Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66550 | A09 | 60766523 | G | A | missense_variant | MODERATE | c.2183C>T|p.Thr728Ile |
S40 S49 |
2 | BAA09g66550 | A09 | 60768279 | G | A | synonymous_variant | LOW | c.1293C>T|p.Ile431Ile |
S130 |
3 | BAA09g66550 | A09 | 60768905 | C | T | missense_variant | MODERATE | c.841G>A|p.Gly281Ser |
S256 |
4 | BAA09g66550 | A09 | 60770954 | G | A | upstream_gene_variant | MODIFIER | c.-782C>T| |
S236 |