| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g19690 | A02 | 10245721 | C | T | intron_variant | MODIFIER | c.702+324G>A| |
S293 |
| 2 | BAA02g19690 | A02 | 10248371 | C | T | intron_variant | MODIFIER | c.386+1282G>A| |
S171 |
| 3 | BAA02g19690 | A02 | 10249263 | G | A | intron_variant | MODIFIER | c.386+390C>T| |
S35 |
| 4 | BAA02g19690 | A02 | 10249668 | G | A | missense_variant | MODERATE | c.371C>T|p.Pro124Leu |
S52 |
| 5 | BAA02g19690 | A02 | 10250325 | C | T | upstream_gene_variant | MODIFIER | c.-287G>A| |
S112 |
| 6 | BAA02g19690 | A02 | 10252937 | C | T | upstream_gene_variant | MODIFIER | c.-2899G>A| |
S284 |