EGFR c.2231T>C ;(p.I744T)

Variant ID: 7-55242461-T-C

NM_005228.3(EGFR):c.2231T>C;(p.I744T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: I744T
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 2
View BVdb publication page



An In Silico Evaluation of Deleterious Nonsynonymous Single Nucleotide Polymorphisms in the ErbB3 Oncogene.

Bioresearch Open Access
Raghav, Dhwani D; Sharma, Vinay V
Publication Date: 2013-06

Variant appearance in text: EGFR: I744T
PubMed Link: 23741632
Variant Present in the following documents:
  • Main text
View BVdb publication page