| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g44600 | A01 | 29693546 | G | A | upstream_gene_variant | MODIFIER | c.-4133G>A| |
S208 S219 |
| 2 | BAA01g44600 | A01 | 29693551 | C | T | upstream_gene_variant | MODIFIER | c.-4128C>T| |
S37 |
| 3 | BAA01g44600 | A01 | 29697331 | G | A | upstream_gene_variant | MODIFIER | c.-348G>A| |
S53 |
| 4 | BAA01g44600 | A01 | 29697612 | C | T | upstream_gene_variant | MODIFIER | c.-67C>T| |
S259 |
| 5 | BAA01g44600 | A01 | 29697758 | C | T | missense_variant&splice_region_variant | MODERATE | c.80C>T|p.Ser27Phe |
S47 |
| 6 | BAA01g44600 | A01 | 29699181 | C | T | missense_variant | MODERATE | c.976C>T|p.Leu326Phe |
S32 |
| 7 | BAA01g44600 | A01 | 29699416 | G | A | missense_variant | MODERATE | c.1141G>A|p.Val381Ile |
S106 S185 |
| 8 | BAA01g44600 | A01 | 29699795 | C | T | synonymous_variant | LOW | c.1363C>T|p.Leu455Leu |
S48 |