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EPHA2 c.2016C>T ;(p.H672=)
Variant ID: 1-16459712-G-A
NM_004431.3(
EPHA2
):c.2016C>T;(p.H672=)
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:
Stemness underpinning all steps of human colorectal cancer defines the core of effective therapeutic strategies.
Ebiomedicine
Visioli, Alberto A; Giani, Fabrizio F; Trivieri, Nadia N; Pracella, Riccardo R; Miccinilli, Elide E; Cariglia, Maria Grazia MG; Palumbo, Orazio O; Arleo, Andrea A; Dezi, Fabio F; Copetti, Massimiliano M; Cajola, Laura L; Restelli, Silvia S; Papa, Valerio V; Sciuto, Antonio A; Latiano, Tiziana Pia TP; Carella, Massimo M; Amadori, Dino D; Gallerani, Giulia G; Ricci, Riccardo R; Alfieri, Sergio S; Pesole, Graziano G; Vescovi, Angelo L AL; Binda, Elena E
Publication Date: 2019-06
Variant appearance in text: EPHA2: 2016C>T; H672H
PubMed Link:
31056474
Variant Present in the following documents:
mmc1.xls, sheet 1
View BVdb publication page
Germ-line and somatic EPHA2 coding variants in lens aging and cataract.
Plos One
Bennett, Thomas M TM; M'Hamdi, Oussama O; Hejtmancik, J Fielding JF; Shiels, Alan A
Publication Date: 2017
Variant appearance in text: EPHA2: 2016C>T; H672H
PubMed Link:
29267365
Variant Present in the following documents:
Main text
pone.0189881.pdf
View BVdb publication page