Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g36910 | A02 | 31583573 | C | T | missense_variant | MODERATE | c.1363G>A|p.Asp455Asn |
S68 |
2 | BAA02g36910 | A02 | 31583610 | G | A | synonymous_variant | LOW | c.1326C>T|p.Phe442Phe |
S23 |
3 | BAA02g36910 | A02 | 31584239 | G | A | stop_gained | HIGH | c.943C>T|p.Arg315* |
S113 |
4 | BAA02g36910 | A02 | 31589594 | C | T | upstream_gene_variant | MODIFIER | c.-1281G>A| |
S144 |
5 | BAA02g36910 | A02 | 31592756 | G | A | upstream_gene_variant | MODIFIER | c.-4443C>T| |
S59 |