| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g23860 | A02 | 13022924 | C | T | synonymous_variant | LOW | c.591G>A|p.Val197Val |
S94 |
| 2 | BAA02g23860 | A02 | 13023141 | C | T | missense_variant | MODERATE | c.374G>A|p.Arg125Lys |
S118 S277 |
| 3 | BAA02g23860 | A02 | 13023370 | G | A | synonymous_variant | LOW | c.207C>T|p.Leu69Leu |
S257 |
| 4 | BAA02g23860 | A02 | 13027114 | C | T | upstream_gene_variant | MODIFIER | c.-3538G>A| |
S171 |
| 5 | BAA02g23860 | A02 | 13027208 | G | A | upstream_gene_variant | MODIFIER | c.-3632C>T| |
S190 |
| 6 | BAA02g23860 | A02 | 13027256 | C | T | upstream_gene_variant | MODIFIER | c.-3680G>A| |
S42 |
| 7 | BAA02g23860 | A02 | 13027447 | G | A | upstream_gene_variant | MODIFIER | c.-3871C>T| |
S136 |
| 8 | BAA02g23860 | A02 | 13027603 | C | T | upstream_gene_variant | MODIFIER | c.-4027G>A| |
S18 |