| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g35620 | A09 | 43999275 | C | T | missense_variant | MODERATE | c.814C>T|p.His272Tyr |
S19 |
| 2 | BAA09g35620 | A09 | 44000141 | C | T | synonymous_variant | LOW | c.1395C>T|p.Val465Val |
S235 |
| 3 | BAA09g35620 | A09 | 44000246 | C | T | synonymous_variant | LOW | c.1500C>T|p.Ile500Ile |
S279 |
| 4 | BAA09g35620 | A09 | 44001469 | G | A | synonymous_variant | LOW | c.2499G>A|p.Lys833Lys |
S100 |
| 5 | BAA09g35620 | A09 | 44001654 | G | A | downstream_gene_variant | MODIFIER | c.*173G>A| |
S298 |
| 6 | BAA09g35620 | A09 | 44001683 | C | T | downstream_gene_variant | MODIFIER | c.*202C>T| |
S240 |
| 7 | BAA09g35620 | A09 | 44003105 | C | T | downstream_gene_variant | MODIFIER | c.*1624C>T| |
S144 |
| 8 | BAA09g35620 | A09 | 44004375 | G | A | downstream_gene_variant | MODIFIER | c.*2894G>A| |
S122 |
| 9 | BAA09g35620 | A09 | 44004808 | C | T | downstream_gene_variant | MODIFIER | c.*3327C>T| |
S100 |