Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29990 | A01 | 19035934 | C | T | missense_variant | MODERATE | c.292G>A|p.Ala98Thr |
S270 |
2 | BAA01g29990 | A01 | 19036153 | C | T | missense_variant | MODERATE | c.73G>A|p.Ala25Thr |
S189 |
3 | BAA01g29990 | A01 | 19038797 | C | T | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S277 |
4 | BAA01g29990 | A01 | 19039193 | G | A | upstream_gene_variant | MODIFIER | c.-2968C>T| |
S199 |
5 | BAA01g29990 | A01 | 19040718 | C | T | upstream_gene_variant | MODIFIER | c.-4493G>A| |
S160 |