| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g20770 | A02 | 11038940 | G | A | upstream_gene_variant | MODIFIER | c.-3768G>A| |
S235 |
| 2 | BAA02g20770 | A02 | 11040669 | C | T | upstream_gene_variant | MODIFIER | c.-2039C>T| |
S152 |
| 3 | BAA02g20770 | A02 | 11042355 | C | T | upstream_gene_variant | MODIFIER | c.-353C>T| |
S218 |
| 4 | BAA02g20770 | A02 | 11042532 | C | T | upstream_gene_variant | MODIFIER | c.-176C>T| |
S255 |
| 5 | BAA02g20770 | A02 | 11043291 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.160-1G>A| |
S197 |
| 6 | BAA02g20770 | A02 | 11043560 | G | A | missense_variant | MODERATE | c.356G>A|p.Arg119Lys |
S263 |
| 7 | BAA02g20770 | A02 | 11043567 | G | A | splice_region_variant&stop_retained_variant | LOW | c.363G>A|p.Ter121Ter |
S228 |