Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09420 | A02 | 4146295 | G | A | missense_variant | MODERATE | c.764C>T|p.Pro255Leu |
S161 |
2 | BAA02g09420 | A02 | 4147242 | C | T | synonymous_variant | LOW | c.36G>A|p.Thr12Thr |
S251 |
3 | BAA02g09420 | A02 | 4147674 | C | T | upstream_gene_variant | MODIFIER | c.-397G>A| |
S273 |
4 | BAA02g09420 | A02 | 4148742 | C | T | upstream_gene_variant | MODIFIER | c.-1465G>A| |
S127 |
5 | BAA02g09420 | A02 | 4150008 | G | A | upstream_gene_variant | MODIFIER | c.-2731C>T| |
S11 |
6 | BAA02g09420 | A02 | 4150432 | C | T | upstream_gene_variant | MODIFIER | c.-3155G>A| |
S97 |