| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g46490 | A02 | 37785663 | G | A | downstream_gene_variant | MODIFIER | c.*3877C>T| |
S133 S172 S202 |
| 2 | BAA02g46490 | A02 | 37789964 | C | T | synonymous_variant | LOW | c.774G>A|p.Gln258Gln |
S296 |
| 3 | BAA02g46490 | A02 | 37793174 | C | T | upstream_gene_variant | MODIFIER | c.-1692G>A| |
S109 |
| 4 | BAA02g46490 | A02 | 37793183 | G | A | upstream_gene_variant | MODIFIER | c.-1701C>T| |
S96 |
| 5 | BAA02g46490 | A02 | 37793278 | C | T | upstream_gene_variant | MODIFIER | c.-1796G>A| |
S39 |
| 6 | BAA02g46490 | A02 | 37793821 | C | T | upstream_gene_variant | MODIFIER | c.-2339G>A| |
S203 |
| 7 | BAA02g46490 | A02 | 37793958 | G | A | upstream_gene_variant | MODIFIER | c.-2476C>T| |
S280 |
| 8 | BAA02g46490 | A02 | 37794436 | C | T | upstream_gene_variant | MODIFIER | c.-2954G>A| |
S4 |