Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45980 | A02 | 37503418 | C | T | stop_gained | HIGH | c.555G>A|p.Trp185* |
S95 |
2 | BAA02g45980 | A02 | 37503693 | C | T | missense_variant | MODERATE | c.280G>A|p.Gly94Ser |
S17 |
3 | BAA02g45980 | A02 | 37505008 | G | A | upstream_gene_variant | MODIFIER | c.-392C>T| |
S302 |
4 | BAA02g45980 | A02 | 37506405 | G | A | upstream_gene_variant | MODIFIER | c.-1789C>T| |
S204 |
5 | BAA02g45980 | A02 | 37508231 | C | T | upstream_gene_variant | MODIFIER | c.-3615G>A| |
S171 |