Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20010 | A02 | 10521221 | C | T | missense_variant | MODERATE | c.49G>A|p.Ala17Thr |
S32 |
2 | BAA02g20010 | A02 | 10521479 | C | T | upstream_gene_variant | MODIFIER | c.-210G>A| |
S216 |
3 | BAA02g20010 | A02 | 10523882 | C | T | upstream_gene_variant | MODIFIER | c.-2613G>A| |
S135 |