| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g16180 | A02 | 7887391 | G | A | downstream_gene_variant | MODIFIER | c.*4747C>T| |
S279 |
| 2 | BAA02g16180 | A02 | 7888483 | C | T | downstream_gene_variant | MODIFIER | c.*3655G>A| |
S128 |
| 3 | BAA02g16180 | A02 | 7889388 | C | T | downstream_gene_variant | MODIFIER | c.*2750G>A| |
S8 |
| 4 | BAA02g16180 | A02 | 7890077 | C | T | downstream_gene_variant | MODIFIER | c.*2061G>A| |
S105 S106 |
| 5 | BAA02g16180 | A02 | 7891788 | C | T | downstream_gene_variant | MODIFIER | c.*350G>A| |
S103 |
| 6 | BAA02g16180 | A02 | 7892873 | G | A | missense_variant | MODERATE | c.994C>T|p.Pro332Ser |
S297 |
| 7 | BAA02g16180 | A02 | 7893281 | C | T | synonymous_variant | LOW | c.822G>A|p.Gln274Gln |
S244 |
| 8 | BAA02g16180 | A02 | 7894056 | G | A | synonymous_variant | LOW | c.423C>T|p.Leu141Leu |
S287 |
| 9 | BAA02g16180 | A02 | 7895569 | G | A | upstream_gene_variant | MODIFIER | c.-844C>T| |
S286 |
| 10 | BAA02g16180 | A02 | 7896770 | G | A | upstream_gene_variant | MODIFIER | c.-2045C>T| |
S148 S30 S31 |
| 11 | BAA02g16180 | A02 | 7897922 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S261 |