| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g00100 | A09 | 229543 | C | T | missense_variant | MODERATE | c.379C>T|p.Leu127Phe |
S67 |
| 2 | BAA09g00100 | A09 | 229899 | C | T | missense_variant | MODERATE | c.647C>T|p.Thr216Ile |
S40 S49 |
| 3 | BAA09g00100 | A09 | 229930 | G | A | synonymous_variant | LOW | c.678G>A|p.Gly226Gly |
S78 S83 |
| 4 | BAA09g00100 | A09 | 230715 | C | T | missense_variant | MODERATE | c.1147C>T|p.His383Tyr |
S148 |