EGFR c.2311_2313delinsGGTTTT ;(p.N771delinsGF)

Variant ID: 7-55249013-AAC-GGTTTT

NM_005228.3(EGFR):c.2311_2313delinsGGTTTT;(p.N771delinsGF)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Frequency, underdiagnosis, and heterogeneity of epidermal growth factor receptor exon 20 insertion mutations using real-world genomic datasets.

Molecular Oncology
Viteri, Santiago S; Minchom, Anna A; Bazhenova, Lyudmila L; Ou, Sai-Hong Ignatius SI; Bauml, Joshua M JM; Shell, Scott A SA; Schaffer, Michael M; Gu, Junchen J; Rose, Jennifer B JB; Curtin, Joshua C JC; Mahadevia, Parthiv P; Girard, Nicolas N
Publication Date: 2022-10-21

Variant appearance in text: EGFR: N771delinsGF
PubMed Link: 36269676
Variant Present in the following documents:
  • MOL2-17-230.pdf
View BVdb publication page



EGFR Exon 20 Insertion Mutations in Sinonasal Squamous Cell Carcinoma.

Cancers
Pacini, Laura L; Cabal, Virginia N VN; Hermsen, Mario A MA; Huang, Paul H PH
Publication Date: 2022-01-13

Variant appearance in text: EGFR: N771delinsGF
PubMed Link: 35053553
Variant Present in the following documents:
  • Main text
  • cancers-14-00394.pdf
View BVdb publication page



EGFR Exon 20 Insertion Mutations in Sinonasal Squamous Cell Carcinoma.

Cancers
Pacini, Laura L; Cabal, Virginia N VN; Hermsen, Mario A MA; Huang, Paul H PH
Publication Date: 2022-01-13

Variant appearance in text: EGFR: N771delinsGF
PubMed Link: 35053553
Variant Present in the following documents:
  • Main text
  • cancers-14-00394.pdf
View BVdb publication page



A Nationwide Study on the Impact of Routine Testing for EGFR Mutations in Advanced NSCLC Reveals Distinct Survival Patterns Based on EGFR Mutation Subclasses.

Cancers
Koopman, Bart B; Cajiao Garcia, Betzabel N BN; Kuijpers, Chantal C H J CCHJ; Damhuis, Ronald A M RAM; van der Wekken, Anthonie J AJ; Groen, Harry J M HJM; Schuuring, Ed E; Willems, Stefan M SM; van Kempen, Léon C LC
Publication Date: 2021-07-20

Variant appearance in text: EGFR: N771delinsGF
PubMed Link: 34298851
Variant Present in the following documents:
  • Main text
  • cancers-13-03641.pdf
View BVdb publication page



EGFR and BRAF mutations in inverted sinonasal papilloma - a more complex landscape?

Virchows Archiv : An International Journal Of Pathology
Zonnur, Sarah S; Erbersdobler, Andreas A; Schneider, Björn B
Publication Date: 2021-05

Variant appearance in text: EGFR: N771delinsGF
PubMed Link: 33048186
Variant Present in the following documents:
  • Main text
  • 428_2020_Article_2945.pdf
View BVdb publication page



Human papillomavirus (HPV) and somatic EGFR mutations are essential, mutually exclusive oncogenic mechanisms for inverted sinonasal papillomas and associated sinonasal squamous cell carcinomas.

Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Udager, A M AM; McHugh, J B JB; Goudsmit, C M CM; Weigelin, H C HC; Lim, M S MS; Elenitoba-Johnson, K S J KSJ; Betz, B L BL; Carey, T E TE; Brown, N A NA
Publication Date: 2018-02-01

Variant appearance in text: EGFR: N771delinsGF
PubMed Link: 29145573
Variant Present in the following documents:
  • Main text
View BVdb publication page