| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g09200 | A10 | 11226867 | C | T | missense_variant | MODERATE | c.776G>A|p.Gly259Asp |
S168 S279 S64 |
| 2 | BAA10g09200 | A10 | 11227122 | A | C | missense_variant | MODERATE | c.627T>G|p.Asp209Glu |
S64 |
| 3 | BAA10g09200 | A10 | 11227300 | C | T | stop_gained | HIGH | c.519G>A|p.Trp173* |
S126 |
| 4 | BAA10g09200 | A10 | 11227572 | G | A | missense_variant | MODERATE | c.332C>T|p.Pro111Leu |
S221 |
| 5 | BAA10g09200 | A10 | 11228564 | C | T | upstream_gene_variant | MODIFIER | c.-301G>A| |
S229 |
| 6 | BAA10g09200 | A10 | 11229593 | C | T | upstream_gene_variant | MODIFIER | c.-1330G>A| |
S51 |
| 7 | BAA10g09200 | A10 | 11230983 | C | T | upstream_gene_variant | MODIFIER | c.-2720G>A| |
S235 |
| 8 | BAA10g09200 | A10 | 11231477 | C | T | upstream_gene_variant | MODIFIER | c.-3214G>A| |
S162 |