|
Mutation Information
|
Mutation Site
|
C1766T |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
BCP |
|
Genotype/Subtype
|
C |
|
Country
|
Iran |
Literature Information
|
PubMed PMID
|
31308922
|
|
Disease
|
Chronic hepatitis B;
Liver cirrhosis
|
|
Published Year
|
2019 |
|
Journal
|
Mediterranean journal of hematology and infectious diseases |
|
Title
|
Nucleotide Substitutions in Hepatitis B Viruses Derived from Chronic HBV Patients. |
|
Author
|
Shokatpour N,Vaezjalali M,Foster GR,Sali S |
|
Evidence
|
In the BCP region, the most common mutations were A1762T (30.0%, 8/26) and G1764T (30.0%, 8/26), followed by G1764A (26.0%, 7/26), C1766G (26.0%, 7/26), C1766T (11.5%, 3/26).
|
|
|
HBV Mutation Detail Information