| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00070 | A02 | 45782 | C | T | missense_variant | MODERATE | c.260G>A|p.Gly87Glu |
S18 |
| 2 | BAA02g00070 | A02 | 48537 | C | T | upstream_gene_variant | MODIFIER | c.-2404G>A| |
S218 |
| 3 | BAA02g00070 | A02 | 48670 | C | T | upstream_gene_variant | MODIFIER | c.-2537G>A| |
S298 |
| 4 | BAA02g00070 | A02 | 49597 | C | T | upstream_gene_variant | MODIFIER | c.-3464G>A| |
S171 |
| 5 | BAA02g00070 | A02 | 49975 | G | A | upstream_gene_variant | MODIFIER | c.-3842C>T| |
S39 |
| 6 | BAA02g00070 | A02 | 50425 | C | G | upstream_gene_variant | MODIFIER | c.-4292G>C| |
S1 |
| 7 | BAA02g00070 | A02 | 50588 | C | T | upstream_gene_variant | MODIFIER | c.-4455G>A| |
S251 |