Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20160 | A02 | 10625699 | C | T | missense_variant | MODERATE | c.793G>A|p.Val265Ile |
S1 S90 |
2 | BAA02g20160 | A02 | 10626822 | G | A | missense_variant | MODERATE | c.101C>T|p.Ala34Val |
S70 |
3 | BAA02g20160 | A02 | 10626830 | G | A | synonymous_variant | LOW | c.93C>T|p.Thr31Thr |
S126 |
4 | BAA02g20160 | A02 | 10629835 | C | T | upstream_gene_variant | MODIFIER | c.-2913G>A| |
S211 S227 |
5 | BAA02g20160 | A02 | 10630303 | C | T | upstream_gene_variant | MODIFIER | c.-3381G>A| |
S6 |
6 | BAA02g20160 | A02 | 10631106 | C | T | upstream_gene_variant | MODIFIER | c.-4184G>A| |
S159 S188 S243 S276 S298 S299 |