EGFR c.2322G>C ;(p.V774=)

Variant ID: 7-55249024-G-C

NM_005228.3(EGFR):c.2322G>C;(p.V774=)

This variant was identified in 3 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: V774V
PubMed Link: 35186718
Variant Present in the following documents:
  • Table_1.xlsx, sheet 2
View BVdb publication page



Formalin fixation increases deamination mutation signature but should not lead to false positive mutations in clinical practice.

Plos One
Prentice, Leah M LM; Miller, Ruth R RR; Knaggs, Jeff J; Mazloomian, Alborz A; Aguirre Hernandez, Rosalia R; Franchini, Patrick P; Parsa, Kourosh K; Tessier-Cloutier, Basile B; Lapuk, Anna A; Huntsman, David D; Schaeffer, David F DF; Sheffield, Brandon S BS
Publication Date: 2018

Variant appearance in text: N/A
PubMed Link: 29698444
Variant Present in the following documents:
View BVdb publication page



Comparison of next generation sequencing, SNaPshot assay and real-time polymerase chain reaction for lung adenocarcinoma EGFR mutation assessment.

Bmc Pulmonary Medicine
Cernomaz, Andrei-Tudor AT; Macovei, Ina Iuliana II; Pavel, Ionut I; Grigoriu, Carmen C; Marinca, Mihai M; Baty, Florent F; Peter, Simona S; Zonda, Radu R; Brutsche, Martin M; Grigoriu, Bogdan- Dragos B
Publication Date: 2016-05-23

Variant appearance in text: EGFR: 2322G>C
PubMed Link: 27215400
Variant Present in the following documents:
  • Main text
  • 12890_2016_Article_250.pdf
View BVdb publication page