Result: Of the 106 P.1 sequences (98 P.1, six P.1.2, two P.1.1), 99 (93.4%) presented most of the 22 P.1 lineage-defining mutations, with exception of one synonymous mutation in the
ORF1ab (
C12778T) and one missense mutation in the
Spike (
R190S), which were present in 44 (41.5%) and 79 (74.5%) sequences, respectively (Table 1).