| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g09600 | A01 | 4273863 | C | T | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S265 |
| 2 | BAA01g09600 | A01 | 4274148 | C | T | missense_variant | MODERATE | c.1021G>A|p.Val341Met |
S242 |
| 3 | BAA01g09600 | A01 | 4274260 | C | T | synonymous_variant | LOW | c.909G>A|p.Leu303Leu |
S133 |
| 4 | BAA01g09600 | A01 | 4274683 | C | T | synonymous_variant | LOW | c.486G>A|p.Gln162Gln |
S8 |
| 5 | BAA01g09600 | A01 | 4275356 | G | A | missense_variant | MODERATE | c.43C>T|p.Pro15Ser |
S183 S198 |
| 6 | BAA01g09600 | A01 | 4275707 | C | T | upstream_gene_variant | MODIFIER | c.-309G>A| |
S152 S68 |
| 7 | BAA01g09600 | A01 | 4276189 | C | T | upstream_gene_variant | MODIFIER | c.-791G>A| |
S8 |
| 8 | BAA01g09600 | A01 | 4276558 | C | T | upstream_gene_variant | MODIFIER | c.-1160G>A| |
S71 |