| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g02350 | A10 | 1107566 | C | T | downstream_gene_variant | MODIFIER | c.*697G>A| |
S50 |
| 2 | BAA10g02350 | A10 | 1107689 | C | T | downstream_gene_variant | MODIFIER | c.*574G>A| |
S131 |
| 3 | BAA10g02350 | A10 | 1108260 | G | A | downstream_gene_variant | MODIFIER | c.*3C>T| |
S282 |
| 4 | BAA10g02350 | A10 | 1109008 | G | A | missense_variant | MODERATE | c.730C>T|p.His244Tyr |
S274 |
| 5 | BAA10g02350 | A10 | 1109034 | G | A | missense_variant | MODERATE | c.704C>T|p.Pro235Leu |
S58 |
| 6 | BAA10g02350 | A10 | 1109099 | G | A | synonymous_variant | LOW | c.639C>T|p.Pro213Pro |
S289 |
| 7 | BAA10g02350 | A10 | 1109195 | G | A | synonymous_variant | LOW | c.543C>T|p.His181His |
S189 |
| 8 | BAA10g02350 | A10 | 1110666 | G | A | upstream_gene_variant | MODIFIER | c.-929C>T| |
S296 |
| 9 | BAA10g02350 | A10 | 1111300 | G | A | upstream_gene_variant | MODIFIER | c.-1563C>T| |
S136 |
| 10 | BAA10g02350 | A10 | 1111533 | C | T | upstream_gene_variant | MODIFIER | c.-1796G>A| |
S74 |
| 11 | BAA10g02350 | A10 | 1114615 | G | A | upstream_gene_variant | MODIFIER | c.-4878C>T| |
S153 S213 |