Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66960 | A09 | 60929212 | G | A | missense_variant | MODERATE | c.47C>T|p.Thr16Met |
S143 |
2 | BAA09g66960 | A09 | 60931802 | C | T | upstream_gene_variant | MODIFIER | c.-2544G>A| |
S20 |
3 | BAA09g66960 | A09 | 60932365 | G | A | upstream_gene_variant | MODIFIER | c.-3107C>T| |
S25 |
4 | BAA09g66960 | A09 | 60932414 | C | T | upstream_gene_variant | MODIFIER | c.-3156G>A| |
S219 S72 |