Mutation Information
Mutation Site
|
G1764T |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
BCP |
Combined Mutation
|
bcp.G1764T+bcp.A1762T |
Genotype/Subtype
|
A;D;E |
Country
|
Morocco |
Literature Information
PubMed PMID
|
22579480
|
Disease
|
Chronic hepatitis B
|
Published Year
|
2012 |
Journal
|
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases |
Title
|
HBV genotypes prevalence, precore and basal core mutants in Morocco. |
Author
|
Baha W,Ennaji MM,Lazar F,Melloul M,El Fahime E,El Malki A,Bennani A |
Evidence
|
BCP mutants were observed in 65.7% of cases, 22.9% were found to have the T1762/1764A double mutation, 18.6% had A1762/1764T mutation and 22.9% of patients showed the A1762T/G1764A double mutation with either A1762T/G1764T mutation.
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