Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05700 | A10 | 2920919 | C | T | synonymous_variant | LOW | c.138C>T|p.Phe46Phe |
S272 |
2 | BAA10g05700 | A10 | 2921037 | C | T | missense_variant | MODERATE | c.256C>T|p.Arg86Cys |
S204 |
3 | BAA10g05700 | A10 | 2921194 | C | T | missense_variant | MODERATE | c.413C>T|p.Ser138Phe |
S92 |
4 | BAA10g05700 | A10 | 2925233 | G | A | downstream_gene_variant | MODIFIER | c.*3966G>A| |
S242 |