| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g39080 | A02 | 33253791 | C | T | missense_variant | MODERATE | c.941G>A|p.Arg314Lys |
S104 S52 |
| 2 | BAA02g39080 | A02 | 33254419 | G | A | missense_variant | MODERATE | c.568C>T|p.Pro190Ser |
S26 |
| 3 | BAA02g39080 | A02 | 33254605 | C | T | synonymous_variant | LOW | c.459G>A|p.Gly153Gly |
S178 |
| 4 | BAA02g39080 | A02 | 33255584 | G | A | upstream_gene_variant | MODIFIER | c.-130C>T| |
S235 |
| 5 | BAA02g39080 | A02 | 33255732 | G | A | upstream_gene_variant | MODIFIER | c.-278C>T| |
S127 |
| 6 | BAA02g39080 | A02 | 33256538 | G | A | upstream_gene_variant | MODIFIER | c.-1084C>T| |
S41 |
| 7 | BAA02g39080 | A02 | 33256647 | C | T | upstream_gene_variant | MODIFIER | c.-1193G>A| |
S75 S81 |
| 8 | BAA02g39080 | A02 | 33256759 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S210 |
| 9 | BAA02g39080 | A02 | 33258867 | C | T | upstream_gene_variant | MODIFIER | c.-3413G>A| |
S54 |
| 10 | BAA02g39080 | A02 | 33260009 | G | T | upstream_gene_variant | MODIFIER | c.-4555C>A| |
S10 S137 S235 S247 S262 S8 S89 |