| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g34780 | A02 | 29940653 | C | T | missense_variant | MODERATE | c.1897G>A|p.Asp633Asn |
S64 |
| 2 | BAA02g34780 | A02 | 29941031 | G | A | missense_variant | MODERATE | c.1706C>T|p.Thr569Ile |
S20 |
| 3 | BAA02g34780 | A02 | 29942448 | G | A | intron_variant | MODIFIER | c.1161+237C>T| |
S223 S95 |
| 4 | BAA02g34780 | A02 | 29942700 | C | T | synonymous_variant | LOW | c.1146G>A|p.Leu382Leu |
S203 |
| 5 | BAA02g34780 | A02 | 29943838 | G | A | synonymous_variant | LOW | c.450C>T|p.Asn150Asn |
S36 |
| 6 | BAA02g34780 | A02 | 29943928 | G | A | synonymous_variant | LOW | c.360C>T|p.Leu120Leu |
S223 |
| 7 | BAA02g34780 | A02 | 29945051 | G | A | upstream_gene_variant | MODIFIER | c.-335C>T| |
S55 |
| 8 | BAA02g34780 | A02 | 29945264 | G | A | upstream_gene_variant | MODIFIER | c.-548C>T| |
S166 S167 |
| 9 | BAA02g34780 | A02 | 29946489 | C | T | upstream_gene_variant | MODIFIER | c.-1773G>A| |
S262 |
| 10 | BAA02g34780 | A02 | 29946559 | G | A | upstream_gene_variant | MODIFIER | c.-1843C>T| |
S264 |
| 11 | BAA02g34780 | A02 | 29947429 | G | A | upstream_gene_variant | MODIFIER | c.-2713C>T| |
S251 |
| 12 | BAA02g34780 | A02 | 29947945 | C | T | upstream_gene_variant | MODIFIER | c.-3229G>A| |
S284 |