HBV Mutation Detail Information

> L101W Search Result


Mutation Information
Mutation Site L101W
Mutation Type Amino acid level
Gene/Protein/Region Type C
Genotype/Subtype C
Viral Reference X72702.1; X70185.1; X01587; GQ377616; D23682; D23680; D16667; D12980; AY247032; AY247030; AY123041; AF286594; AF223957; AF068756; AB100695; AB074755; AB031262
Country Korea
Literature Information
PubMed PMID 23071796
Disease Hepatocellular carcinoma
Published Year 2012
Journal PloS one
Title Naturally occurring precore/core region mutations of hepatitis B virus genotype C related to hepatocellular carcinoma.
Author Kim DW,Lee SA,Hwang ES,Kook YH,Kim BJ
Evidence In the C region, mutation in the 101st codon (leucine to tryptophan or serine, designated C-L101W/S) was found the most frequently (22 patients, 31.4%) (Fig. 1).

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