| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g50120 | A09 | 53134845 | C | T | missense_variant | MODERATE | c.1757G>A|p.Gly586Glu |
S297 |
| 2 | BAA09g50120 | A09 | 53134885 | C | T | splice_region_variant&intron_variant | LOW | c.1724-7G>A| |
S213 |
| 3 | BAA09g50120 | A09 | 53139491 | C | T | upstream_gene_variant | MODIFIER | c.-1142G>A| |
S180 |
| 4 | BAA09g50120 | A09 | 53140675 | C | T | upstream_gene_variant | MODIFIER | c.-2326G>A| |
S61 |
| 5 | BAA09g50120 | A09 | 53143229 | C | T | upstream_gene_variant | MODIFIER | c.-4880G>A| |
S96 |