| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g44830 | A01 | 29864750 | G | A | downstream_gene_variant | MODIFIER | c.*3714C>T| |
S297 |
| 2 | BAA01g44830 | A01 | 29865079 | C | T | downstream_gene_variant | MODIFIER | c.*3385G>A| |
S279 |
| 3 | BAA01g44830 | A01 | 29865224 | G | A | downstream_gene_variant | MODIFIER | c.*3240C>T| |
S153 S213 |
| 4 | BAA01g44830 | A01 | 29865326 | C | T | downstream_gene_variant | MODIFIER | c.*3138G>A| |
S74 |
| 5 | BAA01g44830 | A01 | 29865457 | G | A | downstream_gene_variant | MODIFIER | c.*3007C>T| |
S296 |
| 6 | BAA01g44830 | A01 | 29865710 | A | G | downstream_gene_variant | MODIFIER | c.*2754T>C| |
S256 |
| 7 | BAA01g44830 | A01 | 29866848 | G | A | downstream_gene_variant | MODIFIER | c.*1616C>T| |
S280 |
| 8 | BAA01g44830 | A01 | 29866851 | C | T | downstream_gene_variant | MODIFIER | c.*1613G>A| |
S41 |
| 9 | BAA01g44830 | A01 | 29869454 | C | T | missense_variant&splice_region_variant | MODERATE | c.191G>A|p.Cys64Tyr |
S62 |
| 10 | BAA01g44830 | A01 | 29871713 | G | A | upstream_gene_variant | MODIFIER | c.-2069C>T| |
S149 |
| 11 | BAA01g44830 | A01 | 29872296 | C | T | upstream_gene_variant | MODIFIER | c.-2652G>A| |
S78 S83 |
| 12 | BAA01g44830 | A01 | 29872530 | C | T | upstream_gene_variant | MODIFIER | c.-2886G>A| |
S210 S225 |
| 13 | BAA01g44830 | A01 | 29872639 | C | T | upstream_gene_variant | MODIFIER | c.-2995G>A| |
S112 |
| 14 | BAA01g44830 | A01 | 29873201 | C | T | upstream_gene_variant | MODIFIER | c.-3557G>A| |
S244 |
| 15 | BAA01g44830 | A01 | 29873204 | A | T | upstream_gene_variant | MODIFIER | c.-3560T>A| |
S244 |