| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g05660 | A09 | 3216080 | C | T | missense_variant | MODERATE | c.748G>A|p.Ala250Thr |
S174 S27 |
| 2 | BAA09g05660 | A09 | 3220192 | C | T | upstream_gene_variant | MODIFIER | c.-2437G>A| |
S171 |
| 3 | BAA09g05660 | A09 | 3220635 | C | T | upstream_gene_variant | MODIFIER | c.-2880G>A| |
S135 |
| 4 | BAA09g05660 | A09 | 3222098 | G | A | upstream_gene_variant | MODIFIER | c.-4343C>T| |
S23 |
| 5 | BAA09g05660 | A09 | 3222455 | C | T | upstream_gene_variant | MODIFIER | c.-4700G>A| |
S292 |