Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25690 | A02 | 14100524 | C | T | downstream_gene_variant | MODIFIER | c.*1939G>A| |
S299 |
2 | BAA02g25690 | A02 | 14100678 | G | A | downstream_gene_variant | MODIFIER | c.*1785C>T| |
S278 |
3 | BAA02g25690 | A02 | 14100940 | C | T | downstream_gene_variant | MODIFIER | c.*1523G>A| |
S183 S198 |
4 | BAA02g25690 | A02 | 14103199 | G | A | upstream_gene_variant | MODIFIER | c.-184C>T| |
S232 |
5 | BAA02g25690 | A02 | 14103463 | C | T | upstream_gene_variant | MODIFIER | c.-448G>A| |
S301 S304 |
6 | BAA02g25690 | A02 | 14103506 | C | T | upstream_gene_variant | MODIFIER | c.-491G>A| |
S18 |
7 | BAA02g25690 | A02 | 14103757 | G | A | upstream_gene_variant | MODIFIER | c.-742C>T| |
S153 S213 |
8 | BAA02g25690 | A02 | 14104042 | G | A | upstream_gene_variant | MODIFIER | c.-1027C>T| |
S169 |
9 | BAA02g25690 | A02 | 14104117 | G | A | upstream_gene_variant | MODIFIER | c.-1102C>T| |
S111 |
10 | BAA02g25690 | A02 | 14104143 | G | A | upstream_gene_variant | MODIFIER | c.-1128C>T| |
S188 |
11 | BAA02g25690 | A02 | 14104474 | C | T | upstream_gene_variant | MODIFIER | c.-1459G>A| |
S289 S290 |
12 | BAA02g25690 | A02 | 14104534 | G | A | upstream_gene_variant | MODIFIER | c.-1519C>T| |
S187 |
13 | BAA02g25690 | A02 | 14104880 | G | A | upstream_gene_variant | MODIFIER | c.-1865C>T| |
S230 |
14 | BAA02g25690 | A02 | 14105120 | G | A | upstream_gene_variant | MODIFIER | c.-2105C>T| |
S196 |
15 | BAA02g25690 | A02 | 14105815 | G | A | upstream_gene_variant | MODIFIER | c.-2800C>T| |
S237 |
16 | BAA02g25690 | A02 | 14106164 | G | A | upstream_gene_variant | MODIFIER | c.-3149C>T| |
S25 |
17 | BAA02g25690 | A02 | 14106823 | G | A | upstream_gene_variant | MODIFIER | c.-3808C>T| |
S302 |
18 | BAA02g25690 | A02 | 14107506 | C | T | upstream_gene_variant | MODIFIER | c.-4491G>A| |
S93 |