EGFR c.2241_2248del ;(p.L747Ffs*13)

Variant ID: 7-55242471-TAAGAGAAG-T

NM_005228.3(EGFR):c.2241_2248del;(p.L747Ffs*13)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Complex mutations & subpopulations of deletions at exon 19 of EGFR in NSCLC revealed by next generation sequencing: potential clinical implications.

Plos One
Marchetti, Antonio A; Del Grammastro, Maela M; Filice, Giampaolo G; Felicioni, Lara L; Rossi, Giulio G; Graziano, Paolo P; Sartori, Giuliana G; Leone, Alvaro A; Malatesta, Sara S; Iacono, Michele M; Guetti, Luigi L; Viola, Patrizia P; Mucilli, Felice F; Cuccurullo, Franco F; Buttitta, Fiamma F
Publication Date: 2012

Variant appearance in text: EGFR: 2241_2248del
PubMed Link: 22848739
Variant Present in the following documents:
  • Main text
  • pone.0042164.pdf
View BVdb publication page