| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g25480 | A02 | 13979024 | G | A | upstream_gene_variant | MODIFIER | c.-1461G>A| |
S47 |
| 2 | BAA02g25480 | A02 | 13979781 | C | T | upstream_gene_variant | MODIFIER | c.-704C>T| |
S18 |
| 3 | BAA02g25480 | A02 | 13980106 | G | A | upstream_gene_variant | MODIFIER | c.-379G>A| |
S217 |
| 4 | BAA02g25480 | A02 | 13980464 | G | A | upstream_gene_variant | MODIFIER | c.-21G>A| |
S28 |
| 5 | BAA02g25480 | A02 | 13980750 | G | A | missense_variant | MODERATE | c.266G>A|p.Gly89Glu |
S217 |
| 6 | BAA02g25480 | A02 | 13981570 | G | A | missense_variant | MODERATE | c.943G>A|p.Asp315Asn |
S295 |
| 7 | BAA02g25480 | A02 | 13983497 | C | T | missense_variant | MODERATE | c.2471C>T|p.Ala824Val |
S296 |
| 8 | BAA02g25480 | A02 | 13983708 | G | A | stop_gained | HIGH | c.2610G>A|p.Trp870* |
S148 |
| 9 | BAA02g25480 | A02 | 13983762 | G | A | synonymous_variant | LOW | c.2664G>A|p.Arg888Arg |
S252 S292 |
| 10 | BAA02g25480 | A02 | 13983799 | C | T | missense_variant | MODERATE | c.2701C>T|p.Leu901Phe |
S224 |
| 11 | BAA02g25480 | A02 | 13984525 | G | A | downstream_gene_variant | MODIFIER | c.*427G>A| |
S95 |