|
Mutation Information
|
Mutation Site
|
G1896A |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
PreC |
|
Nucleotide_Mutation
|
W28* |
|
Country
|
Italian |
Literature Information
|
PubMed PMID
|
31846615
|
|
Disease
|
Acute hepatitis B
|
|
Published Year
|
2020 |
|
Journal
|
Virus research |
|
Title
|
The genetic variability of hepatitis B virus subgenotype F1b precore/core gene is related to the outcome of the acute infection. |
|
Author
|
Trinks J,Marciano S,Esposito I,Franco A,Mascardi MF,Mendizabal M,Livellara B,Arrigo D,Calzetta P,Vujacich C,Giunta D,Gadano A,Flichman D |
|
Evidence
|
Mutations T1753C, A1762T, G1764A, C1766T, T1768A G1896A, G2092T and T2107C were associated with acute liver failure and progression to chronic hepatitis.
|
|
|
HBV Mutation Detail Information