| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g19410 | A09 | 11831698 | C | T | upstream_gene_variant | MODIFIER | c.-2309C>T| |
S166 |
| 2 | BAA09g19410 | A09 | 11832080 | C | T | upstream_gene_variant | MODIFIER | c.-1927C>T| |
S218 |
| 3 | BAA09g19410 | A09 | 11832165 | C | T | upstream_gene_variant | MODIFIER | c.-1842C>T| |
S56 |
| 4 | BAA09g19410 | A09 | 11834140 | G | A | missense_variant | MODERATE | c.134G>A|p.Gly45Glu |
S183 S198 |
| 5 | BAA09g19410 | A09 | 11834298 | G | A | missense_variant | MODERATE | c.292G>A|p.Gly98Arg |
S155 S82 |
| 6 | BAA09g19410 | A09 | 11834475 | C | T | missense_variant | MODERATE | c.469C>T|p.Leu157Phe |
S287 |
| 7 | BAA09g19410 | A09 | 11834577 | G | A | missense_variant | MODERATE | c.571G>A|p.Gly191Ser |
S74 |
| 8 | BAA09g19410 | A09 | 11839230 | C | T | downstream_gene_variant | MODIFIER | c.*3733C>T| |
S85 |
| 9 | BAA09g19410 | A09 | 11839390 | C | A | downstream_gene_variant | MODIFIER | c.*3893C>A| |
S221 S239 |
| 10 | BAA09g19410 | A09 | 11839409 | G | A | downstream_gene_variant | MODIFIER | c.*3912G>A| |
S192 |
| 11 | BAA09g19410 | A09 | 11839938 | G | A | downstream_gene_variant | MODIFIER | c.*4441G>A| |
S84 S93 |
| 12 | BAA09g19410 | A09 | 11840116 | G | A | downstream_gene_variant | MODIFIER | c.*4619G>A| |
S225 S73 |
| 13 | BAA09g19410 | A09 | 11840318 | C | T | downstream_gene_variant | MODIFIER | c.*4821C>T| |
S177 |