| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g42440 | A02 | 35352165 | G | A | upstream_gene_variant | MODIFIER | c.-2381G>A| |
S156 |
| 2 | BAA02g42440 | A02 | 35352266 | C | T | upstream_gene_variant | MODIFIER | c.-2280C>T| |
S123 |
| 3 | BAA02g42440 | A02 | 35354141 | C | T | upstream_gene_variant | MODIFIER | c.-405C>T| |
S83 S88 |
| 4 | BAA02g42440 | A02 | 35354555 | G | A | missense_variant | MODERATE | c.10G>A|p.Ala4Thr |
S223 |
| 5 | BAA02g42440 | A02 | 35354637 | C | T | missense_variant | MODERATE | c.92C>T|p.Ser31Phe |
S144 |
| 6 | BAA02g42440 | A02 | 35354695 | G | A | synonymous_variant | LOW | c.150G>A|p.Leu50Leu |
S302 |
| 7 | BAA02g42440 | A02 | 35355568 | G | A | missense_variant | MODERATE | c.881G>A|p.Cys294Tyr |
S186 |
| 8 | BAA02g42440 | A02 | 35358200 | C | T | downstream_gene_variant | MODIFIER | c.*2499C>T| |
S3 |
| 9 | BAA02g42440 | A02 | 35358609 | C | T | downstream_gene_variant | MODIFIER | c.*2908C>T| |
S130 |