| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g51770 | A09 | 53910105 | G | A | missense_variant | MODERATE | c.82G>A|p.Val28Met |
S284 |
| 2 | BAA09g51770 | A09 | 53910423 | G | A | missense_variant | MODERATE | c.400G>A|p.Ala134Thr |
S178 |
| 3 | BAA09g51770 | A09 | 53910494 | C | T | synonymous_variant | LOW | c.471C>T|p.Ile157Ile |
S103 |
| 4 | BAA09g51770 | A09 | 53911163 | C | T | synonymous_variant | LOW | c.1140C>T|p.Ser380Ser |
S256 |
| 5 | BAA09g51770 | A09 | 53911233 | C | T | stop_gained | HIGH | c.1210C>T|p.Arg404* |
S15 S2 S3 |