Table 1. Distribution of coding SNPs selected from resequencing data.
Chr. | Length (Mb) | No. of SNPs | SNPs/kb | No. of predicted genes | Set A (Coding SNPs)a | Set B (Non-synonymous, nonsense and read through coding SNPs)b | Set C (Non-synonymous coding SNPs) c | |||
---|---|---|---|---|---|---|---|---|---|---|
No. of SNPs | SNPs/Gene | No. of SNPs | SNPs/Gene | No. of SNPs | SNPs/Gene | |||||
1 | 55.92 | 268,724 | 4.8 | 2,428 | 7681 | 3.2 | 4374 | 1.8 | 4186 | 1.7 |
2 | 51.66 | 234,553 | 4.5 | 3,158 | 8495 | 2.7 | 4644 | 1.5 | 4463 | 1.4 |
3 | 47.78 | 282,502 | 5.9 | 2,641 | 9145 | 3.5 | 5115 | 1.9 | 4913 | 1.9 |
4 | 49.24 | 240,026 | 4.9 | 2,575 | 7258 | 2.8 | 3984 | 1.5 | 3842 | 1.5 |
5 | 41.94 | 184,474 | 4.4 | 2,636 | 7139 | 2.7 | 3872 | 1.5 | 3741 | 1.4 |
6 | 50.72 | 294,307 | 5.8 | 3,296 | 10797 | 3.3 | 6112 | 1.9 | 5898 | 1.8 |
7 | 44.68 | 235,011 | 5.3 | 2,801 | 8916 | 3.2 | 4980 | 1.8 | 4807 | 1.7 |
8 | 47.00 | 266,154 | 5.7 | 3,867 | 11465 | 3.0 | 6278 | 1.6 | 6052 | 1.6 |
9 | 46.84 | 257,758 | 5.5 | 2,729 | 8583 | 3.1 | 4732 | 1.7 | 4574 | 1.7 |
10 | 50.97 | 247,193 | 4.8 | 2,986 | 8449 | 2.8 | 4595 | 1.5 | 4428 | 1.5 |
11 | 39.17 | 179,976 | 4.6 | 2,866 | 7020 | 2.4 | 3852 | 1.3 | 3717 | 1.3 |
12 | 40.11 | 192,646 | 4.8 | 2,484 | 7061 | 2.8 | 3885 | 1.6 | 3753 | 1.5 |
13 | 44.41 | 277,854 | 6.3 | 3,786 | 10917 | 2.9 | 6002 | 1.6 | 5817 | 1.5 |
14 | 49.71 | 238,506 | 4.8 | 2,201 | 7553 | 3.4 | 4315 | 2.0 | 4161 | 1.9 |
15 | 50.94 | 320,440 | 6.3 | 2,715 | 9510 | 3.5 | 5606 | 2.1 | 5390 | 2.0 |
16 | 37.40 | 251,100 | 6.7 | 2,138 | 10235 | 4.8 | 5927 | 2.8 | 5694 | 2.7 |
17 | 41.91 | 223,989 | 5.3 | 2,685 | 7497 | 2.8 | 3980 | 1.5 | 3831 | 1.4 |
18 | 62.31 | 412,564 | 6.6 | 2,580 | 12887 | 5.0 | 7336 | 2.8 | 7045 | 2.7 |
19 | 50.59 | 254,340 | 5.0 | 2,641 | 7709 | 2.9 | 4240 | 1.6 | 4078 | 1.5 |
20 | 46.77 | 240,127 | 5.1 | 2,369 | 7748 | 3.3 | 4415 | 1.9 | 4231 | 1.8 |
Scaffold | 23.51 | - | - | 205 | - | - | - | - | - | - |
Total | 973.58 | 5,102,244 | 5.2 | 55,787 | 176065 | 3.2 | 98244 | 1.8 | 94621 | 1.7 |
aSet A represented coding SNPs in which all SNPs appeared in coding regions of predicted genes.
bSet B represented SNPs removal of synonymous coding SNPs from Set A, including non-synonymous, nonsense and read through coding SNPs.
cSet C represented only non-synonymous coding SNPs.