| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 180601 | BAA02g20400 | A02 | 10831725 | C | A | upstream_gene_variant | MODIFIER | c.-4875G>T| |
S224 |
| 180602 | BAA02g20410 | A02 | 10833050 | G | A | downstream_gene_variant | MODIFIER | c.*2872C>T| |
S134 |
| 180603 | BAA02g20410 | A02 | 10834479 | G | A | downstream_gene_variant | MODIFIER | c.*1443C>T| |
S296 |
| 180604 | BAA02g20410 | A02 | 10836561 | C | T | upstream_gene_variant | MODIFIER | c.-256G>A| |
S118 |
| 180605 | BAA02g20410 | A02 | 10836581 | C | T | upstream_gene_variant | MODIFIER | c.-276G>A| |
S139 |
| 180606 | BAA02g20410 | A02 | 10836794 | C | T | upstream_gene_variant | MODIFIER | c.-489G>A| |
S140 |
| 180607 | BAA02g20410 | A02 | 10838129 | G | A | upstream_gene_variant | MODIFIER | c.-1824C>T| |
S236 |
| 180608 | BAA02g20410 | A02 | 10839458 | G | A | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S5 |
| 180609 | BAA02g20410 | A02 | 10840274 | G | A | upstream_gene_variant | MODIFIER | c.-3969C>T| |
S289 |
| 180610 | BAA02g20410 | A02 | 10840470 | G | A | upstream_gene_variant | MODIFIER | c.-4165C>T| |
S306 S308 |
| 180611 | BAA02g20410 | A02 | 10840594 | G | A | upstream_gene_variant | MODIFIER | c.-4289C>T| |
S247 |
| 180612 | BAA02g20410 | A02 | 10841227 | G | A | upstream_gene_variant | MODIFIER | c.-4922C>T| |
S259 |
| 180613 | BAA02g20420 | A02 | 10842362 | G | A | stop_gained | HIGH | c.399G>A|p.Trp133* |
S172 S217 |
| 180614 | BAA02g20420 | A02 | 10842389 | G | A | splice_region_variant&synonymous_variant | LOW | c.426G>A|p.Glu142Glu |
S134 |
| 180615 | BAA02g20420 | A02 | 10842410 | C | T | intron_variant | MODIFIER | c.426+21C>T| |
S38 |
| 180616 | BAA02g20420 | A02 | 10842493 | C | T | synonymous_variant | LOW | c.456C>T|p.Asp152Asp |
S131 |
| 180617 | BAA02g20420 | A02 | 10842734 | G | A | missense_variant | MODERATE | c.589G>A|p.Ala197Thr |
S28 |
| 180618 | BAA02g20430 | A02 | 10843088 | C | T | downstream_gene_variant | MODIFIER | c.*4738G>A| |
S119 |
| 180619 | BAA02g20430 | A02 | 10843518 | G | A | downstream_gene_variant | MODIFIER | c.*4308C>T| |
S279 |
| 180620 | BAA02g20430 | A02 | 10844472 | G | A | downstream_gene_variant | MODIFIER | c.*3354C>T| |
S210 |
| 180621 | BAA02g20430 | A02 | 10844680 | G | A | downstream_gene_variant | MODIFIER | c.*3146C>T| |
S110 |
| 180622 | BAA02g20430 | A02 | 10844982 | C | T | downstream_gene_variant | MODIFIER | c.*2844G>A| |
S49 |
| 180623 | BAA02g20420 | A02 | 10845551 | C | T | synonymous_variant | LOW | c.1251C>T|p.Pro417Pro |
S206 |
| 180624 | BAA02g20420 | A02 | 10847360 | C | T | downstream_gene_variant | MODIFIER | c.*1201C>T| |
S5 |
| 180625 | BAA02g20430 | A02 | 10847940 | C | T | synonymous_variant | LOW | c.807G>A|p.Val269Val |
S127 |