EGFR c.2275_2276delinsCCTAG ;(p.I759delinsPS)

Variant ID: 7-55242505-AT-CCTAG

NM_005228.3(EGFR):c.2275_2276delinsCCTAG;(p.I759delinsPS)

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:

Patients harboring uncommon EGFR exon 19 deletion-insertion mutations respond well to first-generation EGFR inhibitors and osimeritinib upon acquisition of T790M.

Bmc Cancer
Wang, Yurong Y; Zheng, Ruipan R; Hu, Peizhu P; Zhang, Ziheng Z; Shen, Shujing S; Li, Xingya X
Publication Date: 2021-11-13

Variant appearance in text: EGFR: I759delinsPS
PubMed Link: 34774017
Variant Present in the following documents:
  • Main text
  • 12885_2021_Article_8942.pdf
View BVdb publication page