Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01200 | A05 | 719213 | C | T | missense_variant | MODERATE | c.293G>A|p.Gly98Asp |
S241 |
2 | BAA05g01200 | A05 | 721581 | C | T | upstream_gene_variant | MODIFIER | c.-1755G>A| |
S189 |
3 | BAA05g01200 | A05 | 722728 | G | A | upstream_gene_variant | MODIFIER | c.-2902C>T| |
S264 |