EGFR c.2292C>T ;(p.Y764=)

Variant ID: 7-55248994-C-T

NM_005228.3(EGFR):c.2292C>T;(p.Y764=)

This variant was identified in 3 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: Y764Y
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 2
  • pone.0196434.s001.xlsx, sheet 3
View BVdb publication page



Missense Mutations in Exons 18-24 of EGFR in Hepatocellular Carcinoma Tissues.

Biomed Research International
Panvichian, Ravat R; Tantiwetrueangdet, Anchalee A; Sornmayura, Pattana P; Leelaudomlipi, Surasak S
Publication Date: 2015

Variant appearance in text: EGFR: Y764Y
PubMed Link: 26436086
Variant Present in the following documents:
  • Main text
  • BMRI2015-171845.pdf
View BVdb publication page



Amplicon sequencing of colorectal cancer: variant calling in frozen and formalin-fixed samples.

Plos One
Betge, Johannes J; Kerr, Grainne G; Miersch, Thilo T; Leible, Svenja S; Erdmann, Gerrit G; Galata, Christian L CL; Zhan, Tianzuo T; Gaiser, Timo T; Post, Stefan S; Ebert, Matthias P MP; Horisberger, Karoline K; Boutros, Michael M
Publication Date: 2015

Variant appearance in text: EGFR: Y764Y
PubMed Link: 26010451
Variant Present in the following documents:
  • pone.0127146.s014.xlsx, sheet 3
View BVdb publication page