| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g09990 | A05 | 5091832 | C | T | upstream_gene_variant | MODIFIER | c.-1905C>T| |
S65 |
| 2 | BAA05g09990 | A05 | 5092239 | G | A | upstream_gene_variant | MODIFIER | c.-1498G>A| |
S132 S137 S215 |
| 3 | BAA05g09990 | A05 | 5092530 | G | A | upstream_gene_variant | MODIFIER | c.-1207G>A| |
S263 |
| 4 | BAA05g09990 | A05 | 5093159 | C | T | upstream_gene_variant | MODIFIER | c.-578C>T| |
S184 |
| 5 | BAA05g09990 | A05 | 5093178 | C | T | upstream_gene_variant | MODIFIER | c.-559C>T| |
S202 |
| 6 | BAA05g09990 | A05 | 5093206 | C | T | upstream_gene_variant | MODIFIER | c.-531C>T| |
S93 |
| 7 | BAA05g09990 | A05 | 5093570 | C | T | upstream_gene_variant | MODIFIER | c.-167C>T| |
S251 |
| 8 | BAA05g09990 | A05 | 5094069 | C | T | synonymous_variant | LOW | c.333C>T|p.Asp111Asp |
S189 |
| 9 | BAA05g09990 | A05 | 5094784 | C | T | missense_variant | MODERATE | c.1048C>T|p.Leu350Phe |
S87 |