| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08980 | A10 | 11073937 | C | T | downstream_gene_variant | MODIFIER | c.*3557G>A| |
S28 |
| 2 | BAA10g08980 | A10 | 11077505 | G | A | missense_variant | MODERATE | c.367C>T|p.Leu123Phe |
S241 |
| 3 | BAA10g08980 | A10 | 11077627 | G | A | synonymous_variant | LOW | c.315C>T|p.Val105Val |
S107 |
| 4 | BAA10g08980 | A10 | 11077886 | G | A | missense_variant | MODERATE | c.56C>T|p.Ser19Leu |
S1 S90 |
| 5 | BAA10g08980 | A10 | 11077917 | G | A | missense_variant | MODERATE | c.25C>T|p.Leu9Phe |
S233 |
| 6 | BAA10g08980 | A10 | 11079153 | C | T | upstream_gene_variant | MODIFIER | c.-1212G>A| |
S175 S177 |
| 7 | BAA10g08980 | A10 | 11079683 | G | A | upstream_gene_variant | MODIFIER | c.-1742C>T| |
S77 S82 |
| 8 | BAA10g08980 | A10 | 11081136 | C | T | upstream_gene_variant | MODIFIER | c.-3195G>A| |
S131 |
| 9 | BAA10g08980 | A10 | 11081510 | G | A | upstream_gene_variant | MODIFIER | c.-3569C>T| |
S219 |
| 10 | BAA10g08980 | A10 | 11081521 | G | A | upstream_gene_variant | MODIFIER | c.-3580C>T| |
S163 |
| 11 | BAA10g08980 | A10 | 11081615 | C | T | upstream_gene_variant | MODIFIER | c.-3674G>A| |
S185 |
| 12 | BAA10g08980 | A10 | 11081629 | C | T | upstream_gene_variant | MODIFIER | c.-3688G>A| |
S247 |
| 13 | BAA10g08980 | A10 | 11081987 | C | T | upstream_gene_variant | MODIFIER | c.-4046G>A| |
S259 |
| 14 | BAA10g08980 | A10 | 11082082 | G | A | upstream_gene_variant | MODIFIER | c.-4141C>T| |
S66 |
| 15 | BAA10g08980 | A10 | 11082145 | C | T | upstream_gene_variant | MODIFIER | c.-4204G>A| |
S269 |