EGFR c.2310_2311insGGTGAC ;(p.D770_N771insGD)

Variant ID: 7-55249009-G-GGACGGT

NM_005228.3(EGFR):c.2310_2311insGGTGAC;(p.D770_N771insGD)

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:

Detection of Targetable Genetic Alterations in Korean Lung Cancer Patients: A Comparison Study of Single-Gene Assays and Targeted Next-Generation Sequencing.

Cancer Research And Treatment
Park, Eunhyang E; Shim, Hyo Sup HS
Publication Date: 2020-04

Variant appearance in text: EGFR: D770_N771insGD
PubMed Link: 31726498
Variant Present in the following documents:
  • Main text
  • crt-2019-305.pdf
View BVdb publication page