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EPHA2 c.2874C>A ;(p.I958=)
Variant ID: 1-16451767-G-T
NM_004431.3(
EPHA2
):c.2874C>A;(p.I958=)
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: I958I
PubMed Link:
31056474
Variant Present in the following documents:
mmc3.xlsx, sheet 1
mmc1.xls, sheet 1
View BVdb publication page
The chronological sequence of somatic mutations in early gastric carcinogenesis inferred from multiregion sequencing of gastric adenomas.
Oncotarget
Lim, Chul-Hyun CH; Cho, Yu Kyung YK; Kim, Sang Woo SW; Choi, Myung-Gyu MG; Rhee, Je-Keun JK; Chung, Yeun-Jun YJ; Lee, Sug-Hyung SH; Kim, Tae-Min TM
Publication Date: 2016-06-28
Variant appearance in text: EPHA2: I958I
PubMed Link:
27175599
Variant Present in the following documents:
oncotarget-07-39758-s006.xlsx, sheet 1
View BVdb publication page