Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04490 | A02 | 1943671 | G | A | missense_variant | MODERATE | c.295G>A|p.Ala99Thr |
S17 |
2 | BAA02g04490 | A02 | 1943811 | G | A | synonymous_variant | LOW | c.435G>A|p.Glu145Glu |
S259 |
3 | BAA02g04490 | A02 | 1943859 | C | T | synonymous_variant | LOW | c.483C>T|p.Thr161Thr |
S88 |
4 | BAA02g04490 | A02 | 1948952 | C | T | downstream_gene_variant | MODIFIER | c.*4724C>T| |
S131 |