Table 1.
Region | % of analyzed sequence | % mutations* | R/S† | P̄n (SD)/P̄s (SD)* |
---|---|---|---|---|
Sec | ||||
FR1 | 25% | 8.6% | 11/7 | 0.028 (0.03)/0.047 (0.05) |
FR3 | 38% | 24% | 40/12 | 0.020 (0.02)/0.019 (0.02) |
CDR1 | 13% | 34% | 61/10 | 0.097 (0.05)/0.073 (0.12)‡ |
CDR2 | 10% | 24% | 43/8 | 0.109 (0.082)/0.126 (0.13) |
CDRs total | 23% | 58.9% ± 7.9§ | ||
Tm | ||||
FR1 | 25% | 15% | 14/3 | 0.02 (0.012)/0.01 (0.033) |
FR3 | 38% | 38% | 26/9 | 0.02 (0.012)/0.03 (0.029) |
CDR1 | 13% | 25% | 18/7 | 0.06 (0.052)/0.09 (0.105) |
CDR2 | 10% | 9.9% | 6/2 | 0.05 (0.024)/0.09 (0.123) |
CDRs total | 23% | 34.7% ± 8.6 |
Mutated clones with fewer than 15 mutations (Sec, n = 66; Tm, n = 60).
Excludes tandem mutations where the type of change depends on which mutation occurred first. These were not excluded from the Pn, Ps analysis. R, replacement; s, silent.
P < 0.05 (Wilcoxon Signed-Ranks Test).
P < 0.05 (G test; Sec clones CDR mutation frequency was higher than Tm clones).