| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g52130 | A03 | 25462115 | C | T | missense_variant | MODERATE | c.413C>T|p.Pro138Leu |
S208 S219 |
| 2 | BAA03g52130 | A03 | 25462949 | G | A | synonymous_variant | LOW | c.816G>A|p.Val272Val |
S278 |
| 3 | BAA03g52130 | A03 | 25466625 | G | A | downstream_gene_variant | MODIFIER | c.*3278G>A| |
S298 |
| 4 | BAA03g52130 | A03 | 25466744 | C | T | downstream_gene_variant | MODIFIER | c.*3397C>T| |
S129 |
| 5 | BAA03g52130 | A03 | 25466938 | C | T | downstream_gene_variant | MODIFIER | c.*3591C>T| |
S228 |
| 6 | BAA03g52130 | A03 | 25466963 | C | T | downstream_gene_variant | MODIFIER | c.*3616C>T| |
S251 |
| 7 | BAA03g52130 | A03 | 25467264 | C | T | downstream_gene_variant | MODIFIER | c.*3917C>T| |
S23 |
| 8 | BAA03g52130 | A03 | 25467989 | G | A | downstream_gene_variant | MODIFIER | c.*4642G>A| |
S284 |
| 9 | BAA03g52130 | A03 | 25468140 | C | T | downstream_gene_variant | MODIFIER | c.*4793C>T| |
S176 |