| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178101 | BAA02g19120 | A02 | 9924433 | G | A | upstream_gene_variant | MODIFIER | c.-1030G>A| |
S238 |
| 178102 | BAA02g19120 | A02 | 9926274 | C | T | missense_variant | MODERATE | c.728C>T|p.Ser243Phe |
S38 |
| 178103 | BAA02g19120 | A02 | 9927055 | G | A | downstream_gene_variant | MODIFIER | c.*103G>A| |
S111 |
| 178104 | BAA02g19120 | A02 | 9928032 | G | A | downstream_gene_variant | MODIFIER | c.*1080G>A| |
S113 |
| 178105 | BAA02g19120 | A02 | 9929156 | G | A | downstream_gene_variant | MODIFIER | c.*2204G>A| |
S113 |
| 178106 | BAA02g19120 | A02 | 9930127 | C | T | downstream_gene_variant | MODIFIER | c.*3175C>T| |
S87 |
| 178107 | BAA02g19120 | A02 | 9930178 | C | T | downstream_gene_variant | MODIFIER | c.*3226C>T| |
S266 |
| 178108 | BAA02g19120 | A02 | 9930270 | G | A | downstream_gene_variant | MODIFIER | c.*3318G>A| |
S149 |
| 178109 | BAA02g19120 | A02 | 9930286 | G | A | downstream_gene_variant | MODIFIER | c.*3334G>A| |
S188 |
| 178110 | BAA02g19120 | A02 | 9930627 | C | T | downstream_gene_variant | MODIFIER | c.*3675C>T| |
S114 |
| 178111 | BAA02g19120 | A02 | 9931278 | G | A | downstream_gene_variant | MODIFIER | c.*4326G>A| |
S206 S26 |
| 178112 | BAA02g19130 | A02 | 9933205 | G | A | upstream_gene_variant | MODIFIER | c.-69C>T| |
S90 |
| 178113 | BAA02g19130 | A02 | 9933374 | C | T | upstream_gene_variant | MODIFIER | c.-238G>A| |
S181 |
| 178114 | BAA02g19130 | A02 | 9934032 | G | A | upstream_gene_variant | MODIFIER | c.-896C>T| |
S125 |
| 178115 | BAA02g19130 | A02 | 9934526 | C | T | upstream_gene_variant | MODIFIER | c.-1390G>A| |
S241 |
| 178116 | BAA02g19130 | A02 | 9934856 | G | A | upstream_gene_variant | MODIFIER | c.-1720C>T| |
S125 |
| 178117 | BAA02g19130 | A02 | 9935158 | C | T | upstream_gene_variant | MODIFIER | c.-2022G>A| |
S63 |
| 178118 | BAA02g19130 | A02 | 9935284 | G | A | upstream_gene_variant | MODIFIER | c.-2148C>T| |
S67 |
| 178119 | BAA02g19130 | A02 | 9935623 | C | T | upstream_gene_variant | MODIFIER | c.-2487G>A| |
S268 |
| 178120 | BAA02g19130 | A02 | 9936514 | C | T | upstream_gene_variant | MODIFIER | c.-3378G>A| |
S118 |
| 178121 | BAA02g19130 | A02 | 9937212 | T | C | upstream_gene_variant | MODIFIER | c.-4076A>G| |
S5 |
| 178122 | BAA02g19130 | A02 | 9937478 | G | A | upstream_gene_variant | MODIFIER | c.-4342C>T| |
S298 |
| 178123 | BAA02g19130 | A02 | 9937867 | G | A | upstream_gene_variant | MODIFIER | c.-4731C>T| |
S51 |
| 178124 | BAA02g19140 | A02 | 9938640 | G | A | upstream_gene_variant | MODIFIER | c.-931G>A| |
S19 S298 |
| 178125 | BAA02g19140 | A02 | 9939833 | C | A | intron_variant | MODIFIER | c.161+12C>A| |
S122 S125 S138 S147 S161 S179 S18 S26 S288 S295 S37 S44 S84 |