EGFR c.2311_2313delinsCATGTA ;(p.N771delinsHV)

Variant ID: 7-55249013-AAC-CATGTA

NM_005228.3(EGFR):c.2311_2313delinsCATGTA;(p.N771delinsHV)

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:

Clinical implementation of circulating tumour DNA testing for EGFR T790M for detection of treatment resistance in non-small cell lung cancer.

Journal Of Clinical Pathology
Spence, Tara T; Perera, Sheron S; Weiss, Jessica J; Grenier, Sylvie S; Ranich, Laura L; Shepherd, Frances F; Stockley, Tracy L TL
Publication Date: 2021-02

Variant appearance in text: EGFR: N771delinsHV
PubMed Link: 32471890
Variant Present in the following documents:
  • Main text
  • jclinpath-2020-206668.pdf
View BVdb publication page