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EGFR c.2353A>T ;(p.T785S)
Variant ID: 7-55249055-A-T
NM_005228.3(
EGFR
):c.2353A>T;(p.T785S)
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:
A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.
Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01
Variant appearance in text: EGFR: T785S
PubMed Link:
34963661
Variant Present in the following documents:
supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page
Integrative Bioinformatics approaches to therapeutic gene target selection in various cancers for Nitroglycerin.
Scientific Reports
Chinnappan, Jayaprakash J; Ramu, Akilandeswari A; V, Vidhya Rajalakshmi VR; S, Akil Kavya AK
Publication Date: 2021-11-11
Variant appearance in text: EGFR: T785S
PubMed Link:
34764329
Variant Present in the following documents:
Main text
41598_2021_Article_1508.pdf
View BVdb publication page