Mutation Information
Mutation Site
|
S91P |
Mutation Type
|
Amino acid level |
Gene/Protein/Region Type
|
P12 |
Country
|
Caribbean; France; North America; Africa; Brazil |
Literature Information
PubMed PMID
|
27553711
|
Disease
|
HTLV-1 associated myelopathy/tropical spastic paraparesis
|
Published Year
|
2016 |
Journal
|
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases |
Title
|
Analyses of HTLV-1 sequences suggest interaction between ORF-I mutations and HAM/TSP outcome. |
Author
|
Barreto FK,Khouri R,Rego FFA,Santos LA,Castro-Amarante MF,Bialuk I,Pise-Masison CA,Galvão-Castro B,Gessain A,Jacobson S,Franchini G,Alcantara LC Jr |
Evidence
|
The mutations P34L and S91P appear most frequently (>than 40% of the sequences analysed) but are not associated with the development of HAM/TSP.
|
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