| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g46190 | A09 | 51058825 | C | T | upstream_gene_variant | MODIFIER | c.-1418C>T| |
S293 |
| 2 | BAA09g46190 | A09 | 51060649 | C | T | missense_variant | MODERATE | c.407C>T|p.Pro136Leu |
S229 |
| 3 | BAA09g46190 | A09 | 51061590 | G | A | missense_variant | MODERATE | c.920G>A|p.Gly307Glu |
S284 |