Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17120 | A09 | 10188216 | C | T | upstream_gene_variant | MODIFIER | c.-3813C>T| |
S62 |
2 | BAA09g17120 | A09 | 10188313 | G | A | upstream_gene_variant | MODIFIER | c.-3716G>A| |
S201 |
3 | BAA09g17120 | A09 | 10188333 | C | T | upstream_gene_variant | MODIFIER | c.-3696C>T| |
S9 |
4 | BAA09g17120 | A09 | 10188626 | C | T | upstream_gene_variant | MODIFIER | c.-3403C>T| |
S187 |
5 | BAA09g17120 | A09 | 10188953 | G | A | upstream_gene_variant | MODIFIER | c.-3076G>A| |
S100 |
6 | BAA09g17120 | A09 | 10189925 | G | A | upstream_gene_variant | MODIFIER | c.-2104G>A| |
S79 S91 |
7 | BAA09g17120 | A09 | 10190301 | C | T | upstream_gene_variant | MODIFIER | c.-1728C>T| |
S206 S26 |
8 | BAA09g17120 | A09 | 10191970 | C | T | upstream_gene_variant | MODIFIER | c.-59C>T| |
S239 |
9 | BAA09g17120 | A09 | 10192143 | C | T | missense_variant | MODERATE | c.115C>T|p.Arg39Trp |
S28 |
10 | BAA09g17120 | A09 | 10194838 | C | T | stop_gained | HIGH | c.1390C>T|p.Gln464* |
S283 |
11 | BAA09g17120 | A09 | 10195694 | G | A | downstream_gene_variant | MODIFIER | c.*627G>A| |
S16 |
12 | BAA09g17120 | A09 | 10195807 | C | T | downstream_gene_variant | MODIFIER | c.*740C>T| |
S306 |
13 | BAA09g17120 | A09 | 10196264 | C | T | downstream_gene_variant | MODIFIER | c.*1197C>T| |
S283 |
14 | BAA09g17120 | A09 | 10196714 | G | A | downstream_gene_variant | MODIFIER | c.*1647G>A| |
S271 |
15 | BAA09g17120 | A09 | 10198043 | G | A | downstream_gene_variant | MODIFIER | c.*2976G>A| |
S189 |