| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g24990 | A09 | 16068589 | G | A | downstream_gene_variant | MODIFIER | c.*1333C>T| |
S116 |
| 2 | BAA09g24990 | A09 | 16069673 | G | A | downstream_gene_variant | MODIFIER | c.*249C>T| |
S301 S304 |
| 3 | BAA09g24990 | A09 | 16070056 | C | T | missense_variant | MODERATE | c.1057G>A|p.Val353Ile |
S269 |
| 4 | BAA09g24990 | A09 | 16072125 | G | A | upstream_gene_variant | MODIFIER | c.-663C>T| |
S180 |
| 5 | BAA09g24990 | A09 | 16072315 | C | T | upstream_gene_variant | MODIFIER | c.-853G>A| |
S282 |
| 6 | BAA09g24990 | A09 | 16072786 | C | T | upstream_gene_variant | MODIFIER | c.-1324G>A| |
S159 S243 S299 |
| 7 | BAA09g24990 | A09 | 16073338 | C | T | upstream_gene_variant | MODIFIER | c.-1876G>A| |
S208 S219 |
| 8 | BAA09g24990 | A09 | 16073552 | G | A | upstream_gene_variant | MODIFIER | c.-2090C>T| |
S40 S49 |
| 9 | BAA09g24990 | A09 | 16074131 | G | A | upstream_gene_variant | MODIFIER | c.-2669C>T| |
S176 |