| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g22460 | A02 | 12136571 | C | T | intron_variant | MODIFIER | c.756+22G>A| |
S123 |
| 2 | BAA02g22460 | A02 | 12137153 | C | T | missense_variant | MODERATE | c.196G>A|p.Gly66Arg |
S25 |
| 3 | BAA02g22460 | A02 | 12137817 | G | A | upstream_gene_variant | MODIFIER | c.-347C>T| |
S287 |
| 4 | BAA02g22460 | A02 | 12140193 | G | A | upstream_gene_variant | MODIFIER | c.-2723C>T| |
S136 |
| 5 | BAA02g22460 | A02 | 12140324 | C | T | upstream_gene_variant | MODIFIER | c.-2854G>A| |
S6 |
| 6 | BAA02g22460 | A02 | 12141571 | G | A | upstream_gene_variant | MODIFIER | c.-4101C>T| |
S288 |
| 7 | BAA02g22460 | A02 | 12142460 | C | T | upstream_gene_variant | MODIFIER | c.-4990G>A| |
S234 |