Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03860 | A02 | 1697376 | C | T | missense_variant | MODERATE | c.571G>A|p.Gly191Arg |
S2 |
2 | BAA02g03860 | A02 | 1697540 | G | A | synonymous_variant | LOW | c.498C>T|p.Asp166Asp |
S221 |
3 | BAA02g03860 | A02 | 1698430 | C | T | missense_variant | MODERATE | c.197G>A|p.Gly66Glu |
S178 |
4 | BAA02g03860 | A02 | 1701635 | C | T | upstream_gene_variant | MODIFIER | c.-2832G>A| |
S186 |
5 | BAA02g03860 | A02 | 1701754 | G | A | upstream_gene_variant | MODIFIER | c.-2951C>T| |
S148 S210 S30 S31 |