HBV Mutation Detail Information

> W182* Search Result

Mutation Information

Mutation Site	W182*
Mutation Type	Amino acid level
Gene/Protein/Region Type	S
Genotype/Subtype	C
Country	China

Literature Information

PubMed PMID	28198078
Disease	Chronic hepatitis B
Published Year	2017
Journal	Journal of medical virology
Title	Mutation in the S gene of hepatitis B virus and anti-HBs subtype-nonspecificity contributed to the co-existence of HBsAg and anti-HBs in patients with chronic hepatitis B virus infection.
Author	Fu X,Chen J,Chen H,Lin J,Xun Z,Li S,Liu C,Zeng Y,Chen T,Yang B,Ou Q
Evidence	Two termination mutations were observed in patients with genotype C (Fig. 1), sC69* (8.69% vs 4.17%, P > 0.05) and sW182* (8.69% vs 4.17%, P > 0.05).

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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