Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13770 | A09 | 7930234 | C | T | missense_variant | MODERATE | c.745G>A|p.Ala249Thr |
S33 |
2 | BAA09g13770 | A09 | 7930556 | C | T | missense_variant | MODERATE | c.520G>A|p.Ala174Thr |
S270 |
3 | BAA09g13770 | A09 | 7932495 | C | T | upstream_gene_variant | MODIFIER | c.-947G>A| |
S6 |
4 | BAA09g13770 | A09 | 7933957 | G | A | upstream_gene_variant | MODIFIER | c.-2409C>T| |
S170 |