Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39660 | A02 | 33662170 | C | T | missense_variant | MODERATE | c.1337C>T|p.Ala446Val |
S122 |
2 | BAA02g39660 | A02 | 33664825 | C | T | stop_gained | HIGH | c.2785C>T|p.Arg929* |
S212 |
3 | BAA02g39660 | A02 | 33665317 | C | T | missense_variant | MODERATE | c.3188C>T|p.Ser1063Phe |
S216 |
4 | BAA02g39660 | A02 | 33665657 | G | A | downstream_gene_variant | MODIFIER | c.*264G>A| |
S19 |