EGFR c.2317_2319delinsTATAACCCTTAT ;(p.H773delinsYNPY)

Variant ID: 7-55249019-CAC-TATAACCCTTAT

NM_005228.3(EGFR):c.2317_2319delinsTATAACCCTTAT;(p.H773delinsYNPY)

This variant was identified in 2 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: H773delinsYNPY
PubMed Link: 36269676
Variant Present in the following documents:
  • MOL2-17-230.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: H773delinsYNPY
PubMed Link: 34298851
Variant Present in the following documents:
  • Main text
  • cancers-13-03641.pdf
View BVdb publication page