| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g13170 | A09 | 7568488 | G | A | synonymous_variant | LOW | c.1225C>T|p.Leu409Leu |
S245 |
| 2 | BAA09g13170 | A09 | 7569499 | G | A | splice_region_variant&intron_variant | LOW | c.792+4C>T| |
S198 |
| 3 | BAA09g13170 | A09 | 7569806 | C | T | missense_variant | MODERATE | c.686G>A|p.Gly229Glu |
S212 |
| 4 | BAA09g13170 | A09 | 7571238 | G | A | upstream_gene_variant | MODIFIER | c.-186C>T| |
S151 S263 |
| 5 | BAA09g13170 | A09 | 7571367 | C | T | upstream_gene_variant | MODIFIER | c.-315G>A| |
S295 |
| 6 | BAA09g13170 | A09 | 7571483 | C | T | upstream_gene_variant | MODIFIER | c.-431G>A| |
S58 |
| 7 | BAA09g13170 | A09 | 7573875 | G | A | upstream_gene_variant | MODIFIER | c.-2823C>T| |
S199 |
| 8 | BAA09g13170 | A09 | 7575049 | G | A | upstream_gene_variant | MODIFIER | c.-3997C>T| |
S281 |
| 9 | BAA09g13170 | A09 | 7575133 | C | T | upstream_gene_variant | MODIFIER | c.-4081G>A| |
S85 |
| 10 | BAA09g13170 | A09 | 7575439 | C | T | upstream_gene_variant | MODIFIER | c.-4387G>A| |
S172 S217 |
| 11 | BAA09g13170 | A09 | 7575495 | C | A | upstream_gene_variant | MODIFIER | c.-4443G>T| |
S292 |
| 12 | BAA09g13170 | A09 | 7575666 | C | T | upstream_gene_variant | MODIFIER | c.-4614G>A| |
S117 |