Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46650 | A02 | 37865124 | C | T | upstream_gene_variant | MODIFIER | c.-4798C>T| |
S252 |
2 | BAA02g46650 | A02 | 37867162 | G | A | upstream_gene_variant | MODIFIER | c.-2760G>A| |
S204 |
3 | BAA02g46650 | A02 | 37870010 | C | T | missense_variant | MODERATE | c.89C>T|p.Ser30Phe |
S283 |
4 | BAA02g46650 | A02 | 37870130 | C | T | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S201 |