Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03540 | A02 | 1563859 | C | T | missense_variant | MODERATE | c.856C>T|p.His286Tyr |
S233 |
2 | BAA02g03540 | A02 | 1564912 | C | T | downstream_gene_variant | MODIFIER | c.*343C>T| |
S200 |
3 | BAA02g03540 | A02 | 1565056 | G | A | downstream_gene_variant | MODIFIER | c.*487G>A| |
S50 |