HBV Mutation Detail Information

> G1896A Search Result


Mutation Information
Mutation Site G1896A
Mutation Type Nucleotide level
Gene/Protein/Region Type PreC
Country india
Literature Information
PubMed PMID 12794713
Disease Chronic hepatitis B
Published Year 2003
Journal Journal of medical virology
Title Molecular epidemiology and transmission of hepatitis B virus in close family contacts of HBV-related chronic liver disease patients.
Author Thakur V,Kazim SN,Guptan RC,Malhotra V,Sarin SK
Evidence G1896A mutation was found in 7 of 11 (64%) specimens changing amino acid tryptophane (W) to stop codon.

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