EGFR c.2312_2313delinsGCGGT ;(p.N771delinsSG)

Variant ID: 7-55249014-AC-GCGGT

NM_005228.3(EGFR):c.2312_2313delinsGCGGT;(p.N771delinsSG)

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 Sinonasal Squamous Cell Carcinoma.

Cancers
Pacini, Laura L; Cabal, Virginia N VN; Hermsen, Mario A MA; Huang, Paul H PH
Publication Date: 2022-01-13

Variant appearance in text: EGFR: N771delinsSG
PubMed Link: 35053553
Variant Present in the following documents:
  • Main text
  • cancers-14-00394.pdf
View BVdb publication page


EGFR Exon 20 Insertion Mutations in Sinonasal Squamous Cell Carcinoma.

Cancers
Pacini, Laura L; Cabal, Virginia N VN; Hermsen, Mario A MA; Huang, Paul H PH
Publication Date: 2022-01-13

Variant appearance in text: EGFR: N771delinsSG
PubMed Link: 35053553
Variant Present in the following documents:
  • Main text
  • cancers-14-00394.pdf
View BVdb publication page