Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05450 | A10 | 2786751 | G | A | missense_variant | MODERATE | c.515C>T|p.Ala172Val |
S25 |
2 | BAA10g05450 | A10 | 2790794 | G | A | upstream_gene_variant | MODIFIER | c.-2926C>T| |
S66 |
3 | BAA10g05450 | A10 | 2790839 | C | A | upstream_gene_variant | MODIFIER | c.-2971G>T| |
S179 |