Table 5. Frequency of significant mutations (>0.001) identified in tissue culture passaged viral populations.
GenomeRegion | nt Position | nt Change | AA Change | C6/36-1 | C6/36-2 | C6/36-3 | C6/36-4 | C6/36-5 | Vero-1 | Vero-2 | Vero-3 | Vero-4 | Vero-5 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
nsp1 | 479 | T>C | syn>L | 0.010 | 1.000 | 1.000 | |||||||
nsp1 | 1525 | C>T | syn>Y | 0.006 | 0.996 | 0.973 | 0.978 | 0.012 | |||||
nsp2 | 2716 | A>G | syn>T | 0.996 | 0.999 | 0.997 | 0.997 | 0.997 | 0.999 | 0.999 | 0.999 | 0.999 | 0.999 |
nsp2 | 3059 | G>A | G460S | 0.371 | |||||||||
nsp3 | 4507 | C>A | syn>R | 0.998 | 0.998 | 0.998 | 0.997 | 0.998 | |||||
nsp3 | 4513 | A>G | syn>K | 0.999 | 0.999 | 0.999 | 0.999 | 0.996 | |||||
nsp3 | 4864 | T>A | syn>L | 0.007 | 0.003 | 0.004 | 0.999 | 0.003 | 0.012 | 0.011 | 0.990 | 0.009 | 0.011 |
nsp4 | 7016 | C>A | L455M | 0.951 | 0.020 | 0.081 | |||||||
E2 | 8874 | C>T | syn>F | 0.005 | 0.002 | 0.002 | 0.002 | 0.990 | |||||
E2 | 8892 | T>C | syn>I | 0.999 | 0.998 | 0.998 | 1.000 | 1.000 | 1.000 | 0.999 | 1.000 | ||
E1 | 10104 | G>A | syn>T | 0.979 | 0.002 | 0.003 | 0.004 | 0.002 | 0.002 | 0.003 | 0.002 | 0.968 | |
E1 | 10802 | G>T | G274V | 0.044 | 0.041 | 0.096 | 0.093 | 0.088 | 0.959 | ||||
3UTR | 11775 | C>T | 0.978 | 0.952 | 0.985 | 0.981 | |||||||
3UTR | 11776 | G>A | 0.999 | 0.995 | 0.994 | ||||||||
3UTR | 11791 | C>T | 0.359 | 0.291 | 0.499 | 0.539 |
nt = nucleotide, AA = amino acid, syn = synonymous, The table shows any mutation present above 0.1 in at least one individual, and any mutation above 0.001 found in more than one individual.