| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g47370 | A02 | 38222150 | C | T | missense_variant | MODERATE | c.1342G>A|p.Val448Met |
S42 |
| 2 | BAA02g47370 | A02 | 38222328 | C | T | synonymous_variant | LOW | c.1164G>A|p.Arg388Arg |
S42 |
| 3 | BAA02g47370 | A02 | 38222918 | C | T | missense_variant | MODERATE | c.574G>A|p.Ala192Thr |
S189 |
| 4 | BAA02g47370 | A02 | 38223282 | G | A | synonymous_variant | LOW | c.210C>T|p.Pro70Pro |
S174 S27 |
| 5 | BAA02g47370 | A02 | 38223662 | C | T | upstream_gene_variant | MODIFIER | c.-171G>A| |
S100 |
| 6 | BAA02g47370 | A02 | 38223844 | A | T | upstream_gene_variant | MODIFIER | c.-353T>A| |
S109 |
| 7 | BAA02g47370 | A02 | 38223909 | G | A | upstream_gene_variant | MODIFIER | c.-418C>T| |
S155 |
| 8 | BAA02g47370 | A02 | 38224433 | C | T | upstream_gene_variant | MODIFIER | c.-942G>A| |
S144 |
| 9 | BAA02g47370 | A02 | 38226380 | C | A | upstream_gene_variant | MODIFIER | c.-2889G>T| |
S44 |
| 10 | BAA02g47370 | A02 | 38227383 | C | T | upstream_gene_variant | MODIFIER | c.-3892G>A| |
S295 |