Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25980 | A02 | 14394112 | G | A | upstream_gene_variant | MODIFIER | c.-2430G>A| |
S247 |
2 | BAA02g25980 | A02 | 14394571 | G | A | upstream_gene_variant | MODIFIER | c.-1971G>A| |
S293 |
3 | BAA02g25980 | A02 | 14394666 | G | A | upstream_gene_variant | MODIFIER | c.-1876G>A| |
S259 |
4 | BAA02g25980 | A02 | 14395194 | G | A | upstream_gene_variant | MODIFIER | c.-1348G>A| |
S187 |
5 | BAA02g25980 | A02 | 14395534 | C | T | upstream_gene_variant | MODIFIER | c.-1008C>T| |
S25 S264 |
6 | BAA02g25980 | A02 | 14395722 | C | T | upstream_gene_variant | MODIFIER | c.-820C>T| |
S195 |
7 | BAA02g25980 | A02 | 14396554 | G | A | missense_variant | MODERATE | c.13G>A|p.Gly5Arg |
S294 |
8 | BAA02g25980 | A02 | 14396623 | C | T | missense_variant | MODERATE | c.82C>T|p.Leu28Phe |
S135 |
9 | BAA02g25980 | A02 | 14396894 | C | T | missense_variant | MODERATE | c.278C>T|p.Ala93Val |
S112 |
10 | BAA02g25980 | A02 | 14396972 | C | T | missense_variant | MODERATE | c.356C>T|p.Pro119Leu |
S100 S104 |