| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g39490 | A01 | 26254444 | G | A | upstream_gene_variant | MODIFIER | c.-4760G>A| |
S47 |
| 2 | BAA01g39490 | A01 | 26255466 | C | T | upstream_gene_variant | MODIFIER | c.-3738C>T| |
S261 |
| 3 | BAA01g39490 | A01 | 26255476 | G | A | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S143 |
| 4 | BAA01g39490 | A01 | 26256226 | G | A | upstream_gene_variant | MODIFIER | c.-2978G>A| |
S143 S150 |
| 5 | BAA01g39490 | A01 | 26256425 | A | T | upstream_gene_variant | MODIFIER | c.-2779A>T| |
S261 |
| 6 | BAA01g39490 | A01 | 26257060 | C | A | upstream_gene_variant | MODIFIER | c.-2144C>A| |
S160 |
| 7 | BAA01g39490 | A01 | 26257751 | G | A | upstream_gene_variant | MODIFIER | c.-1453G>A| |
S284 |
| 8 | BAA01g39490 | A01 | 26259449 | G | A | synonymous_variant | LOW | c.246G>A|p.Ala82Ala |
S262 |
| 9 | BAA01g39490 | A01 | 26259825 | G | A | intron_variant | MODIFIER | c.484+138G>A| |
S202 |
| 10 | BAA01g39490 | A01 | 26260937 | C | T | downstream_gene_variant | MODIFIER | c.*114C>T| |
S54 |