| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00100 | A02 | 88381 | C | T | missense_variant | MODERATE | c.625G>A|p.Gly209Ser |
S8 |
| 2 | BAA02g00100 | A02 | 92184 | C | T | upstream_gene_variant | MODIFIER | c.-3179G>A| |
S13 |
| 3 | BAA02g00100 | A02 | 93423 | C | T | upstream_gene_variant | MODIFIER | c.-4418G>A| |
S200 |
| 4 | BAA02g00100 | A02 | 93717 | G | A | upstream_gene_variant | MODIFIER | c.-4712C>T| |
S282 |