| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 176501 | BAA02g18380-BAA02g18390 | A02 | 9331065 | G | A | intergenic_region | MODIFIER | n.9331065G>A| |
S172 S217 |
| 176502 | BAA02g18380-BAA02g18390 | A02 | 9380732 | C | T | intergenic_region | MODIFIER | n.9380732C>T| |
S266 |
| 176503 | BAA02g18380-BAA02g18390 | A02 | 9380782 | C | T | intergenic_region | MODIFIER | n.9380782C>T| |
S138 |
| 176504 | BAA02g18380-BAA02g18390 | A02 | 9386590 | G | A | intergenic_region | MODIFIER | n.9386590G>A| |
S125 |
| 176505 | BAA02g18380-BAA02g18390 | A02 | 9390405 | C | T | intergenic_region | MODIFIER | n.9390405C>T| |
S260 |
| 176506 | BAA02g18380-BAA02g18390 | A02 | 9390982 | C | T | intergenic_region | MODIFIER | n.9390982C>T| |
S174 S27 |
| 176507 | BAA02g18380-BAA02g18390 | A02 | 9391356 | C | T | intergenic_region | MODIFIER | n.9391356C>T| |
S212 |
| 176508 | BAA02g18380-BAA02g18390 | A02 | 9391754 | C | T | intergenic_region | MODIFIER | n.9391754C>T| |
S42 |
| 176509 | BAA02g18380-BAA02g18390 | A02 | 9391853 | C | T | intergenic_region | MODIFIER | n.9391853C>T| |
S181 |
| 176510 | BAA02g18380-BAA02g18390 | A02 | 9392224 | C | T | intergenic_region | MODIFIER | n.9392224C>T| |
S75 |
| 176511 | BAA02g18380-BAA02g18390 | A02 | 9392252 | C | T | intergenic_region | MODIFIER | n.9392252C>T| |
S32 |
| 176512 | BAA02g18390 | A02 | 9394188 | C | T | upstream_gene_variant | MODIFIER | c.-3870C>T| |
S127 |
| 176513 | BAA02g18390 | A02 | 9394747 | C | T | upstream_gene_variant | MODIFIER | c.-3311C>T| |
S272 |
| 176514 | BAA02g18390 | A02 | 9395062 | G | A | upstream_gene_variant | MODIFIER | c.-2996G>A| |
S184 |
| 176515 | BAA02g18390 | A02 | 9395642 | G | A | upstream_gene_variant | MODIFIER | c.-2416G>A| |
S125 |
| 176516 | BAA02g18390 | A02 | 9397951 | C | T | upstream_gene_variant | MODIFIER | c.-107C>T| |
S49 |
| 176517 | BAA02g18390 | A02 | 9398190 | C | T | missense_variant | MODERATE | c.133C>T|p.Leu45Phe |
S42 |
| 176518 | BAA02g18400 | A02 | 9399562 | G | A | synonymous_variant | LOW | c.492G>A|p.Leu164Leu |
S13 S140 S168 S279 S64 |
| 176519 | BAA02g18400 | A02 | 9399747 | G | A | synonymous_variant | LOW | c.591G>A|p.Lys197Lys |
S296 |
| 176520 | BAA02g18410 | A02 | 9400872 | G | A | missense_variant | MODERATE | c.1033C>T|p.Leu345Phe |
S203 |
| 176521 | BAA02g18410 | A02 | 9400912 | G | A | synonymous_variant | LOW | c.993C>T|p.Val331Val |
S303 |
| 176522 | BAA02g18410 | A02 | 9401449 | C | T | synonymous_variant | LOW | c.456G>A|p.Lys152Lys |
S64 |
| 176523 | BAA02g18410 | A02 | 9401536 | C | T | synonymous_variant | LOW | c.369G>A|p.Lys123Lys |
S208 S219 |
| 176524 | BAA02g18390 | A02 | 9401788 | G | A | downstream_gene_variant | MODIFIER | c.*3569G>A| |
S189 |
| 176525 | BAA02g18390 | A02 | 9401867 | G | A | downstream_gene_variant | MODIFIER | c.*3648G>A| |
S191 |