| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g21660 | A09 | 13500125 | G | A | synonymous_variant | LOW | c.897C>T|p.Phe299Phe |
S86 |
| 2 | BAA09g21660 | A09 | 13502883 | C | T | missense_variant | MODERATE | c.368G>A|p.Gly123Asp |
S108 |
| 3 | BAA09g21660 | A09 | 13505195 | G | A | upstream_gene_variant | MODIFIER | c.-1945C>T| |
S45 |
| 4 | BAA09g21660 | A09 | 13506550 | A | C | upstream_gene_variant | MODIFIER | c.-3300T>G| |
S103 S111 S142 S152 S171 S193 S209 S303 S87 |
| 5 | BAA09g21660 | A09 | 13507110 | C | T | upstream_gene_variant | MODIFIER | c.-3860G>A| |
S28 |
| 6 | BAA09g21660 | A09 | 13507425 | C | T | upstream_gene_variant | MODIFIER | c.-4175G>A| |
S143 |
| 7 | BAA09g21660 | A09 | 13508173 | C | T | upstream_gene_variant | MODIFIER | c.-4923G>A| |
S108 |