Mutation Information
Mutation Site
|
M197T |
Mutation Type
|
Amino acid level |
Gene/Protein/Region Type
|
S |
Combined Mutation
|
s.M197T+s.Y206F |
Genotype/Subtype
|
D |
Viral Reference
|
X65259.1
|
Country
|
Italy; United Kingdom and Germany |
Literature Information
PubMed PMID
|
32312174
|
Disease
|
Chronic hepatitis B
|
Published Year
|
2020 |
Journal
|
Emerging microbes & infections |
Title
|
Key mutations in the C-terminus of the HBV surface glycoprotein correlate with lower HBsAg levels in vivo, hinder HBsAg secretion in vitro and reduce HBsAg structural stability in the setting of HBeAg-negative chronic HBV genotype-D infection. |
Author
|
Salpini R,Battisti A,Piermatteo L,Carioti L,Anastasiou OE,Gill US,Di Carlo D,Colagrossi L,Duca L,Bertoli A,La Rosa KY,Fabeni L,Iuvara A,Malagnino V,Cerva C,Lichtner M,Mastroianni CM,De Sanctis GM,Paoloni M,Marignani M,Pasquazzi C,Iapadre N,Parruti G,Vecchiet J,Sarmati L,Andreoni M,Angelico M,Grelli S,T Kennedy P,Verheyen J,Aquaro S,Silberstein FC,Perno CF,Svicher V |
Evidence
|
The following mutations were introduced: V190A, V190A + F220L, S204N, S204N + L205P, Y206F, Y206F + S210R, Y206F + V194A, Y206F + S204T, Y206F + M197T, S210N, S210N + F220L.
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