Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40980 | A05 | 39392509 | G | A | missense_variant | MODERATE | c.838C>T|p.Leu280Phe |
S264 |
2 | BAA05g40980 | A05 | 39392561 | G | A | synonymous_variant | LOW | c.786C>T|p.Leu262Leu |
S255 |
3 | BAA05g40980 | A05 | 39395409 | G | A | upstream_gene_variant | MODIFIER | c.-1227C>T| |
S180 |
4 | BAA05g40980 | A05 | 39396286 | C | T | upstream_gene_variant | MODIFIER | c.-2104G>A| |
S9 |