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Mutation Information
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Mutation Site
|
C1799G |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
C Promoter |
|
Combined Mutation
|
c promoter.T1800C+c promoter.C1799G |
|
Genotype/Subtype
|
A;B;C;D |
|
Country
|
Sweden |
Literature Information
|
PubMed PMID
|
24249691
|
|
Disease
|
HBV infection
|
|
Published Year
|
2014 |
|
Journal
|
Journal of medical virology |
|
Title
|
Variability in the precore and core promoter region of the hepatitis B virus genome. |
|
Author
|
Nordin M,Ingman M,Lindqvist B,Kidd-Ljunggren K |
|
Evidence
|
The mutation C1799G was found significantly more often in genotype B strains (43%, n = 23) than in genotype A strains (n = 0), genotype C strains (4%, n = 3), or genotype D strains (1%, n = 3) (all P < 0.0001).
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HBV Mutation Detail Information