EGFR c.2532G>A ;(p.L844=)

Variant ID: 7-55259474-G-A

NM_005228.3(EGFR):c.2532G>A;(p.L844=)

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: L844L
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 3
  • pone.0196434.s001.xlsx, sheet 1
  • pone.0196434.s001.xlsx, sheet 2
View BVdb publication page



Limited copy number-high resolution melting (LCN-HRM) enables the detection and identification by sequencing of low level mutations in cancer biopsies.

Molecular Cancer
Do, Hongdo H; Dobrovic, Alexander A
Publication Date: 2009-10-08

Variant appearance in text: EGFR: 2532G>A; L844L
PubMed Link: 19811662
Variant Present in the following documents:
  • Main text
  • 1476-4598-8-82.pdf
View BVdb publication page