Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66880 | A09 | 60890502 | C | T | upstream_gene_variant | MODIFIER | c.-827C>T| |
S173 |
2 | BAA09g66880 | A09 | 60890660 | G | A | upstream_gene_variant | MODIFIER | c.-669G>A| |
S4 |
3 | BAA09g66880 | A09 | 60891437 | G | A | missense_variant | MODERATE | c.109G>A|p.Gly37Ser |
S274 |
4 | BAA09g66880 | A09 | 60895017 | C | T | intron_variant | MODIFIER | c.1645-10C>T| |
S271 |