EGFR c.2360A>C ;(p.Q787P)

Variant ID: 7-55249062-A-C

NM_005228.3(EGFR):c.2360A>C;(p.Q787P)

This variant was identified in 4 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: EGFR: Q787P
PubMed Link: 36561320
Variant Present in the following documents:
  • Table3.xlsx, sheet 1
  • Table2.xlsx, sheet 4
View BVdb publication page



Contribution of the IdyllaTM System to Improving the Therapeutic Care of Patients with NSCLC through Early Screening of EGFR Mutations.

Current Oncology (Toronto, Ont.)
Petiteau, Constance C; Robinet-Zimmermann, Gwladys G; Riot, Adèle A; Dorbeau, Marine M; Richard, Nicolas N; Blanc-Fournier, Cécile C; Bibeau, Frédéric F; Deshayes, Simon S; Bergot, Emmanuel E; Gervais, Radj R; Levallet, Guénaëlle G
Publication Date: 2021-11-03

Variant appearance in text: EGFR: 2360A>C; Gln787Pro
PubMed Link: 34898548
Variant Present in the following documents:
  • Main text
  • curroncol-28-00376.pdf
View BVdb publication page



Contribution of the IdyllaTM System to Improving the Therapeutic Care of Patients with NSCLC through Early Screening of EGFR Mutations.

Current Oncology (Toronto, Ont.)
Petiteau, Constance C; Robinet-Zimmermann, Gwladys G; Riot, Adèle A; Dorbeau, Marine M; Richard, Nicolas N; Blanc-Fournier, Cécile C; Bibeau, Frédéric F; Deshayes, Simon S; Bergot, Emmanuel E; Gervais, Radj R; Levallet, Guénaëlle G
Publication Date: 2021-11-03

Variant appearance in text: EGFR: 2360A>C; Gln787Pro
PubMed Link: 34898548
Variant Present in the following documents:
  • Main text
  • curroncol-28-00376.pdf
View BVdb publication page



Identification of pathogenic missense mutations using protein stability predictors.

Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21

Variant appearance in text: EGFR: Q787P
PubMed Link: 32958805
Variant Present in the following documents:
  • 41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page