Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22280 | A02 | 12043983 | C | T | upstream_gene_variant | MODIFIER | c.-3010C>T| |
S241 S276 |
2 | BAA02g22280 | A02 | 12044268 | G | A | upstream_gene_variant | MODIFIER | c.-2725G>A| |
S298 |
3 | BAA02g22280 | A02 | 12044627 | G | A | upstream_gene_variant | MODIFIER | c.-2366G>A| |
S28 |
4 | BAA02g22280 | A02 | 12045250 | G | A | upstream_gene_variant | MODIFIER | c.-1743G>A| |
S89 |
5 | BAA02g22280 | A02 | 12045569 | G | A | upstream_gene_variant | MODIFIER | c.-1424G>A| |
S288 |
6 | BAA02g22280 | A02 | 12046044 | G | A | upstream_gene_variant | MODIFIER | c.-949G>A| |
S236 |
7 | BAA02g22280 | A02 | 12046820 | C | T | upstream_gene_variant | MODIFIER | c.-173C>T| |
S185 |
8 | BAA02g22280 | A02 | 12047158 | G | A | missense_variant | MODERATE | c.166G>A|p.Glu56Lys |
S125 |
9 | BAA02g22280 | A02 | 12047795 | C | T | missense_variant | MODERATE | c.803C>T|p.Ser268Phe |
S99 |