EGFR c.2298G>A ;(p.M766I)

Variant ID: 7-55249000-G-A

NM_005228.3(EGFR):c.2298G>A;(p.M766I)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022

Variant appearance in text: rs1322818258
PubMed Link: 36561320
Variant Present in the following documents:
  • Table2.xlsx, sheet 4
View BVdb publication page



Presentation of EGFR mutations in 162 family probands with multiple primary lung cancer.

Translational Lung Cancer Research
Li, Chunxiang C; Wang, Yalong Y; Su, Kai K; Liu, Yu Y; Wang, Liyu L; Zheng, Bo B; Yan, Na N; Yuan, Dawei D; Zhang, Yanxiang Y; Xue, Liyan L; Gao, Shugeng S; He, Jie J
Publication Date: 2021-04

Variant appearance in text: EGFR: M766i
PubMed Link: 34012789
Variant Present in the following documents:
  • Main text
  • tlcr-10-04-1734.pdf
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: EGFR: M766I
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 3
View BVdb publication page



CA 19-9 and CA 125 as potential predictors of disease recurrence in resectable lung adenocarcinoma.

Plos One
Isaksson, Sofi S; Jönsson, Per P; Monsef, Nastaran N; Brunnström, Hans H; Bendahl, Pär-Ola PO; Jönsson, Mats M; Staaf, Johan J; Planck, Maria M
Publication Date: 2017

Variant appearance in text: EGFR: M766I
PubMed Link: 29049328
Variant Present in the following documents:
  • Main text
  • pone.0186284.pdf
View BVdb publication page



Beyond BRAF(V600): clinical mutation panel testing by next-generation sequencing in advanced melanoma.

The Journal Of Investigative Dermatology
Siroy, Alan E AE; Boland, Genevieve M GM; Milton, Denái R DR; Roszik, Jason J; Frankian, Silva S; Malke, Jared J; Haydu, Lauren L; Prieto, Victor G VG; Tetzlaff, Michael M; Ivan, Doina D; Wang, Wei-Lien WL; Torres-Cabala, Carlos C; Curry, Jonathan J; Roy-Chowdhuri, Sinchita S; Broaddus, Russell R; Rashid, Asif A; Stewart, John J; Gershenwald, Jeffrey E JE; Amaria, Rodabe N RN; Patel, Sapna P SP; Papadopoulos, Nicholas E NE; Bedikian, Agop A; Hwu, Wen-Jen WJ; Hwu, Patrick P; Diab, Adi A; Woodman, Scott E SE; Aldape, Kenneth D KD; Luthra, Rajyalakshmi R; Patel, Keyur P KP; Shaw, Kenna R KR; Mills, Gordon B GB; Mendelsohn, John J; Meric-Bernstam, Funda F; Kim, Kevin B KB; Routbort, Mark J MJ; Lazar, Alexander J AJ; Davies, Michael A MA
Publication Date: 2015-02

Variant appearance in text: EGFR: 2298G>A; M766I
PubMed Link: 25148578
Variant Present in the following documents:
  • NIHMS622327-supplement-supplement_1.pdf
View BVdb publication page



EGFR and KRAS mutations in patients with adenocarcinoma of the lung.

The Korean Journal Of Internal Medicine
Jang, Tae Won TW; Oak, Chul Ho CH; Chang, Hee Kyung HK; Suo, Soon Jung SJ; Jung, Mann Hong MH
Publication Date: 2009-03

Variant appearance in text: EGFR: M766I
PubMed Link: 19270482
Variant Present in the following documents:
  • kjim-24-48.pdf
View BVdb publication page