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. 2022 Jun 25;13:3645. doi: 10.1038/s41467-022-31247-x

Table 2.

Lineage defining mutations and their frequency in the index case (NYCPHL-002130) and named contact partner (NYCPHL-002461).

Lineage Defining mutations Frequency
NYCPHL-002130 NYCPHL-002461
B.1 C241T 0.940 0.916
C3037T 0.939 0.934
C14408T 0.966 0.931
A23403G 0.949 0.945
Alpha C913T 0.946 0.736
C3267T 0.973 0.755
A5388C 0.949 0.761
C5986T 0.983 0.771
T6954C 0.977 0.787
ORF1a: Δ3675-3677 0.983 0.806
C14676T 0.945 0.625
C15279T 1.000 0.772
T16176C 0.985 0.785
S: Δ69-70 1.000 0.983
S: Δ144 0.990 0.978
A23063T 0.944 0.776
C23271A 0.968 0.737
C23604A 0.902 0.711
C23709T 0.939 0.780
T24506G 0.971 0.766
G24914C 0.947 0.751
C27972T 0.978 0.706
G28048T 0.982 0.723
A28111G 0.978 0.718
G28280C 0.945 0.726
A28281T 0.963 0.727
T28282A 0.963 0.736
C28977T 0.962 0.704
Epsilon C1059T 0.000 0.214
A12878G 0.000 0.172
G17014T 0.000 0.169
G21600T 0.000 0.170
G22018T 0.000 0.124
T22917G 0.000 0.181
T24349C 0.000 0.164
G25563T 0.000 0.178
C26681T 0.000 0.182
G27890T 0.000 0.235
A28272T 0.000 0.000
C28887T 0.000 0.227

Δ in-frame codon deletion.