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KIT c.2368C>T ;(p.H790Y)
Variant ID: 4-55599242-C-T
NM_000222.2(
KIT
):c.2368C>T;(p.H790Y)
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:
Clinical and Molecular-Based Approach in the Evaluation of Hepatocellular Carcinoma Recurrence after Radical Liver Resection.
Cancers
Gruttadauria, Salvatore S; Barbera, Floriana F; Conaldi, Pier Giulio PG; Pagano, Duilio D; Liotta, Rosa R; Gringeri, Enrico E; Miraglia, Roberto R; Burgio, Gaetano G; Barbara, Marco M; Pietrosi, Giada G; Cammà, Calogero C; Di Francesco, Fabrizio F
Publication Date: 2021-01-29
Variant appearance in text: KIT: His790Tyr
PubMed Link:
33572904
Variant Present in the following documents:
Main text
cancers-13-00518.pdf
View BVdb publication page
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: KIT: H790Y
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page