| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS13g01700 | Scaffold13 | 13907465 | C | T | upstream_gene_variant | MODIFIER | c.-4972C>T| |
S122 S7 |
| 2 | BAS13g01700 | Scaffold13 | 13907644 | G | A | upstream_gene_variant | MODIFIER | c.-4793G>A| |
S67 |
| 3 | BAS13g01700 | Scaffold13 | 13907815 | G | A | upstream_gene_variant | MODIFIER | c.-4622G>A| |
S42 |
| 4 | BAS13g01700 | Scaffold13 | 13907998 | C | T | upstream_gene_variant | MODIFIER | c.-4439C>T| |
S11 |
| 5 | BAS13g01700 | Scaffold13 | 13909377 | C | T | upstream_gene_variant | MODIFIER | c.-3060C>T| |
S125 |
| 6 | BAS13g01700 | Scaffold13 | 13909596 | G | A | upstream_gene_variant | MODIFIER | c.-2841G>A| |
S124 |
| 7 | BAS13g01700 | Scaffold13 | 13910236 | G | A | upstream_gene_variant | MODIFIER | c.-2201G>A| |
S243 S299 |
| 8 | BAS13g01700 | Scaffold13 | 13910611 | G | A | upstream_gene_variant | MODIFIER | c.-1826G>A| |
S168 |
| 9 | BAS13g01700 | Scaffold13 | 13910899 | G | A | upstream_gene_variant | MODIFIER | c.-1538G>A| |
S245 |
| 10 | BAS13g01700 | Scaffold13 | 13911872 | G | A | upstream_gene_variant | MODIFIER | c.-565G>A| |
S74 |
| 11 | BAS13g01700 | Scaffold13 | 13912009 | C | T | upstream_gene_variant | MODIFIER | c.-428C>T| |
S35 |
| 12 | BAS13g01700 | Scaffold13 | 13912936 | G | A | downstream_gene_variant | MODIFIER | c.*122G>A| |
S208 S93 |
| 13 | BAS13g01700 | Scaffold13 | 13913171 | G | A | downstream_gene_variant | MODIFIER | c.*357G>A| |
S243 S299 |
| 14 | BAS13g01700 | Scaffold13 | 13913323 | G | A | downstream_gene_variant | MODIFIER | c.*509G>A| |
S283 |
| 15 | BAS13g01700 | Scaffold13 | 13913655 | C | T | downstream_gene_variant | MODIFIER | c.*841C>T| |
S44 |
| 16 | BAS13g01700 | Scaffold13 | 13913675 | G | A | downstream_gene_variant | MODIFIER | c.*861G>A| |
S79 S91 |