Mutation Information
Mutation Site
|
T1753A |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
BCP |
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 A1762T/G1764A, A1846T, and G1896A were the most prevalent mutations in patients with genotype B, while T1753V and A1762T/G1764A had a high prevalence in genotype C, especially in patients with HCC.
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