Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00080 | A02 | 68632 | C | T | downstream_gene_variant | MODIFIER | c.*4726G>A| |
S239 |
2 | BAA02g00080 | A02 | 68728 | G | A | downstream_gene_variant | MODIFIER | c.*4630C>T| |
S107 |
3 | BAA02g00080 | A02 | 69069 | G | A | downstream_gene_variant | MODIFIER | c.*4289C>T| |
S51 |
4 | BAA02g00080 | A02 | 69223 | C | T | downstream_gene_variant | MODIFIER | c.*4135G>A| |
S73 |
5 | BAA02g00080 | A02 | 69382 | G | A | downstream_gene_variant | MODIFIER | c.*3976C>T| |
S265 |
6 | BAA02g00080 | A02 | 70540 | C | T | downstream_gene_variant | MODIFIER | c.*2818G>A| |
S142 |
7 | BAA02g00080 | A02 | 71333 | C | T | downstream_gene_variant | MODIFIER | c.*2025G>A| |
S240 |
8 | BAA02g00080 | A02 | 71336 | C | T | downstream_gene_variant | MODIFIER | c.*2022G>A| |
S192 |
9 | BAA02g00080 | A02 | 71885 | C | T | downstream_gene_variant | MODIFIER | c.*1473G>A| |
S138 |
10 | BAA02g00080 | A02 | 73487 | C | T | synonymous_variant | LOW | c.663G>A|p.Glu221Glu |
S183 S198 |