Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09990 | A02 | 4415080 | C | T | upstream_gene_variant | MODIFIER | c.-474C>T| |
S250 |
2 | BAA02g09990 | A02 | 4415724 | C | T | synonymous_variant | LOW | c.171C>T|p.Phe57Phe |
S209 |
3 | BAA02g09990 | A02 | 4415827 | C | T | missense_variant | MODERATE | c.274C>T|p.Pro92Ser |
S209 |
4 | BAA02g09990 | A02 | 4420945 | G | A | downstream_gene_variant | MODIFIER | c.*4480G>A| |
S161 |