Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGFR c.2311_2312delinsGGTAG ;(p.N771delinsGS)
Variant ID: 7-55249013-AA-GGTAG
NM_005228.3(
EGFR
):c.2311_2312delinsGGTAG;(p.N771delinsGS)
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: N771delinsGS
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: N771delinsGS
PubMed Link:
35053553
Variant Present in the following documents:
Main text
cancers-14-00394.pdf
View BVdb publication page