| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g07760 | A05 | 3856430 | C | T | missense_variant | MODERATE | c.125C>T|p.Thr42Ile |
S98 |
| 2 | BAA05g07760 | A05 | 3857302 | C | T | synonymous_variant | LOW | c.438C>T|p.Tyr146Tyr |
S19 |
| 3 | BAA05g07760 | A05 | 3857360 | C | T | stop_gained | HIGH | c.496C>T|p.Gln166* |
S204 |
| 4 | BAA05g07760 | A05 | 3857390 | G | A | missense_variant | MODERATE | c.526G>A|p.Glu176Lys |
S240 |
| 5 | BAA05g07760 | A05 | 3861493 | C | T | downstream_gene_variant | MODIFIER | c.*4071C>T| |
S127 |
| 6 | BAA05g07760 | A05 | 3861525 | C | T | downstream_gene_variant | MODIFIER | c.*4103C>T| |
S87 |
| 7 | BAA05g07760 | A05 | 3861539 | C | T | downstream_gene_variant | MODIFIER | c.*4117C>T| |
S280 |
| 8 | BAA05g07760 | A05 | 3861613 | C | T | downstream_gene_variant | MODIFIER | c.*4191C>T| |
S136 |