| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g05960 | A02 | 2526111 | C | T | missense_variant | MODERATE | c.1406G>A|p.Gly469Asp |
S138 |
| 2 | BAA02g05960 | A02 | 2527735 | C | T | missense_variant | MODERATE | c.526G>A|p.Val176Met |
S306 S308 |
| 3 | BAA02g05960 | A02 | 2528854 | C | T | upstream_gene_variant | MODIFIER | c.-31G>A| |
S172 |
| 4 | BAA02g05960 | A02 | 2530258 | C | T | upstream_gene_variant | MODIFIER | c.-1435G>A| |
S221 |
| 5 | BAA02g05960 | A02 | 2530505 | G | A | upstream_gene_variant | MODIFIER | c.-1682C>T| |
S60 |
| 6 | BAA02g05960 | A02 | 2530776 | C | T | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S181 |