Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10850 | A01 | 5003456 | C | T | upstream_gene_variant | MODIFIER | c.-126C>T| |
S166 |
2 | BAA01g10850 | A01 | 5003629 | C | T | synonymous_variant | LOW | c.48C>T|p.Thr16Thr |
S112 |
3 | BAA01g10850 | A01 | 5003637 | C | T | missense_variant | MODERATE | c.56C>T|p.Ala19Val |
S185 |
4 | BAA01g10850 | A01 | 5006054 | G | A | downstream_gene_variant | MODIFIER | c.*78G>A| |
S187 |