Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08060 | A02 | 3445601 | C | T | missense_variant | MODERATE | c.503G>A|p.Arg168Lys |
S116 |
2 | BAA02g08060 | A02 | 3445845 | C | T | missense_variant | MODERATE | c.352G>A|p.Ala118Thr |
S130 |
3 | BAA02g08060 | A02 | 3445994 | G | A | synonymous_variant | LOW | c.297C>T|p.Ile99Ile |
S191 |
4 | BAA02g08060 | A02 | 3447172 | G | A | upstream_gene_variant | MODIFIER | c.-665C>T| |
S105 S106 |
5 | BAA02g08060 | A02 | 3447417 | G | A | upstream_gene_variant | MODIFIER | c.-910C>T| |
S305 |
6 | BAA02g08060 | A02 | 3447599 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S292 |
7 | BAA02g08060 | A02 | 3447907 | G | A | upstream_gene_variant | MODIFIER | c.-1400C>T| |
S60 |
8 | BAA02g08060 | A02 | 3450034 | G | A | upstream_gene_variant | MODIFIER | c.-3527C>T| |
S289 S290 |
9 | BAA02g08060 | A02 | 3451355 | C | T | upstream_gene_variant | MODIFIER | c.-4848G>A| |
S97 |