Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25620 | A02 | 14052379 | C | T | upstream_gene_variant | MODIFIER | c.-2803C>T| |
S46 |
2 | BAA02g25620 | A02 | 14052680 | G | A | upstream_gene_variant | MODIFIER | c.-2502G>A| |
S239 |
3 | BAA02g25620 | A02 | 14052710 | G | A | upstream_gene_variant | MODIFIER | c.-2472G>A| |
S264 |
4 | BAA02g25620 | A02 | 14053189 | G | A | upstream_gene_variant | MODIFIER | c.-1993G>A| |
S11 |
5 | BAA02g25620 | A02 | 14054306 | C | T | upstream_gene_variant | MODIFIER | c.-876C>T| |
S172 S217 |
6 | BAA02g25620 | A02 | 14054346 | G | A | upstream_gene_variant | MODIFIER | c.-836G>A| |
S68 |
7 | BAA02g25620 | A02 | 14055241 | G | A | synonymous_variant | LOW | c.60G>A|p.Ser20Ser |
S191 |
8 | BAA02g25620 | A02 | 14055377 | G | A | missense_variant | MODERATE | c.196G>A|p.Val66Met |
S189 |
9 | BAA02g25620 | A02 | 14055473 | G | A | missense_variant | MODERATE | c.292G>A|p.Val98Met |
S155 S211 |
10 | BAA02g25620 | A02 | 14059061 | G | A | downstream_gene_variant | MODIFIER | c.*3295G>A| |
S256 |
11 | BAA02g25620 | A02 | 14059494 | G | A | downstream_gene_variant | MODIFIER | c.*3728G>A| |
S10 |