Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47730 | A02 | 38467193 | C | T | upstream_gene_variant | MODIFIER | c.-318G>A| |
S61 |
2 | BAA02g47730 | A02 | 38467530 | G | A | upstream_gene_variant | MODIFIER | c.-655C>T| |
S113 |
3 | BAA02g47730 | A02 | 38467556 | G | A | upstream_gene_variant | MODIFIER | c.-681C>T| |
S68 |
4 | BAA02g47730 | A02 | 38468778 | C | T | upstream_gene_variant | MODIFIER | c.-1903G>A| |
S216 |
5 | BAA02g47730 | A02 | 38469176 | C | T | upstream_gene_variant | MODIFIER | c.-2301G>A| |
S100 |
6 | BAA02g47730 | A02 | 38469190 | C | T | upstream_gene_variant | MODIFIER | c.-2315G>A| |
S176 |
7 | BAA02g47730 | A02 | 38469417 | C | A | upstream_gene_variant | MODIFIER | c.-2542G>T| |
S277 |
8 | BAA02g47730 | A02 | 38469511 | G | A | upstream_gene_variant | MODIFIER | c.-2636C>T| |
S288 |
9 | BAA02g47730 | A02 | 38469638 | G | A | upstream_gene_variant | MODIFIER | c.-2763C>T| |
S302 |
10 | BAA02g47730 | A02 | 38471144 | C | T | upstream_gene_variant | MODIFIER | c.-4269G>A| |
S249 |
11 | BAA02g47730 | A02 | 38471578 | C | T | upstream_gene_variant | MODIFIER | c.-4703G>A| |
S16 |