| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00060 | A02 | 42029 | C | T | missense_variant | MODERATE | c.676G>A|p.Asp226Asn |
S233 |
| 2 | BAA02g00060 | A02 | 45186 | G | A | upstream_gene_variant | MODIFIER | c.-2482C>T| |
S225 |
| 3 | BAA02g00060 | A02 | 46852 | G | A | upstream_gene_variant | MODIFIER | c.-4148C>T| |
S69 |
| 4 | BAA02g00060 | A02 | 47323 | G | A | upstream_gene_variant | MODIFIER | c.-4619C>T| |
S35 |