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EGFR c.2398_2399delinsCT ;(p.D800L)
Variant ID: 7-55249100-GA-CT
NM_005228.3(
EGFR
):c.2398_2399delinsCT;(p.D800L)
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:
A platinum-based hybrid drug design approach to circumvent acquired resistance to molecular targeted tyrosine kinase inhibitors.
Scientific Reports
Wei, Yuming Y; Poon, Daniel C DC; Fei, Rong R; Lam, Amy S M AS; Au-Yeung, Steve C F SC; To, Kenneth K W KK
Publication Date: 2016-05-06
Variant appearance in text: EGFR: D800L
PubMed Link:
27150583
Variant Present in the following documents:
Main text
srep25363-s1.pdf
srep25363.pdf
View BVdb publication page