Table 1.
Mutation | Nucleotide | Amino acid | No. of |
site | changes | changes | isolates |
-11 | A to Gb | Mutation in promoter | 3 |
23 | TCG insertion | Slipped-strand mispairing | 1 |
41 | G41A | Missense (Cys14 Tyr) | 1 |
56 | 234-bp deletion | Frameshift | 1 |
172 | T172Cc | Missense (Phe58 Leu) | 1 |
190 | T190G | Missense (Tyr64 Asp) | 1 |
212 | A212Gd | Missense (His71 Arg) | 1 |
227 | C227Te | Missense (Thr76 Ile) | 1 |
317 | CT insertion | Frameshift | 1 |
382 | AG insertion | Frameshift | 1 |
393 | GT insertion | Frameshift | 1 |
393 | T insertion | Frameshift | 1 |
395 | G395T | Missense (Gly132 Val) | 2 |
403 | A403Cd | Missense (Thr135 Pro) | 1 |
407 | A407G | Missense (Asp136 Gly) | 1 |
421 | C421T | Nonsense (Gln141 Termination) | 1 |
425, 180a | C425Tf, C180T | Missense (Thr142 Met), Silent (Gly60 Gly) | 1 |
513 | GC deletion | Frameshift | 1 |