EGFR c.2125_2127delinsATG ;(p.E709M)

Variant ID: 7-55241677-GAA-ATG

NM_005228.3(EGFR):c.2125_2127delinsATG;(p.E709M)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

ErbB Family Signalling: A Paradigm for Oncogene Addiction and Personalized Oncology.

Cancers
Jacobi, Nico N; Seeboeck, Rita R; Hofmann, Elisabeth E; Eger, Andreas A
Publication Date: 2017-04-12

Variant appearance in text: EGFR: E709m
PubMed Link: 28417948
Variant Present in the following documents:
  • Main text
  • cancers-09-00033.pdf
View BVdb publication page