| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g47230 | A02 | 38134922 | C | T | missense_variant | MODERATE | c.62G>A|p.Gly21Glu |
S187 S188 S243 S276 S299 |
| 2 | BAA02g47230 | A02 | 38135590 | C | T | upstream_gene_variant | MODIFIER | c.-607G>A| |
S263 |
| 3 | BAA02g47230 | A02 | 38135592 | G | A | upstream_gene_variant | MODIFIER | c.-609C>T| |
S1 S19 |
| 4 | BAA02g47230 | A02 | 38135862 | C | T | upstream_gene_variant | MODIFIER | c.-879G>A| |
S203 |
| 5 | BAA02g47230 | A02 | 38136801 | C | T | upstream_gene_variant | MODIFIER | c.-1818G>A| |
S159 |
| 6 | BAA02g47230 | A02 | 38137065 | G | A | upstream_gene_variant | MODIFIER | c.-2082C>T| |
S280 |
| 7 | BAA02g47230 | A02 | 38137578 | C | T | upstream_gene_variant | MODIFIER | c.-2595G>A| |
S233 |
| 8 | BAA02g47230 | A02 | 38138416 | G | A | upstream_gene_variant | MODIFIER | c.-3433C>T| |
S302 |
| 9 | BAA02g47230 | A02 | 38138998 | C | T | upstream_gene_variant | MODIFIER | c.-4015G>A| |
S183 S198 |