Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04790 | A02 | 2082108 | C | T | missense_variant | MODERATE | c.7G>A|p.Ala3Thr |
S287 |
2 | BAA02g04790 | A02 | 2082645 | C | T | upstream_gene_variant | MODIFIER | c.-531G>A| |
S37 |
3 | BAA02g04790 | A02 | 2082992 | G | A | upstream_gene_variant | MODIFIER | c.-878C>T| |
S7 |
4 | BAA02g04790 | A02 | 2084398 | G | A | upstream_gene_variant | MODIFIER | c.-2284C>T| |
S60 |
5 | BAA02g04790 | A02 | 2085128 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S127 |