| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g21860 | A02 | 11777305 | G | A | synonymous_variant | LOW | c.507C>T|p.Leu169Leu |
S192 |
| 2 | BAA02g21860 | A02 | 11777405 | G | A | missense_variant | MODERATE | c.407C>T|p.Thr136Ile |
S291 |
| 3 | BAA02g21860 | A02 | 11778672 | G | A | upstream_gene_variant | MODIFIER | c.-756C>T| |
S204 |
| 4 | BAA02g21860 | A02 | 11778817 | G | A | upstream_gene_variant | MODIFIER | c.-901C>T| |
S149 |
| 5 | BAA02g21860 | A02 | 11778828 | G | A | upstream_gene_variant | MODIFIER | c.-912C>T| |
S126 |
| 6 | BAA02g21860 | A02 | 11781179 | G | A | upstream_gene_variant | MODIFIER | c.-3263C>T| |
S20 |
| 7 | BAA02g21860 | A02 | 11782496 | C | T | upstream_gene_variant | MODIFIER | c.-4580G>A| |
S203 |
| 8 | BAA02g21860 | A02 | 11782603 | C | T | upstream_gene_variant | MODIFIER | c.-4687G>A| |
S296 |