| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g14660 | A02 | 6849734 | C | T | missense_variant | MODERATE | c.107G>A|p.Gly36Glu |
S182 |
| 2 | BAA02g14660 | A02 | 6849750 | G | A | missense_variant | MODERATE | c.91C>T|p.Leu31Phe |
S223 |
| 3 | BAA02g14660 | A02 | 6851192 | C | T | upstream_gene_variant | MODIFIER | c.-1352G>A| |
S73 |
| 4 | BAA02g14660 | A02 | 6851230 | C | T | upstream_gene_variant | MODIFIER | c.-1390G>A| |
S130 |
| 5 | BAA02g14660 | A02 | 6854601 | C | T | upstream_gene_variant | MODIFIER | c.-4761G>A| |
S40 S49 |