Table 1.
Gene | Protein | Nucleotide Change | Amino Acid Change | Variant Allele Frequency (%) | ||
---|---|---|---|---|---|---|
Initial Infection | Reinfection | |||||
Initial Diagnosis | Follow-up | |||||
5’UTR | 241C>Ta | .0 | .0 | 79.4 | ||
ORF1ab | nsp1 | 526G>T | Q87D | 99.9 | 99.1 | 19.0 |
ORF1ab | nsp1 | 635C>T | R124C | .0 | .0 | 28.6 |
ORF1ab | nsp2 | 1059C>T | T85I | .0 | .0 | 66.0 |
ORF1ab | nsp3 | 3037C>Ta | F106= | .0 | .0 | 88.7 |
ORF1ab | nsp3 | 4951G>C | L744F | .0 | .0 | 20.5 |
ORF1ab | nsp3 | 5572G>T | M951I | 99.9 | NAb | 45.7 |
ORF1ab | nsp3 | 5822C>T | L1035F | .0 | NAb | 23.3 |
ORF1ab | nsp3 | 6262T>C | N1181= | 99.9 | 99.8 | 26.7 |
ORF1ab | nsp3 | 6719A>G | T1334A | 99.8 | 99.9 | 24.9 |
ORF1ab | nsp4 | 9773delT | V407fs | .0 | .0 | 25.2 |
ORF1ab | nsp4 | 9996C>T | S481L | .0 | .0 | 23.3 |
ORF1ab | nsp6 | 11083G>Tc | L37F | 99.5 | 99.2 | 8.0 |
ORF1ab | nsp9 | 12810T>C | L42P | .0 | .0 | 32.0 |
ORF1ab | nsp12 | 14408C>Ta | P323L | .0 | .0 | 92.1 |
ORF1ab | nsp12 | 14805C>T | Y455= | 99.7 | 99.4 | 59.4 |
ORF1ab | nsp13 | 16580C>T | T115I | .0 | .0 | 34.5 |
S | S | 23403A>Ga | D614G | .0 | .0 | 84.8 |
ORF3a | ORF3a | 25563G>Ta | Q57H | .0 | .0 | 80.0 |
ORF3a | ORF3a | 26060C>T | T223I | 99.8 | 99.5 | 10.0 |
ORF3a | ORF3a | 26144G>Tc | G251V | 99.9 | 98.6 | 10.0 |
N | N | 28768A>G | T165= | .0 | .0 | 47.5 |
Abbreviation: NA, not available.
aThe variant that characterizes the clade G.
bNot available because the region between 5214 and 5931 of the reference genome was not well covered by aligned sequencing reads.
cThe variant that characterizes the clade V.