| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g49050 | A09 | 52611533 | G | A | missense_variant | MODERATE | c.71C>T|p.Thr24Ile |
S216 |
| 2 | BAA09g49050 | A09 | 52612496 | G | A | upstream_gene_variant | MODIFIER | c.-893C>T| |
S135 |
| 3 | BAA09g49050 | A09 | 52614775 | C | T | upstream_gene_variant | MODIFIER | c.-3172G>A| |
S28 |
| 4 | BAA09g49050 | A09 | 52615308 | G | A | upstream_gene_variant | MODIFIER | c.-3705C>T| |
S161 |