|
Mutation Information
|
Mutation Site
|
G1862T |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
PreC |
|
Nucleotide_Mutation
|
V17F |
|
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
|
G1862T mutation was observed in the two HBV/A1 patients, resulting in the pre-core amino acid substitution with a switch from valine (Val) to phenylalanine (Phe).
|
|
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HBV Mutation Detail Information