HBV Mutation Detail Information

> C1913A Search Result

Mutation Information

Mutation Site	C1913A
Mutation Type	Nucleotide level
Gene/Protein/Region Type	C
Genotype/Subtype	B;C
Country	China

Literature Information

PubMed PMID	26202756
Disease	Acute on chronic liver failure
Published Year	2014
Journal	Hepatology international
Title	Hepatitis B virus genotype B and mutations in basal core promoter and pre-core/core genes associated with acute-on-chronic liver failure: a multicenter cross-sectional study in China.
Author	Yang G,Han M,Chen F,Xu Y,Chen E,Wang X,Liu Y,Sun J,Hou J,Ning Q,Wang Z
Evidence	The A1762T/G1764A, A1846T and G1896A mutations were significantly more common in HB-ACLF patients infected with either genotype B or C as compared with CHB-M, whereas the C1913A/G and A2159G mutations were more associated with HB-ACLF in genotype C patients.

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Description

Mutation Information Note

Gene/Protein/Region Type: Virus Gene (e.g. LMP-1) or Virus Protein (e.g. Rep 68) or Virus Region (e.g. S, X)

Literature Information Note

Evidence: sentence contains this mutation information in the citation