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. 2021 May 31;13(6):e14062. doi: 10.15252/emmm.202114062

Table 1.

Mutations associated with variants B.1.1.7 (UK), B.1.135 (South Africa), P.1 (Brazil), P.2 (Brazil), B.1.525 (New York), B.1.526 (New York), B.1.427 (California), and B.1.429 (California).

Gene B. 1. 1.7 B.1.135 P.1 P.2 B.1.525 B.1.526 B.1.427 B.1.429
Mutation Mutation Mutation Mutation Mutation Mutation Mutation Mutation
ORF1ab T1001I P314F P314L L452R S13I
A1708D T2007O Q1011H D614G W152C
I2230T T265I L452R
L3201P D614G
SGF 3675‐3677 del SGF 3675‐3677 del SGF 3675‐3677 del 3575‐3677 del
nsp5 L205V
nsp6
Spike H69/V70 del L18F A67V L5F*
Y144 del D80A H68/V70del T95I
N501Y D215G Y144del D253G
A570D R246I S477N*
P681H K417N K417N
T716I E484K E484K E484K E484K E484K*
S982A N501Y N501Y D614G
D118H A701Y V1176F Q677H *not in all sequences
F888L
Orf8 Q27stop
R52I
Y73C
Nucleocapsid D3L A119S A12G
S235F R203K T205I
G204R
M234I