| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g01560 | A02 | 702333 | G | A | missense_variant | MODERATE | c.260C>T|p.Thr87Ile |
S288 |
| 2 | BAA02g01560 | A02 | 702359 | G | A | synonymous_variant | LOW | c.234C>T|p.Asp78Asp |
S105 S106 |
| 3 | BAA02g01560 | A02 | 702538 | C | T | missense_variant | MODERATE | c.55G>A|p.Val19Met |
S100 |
| 4 | BAA02g01560 | A02 | 706014 | C | T | upstream_gene_variant | MODIFIER | c.-3422G>A| |
S14 S224 |
| 5 | BAA02g01560 | A02 | 706127 | C | A | upstream_gene_variant | MODIFIER | c.-3535G>T| |
S132 S137 S215 S89 |
| 6 | BAA02g01560 | A02 | 706212 | G | A | upstream_gene_variant | MODIFIER | c.-3620C>T| |
S297 |
| 7 | BAA02g01560 | A02 | 707253 | C | T | upstream_gene_variant | MODIFIER | c.-4661G>A| |
S195 |