| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g31590 | A02 | 19024875 | G | A | missense_variant | MODERATE | c.281G>A|p.Gly94Glu |
S197 |
| 2 | BAA02g31590 | A02 | 19025127 | G | A | missense_variant | MODERATE | c.451G>A|p.Val151Ile |
S278 |
| 3 | BAA02g31590 | A02 | 19026683 | C | T | missense_variant | MODERATE | c.1192C>T|p.Pro398Ser |
S118 |
| 4 | BAA02g31590 | A02 | 19026764 | G | A | missense_variant | MODERATE | c.1273G>A|p.Val425Met |
S156 |
| 5 | BAA02g31590 | A02 | 19029111 | G | A | downstream_gene_variant | MODIFIER | c.*2324G>A| |
S168 S259 |
| 6 | BAA02g31590 | A02 | 19029682 | C | T | downstream_gene_variant | MODIFIER | c.*2895C>T| |
S180 |
| 7 | BAA02g31590 | A02 | 19029860 | C | A | downstream_gene_variant | MODIFIER | c.*3073C>A| |
|
| 8 | BAA02g31590 | A02 | 19029884 | C | T | downstream_gene_variant | MODIFIER | c.*3097C>T| |
S157 S163 |