| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g05120 | A02 | 2254296 | C | T | missense_variant | MODERATE | c.824C>T|p.Thr275Ile |
S202 |
| 2 | BAA02g05120 | A02 | 2254314 | C | T | missense_variant | MODERATE | c.842C>T|p.Ser281Phe |
S174 S265 S39 |
| 3 | BAA02g05120 | A02 | 2254912 | C | T | missense_variant | MODERATE | c.1345C>T|p.Leu449Phe |
S73 |
| 4 | BAA02g05120 | A02 | 2255179 | G | A | missense_variant | MODERATE | c.1612G>A|p.Gly538Ser |
S259 |
| 5 | BAA02g05120 | A02 | 2257381 | G | A | downstream_gene_variant | MODIFIER | c.*2101G>A| |
S158 |