| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g27240 | A02 | 15272530 | G | A | synonymous_variant | LOW | c.1483C>T|p.Leu495Leu |
S136 |
| 2 | BAA02g27240 | A02 | 15273377 | G | A | synonymous_variant | LOW | c.636C>T|p.Phe212Phe |
S188 |
| 3 | BAA02g27240 | A02 | 15273726 | G | A | missense_variant | MODERATE | c.287C>T|p.Ser96Phe |
S186 |
| 4 | BAA02g27240 | A02 | 15273776 | G | A | synonymous_variant | LOW | c.237C>T|p.Ile79Ile |
S200 |
| 5 | BAA02g27240 | A02 | 15276161 | G | A | upstream_gene_variant | MODIFIER | c.-2149C>T| |
S177 |
| 6 | BAA02g27240 | A02 | 15276362 | G | A | upstream_gene_variant | MODIFIER | c.-2350C>T| |
S98 |
| 7 | BAA02g27240 | A02 | 15277074 | G | A | upstream_gene_variant | MODIFIER | c.-3062C>T| |
S45 |
| 8 | BAA02g27240 | A02 | 15277635 | G | A | upstream_gene_variant | MODIFIER | c.-3623C>T| |
S303 |
| 9 | BAA02g27240 | A02 | 15277736 | G | A | upstream_gene_variant | MODIFIER | c.-3724C>T| |
S56 |
| 10 | BAA02g27240 | A02 | 15277786 | C | T | upstream_gene_variant | MODIFIER | c.-3774G>A| |
S135 |
| 11 | BAA02g27240 | A02 | 15277795 | C | T | upstream_gene_variant | MODIFIER | c.-3783G>A| |
S124 |
| 12 | BAA02g27240 | A02 | 15277953 | C | T | upstream_gene_variant | MODIFIER | c.-3941G>A| |
S11 |
| 13 | BAA02g27240 | A02 | 15277979 | C | T | upstream_gene_variant | MODIFIER | c.-3967G>A| |
S162 |
| 14 | BAA02g27240 | A02 | 15278168 | G | A | upstream_gene_variant | MODIFIER | c.-4156C>T| |
S116 |
| 15 | BAA02g27240 | A02 | 15278250 | C | T | upstream_gene_variant | MODIFIER | c.-4238G>A| |
S64 |
| 16 | BAA02g27240 | A02 | 15278643 | G | A | upstream_gene_variant | MODIFIER | c.-4631C>T| |
S186 |
| 17 | BAA02g27240 | A02 | 15278652 | C | T | upstream_gene_variant | MODIFIER | c.-4640G>A| |
S176 |
| 18 | BAA02g27240 | A02 | 15278666 | G | A | upstream_gene_variant | MODIFIER | c.-4654C>T| |
S173 |
| 19 | BAA02g27240 | A02 | 15278759 | C | T | upstream_gene_variant | MODIFIER | c.-4747G>A| |
S46 |