HBV Mutation Detail Information

> C1766T Search Result

Mutation Information

Mutation Site	C1766T
Mutation Type	Nucleotide level
Gene/Protein/Region Type	BCP
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).

Contents
Description

Mutation Information Note

Gene/Protein/Region Type: Virus Gene (e.g. LMP-1) or Virus Protein (e.g. Rep 68) or Virus Region (e.g. S, X)

Literature Information Note

Evidence: sentence contains this mutation information in the citation