Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16100 | A02 | 7828168 | C | T | missense_variant | MODERATE | c.1126G>A|p.Gly376Arg |
S121 |
2 | BAA02g16100 | A02 | 7832532 | C | T | upstream_gene_variant | MODIFIER | c.-2696G>A| |
S299 |
3 | BAA02g16100 | A02 | 7832550 | C | T | upstream_gene_variant | MODIFIER | c.-2714G>A| |
S131 |
4 | BAA02g16100 | A02 | 7833229 | G | A | upstream_gene_variant | MODIFIER | c.-3393C>T| |
S159 S243 |