HBV Mutation Detail Information

> C1766T Search Result


Mutation Information
Mutation Site C1766T
Mutation Type Nucleotide level
Gene/Protein/Region Type BCP
Genotype/Subtype B;C
Viral Reference AY090460; AY090457; AY090454; AF405706; AB064310; AF160501; AF223965; AB036910; X69798; AB032431; X75657; X85254; M32138; X65259; AB014381; M12906; X04615; AB033554; AF100309; D00329; AF090842; X51970; X02763
Country China
Literature Information
PubMed PMID 20848146
Disease Chronic hepatitis B; Acute on chronic liver failure
Published Year 2011
Journal Journal of gastroenterology
Title Association of hepatitis B virus mutations in basal core promoter and precore regions with severity of liver disease: an investigation of 793 Chinese patients with mild and severe chronic hepatitis B and acute-on-chronic liver failure.
Author Xu Z,Ren X,Liu Y,Li X,Bai S,Zhong Y,Wang L,Mao P,Wang H,Xin S,Wong VW,Chan HL,Zoulim F,Xu D
Evidence Compared to CHB patients, ACLF patients had significantly higher mutation incidences at eight of the ten sites of interest, including T1753V (C/A/G), A1762T, G1764A, C1766T, and T1768A in the BCP region and G1862T, G1896A, and G1899A in the PC region.

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