| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g44860 | A01 | 29876161 | C | T | missense_variant | MODERATE | c.1051G>A|p.Val351Ile |
S200 |
| 2 | BAA01g44860 | A01 | 29876806 | C | T | missense_variant | MODERATE | c.1006G>A|p.Val336Ile |
S242 |
| 3 | BAA01g44860 | A01 | 29879057 | C | T | upstream_gene_variant | MODIFIER | c.-1246G>A| |
S68 |
| 4 | BAA01g44860 | A01 | 29879167 | C | T | upstream_gene_variant | MODIFIER | c.-1356G>A| |
S35 |
| 5 | BAA01g44860 | A01 | 29879321 | C | T | upstream_gene_variant | MODIFIER | c.-1510G>A| |
S134 |
| 6 | BAA01g44860 | A01 | 29879691 | C | T | upstream_gene_variant | MODIFIER | c.-1880G>A| |
S183 S198 |
| 7 | BAA01g44860 | A01 | 29879921 | C | T | upstream_gene_variant | MODIFIER | c.-2110G>A| |
S305 |
| 8 | BAA01g44860 | A01 | 29880561 | C | T | upstream_gene_variant | MODIFIER | c.-2750G>A| |
S239 |
| 9 | BAA01g44860 | A01 | 29881262 | C | T | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S192 |
| 10 | BAA01g44860 | A01 | 29882187 | A | G | upstream_gene_variant | MODIFIER | c.-4376T>C| |
S186 |