HBV Mutation Detail Information

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Mutation Information
Mutation Site G1764A
Mutation Type Nucleotide level
Gene/Protein/Region Type X
Combined Mutation x.V131I+x.K130M
Nucleotide_Mutation V131I
Genotype/Subtype C
Country Korea
Literature Information
PubMed PMID 18551606
Disease Hepatocellular carcinoma; Liver cirrhosis; Chronic hepatitis B
Published Year 2008
Journal Journal of medical virology
Title Hepatitis B virus X mutations occurring naturally associated with clinical severity of liver disease among Korean patients with chronic genotype C infection.
Author Kim HJ,Park JH,Jee Y,Lee SA,Kim H,Song BC,Yang S,Lee M,Yoon JH,Kim YJ,Lee HS,Hwang ES,Kook YH,Kim BJ
Evidence Mutation rates in the X region in patients with more severe liver disease, hepatocellular carcinoma (HCC) (3.6%) or liver cirrhosis (4%) were always significantly higher than in patients with corresponding less severe forms, chronic hepatitis (2.9%) or asymptomatic carriers (2.1%), but no significant difference in mutation rates was found in terms of HBeAg serostatus. All five mutation types (V5M/L, P38S, H94Y, I127T/N, and K130M and V131I) affecting the six codons were found to be related significantly to clinical severity.

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