| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g44650 | A02 | 36731591 | C | T | upstream_gene_variant | MODIFIER | c.-3609C>T| |
S259 |
| 2 | BAA02g44650 | A02 | 36732117 | C | T | upstream_gene_variant | MODIFIER | c.-3083C>T| |
S131 S269 S303 |
| 3 | BAA02g44650 | A02 | 36733329 | C | T | upstream_gene_variant | MODIFIER | c.-1871C>T| |
S100 |
| 4 | BAA02g44650 | A02 | 36736034 | C | T | missense_variant | MODERATE | c.536C>T|p.Thr179Met |
S121 |
| 5 | BAA02g44650 | A02 | 36737284 | C | T | missense_variant | MODERATE | c.1426C>T|p.Leu476Phe |
S267 |
| 6 | BAA02g44650 | A02 | 36739479 | C | T | downstream_gene_variant | MODIFIER | c.*2154C>T| |
S144 |