| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 24851 | BAA01g17940 | A01 | 8743393 | G | A | intron_variant | MODIFIER | c.1533+3564G>A| |
S152 |
| 24852 | BAA01g17940 | A01 | 8744118 | C | T | intron_variant | MODIFIER | c.1533+4289C>T| |
S136 |
| 24853 | BAA01g17940 | A01 | 8744218 | C | T | intron_variant | MODIFIER | c.1533+4389C>T| |
S177 |
| 24854 | BAA01g17940 | A01 | 8746024 | C | T | intron_variant | MODIFIER | c.1533+6195C>T| |
S208 S93 |
| 24855 | BAA01g17940 | A01 | 8746142 | C | T | intron_variant | MODIFIER | c.1533+6313C>T| |
S135 |
| 24856 | BAA01g17940 | A01 | 8746348 | G | A | intron_variant | MODIFIER | c.1533+6519G>A| |
S163 |
| 24857 | BAA01g17940 | A01 | 8747185 | A | T | intron_variant | MODIFIER | c.1533+7356A>T| |
S278 |
| 24858 | BAA01g17940 | A01 | 8747489 | C | T | intron_variant | MODIFIER | c.1533+7660C>T| |
S231 |
| 24859 | BAA01g17940 | A01 | 8747912 | C | T | intron_variant | MODIFIER | c.1533+8083C>T| |
S176 |
| 24860 | BAA01g17940 | A01 | 8748082 | G | A | intron_variant | MODIFIER | c.1533+8253G>A| |
S105 S106 |
| 24861 | BAA01g17940 | A01 | 8749045 | G | A | intron_variant | MODIFIER | c.1533+9216G>A| |
S251 |
| 24862 | BAA01g17940 | A01 | 8749781 | G | A | intron_variant | MODIFIER | c.1533+9952G>A| |
S38 |
| 24863 | BAA01g17940 | A01 | 8750661 | G | A | intron_variant | MODIFIER | c.1533+10832G>A| |
S87 |
| 24864 | BAA01g17940 | A01 | 8751397 | G | A | intron_variant | MODIFIER | c.1534-10226G>A| |
S59 |
| 24865 | BAA01g17940 | A01 | 8752284 | G | A | intron_variant | MODIFIER | c.1534-9339G>A| |
S196 |
| 24866 | BAA01g17940 | A01 | 8752419 | G | A | intron_variant | MODIFIER | c.1534-9204G>A| |
S169 |
| 24867 | BAA01g17940 | A01 | 8752483 | G | A | intron_variant | MODIFIER | c.1534-9140G>A| |
S98 |
| 24868 | BAA01g17940 | A01 | 8752980 | G | A | intron_variant | MODIFIER | c.1534-8643G>A| |
S229 |
| 24869 | BAA01g17940 | A01 | 8753917 | G | A | intron_variant | MODIFIER | c.1534-7706G>A| |
S52 |
| 24870 | BAA01g17940 | A01 | 8754252 | G | A | intron_variant | MODIFIER | c.1534-7371G>A| |
S12 |
| 24871 | BAA01g17940 | A01 | 8754331 | C | T | intron_variant | MODIFIER | c.1534-7292C>T| |
S69 |
| 24872 | BAA01g17940 | A01 | 8756102 | C | T | intron_variant | MODIFIER | c.1534-5521C>T| |
S210 |
| 24873 | BAA01g17940 | A01 | 8756677 | C | T | intron_variant | MODIFIER | c.1534-4946C>T| |
S69 |
| 24874 | BAA01g17940 | A01 | 8757399 | C | T | intron_variant | MODIFIER | c.1534-4224C>T| |
S33 |
| 24875 | BAA01g17940 | A01 | 8757511 | G | A | intron_variant | MODIFIER | c.1534-4112G>A| |
S203 |