Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17580 | A02 | 8766925 | C | T | missense_variant | MODERATE | c.436G>A|p.Val146Met |
S135 |
2 | BAA02g17580 | A02 | 8766943 | G | A | missense_variant | MODERATE | c.418C>T|p.Arg140Cys |
S4 |
3 | BAA02g17580 | A02 | 8769459 | C | T | upstream_gene_variant | MODIFIER | c.-2099G>A| |
S32 |
4 | BAA02g17580 | A02 | 8771137 | C | T | upstream_gene_variant | MODIFIER | c.-3777G>A| |
S96 |
5 | BAA02g17580 | A02 | 8772221 | C | T | upstream_gene_variant | MODIFIER | c.-4861G>A| |
S246 |