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KIT c.207G>C ;(p.E69D)
Variant ID: 4-55561817-G-C
NM_000222.2(
KIT
):c.207G>C;(p.E69D)
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:
Evolving neoantigen profiles in colorectal cancers with DNA repair defects.
Genome Medicine
Rospo, Giuseppe G; Lorenzato, Annalisa A; Amirouchene-Angelozzi, Nabil N; Magrì, Alessandro A; Cancelliere, Carlotta C; Corti, Giorgio G; Negrino, Carola C; Amodio, Vito V; Montone, Monica M; Bartolini, Alice A; Barault, Ludovic L; Novara, Luca L; Isella, Claudio C; Medico, Enzo E; Bertotti, Andrea A; Trusolino, Livio L; Germano, Giovanni G; Di Nicolantonio, Federica F; Bardelli, Alberto A
Publication Date: 2019-06-28
Variant appearance in text: KIT: E69D
PubMed Link:
31253177
Variant Present in the following documents:
13073_2019_654_MOESM2_ESM.xlsx, sheet 24
View BVdb publication page
Adherence to the guidelines and the pathological diagnosis of high-risk gastrointestinal stromal tumors in the real world.
Gastric Cancer : Official Journal Of The International Gastric Cancer Association And The Japanese Gastric Cancer Association
Nishida, Toshirou T; Sakai, Yoshiharu Y; Takagi, Masakazu M; Ozaka, Masato M; Kitagawa, Yuko Y; Kurokawa, Yukinori Y; Masuzawa, Toru T; Naito, Yoichi Y; Kagimura, Tatsuo T; Hirota, Seiichi S; ,
Publication Date: 2020-01
Variant appearance in text: KIT: E69D
PubMed Link:
31041650
Variant Present in the following documents:
Main text
View BVdb publication page