Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11500 | A02 | 5194480 | C | T | missense_variant | MODERATE | c.367G>A|p.Glu123Lys |
S124 |
2 | BAA02g11500 | A02 | 5194946 | G | A | upstream_gene_variant | MODIFIER | c.-31C>T| |
S235 |
3 | BAA02g11500 | A02 | 5195014 | G | A | upstream_gene_variant | MODIFIER | c.-99C>T| |
S288 |
4 | BAA02g11500 | A02 | 5195625 | C | T | upstream_gene_variant | MODIFIER | c.-710G>A| |
S6 |
5 | BAA02g11500 | A02 | 5196596 | G | A | upstream_gene_variant | MODIFIER | c.-1681C>T| |
S247 |
6 | BAA02g11500 | A02 | 5196714 | G | A | upstream_gene_variant | MODIFIER | c.-1799C>T| |
S217 |
7 | BAA02g11500 | A02 | 5198022 | A | T | upstream_gene_variant | MODIFIER | c.-3107T>A| |
S298 |
8 | BAA02g11500 | A02 | 5198174 | C | T | upstream_gene_variant | MODIFIER | c.-3259G>A| |
S270 |
9 | BAA02g11500 | A02 | 5198360 | G | A | upstream_gene_variant | MODIFIER | c.-3445C>T| |
S158 |
10 | BAA02g11500 | A02 | 5198443 | C | T | upstream_gene_variant | MODIFIER | c.-3528G>A| |
S123 |
11 | BAA02g11500 | A02 | 5199042 | G | A | upstream_gene_variant | MODIFIER | c.-4127C>T| |
S282 |
12 | BAA02g11500 | A02 | 5199460 | G | A | upstream_gene_variant | MODIFIER | c.-4545C>T| |
S99 |
13 | BAA02g11500 | A02 | 5199583 | C | A | upstream_gene_variant | MODIFIER | c.-4668G>T| |
S272 |
14 | BAA02g11500 | A02 | 5199586 | C | T | upstream_gene_variant | MODIFIER | c.-4671G>A| |
S278 |