EGFR c.2257_2259delinsAGCAACATCAGCGGT ;(p.P753delinsSNISG)

Variant ID: 7-55242487-CCG-AGCAACATCAGCGGT

NM_005228.3(EGFR):c.2257_2259delinsAGCAACATCAGCGGT;(p.P753delinsSNISG)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: P753delinsSNISG
PubMed Link: 34298851
Variant Present in the following documents:
  • Main text
  • cancers-13-03641.pdf
View BVdb publication page