| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g28450 | A02 | 15995756 | C | T | upstream_gene_variant | MODIFIER | c.-1404C>T| |
S63 |
| 2 | BAA02g28450 | A02 | 15995983 | G | A | upstream_gene_variant | MODIFIER | c.-1177G>A| |
S265 |
| 3 | BAA02g28450 | A02 | 15997200 | G | A | missense_variant | MODERATE | c.41G>A|p.Gly14Glu |
S192 |
| 4 | BAA02g28450 | A02 | 15999809 | G | A | synonymous_variant | LOW | c.633G>A|p.Pro211Pro |
S92 |
| 5 | BAA02g28450 | A02 | 16003727 | C | T | downstream_gene_variant | MODIFIER | c.*3876C>T| |
S2 |
| 6 | BAA02g28450 | A02 | 16003837 | C | T | downstream_gene_variant | MODIFIER | c.*3986C>T| |
S282 |
| 7 | BAA02g28450 | A02 | 16003964 | C | T | downstream_gene_variant | MODIFIER | c.*4113C>T| |
S286 |
| 8 | BAA02g28450 | A02 | 16004707 | C | T | downstream_gene_variant | MODIFIER | c.*4856C>T| |
S221 |
| 9 | BAA02g28450 | A02 | 16004828 | C | T | downstream_gene_variant | MODIFIER | c.*4977C>T| |
S2 |