Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40750 | A02 | 34223568 | C | T | missense_variant | MODERATE | c.79G>A|p.Gly27Ser |
S183 S198 |
2 | BAA02g40750 | A02 | 34227295 | G | A | upstream_gene_variant | MODIFIER | c.-3649C>T| |
S1 S90 |
3 | BAA02g40750 | A02 | 34227586 | G | A | upstream_gene_variant | MODIFIER | c.-3940C>T| |
S302 |
4 | BAA02g40750 | A02 | 34227777 | C | T | upstream_gene_variant | MODIFIER | c.-4131G>A| |
S114 |
5 | BAA02g40750 | A02 | 34227904 | G | A | upstream_gene_variant | MODIFIER | c.-4258C>T| |
S302 |
6 | BAA02g40750 | A02 | 34228421 | G | A | upstream_gene_variant | MODIFIER | c.-4775C>T| |
S72 S78 |
7 | BAA02g40750 | A02 | 34228492 | G | A | upstream_gene_variant | MODIFIER | c.-4846C>T| |
S199 |