Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06080 | A02 | 2587726 | G | A | synonymous_variant | LOW | c.478C>T|p.Leu160Leu |
S174 |
2 | BAA02g06080 | A02 | 2587991 | G | A | missense_variant | MODERATE | c.409C>T|p.Leu137Phe |
S110 |
3 | BAA02g06080 | A02 | 2588178 | C | T | synonymous_variant | LOW | c.336G>A|p.Thr112Thr |
S46 |
4 | BAA02g06080 | A02 | 2590189 | G | A | upstream_gene_variant | MODIFIER | c.-1261C>T| |
S5 |
5 | BAA02g06080 | A02 | 2592829 | C | T | upstream_gene_variant | MODIFIER | c.-3901G>A| |
S138 |