| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g42650 | A02 | 35499778 | C | T | upstream_gene_variant | MODIFIER | c.-4801C>T| |
S93 |
| 2 | BAA02g42650 | A02 | 35499855 | G | A | upstream_gene_variant | MODIFIER | c.-4724G>A| |
S69 |
| 3 | BAA02g42650 | A02 | 35500593 | G | A | upstream_gene_variant | MODIFIER | c.-3986G>A| |
S35 |
| 4 | BAA02g42650 | A02 | 35501762 | C | T | upstream_gene_variant | MODIFIER | c.-2817C>T| |
S144 S158 |
| 5 | BAA02g42650 | A02 | 35504627 | G | A | missense_variant | MODERATE | c.49G>A|p.Glu17Lys |
S288 |
| 6 | BAA02g42650 | A02 | 35504761 | T | A | intron_variant | MODIFIER | c.150+33T>A| |
S195 |
| 7 | BAA02g42650 | A02 | 35504786 | G | A | intron_variant | MODIFIER | c.150+58G>A| |
S236 |
| 8 | BAA02g42650 | A02 | 35505986 | G | A | downstream_gene_variant | MODIFIER | c.*920G>A| |
S9 |
| 9 | BAA02g42650 | A02 | 35506729 | C | T | downstream_gene_variant | MODIFIER | c.*1663C>T| |
S275 |
| 10 | BAA02g42650 | A02 | 35507054 | C | T | downstream_gene_variant | MODIFIER | c.*1988C>T| |
S176 |
| 11 | BAA02g42650 | A02 | 35507694 | G | A | downstream_gene_variant | MODIFIER | c.*2628G>A| |
S238 |
| 12 | BAA02g42650 | A02 | 35508685 | A | T | downstream_gene_variant | MODIFIER | c.*3619A>T| |
S183 |