Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35140 | A09 | 43510313 | C | T | missense_variant | MODERATE | c.952G>A|p.Ala318Thr |
S159 S162 S243 S299 |
2 | BAA09g35140 | A09 | 43510856 | G | A | synonymous_variant | LOW | c.409C>T|p.Leu137Leu |
S185 |
3 | BAA09g35140 | A09 | 43512389 | C | T | upstream_gene_variant | MODIFIER | c.-749G>A| |
S30 S31 |
4 | BAA09g35140 | A09 | 43512442 | C | T | upstream_gene_variant | MODIFIER | c.-802G>A| |
S256 |
5 | BAA09g35140 | A09 | 43513972 | G | A | upstream_gene_variant | MODIFIER | c.-2332C>T| |
S177 |
6 | BAA09g35140 | A09 | 43515362 | G | A | upstream_gene_variant | MODIFIER | c.-3722C>T| |
S172 S217 |
7 | BAA09g35140 | A09 | 43515434 | C | T | upstream_gene_variant | MODIFIER | c.-3794G>A| |
S202 |
8 | BAA09g35140 | A09 | 43515661 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S61 |
9 | BAA09g35140 | A09 | 43515708 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S43 |
10 | BAA09g35140 | A09 | 43515740 | G | A | upstream_gene_variant | MODIFIER | c.-4100C>T| |
S216 |