HTLV1 Mutation Detail Information

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Mutation Information
Mutation Site C268T
Mutation Type Nucleotide level
Gene/Protein/Region Type 5′LTR
Viral Reference J02029.1
Country Brazil
Literature Information
PubMed PMID 26472535
Disease HTLV-1 associated myelopathy/tropical spastic paraparesis
Published Year 2016
Journal AIDS research and human retroviruses
Title Deep Sequencing Analysis of Human T Cell Lymphotropic Virus Type 1 Long Terminal Repeat 5' Region from Patients with Tropical Spastic Paraparesis/Human T Cell Lymphotropic Virus Type 1-Associated Myelopathy and Asymptomatic Carriers.
Author Rego FF,de Oliveira T,Giovanetti M,Galvão-Castro B,Gonçalves Mde S,Alcantara LC
Evidence We found that A153G, C167T, G199A, A207G, C215T, C219G/T, C268T, and G306C abrogated possible TFBS while T165C, C219G/T, T301A/C, and G306C/A created new possible TFBS (Table 2).

Contents
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