| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g17990 | A01 | 8805471 | G | A | missense_variant | MODERATE | c.1043C>T|p.Pro348Leu |
S94 |
| 2 | BAA01g17990 | A01 | 8805777 | C | T | missense_variant | MODERATE | c.737G>A|p.Gly246Glu |
S39 |
| 3 | BAA01g17990 | A01 | 8806480 | C | T | missense_variant | MODERATE | c.34G>A|p.Glu12Lys |
S150 |
| 4 | BAA01g17990 | A01 | 8807516 | G | A | upstream_gene_variant | MODIFIER | c.-1003C>T| |
S271 |
| 5 | BAA01g17990 | A01 | 8807855 | C | T | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S182 |
| 6 | BAA01g17990 | A01 | 8808198 | G | A | upstream_gene_variant | MODIFIER | c.-1685C>T| |
S38 |
| 7 | BAA01g17990 | A01 | 8809025 | C | T | upstream_gene_variant | MODIFIER | c.-2512G>A| |
S136 |
| 8 | BAA01g17990 | A01 | 8810132 | C | T | upstream_gene_variant | MODIFIER | c.-3619G>A| |
S267 |
| 9 | BAA01g17990 | A01 | 8811207 | G | A | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S157 S163 |