|
Mutation Information
|
Mutation Site
|
G1899A |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
PreC |
|
Genotype/Subtype
|
B;C |
|
Country
|
China |
Literature Information
|
PubMed PMID
|
21739444
|
|
Disease
|
Acute on chronic liver failure
|
|
Published Year
|
2011 |
|
Journal
|
Journal of medical virology |
|
Title
|
Hepatitis B virus genotype B with G1896A and A1762T/G1764A mutations is associated with hepatitis B related acute-on-chronic liver failure. |
|
Author
|
Xiao L,Zhou B,Gao H,Ma S,Yang G,Xu M,Abbott WG,Chen J,Sun J,Wang Z,Hou J |
|
Evidence
|
The frequencies of the T1753V, C1766T, T1768A, G1862T, and G1899A mutations were low in the patients.
|
|
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HBV Mutation Detail Information