Mutation detail:
| Mutation site | F486R |
| Virus | SARS-CoV-2 |
Mutation level  |
Amino acid level |
| Gene/protein/region type | S |
| Gene ID | 43740568 |
| Country | - |
| Mutation type |
nonsynonymous mutation |
| Genotype/subtype/clade | - |
| Sample |
cell line |
| Variants | - |
| Viral reference sequence | MN908947.3 |
| Drug/antibody/vaccine | REGN10933-resistant, mAb_COC2-2832-resistant, Plasma samples from patients-resistant, mAb_2B04-resistant, mAb_1B07-resistant, mAb_SARS2-21-resistant, mAb_SARS2-58-resistant, mAb_SARS2-71-resistant, mAb_COV2-2196/AZD8895/Tixagevimab-resistant |
| Transmissibility |
- |
| Transmission mechanism | - |
| Pathogenicity |
- |
| Pathogenicity mechanism | - |
| Immune escape mutation | Yes |
| Immune escape mechanism | - |
| RT-PCR primers probes | - |
Protein detail:
| Protein name | Spike glycoprotein |
| Uniprot protein ID | P0DTC2 |
| Protein length | 1273 amino acids |
| Protein description | Spike protein is one of the structural proteins of SARS-CoV-2. The monomeric protein consists of one large ectodomain, a single-pass transmembrane anchor, and a short intracellular tail at C-terminus. It encompasses 22 glycosylation sites. S protein cleaves into two subunits namely S1 and S2 following receptor recognition. Receptor Binding Domain (RBD) in S1 subunit plays a major role in ACE2 receptor binding. |
Literature information:
| Pubmed ID | 33592168 |
| Clinical information | No |
| Disease | - |
| Published year | 2021 |
| Journal | Cell Host & Microbe |
| Title | Comprehensive mapping of mutations in the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human plasma antibodies |
| Author | Allison J Greaney, Andrea N Loes, Katharine H D Crawford, Tyler N Starr, Keara D Malone |
| Evidence | TableS3 |