|
Mutation Information
|
Mutation Site
|
T1768A |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
BCP |
|
Combined Mutation
|
bcp.T1768A+bcp.C1766G |
|
Genotype/Subtype
|
D |
|
Country
|
Belgium |
Literature Information
|
PubMed PMID
|
20087936
|
|
Disease
|
Chronic hepatitis B;
Liver cirrhosis
|
|
Published Year
|
2010 |
|
Journal
|
Journal of medical virology |
|
Title
|
Molecular evolutionary analysis and mutational pattern of full-length genomes of hepatitis B virus isolated from Belgian patients with different clinical manifestations. |
|
Author
|
Pourkarim MR,Amini-Bavil-Olyaee S,Verbeeck J,Lemey P,Zeller M,Rahman M,Maes P,Nevens F,Van Ranst M |
|
Evidence
|
Of note,62.5% of HBV genotype D showed a PC mutation(G1896A) and also novel BCP mutations C1766G/T+T1768A were detected in this genotype
|
|
|
HBV Mutation Detail Information