| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g33120 | A09 | 41746685 | C | T | missense_variant | MODERATE | c.629C>T|p.Pro210Leu |
S246 |
| 2 | BAA09g33120 | A09 | 41747341 | C | T | synonymous_variant | LOW | c.1209C>T|p.Leu403Leu |
S256 |
| 3 | BAA09g33120 | A09 | 41750758 | G | A | downstream_gene_variant | MODIFIER | c.*2914G>A| |
S87 |
| 4 | BAA09g33120 | A09 | 41750887 | C | T | downstream_gene_variant | MODIFIER | c.*3043C>T| |
S182 |
| 5 | BAA09g33120 | A09 | 41751433 | C | T | downstream_gene_variant | MODIFIER | c.*3589C>T| |
S302 |
| 6 | BAA09g33120 | A09 | 41751783 | C | T | downstream_gene_variant | MODIFIER | c.*3939C>T| |
S36 |
| 7 | BAA09g33120 | A09 | 41752606 | C | T | downstream_gene_variant | MODIFIER | c.*4762C>T| |
S293 |
| 8 | BAA09g33120 | A09 | 41752731 | C | T | downstream_gene_variant | MODIFIER | c.*4887C>T| |
S303 |