| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g47590 | A02 | 38324012 | C | A | missense_variant | MODERATE | c.520G>T|p.Gly174Cys |
S177 |
| 2 | BAA02g47590 | A02 | 38324319 | C | T | stop_gained | HIGH | c.213G>A|p.Trp71* |
S108 |
| 3 | BAA02g47590 | A02 | 38326258 | C | T | upstream_gene_variant | MODIFIER | c.-1727G>A| |
S201 |
| 4 | BAA02g47590 | A02 | 38326550 | C | T | upstream_gene_variant | MODIFIER | c.-2019G>A| |
S264 |
| 5 | BAA02g47590 | A02 | 38328131 | G | A | upstream_gene_variant | MODIFIER | c.-3600C>T| |
S187 |
| 6 | BAA02g47590 | A02 | 38328171 | C | T | upstream_gene_variant | MODIFIER | c.-3640G>A| |
S299 |
| 7 | BAA02g47590 | A02 | 38328174 | C | T | upstream_gene_variant | MODIFIER | c.-3643G>A| |
S263 |