Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19470 | A02 | 10101083 | C | T | upstream_gene_variant | MODIFIER | c.-1269C>T| |
S79 |
2 | BAA02g19470 | A02 | 10101952 | G | A | upstream_gene_variant | MODIFIER | c.-400G>A| |
S247 |
3 | BAA02g19470 | A02 | 10102776 | C | T | missense_variant | MODERATE | c.257C>T|p.Thr86Ile |
S167 |