HBV Mutation Detail Information

> A181T Search Result


Mutation Information
Mutation Site A181T
Mutation Type Amino acid level
Gene/Protein/Region Type RT
Combined Mutation rt.N236T+rt.A181T;rt.M250L+rt.N236T+rt.A181T;rt.A181T+rt.I169V
Relevant Drug adefovir dipivoxil (ADV);lamivudine (LAM)
Country China
Literature Information
PubMed PMID 28300730
Disease Chronic hepatitis B
Published Year 2017
Journal Antiviral therapy
Title The enrichment of HBV immune-escape mutations during nucleoside/nucleotide analogue therapy.
Author Shan M,Shen Z,Sun H,Zheng J,Zhang M
Evidence The substitution of rtA181T is another frequently detected primary mutation, conferring resistance to LMV and ADV, and leading to a premature stop codon sW172* in the corresponding S protein, while no significant difference in serum HBsAg level was observed in patients with or without this 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