| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 153301 | BAA02g01810 | A02 | 797737 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S217 |
| 153302 | BAA02g01810 | A02 | 798442 | G | A | upstream_gene_variant | MODIFIER | c.-3772C>T| |
S105 S106 |
| 153303 | BAA02g01810 | A02 | 798821 | C | T | upstream_gene_variant | MODIFIER | c.-4151G>A| |
S115 |
| 153304 | BAA02g01810 | A02 | 799253 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S78 S83 |
| 153305 | BAA02g01820 | A02 | 799704 | G | A | upstream_gene_variant | MODIFIER | c.-1644G>A| |
S187 |
| 153306 | BAA02g01830 | A02 | 801799 | G | A | upstream_gene_variant | MODIFIER | c.-2630G>A| |
S155 S211 |
| 153307 | BAA02g01820 | A02 | 801861 | G | A | missense_variant | MODERATE | c.275G>A|p.Gly92Glu |
S107 |
| 153308 | BAA02g01820 | A02 | 802032 | C | T | missense_variant | MODERATE | c.446C>T|p.Ser149Phe |
S15 S3 |
| 153309 | BAA02g01830 | A02 | 804832 | C | T | missense_variant | MODERATE | c.404C>T|p.Ser135Phe |
S108 |
| 153310 | BAA02g01820 | A02 | 805251 | G | A | downstream_gene_variant | MODIFIER | c.*1665G>A| |
S209 |
| 153311 | BAA02g01820 | A02 | 805485 | C | T | downstream_gene_variant | MODIFIER | c.*1899C>T| |
S108 |
| 153312 | BAA02g01820 | A02 | 805650 | G | A | downstream_gene_variant | MODIFIER | c.*2064G>A| |
S41 |
| 153313 | BAA02g01820 | A02 | 805859 | G | A | downstream_gene_variant | MODIFIER | c.*2273G>A| |
S127 |
| 153314 | BAA02g01820 | A02 | 805976 | G | A | downstream_gene_variant | MODIFIER | c.*2390G>A| |
S17 |
| 153315 | BAA02g01820 | A02 | 806009 | G | A | downstream_gene_variant | MODIFIER | c.*2423G>A| |
S122 |
| 153316 | BAA02g01820 | A02 | 806247 | C | T | downstream_gene_variant | MODIFIER | c.*2661C>T| |
S56 |
| 153317 | BAA02g01820 | A02 | 806511 | C | T | downstream_gene_variant | MODIFIER | c.*2925C>T| |
S108 S171 |
| 153318 | BAA02g01820 | A02 | 806598 | G | A | downstream_gene_variant | MODIFIER | c.*3012G>A| |
S221 |
| 153319 | BAA02g01820 | A02 | 807230 | C | A | downstream_gene_variant | MODIFIER | c.*3644C>A| |
S43 |
| 153320 | BAA02g01840 | A02 | 807675 | C | T | upstream_gene_variant | MODIFIER | c.-4898C>T| |
S200 |
| 153321 | BAA02g01840 | A02 | 808101 | C | T | upstream_gene_variant | MODIFIER | c.-4472C>T| |
S292 |
| 153322 | BAA02g01840 | A02 | 808176 | C | T | upstream_gene_variant | MODIFIER | c.-4397C>T| |
S152 |
| 153323 | BAA02g01840 | A02 | 808444 | G | A | upstream_gene_variant | MODIFIER | c.-4129G>A| |
S295 |
| 153324 | BAA02g01830 | A02 | 808597 | C | T | missense_variant | MODERATE | c.935C>T|p.Ser312Phe |
S38 |
| 153325 | BAA02g01830 | A02 | 809242 | G | A | missense_variant | MODERATE | c.1301G>A|p.Gly434Glu |
S25 |