TABLE 1.
Classification a | WHO label | Pango lineage | Mutations in RBD of the spike protein a | Mutations in the rest of the spike protein a |
---|---|---|---|---|
VOC | Omicron | B.1.1.529 (BA.1) | G339D, S371L, S373P, S375F, K417N, N440K, G446S, S477N, T478K, E484A, Q493R, G496S, Q498R, N501Y, Y505H | A67V, HV69‐70Del, T95I, G142D, VYY143‐145Del, N211Del, L212I, Ins214EPE, T547K, D614G, H655Y, N679K, P681H, N764K, D796Y, N856K, Q954H, N969K, L981F |
BA.2 | G339D, S371F, S373P, S375F,T376A, D405N, R408S, K417N, N440K, S477N, T478K, E484A, Q493R, Q498R, N501Y, Y505H | T19I, LPP24‐26Del, A27S, G142D, V213G, D614G, H655Y, N679K, P681H, N764K, D796Y, Q954H, N969K | ||
BA.3 | G339D, S371F, S373P, S375F, D405N, K417N, N440K, G446S, S477N, T478K, E484A, Q493R, Q498R, N501Y, Y505H | A67V, HV69‐70Del, T95I, G142D, VYY143‐145Del, N211Del, L212I, D614G, H655Y, N679K, P681H, N764K, D796Y, Q954H, N969K | ||
Alpha | B.1.1.7 | N501Y | HV69‐70Del, Y144Del, A570D, D614G, P681H, T716I, S982A, D1118H | |
Beta | B.1.351 | K417N, E484K, N501Y | L18F, D80A, D215G, LAL242‐244Del, D614G, A701V | |
Gamma | P.1 | K417T, E484K, N501Y | L18F, T20N, P26S, D138Y, R190S, D614G, H655Y, T1027I, V1176F | |
Delta | B.1.617.2 | L452R, T478K | T19R, G142D, EF156‐157Del, R158G, D614G, P681R, D950N | |
VOI | Lambda | C.37 | L452Q, F490S | G75V, T76I, RSYLTPG246‐252Del, D253N, D614G, T859N |
Mu | B.1.621 | R346K, E484K, N501Y | T95I, Y144S, Y145N, D614G, P681H, D950N | |
VUM | C.1.2 | Y449H, E484K, N501Y | P9L, C136F, Y144Del, R190S, D215G, AL243‐244Del, D614G, H655Y, N679K, T716I, T859N | |
B.1.630 | L452R, T478R, E484Q | P9L, C136F, Y144Del, A222V, AL243‐244Del, D614G, H655Y, D950N | ||
B.1.640.1 | R346S, N394S, Y449N, F490R, N501Y | P9L, E96Q, CNDPFLGVY136‐144 Del, R190S, I210T, D614G, P681H, T859N, D936H | ||
B.1.640.2 | R346S, N394S, Y449N, E484K, F490S, N501Y | P9L, E96Q, CNDPFLGVY136‐144 Del, R190S, D215H, D614G, P681H, T859N, D1139H |
Note: The spike protein mutations of the SARS‐CoV‐2 variants used in this study are listed.
Abbreviations: RBD, receptor‐binding domain; VOC, variants of concern; VOI, variants of interest; VUM, variants under monitoring.
The classification of variant strains is regularly adjusted based on the SARS‐CoV‐2 continuous evolution and spread, as well as a better understanding of the impact of the variants. As a result, the classification of variants is dynamic, constantly being removed or added.
The mutation sites of the variants represent the characteristics of most sequences, and individual mutation sites can only be detected in partial sequences, which are not shown here.