Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47930 | A02 | 38612048 | C | T | downstream_gene_variant | MODIFIER | c.*4905G>A| |
S170 |
2 | BAA02g47930 | A02 | 38613280 | C | T | downstream_gene_variant | MODIFIER | c.*3673G>A| |
S178 |
3 | BAA02g47930 | A02 | 38613288 | G | A | downstream_gene_variant | MODIFIER | c.*3665C>T| |
S166 |
4 | BAA02g47930 | A02 | 38613590 | C | T | downstream_gene_variant | MODIFIER | c.*3363G>A| |
S38 |
5 | BAA02g47930 | A02 | 38613720 | C | T | downstream_gene_variant | MODIFIER | c.*3233G>A| |
S184 |
6 | BAA02g47930 | A02 | 38614033 | C | T | downstream_gene_variant | MODIFIER | c.*2920G>A| |
S63 |
7 | BAA02g47930 | A02 | 38614396 | T | A | downstream_gene_variant | MODIFIER | c.*2557A>T| |
S252 |
8 | BAA02g47930 | A02 | 38615076 | G | A | downstream_gene_variant | MODIFIER | c.*1877C>T| |
S113 |
9 | BAA02g47930 | A02 | 38616426 | C | T | downstream_gene_variant | MODIFIER | c.*527G>A| |
S133 |
10 | BAA02g47930 | A02 | 38618600 | C | T | upstream_gene_variant | MODIFIER | c.-1348G>A| |
S256 |
11 | BAA02g47930 | A02 | 38618640 | G | A | upstream_gene_variant | MODIFIER | c.-1388C>T| |
S207 |
12 | BAA02g47930 | A02 | 38618686 | G | A | upstream_gene_variant | MODIFIER | c.-1434C>T| |
S126 |
13 | BAA02g47930 | A02 | 38618811 | G | A | upstream_gene_variant | MODIFIER | c.-1559C>T| |
S279 |
14 | BAA02g47930 | A02 | 38618857 | G | A | upstream_gene_variant | MODIFIER | c.-1605C>T| |
S139 |
15 | BAA02g47930 | A02 | 38619352 | C | T | upstream_gene_variant | MODIFIER | c.-2100G>A| |
S233 |
16 | BAA02g47930 | A02 | 38620696 | G | A | upstream_gene_variant | MODIFIER | c.-3444C>T| |
S37 |
17 | BAA02g47930 | A02 | 38621784 | C | T | upstream_gene_variant | MODIFIER | c.-4532G>A| |
S33 |
18 | BAA02g47930 | A02 | 38621970 | G | A | upstream_gene_variant | MODIFIER | c.-4718C>T| |
S177 |