| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g44990 | A02 | 36962121 | C | T | missense_variant | MODERATE | c.49G>A|p.Asp17Asn |
S25 S264 |
| 2 | BAA02g44990 | A02 | 36963970 | C | T | upstream_gene_variant | MODIFIER | c.-1801G>A| |
S183 S198 |
| 3 | BAA02g44990 | A02 | 36964394 | C | T | upstream_gene_variant | MODIFIER | c.-2225G>A| |
S261 S303 |
| 4 | BAA02g44990 | A02 | 36965344 | C | T | upstream_gene_variant | MODIFIER | c.-3175G>A| |
S157 |
| 5 | BAA02g44990 | A02 | 36965549 | T | C | upstream_gene_variant | MODIFIER | c.-3380A>G| |
S305 |
| 6 | BAA02g44990 | A02 | 36965620 | C | T | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S203 |
| 7 | BAA02g44990 | A02 | 36965923 | C | T | upstream_gene_variant | MODIFIER | c.-3754G>A| |
S116 |
| 8 | BAA02g44990 | A02 | 36966813 | C | T | upstream_gene_variant | MODIFIER | c.-4644G>A| |
S249 |
| 9 | BAA02g44990 | A02 | 36967024 | C | T | upstream_gene_variant | MODIFIER | c.-4855G>A| |
S299 |