HBV Mutation Detail Information

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Mutation Information
Mutation Site G1764T
Mutation Type Nucleotide level
Gene/Protein/Region Type BCP
Combined Mutation bcp.G1764T+bcp.A1762T
Genotype/Subtype A;D;E
Country Morocco
Literature Information
PubMed PMID 22579480
Disease Chronic hepatitis B
Published Year 2012
Journal Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
Title HBV genotypes prevalence, precore and basal core mutants in Morocco.
Author Baha W,Ennaji MM,Lazar F,Melloul M,El Fahime E,El Malki A,Bennani A
Evidence BCP mutants were observed in 65.7% of cases, 22.9% were found to have the T1762/1764A double mutation, 18.6% had A1762/1764T mutation and 22.9% of patients showed the A1762T/G1764A double mutation with either A1762T/G1764T mutation.

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