Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00840 | A02 | 403661 | C | T | missense_variant | MODERATE | c.635G>A|p.Arg212His |
S262 |
2 | BAA02g00840 | A02 | 403869 | C | T | missense_variant | MODERATE | c.427G>A|p.Ala143Thr |
S177 |
3 | BAA02g00840 | A02 | 405024 | G | A | upstream_gene_variant | MODIFIER | c.-633C>T| |
S11 |
4 | BAA02g00840 | A02 | 405026 | G | A | upstream_gene_variant | MODIFIER | c.-635C>T| |
S122 |
5 | BAA02g00840 | A02 | 409150 | C | T | upstream_gene_variant | MODIFIER | c.-4759G>A| |
S133 |