| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g32000 | A02 | 26038828 | C | T | missense_variant | MODERATE | c.187G>A|p.Asp63Asn |
S188 |
| 2 | BAA02g32000 | A02 | 26039017 | C | T | upstream_gene_variant | MODIFIER | c.-3G>A| |
S125 |
| 3 | BAA02g32000 | A02 | 26039635 | G | A | upstream_gene_variant | MODIFIER | c.-621C>T| |
S231 |
| 4 | BAA02g32000 | A02 | 26040383 | C | T | upstream_gene_variant | MODIFIER | c.-1369G>A| |
S35 |
| 5 | BAA02g32000 | A02 | 26042442 | C | T | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S69 |
| 6 | BAA02g32000 | A02 | 26042669 | G | A | upstream_gene_variant | MODIFIER | c.-3655C>T| |
S130 |
| 7 | BAA02g32000 | A02 | 26042680 | C | T | upstream_gene_variant | MODIFIER | c.-3666G>A| |
S184 |