EGFR c.2316_2317insAACCCT ;(p.N771_P772dup)

Variant ID: 7-55249018-C-CAACCCT

NM_005228.3(EGFR):c.2316_2317insAACCCT;(p.N771_P772dup)

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:

EGFR exon 20 insertion mutations in lung adenocarcinomas: prevalence, molecular heterogeneity, and clinicopathologic characteristics.

Molecular Cancer Therapeutics
Arcila, Maria E ME; Nafa, Khedoudja K; Chaft, Jamie E JE; Rekhtman, Natasha N; Lau, Christopher C; Reva, Boris A BA; Zakowski, Maureen F MF; Kris, Mark G MG; Ladanyi, Marc M
Publication Date: 2013-02

Variant appearance in text: EGFR: P772_H773insNP
PubMed Link: 23371856
Variant Present in the following documents:
  • Main text
View BVdb publication page