HBV Mutation Detail Information

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Mutation Information

Mutation Site	G1899A
Mutation Type	Nucleotide level
Gene/Protein/Region Type	PreC

Literature Information

PubMed PMID	21742757
Clinical information	Yes
Disease	Chronic hepatitis B
Published Year	2011
Journal	Nucleic acids research
Title	Ultra-deep pyrosequencing analysis of the hepatitis B virus preCore region and main catalytic motif of the viral polymerase in the same viral genome.
Author	Homs M,Buti M,Quer J,Jardí R,Schaper M,Tabernero D,Ortega I,Sanchez A,Esteban R,Rodriguez-Frias F
Evidence	The second most frequent nucleotide substitution, G1899A (28.35%), was paired with T1855 in 99.3% of cases, and was observed in the presence of G1896A in 99.6% of cases.

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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