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. 2021 Jul 2;13(7):1295. doi: 10.3390/v13071295

Table 2.

Time trends for missense mutations in spike protein.

Spike Mutation Frequency in Analyzed Dataset n = 1106 OR 95% CI p
Nov 20 Dec 20 Jan 21 Feb 21
delH69V70 30 (26.31%) 47 (29.19%) 110 (24.66%) 94 (60.65%) 1.54 1.30–1.83 <0.0001
delY144 0 2 (1.23%) 43 (9.75%) 78 (51.32%) 9.52 6.46–14.35 <0.0001
P681H 1 (0.88%) 15 (9.20%) 110 (24.66%) 93 (60.00%) 4.30 3.32–5.67 <0.0001
T716I 0 1 (0.88%) 43 (9.64%) 80 (51.61%) 10.59 7.13–16.11 <0.0001
S982A 0 1 (0.88%) 43 (9.64%) 79 (50.97%) 10.35 6.97–15.72 <0.0001
A570D 0 1 (0.88%) 43 (9.64%) 78 (51.32%) 10.12 6.83–15.37 <0.0001
N501Y 0 1 (0.88%) 43 (9.64%) 78 (51.32%) 10.12 6.83–15.37 <0.0001
D1118H 0 1 (0.88%) 43 (9.64%) 77 (49.68%) 9.90 6.68–15.01 <0.0001
N439K 30 (26.31%) 47 (29.19%) 76 (17.23%) 17 (10.97%) 0.68 0.57–0.82 <0.0001

ΔH69V70 was found in lineage B.1.1.7 (Clade 1), and in B.1.258 (Clade 2). ΔY144, T716I, S982A, A570D, N501Y, and D1118H was a signature mutation of B.1.1.7 (Clade 1) lineage. P681H was related to B.1.1.7 and B.1.1.29 (Clade 1) lineages. Finally, N439K persisted in the B.1.258 (Clade 2) lineage.