ERBB2 c.2339_2340insGGCTCCCCA ;(p.P780_Y781insAPQ)

Variant ID: 17-37881010-C-CGGCTCCCCA

NM_004448.2(ERBB2):c.2339_2340insGGCTCCCCA;(p.P780_Y781insAPQ)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Analysis of the frequency of oncogenic driver mutations and correlation with clinicopathological characteristics in patients with lung adenocarcinoma from Northeastern Switzerland.

Diagnostic Pathology
Grosse, Alexandra A; Grosse, Claudia C; Rechsteiner, Markus M; Soltermann, Alex A
Publication Date: 2019-02-11

Variant appearance in text: ERBB2: 2339_2340insGGCTCCCCA
PubMed Link: 30744664
Variant Present in the following documents:
  • Main text
  • 13000_2019_Article_789.pdf
View BVdb publication page