Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26340 | A02 | 14634688 | G | A | downstream_gene_variant | MODIFIER | c.*4951C>T| |
S68 |
2 | BAA02g26340 | A02 | 14635358 | C | T | downstream_gene_variant | MODIFIER | c.*4281G>A| |
S175 |
3 | BAA02g26340 | A02 | 14636053 | C | T | downstream_gene_variant | MODIFIER | c.*3586G>A| |
S117 |
4 | BAA02g26340 | A02 | 14636699 | G | A | downstream_gene_variant | MODIFIER | c.*2940C>T| |
S263 |
5 | BAA02g26340 | A02 | 14636837 | G | A | downstream_gene_variant | MODIFIER | c.*2802C>T| |
S189 |
6 | BAA02g26340 | A02 | 14636945 | G | A | downstream_gene_variant | MODIFIER | c.*2694C>T| |
S158 |
7 | BAA02g26340 | A02 | 14638351 | C | T | downstream_gene_variant | MODIFIER | c.*1288G>A| |
S284 |
8 | BAA02g26340 | A02 | 14638503 | G | A | downstream_gene_variant | MODIFIER | c.*1136C>T| |
S247 |
9 | BAA02g26340 | A02 | 14638636 | G | A | downstream_gene_variant | MODIFIER | c.*1003C>T| |
S155 S211 |
10 | BAA02g26340 | A02 | 14639794 | G | A | intron_variant | MODIFIER | c.235-15C>T| |
S95 |
11 | BAA02g26340 | A02 | 14640729 | C | T | upstream_gene_variant | MODIFIER | c.-430G>A| |
S66 |
12 | BAA02g26340 | A02 | 14640908 | C | T | upstream_gene_variant | MODIFIER | c.-609G>A| |
S41 |
13 | BAA02g26340 | A02 | 14642649 | C | T | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S140 |