Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGFR c.894T>G ;(p.N298K)
Variant ID: 7-55223527-T-G
NM_005228.3(
EGFR
):c.894T>G;(p.N298K)
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:
In vitro anticancer activity of hydrogen sulfide and nitric oxide alongside nickel nanoparticle and novel mutations in their genes in CRC patients.
Scientific Reports
Housein, Zjwan Z; Kareem, Tayeb Sabir TS; Salihi, Abbas A
Publication Date: 2021-01-28
Variant appearance in text: EGFR: 894T>G
PubMed Link:
33510426
Variant Present in the following documents:
Main text
41598_2021_Article_82244.pdf
View BVdb publication page