| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g02320 | A02 | 1039505 | G | A | missense_variant | MODERATE | c.2353C>T|p.Pro785Ser |
S297 |
| 2 | BAA02g02320 | A02 | 1039880 | G | A | missense_variant | MODERATE | c.1978C>T|p.Pro660Ser |
S10 |
| 3 | BAA02g02320 | A02 | 1040349 | C | T | synonymous_variant | LOW | c.1509G>A|p.Glu503Glu |
S270 |
| 4 | BAA02g02320 | A02 | 1041609 | G | A | synonymous_variant | LOW | c.552C>T|p.Ser184Ser |
S265 |
| 5 | BAA02g02320 | A02 | 1041756 | G | A | synonymous_variant | LOW | c.405C>T|p.Ser135Ser |
S10 |
| 6 | BAA02g02320 | A02 | 1041888 | G | A | synonymous_variant | LOW | c.273C>T|p.Leu91Leu |
S295 |
| 7 | BAA02g02320 | A02 | 1041990 | C | T | stop_gained | HIGH | c.171G>A|p.Trp57* |
S63 |
| 8 | BAA02g02320 | A02 | 1047152 | C | T | upstream_gene_variant | MODIFIER | c.-4992G>A| |
S306 |