EGFR c.2302_2303insCACTTGCAA ;(p.A767_S768insTLA)

Variant ID: 7-55249003-C-CACACTTGCA

NM_005228.3(EGFR):c.2302_2303insCACTTGCAA;(p.A767_S768insTLA)

This variant was identified in 2 publications

View GRCh38 version.



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

Publications:

Real-world clinical treatment outcomes in Chinese non-small cell lung cancer with EGFR exon 20 insertion mutations.

Frontiers In Oncology
Shi, Chao C; Xing, Ruyue R; Li, Mengmeng M; Feng, Junnan J; Sun, Rui R; Wei, Bing B; Guo, Yongjun Y; Ma, Jie J; Wang, Huijuan H
Publication Date: 2022

Variant appearance in text: EGFR: A767_S768insTLA
PubMed Link: 36119499
Variant Present in the following documents:
  • Main text
  • fonc-12-949304.pdf
View BVdb publication page


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: A767_S768insTLA
PubMed Link: 23371856
Variant Present in the following documents:
  • Main text
View BVdb publication page