| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g40860 | A02 | 34270780 | C | T | missense_variant | MODERATE | c.1663G>A|p.Glu555Lys |
S167 |
| 2 | BAA02g40860 | A02 | 34270813 | C | T | missense_variant | MODERATE | c.1630G>A|p.Asp544Asn |
S117 |
| 3 | BAA02g40860 | A02 | 34276844 | C | T | intron_variant | MODIFIER | c.445-1027G>A| |
S167 |
| 4 | BAA02g40860 | A02 | 34279526 | G | A | upstream_gene_variant | MODIFIER | c.-592C>T| |
S280 |
| 5 | BAA02g40860 | A02 | 34279869 | G | A | upstream_gene_variant | MODIFIER | c.-935C>T| |
S81 S85 |
| 6 | BAA02g40860 | A02 | 34283655 | G | A | upstream_gene_variant | MODIFIER | c.-4721C>T| |
S125 |
| 7 | BAA02g40860 | A02 | 34283873 | T | C | upstream_gene_variant | MODIFIER | c.-4939A>G| |
S157 |
| 8 | BAA02g40860 | A02 | 34283934 | G | A | upstream_gene_variant | MODIFIER | c.-5000C>T| |
S268 |