| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g44690 | A02 | 36751586 | C | T | upstream_gene_variant | MODIFIER | c.-734C>T| |
S35 |
| 2 | BAA02g44690 | A02 | 36751774 | C | T | upstream_gene_variant | MODIFIER | c.-546C>T| |
S116 |
| 3 | BAA02g44690 | A02 | 36752110 | C | T | upstream_gene_variant | MODIFIER | c.-210C>T| |
S273 |
| 4 | BAA02g44690 | A02 | 36752250 | G | A | upstream_gene_variant | MODIFIER | c.-70G>A| |
S146 |
| 5 | BAA02g44690 | A02 | 36752401 | G | A | missense_variant | MODERATE | c.82G>A|p.Gly28Arg |
S107 |
| 6 | BAA02g44690 | A02 | 36753036 | G | A | missense_variant | MODERATE | c.625G>A|p.Val209Ile |
S44 |
| 7 | BAA02g44690 | A02 | 36755055 | C | T | synonymous_variant | LOW | c.1269C>T|p.Ser423Ser |
S133 |
| 8 | BAA02g44690 | A02 | 36755978 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2113-1G>A| |
S164 |