HBV Mutation Detail Information

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Mutation Information
Mutation Site W123L
Mutation Type Amino acid level
Gene/Protein/Region Type X
Amino acid_Mutation G1742T
Genotype/Subtype C
Viral Reference M12906
Country China
Literature Information
PubMed PMID 19272629
Clinical information Yes
Disease HBV infection
Published Year 2009
Journal Virology
Title Association between genomic heterogeneity of hepatitis B virus and intrauterine infection.
Author Cheng H,Su H,Wang S,Shao Z,Men K,Li M,Li S,Zhang J,Xu J,Zhang H,Yan Y,Xu D
Evidence Because of overlapping with HBx open reading frame (ORF), the mutations of C1637G, G1658A, G1719T, G1742T, A1762T and G1764A in CP were non-synonymous in HBx ORF and resulted in the amino acid substitutions of S88C, R95K, K118R, W123L, K130M and V131I, respectively.

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