Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21600 | A02 | 11612774 | C | T | upstream_gene_variant | MODIFIER | c.-3161C>T| |
S171 |
2 | BAA02g21600 | A02 | 11612955 | G | A | upstream_gene_variant | MODIFIER | c.-2980G>A| |
S82 S92 |
3 | BAA02g21600 | A02 | 11613016 | C | T | upstream_gene_variant | MODIFIER | c.-2919C>T| |
S266 |
4 | BAA02g21600 | A02 | 11614295 | C | T | upstream_gene_variant | MODIFIER | c.-1640C>T| |
S49 |
5 | BAA02g21600 | A02 | 11614797 | G | A | upstream_gene_variant | MODIFIER | c.-1138G>A| |
S103 |
6 | BAA02g21600 | A02 | 11614878 | C | T | upstream_gene_variant | MODIFIER | c.-1057C>T| |
S40 S49 |
7 | BAA02g21600 | A02 | 11618313 | G | A | downstream_gene_variant | MODIFIER | c.*1770G>A| |
S247 |
8 | BAA02g21600 | A02 | 11619570 | G | A | downstream_gene_variant | MODIFIER | c.*3027G>A| |
S235 |
9 | BAA02g21600 | A02 | 11619783 | G | A | downstream_gene_variant | MODIFIER | c.*3240G>A| |
S34 |