EGFR c.2367C>T ;(p.I789=)

Variant ID: 7-55249069-C-T

NM_005228.3(EGFR):c.2367C>T;(p.I789=)

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: I789I
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 3
View BVdb publication page



Urothelial Cancer With Occult Bone Marrow Metastases and Isolated Thrombocytopenia.

Urology Case Reports
Alva, Ajjai A; Davis, Elizabeth E; Chinnaiyan, Arul M AM; Dhanasekaran, Saravana S; Mehra, Rohit R
Publication Date: 2015-07

Variant appearance in text: EGFR: 2367C>T
PubMed Link: 26793516
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page