Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11770 | A02 | 5322626 | C | T | upstream_gene_variant | MODIFIER | c.-435C>T| |
S34 |
2 | BAA02g11770 | A02 | 5322778 | C | T | upstream_gene_variant | MODIFIER | c.-283C>T| |
S277 |
3 | BAA02g11770 | A02 | 5323155 | C | T | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S123 |
4 | BAA02g11770 | A02 | 5323314 | C | T | missense_variant | MODERATE | c.254C>T|p.Pro85Leu |
S135 |
5 | BAA02g11770 | A02 | 5323663 | G | A | stop_gained | HIGH | c.603G>A|p.Trp201* |
S276 |
6 | BAA02g11770 | A02 | 5323852 | G | A | synonymous_variant | LOW | c.792G>A|p.Glu264Glu |
S229 |