifying Actionable Variants Using Capture-Based Targeted Sequencing in 563 Patients With Non-Small Cell Lung Carcinoma.

Frontiers In Oncology
Jiang, Haiping H; Wang, Yinan Y; Xu, Hanlin H; Lei, Wei W; Yu, Xiaoyun X; Tian, Haiying H; Meng, Cong C; Wang, Xueying X; Zhao, Zicheng Z; Jin, Xiangfeng X
Publication Date: 2021

Variant appearance in text: EGFR: 1495_1496insTGGCCAGCG
PubMed Link: 35186718
Variant Present in the following documents:
  • Table_1.xlsx, sheet 2
View BVdb publication page



Exome sequencing identifies somatic mutations in novel driver genes in non-small cell lung cancer.

Aging
Zhang, Manman M; Zhang, Lele L; Li, Yan Y; Sun, Feng F; Fang, Ya Y; Zhang, Ruijia R; Wu, Jin J; Zhou, Guanbiao G; Song, Huaidong H; Xue, Liqiong L; Han, Bing B; Zheng, Cuixia C
Publication Date: 2020-07-06

Variant appearance in text: EGFR: 1495_1496insTGGCCAGCG
PubMed Link: 32629428
Variant Present in the following documents:
  • aging-12-103500-s002..xlsx, sheet 1
View BVdb publication page