Mutation Information
Mutation Site
|
V17F |
Mutation Type
|
Amino acid level |
Gene/Protein/Region Type
|
PreC |
Amino acid_Mutation
|
G1862T |
Genotype/Subtype
|
A |
Country
|
Japan |
Literature Information
PubMed PMID
|
17607789
|
Disease
|
HBV infection
|
Published Year
|
2007 |
Journal
|
Journal of medical virology |
Title
|
Virological features of hepatitis B virus-associated nephropathy in Japan. |
Author
|
Kusakabe A,Tanaka Y,Kurbanov F,Goto K,Tajiri H,Murakami J,Okuse C,Yotsuyanagi H,Joh T,Mizokami M |
Evidence
|
In both patients with HBV/A1 (Patients 1 and 2), G1862T mutation was observed in the pre-core region resulting in an amino acid change from valine (Val)17to phenyl-alanine (Phe)17(Fig. 2).
|
|
|