Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26990 | A02 | 15130125 | C | T | missense_variant | MODERATE | c.676G>A|p.Glu226Lys |
S274 |
2 | BAA02g26990 | A02 | 15130148 | G | A | missense_variant | MODERATE | c.653C>T|p.Pro218Leu |
S86 |
3 | BAA02g26990 | A02 | 15130581 | C | T | stop_gained | HIGH | c.576G>A|p.Trp192* |
S305 |
4 | BAA02g26990 | A02 | 15134884 | G | A | upstream_gene_variant | MODIFIER | c.-3365C>T| |
S236 |
5 | BAA02g26990 | A02 | 15135204 | C | T | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S162 |