AVM v1, released 02-OCT-22

A manually curated database of aerosol-transmitted virus mutations, human diseases, and drugs

Mutation detail:


Mutation site T120I
Virus SARS-CoV-2
Mutation level Amino acid level
Gene/protein/region type ORF7a
Gene ID 43740573
Country -
Mutation type nonsynonymous mutation
Genotype/subtype/clade -
Sample Human
Variants Delta
Viral reference sequence NC_045512.2
Drug/antibody/vaccine -
Transmissibility -
Transmission mechanism -
Pathogenicity -
Pathogenicity mechanism -
Immune escape mutation -
Immune escape mechanism -
RT-PCR primers probes -

Protein detail:


Protein name ORF7a protein
Uniprot protein ID P0DTC7
Protein length 121 amino acids
Protein description The orf 7a of SARS-CoV-2 is a transmembrane protein with four regions from the N-terminal: 1) the first 15 amino acids form a signal peptide which is hydrolyzed by the infected host cells; 2) the amino acids from 16 to 96 constitute the intracellular domain; 3) the 97- 117 amino acids are hydrophobic amino acids constituting a transmembrane domain; and 4) the last five amino acids constitute the C- terminal of the orf7a. The orf7a interacts with the S, M, E, and the orf3a proteins, which suggest a role of the protein in the assembling of the virus and in the binding and invasion of the virus to the host cells.

Literature information:


Pubmed ID 34399188
Clinical information No
Disease -
Published year 2021
Journal JOURNAL OF AUTOIMMUNITY
Title Evolutionary analysis of the Delta and Delta Plus variants of the SARS-CoV-2 viruses
Author Saathvik R Kannan, Austin N Spratt, Alisha R Cohen, S Hasan Naqvi, Hitendra S Chand
Evidence The Delta Plus variant had a significant number of high-prevalence mutations (-20 %) than in the Delta variant. Signature mutations in Spike (G142D, A222V, and T95I) existed at a more significant percentage in the Delta Plus variant than the Delta variant. Three mutations in Spike (K417N, V70F, and W258L) were exclusively present in the Delta Plus variant. A new mutation was identified in ORF1a (A1146T), which was only present in the Delta Plus variant with ~58 % prevalence. Furthermore, five key mutations (T95I, A222V, G142D, R158G, and K417N) were significantly more prevalent in the Delta Plus than in the Delta variant.