| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g26130 | A02 | 14473866 | C | T | synonymous_variant | LOW | c.183C>T|p.Asp61Asp |
S32 |
| 2 | BAA02g26130 | A02 | 14474187 | G | A | synonymous_variant | LOW | c.504G>A|p.Ala168Ala |
S80 |
| 3 | BAA02g26130 | A02 | 14474247 | C | T | synonymous_variant | LOW | c.564C>T|p.Phe188Phe |
S2 |
| 4 | BAA02g26130 | A02 | 14475114 | G | A | missense_variant | MODERATE | c.730G>A|p.Asp244Asn |
S80 |
| 5 | BAA02g26130 | A02 | 14478581 | C | T | downstream_gene_variant | MODIFIER | c.*2779C>T| |
S16 |