Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41490 | A02 | 34814945 | C | T | downstream_gene_variant | MODIFIER | c.*581G>A| |
S277 |
2 | BAA02g41490 | A02 | 34816132 | G | A | synonymous_variant | LOW | c.1269C>T|p.Ser423Ser |
S58 |
3 | BAA02g41490 | A02 | 34816486 | C | T | synonymous_variant | LOW | c.915G>A|p.Glu305Glu |
S284 |
4 | BAA02g41490 | A02 | 34816966 | C | T | synonymous_variant | LOW | c.783G>A|p.Lys261Lys |
S100 |
5 | BAA02g41490 | A02 | 34817042 | C | T | missense_variant | MODERATE | c.707G>A|p.Gly236Asp |
S64 |
6 | BAA02g41490 | A02 | 34817299 | G | A | synonymous_variant | LOW | c.450C>T|p.Thr150Thr |
S125 |
7 | BAA02g41490 | A02 | 34817788 | G | A | upstream_gene_variant | MODIFIER | c.-40C>T| |
S167 |
8 | BAA02g41490 | A02 | 34818233 | C | T | upstream_gene_variant | MODIFIER | c.-485G>A| |
S167 |
9 | BAA02g41490 | A02 | 34818743 | C | T | upstream_gene_variant | MODIFIER | c.-995G>A| |
S228 |
10 | BAA02g41490 | A02 | 34818856 | C | T | upstream_gene_variant | MODIFIER | c.-1108G>A| |
S63 |
11 | BAA02g41490 | A02 | 34820462 | C | T | upstream_gene_variant | MODIFIER | c.-2714G>A| |
S83 S88 |
12 | BAA02g41490 | A02 | 34820491 | C | T | upstream_gene_variant | MODIFIER | c.-2743G>A| |
S231 |