Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45790 | A02 | 37393636 | G | A | missense_variant | MODERATE | c.35C>T|p.Pro12Leu |
S276 |
2 | BAA02g45790 | A02 | 37393643 | C | T | missense_variant | MODERATE | c.28G>A|p.Ala10Thr |
S277 |
3 | BAA02g45790 | A02 | 37395905 | G | A | upstream_gene_variant | MODIFIER | c.-2235C>T| |
S34 |
4 | BAA02g45790 | A02 | 37396190 | G | T | upstream_gene_variant | MODIFIER | c.-2520C>A| |
S55 |
5 | BAA02g45790 | A02 | 37396650 | C | T | upstream_gene_variant | MODIFIER | c.-2980G>A| |
S205 |