| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 175551 | BAA02g17890-BAA02g17900 | A02 | 8971761 | G | A | intergenic_region | MODIFIER | n.8971761G>A| |
S282 |
| 175552 | BAA02g17890-BAA02g17900 | A02 | 8972951 | C | T | intergenic_region | MODIFIER | n.8972951C>T| |
S244 |
| 175553 | BAA02g17890-BAA02g17900 | A02 | 8973429 | G | A | intergenic_region | MODIFIER | n.8973429G>A| |
S238 |
| 175554 | BAA02g17890-BAA02g17900 | A02 | 8973589 | C | T | intergenic_region | MODIFIER | n.8973589C>T| |
S163 |
| 175555 | BAA02g17890-BAA02g17900 | A02 | 8974167 | C | T | intergenic_region | MODIFIER | n.8974167C>T| |
S120 |
| 175556 | BAA02g17890-BAA02g17900 | A02 | 8974590 | C | T | intergenic_region | MODIFIER | n.8974590C>T| |
S8 |
| 175557 | BAA02g17890-BAA02g17900 | A02 | 8974716 | C | T | intergenic_region | MODIFIER | n.8974716C>T| |
S301 S304 |
| 175558 | BAA02g17900 | A02 | 8977404 | G | A | downstream_gene_variant | MODIFIER | c.*2599C>T| |
S188 |
| 175559 | BAA02g17900 | A02 | 8977905 | C | T | downstream_gene_variant | MODIFIER | c.*2098G>A| |
S261 |
| 175560 | BAA02g17900 | A02 | 8978472 | G | A | downstream_gene_variant | MODIFIER | c.*1531C>T| |
S231 |
| 175561 | BAA02g17900 | A02 | 8979839 | G | A | downstream_gene_variant | MODIFIER | c.*164C>T| |
S122 |
| 175562 | BAA02g17900 | A02 | 8980730 | G | A | intron_variant | MODIFIER | c.790-71C>T| |
S60 |
| 175563 | BAA02g17900 | A02 | 8981070 | C | T | intron_variant | MODIFIER | c.790-411G>A| |
S75 S81 |
| 175564 | BAA02g17900 | A02 | 8981249 | G | A | intron_variant | MODIFIER | c.789+277C>T| |
S109 |
| 175565 | BAA02g17900 | A02 | 8982684 | G | A | intron_variant | MODIFIER | c.335-181C>T| |
S265 |
| 175566 | BAA02g17900 | A02 | 8983483 | G | A | intron_variant | MODIFIER | c.334+760C>T| |
S33 |
| 175567 | BAA02g17900 | A02 | 8984060 | C | T | intron_variant | MODIFIER | c.334+183G>A| |
S135 |
| 175568 | BAA02g17900 | A02 | 8984172 | G | A | intron_variant | MODIFIER | c.334+71C>T| |
S168 |
| 175569 | BAA02g17900 | A02 | 8984659 | C | T | intron_variant | MODIFIER | c.100+169G>A| |
S206 S26 |
| 175570 | BAA02g17900 | A02 | 8984783 | G | A | intron_variant | MODIFIER | c.100+45C>T| |
S274 |
| 175571 | BAA02g17900 | A02 | 8984890 | G | A | missense_variant | MODERATE | c.38C>T|p.Thr13Ile |
S59 |
| 175572 | BAA02g17900 | A02 | 8986167 | G | A | upstream_gene_variant | MODIFIER | c.-1240C>T| |
S20 |
| 175573 | BAA02g17900 | A02 | 8986282 | G | A | upstream_gene_variant | MODIFIER | c.-1355C>T| |
S129 |
| 175574 | BAA02g17900 | A02 | 8988000 | G | A | upstream_gene_variant | MODIFIER | c.-3073C>T| |
S67 |
| 175575 | BAA02g17900 | A02 | 8988352 | C | T | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S103 |