| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g66060 | A09 | 60556598 | G | A | synonymous_variant | LOW | c.486C>T|p.Tyr162Tyr |
S297 |
| 2 | BAA09g66060 | A09 | 60556815 | C | T | missense_variant | MODERATE | c.338G>A|p.Gly113Asp |
S293 |
| 3 | BAA09g66060 | A09 | 60559737 | C | T | upstream_gene_variant | MODIFIER | c.-2472G>A| |
S136 |
| 4 | BAA09g66060 | A09 | 60560189 | G | A | upstream_gene_variant | MODIFIER | c.-2924C>T| |
S180 |
| 5 | BAA09g66060 | A09 | 60560944 | C | T | upstream_gene_variant | MODIFIER | c.-3679G>A| |
S60 |
| 6 | BAA09g66060 | A09 | 60562180 | C | T | upstream_gene_variant | MODIFIER | c.-4915G>A| |
S45 |