Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34050 | A02 | 29186164 | C | T | missense_variant | MODERATE | c.2683G>A|p.Ala895Thr |
S177 |
2 | BAA02g34050 | A02 | 29186624 | G | A | synonymous_variant | LOW | c.2223C>T|p.Leu741Leu |
S278 |
3 | BAA02g34050 | A02 | 29190068 | C | T | upstream_gene_variant | MODIFIER | c.-492G>A| |
S255 |