|
Basic Characteristics of Mutations
|
|
Mutation Site
|
C1059T |
|
Mutation Site Sentence
|
Table 1 |
|
Mutation Level
|
Nucleotide level |
|
Mutation Type
|
Nonsynonymous substitution |
|
Gene/Protein/Region
|
ORF1a |
|
Standardized Encoding Gene
|
ORF1a
|
|
Genotype/Subtype
|
- |
|
Viral Reference
|
NC_045512.2
|
|
Functional Impact and Mechanisms
|
|
Disease
|
COVID-19
|
|
Immune
|
- |
|
Target Gene
|
-
|
|
Clinical and Epidemiological Correlations
|
|
Clinical Information
|
- |
|
Treatment
|
- |
|
Location
|
- |
|
Literature Information
|
|
PMID
|
36343703
|
|
Title
|
Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
|
|
Author
|
Khalid M,Murphy D,Shoai M,George-William JN,Al-Ebini Y
|
|
Journal
|
Gene
|
|
Journal Info
|
2023 Jan 30;851:147020
|
|
Abstract
|
PURPOSE: To assess, if the SARS-CoV-2 mutate in a similar pattern globally or has a specific pattern in any given population. RESULTS: We report, the insertion of TTT at 11085, which adds an extra amino acid, F to the NSP6 at amino acid position 38. The highest occurrence of TTT insertion at 11,085 position was found in UK derived samples (65.97%). The second and third highest occurrence of the mutation were found in Australia (8.3%) and USA (4.16%) derived samples, respectively. Another important discovery of this study is the C27945T mutation, which translates into the termination of ORF-8 after 17 amino acids, reveals that the SARS-CoV-2 can replicate without the intact ORF-8 protein. We found that the 97% of C27945T mutation of global occurrence, occurred in Europe and the USA derived samples. CONCLUSIONS: Two of the reported mutations (11085TTT insertion and C27945T nonsense), which seemed to reduce Type I interferon response are linked to specific geographical locations of the host and implicate region-specific mutations in the virus. The findings of this study signify that SARS-CoV-2 has the potential to adapt differently to different populations.
|
|
Sequence Data
|
-
|
|
|