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EGFR c.2634C>T ;(p.I878=)
Variant ID: 7-55260467-C-T
NM_005228.3(
EGFR
):c.2634C>T;(p.I878=)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Meta-Data Analysis to Explore the Hub of the Hub-Genes That Influence SARS-CoV-2 Infections Highlighting Their Pathogenetic Processes and Drugs Repurposing.
Vaccines
Mosharaf, Md Parvez MP; Kibria, Md Kaderi MK; Hossen, Md Bayazid MB; Islam, Md Ariful MA; Reza, Md Selim MS; Mahumud, Rashidul Alam RA; Alam, Khorshed K; Gow, Jeff J; Mollah, Md Nurul Haque MNH
Publication Date: 2022-08-03
Variant appearance in text: EGFR: ILE878ILE
PubMed Link:
36016137
Variant Present in the following documents:
vaccines-10-01248.pdf
View BVdb publication page
Missense Mutations in Exons 18-24 of EGFR in Hepatocellular Carcinoma Tissues.
Biomed Research International
Panvichian, Ravat R; Tantiwetrueangdet, Anchalee A; Sornmayura, Pattana P; Leelaudomlipi, Surasak S
Publication Date: 2015
Variant appearance in text: EGFR: 2634C>T; I878I
PubMed Link:
26436086
Variant Present in the following documents:
Main text
BMRI2015-171845.pdf
View BVdb publication page