| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g39000 | A01 | 25959344 | C | T | synonymous_variant | LOW | c.951G>A|p.Val317Val |
S198 |
| 2 | BAA01g39000 | A01 | 25959438 | G | A | missense_variant | MODERATE | c.857C>T|p.Ser286Phe |
S259 |
| 3 | BAA01g39000 | A01 | 25959892 | G | A | missense_variant | MODERATE | c.403C>T|p.Pro135Ser |
S169 |
| 4 | BAA01g39000 | A01 | 25960123 | G | A | missense_variant | MODERATE | c.172C>T|p.Pro58Ser |
S224 |
| 5 | BAA01g39000 | A01 | 25960160 | C | T | synonymous_variant | LOW | c.135G>A|p.Arg45Arg |
S293 |
| 6 | BAA01g39000 | A01 | 25960823 | G | A | upstream_gene_variant | MODIFIER | c.-529C>T| |
S190 |
| 7 | BAA01g39000 | A01 | 25960898 | G | A | upstream_gene_variant | MODIFIER | c.-604C>T| |
S34 |
| 8 | BAA01g39000 | A01 | 25962554 | C | T | upstream_gene_variant | MODIFIER | c.-2260G>A| |
S192 |
| 9 | BAA01g39000 | A01 | 25963828 | C | T | upstream_gene_variant | MODIFIER | c.-3534G>A| |
S239 |
| 10 | BAA01g39000 | A01 | 25964716 | C | T | upstream_gene_variant | MODIFIER | c.-4422G>A| |
S256 |