Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29960 | A02 | 17258376 | G | A | missense_variant | MODERATE | c.139G>A|p.Ala47Thr |
S94 |
2 | BAA02g29960 | A02 | 17258563 | C | T | synonymous_variant | LOW | c.240C>T|p.Leu80Leu |
S216 |
3 | BAA02g29960 | A02 | 17262362 | G | A | downstream_gene_variant | MODIFIER | c.*3553G>A| |
S298 |
4 | BAA02g29960 | A02 | 17262551 | C | T | downstream_gene_variant | MODIFIER | c.*3742C>T| |
S216 |
5 | BAA02g29960 | A02 | 17262919 | C | T | downstream_gene_variant | MODIFIER | c.*4110C>T| |
S299 |