| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g30130 | A02 | 17478214 | C | T | missense_variant | MODERATE | c.575G>A|p.Arg192His |
S112 |
| 2 | BAA02g30130 | A02 | 17478245 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.545-1G>A| |
S177 |
| 3 | BAA02g30130 | A02 | 17478379 | G | A | missense_variant | MODERATE | c.475C>T|p.Leu159Phe |
S247 |
| 4 | BAA02g30130 | A02 | 17478426 | G | A | missense_variant | MODERATE | c.428C>T|p.Pro143Leu |
S197 |