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HBV Mutation Detail Information

> V17F Search Result


Mutation Information
Mutation Site V17F
Mutation Type Amino acid level
Gene/Protein/Region Type PreC
Amino acid_Mutation G1862T
Genotype/Subtype D
Literature Information
PubMed PMID 18201182
Published Year 2008
Journal Hepatology research : the official journal of the Japan Society of Hepatology
Title A valine to phenylalanine mutation in the precore region of hepatitis B virus causes intracellular retention and impaired secretion of HBe-antigen.
Author Chen CY,Crowther C,Kew MC,Kramvis A
Evidence The G1862T mutation in the bulge of the RNA encapsidation signal (codon 17) changes the valine at the −3 position to the signal peptide cleavage site at position 19 to phenylalanine
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