| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g26990 | A05 | 31464568 | C | T | missense_variant | MODERATE | c.386G>A|p.Gly129Asp |
S35 |
| 2 | BAA05g26990 | A05 | 31465158 | C | T | upstream_gene_variant | MODIFIER | c.-52G>A| |
S116 |
| 3 | BAA05g26990 | A05 | 31468520 | C | T | upstream_gene_variant | MODIFIER | c.-3414G>A| |
S189 |
| 4 | BAA05g26990 | A05 | 31468995 | G | A | upstream_gene_variant | MODIFIER | c.-3889C>T| |
S144 |
| 5 | BAA05g26990 | A05 | 31469052 | A | G | upstream_gene_variant | MODIFIER | c.-3946T>C| |
S190 |
| 6 | BAA05g26990 | A05 | 31469278 | C | T | upstream_gene_variant | MODIFIER | c.-4172G>A| |
S236 |