Mutation Information
Mutation Site
|
G1899A |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
PreC |
Country
|
China |
Literature Information
PubMed PMID
|
26202756
|
Disease
|
Acute on chronic liver failure
|
Published Year
|
2014 |
Journal
|
Hepatology international |
Title
|
Hepatitis B virus genotype B and mutations in basal core promoter and pre-core/core genes associated with acute-on-chronic liver failure: a multicenter cross-sectional study in China. |
Author
|
Yang G,Han M,Chen F,Xu Y,Chen E,Wang X,Liu Y,Sun J,Hou J,Ning Q,Wang Z |
Evidence
|
The occurrences of T1753 V, C1766T, T1768A, G1862T and G1899A mutations were low in the three patients groups and the frequency of almost all of these mutations did not even reach 20 % (Table 2).
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