Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05980 | A02 | 2536143 | C | T | missense_variant | MODERATE | c.382G>A|p.Asp128Asn |
S112 |
2 | BAA02g05980 | A02 | 2538748 | C | T | upstream_gene_variant | MODIFIER | c.-2224G>A| |
S128 S60 |
3 | BAA02g05980 | A02 | 2539563 | C | T | upstream_gene_variant | MODIFIER | c.-3039G>A| |
S85 |
4 | BAA02g05980 | A02 | 2539975 | C | T | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S6 |
5 | BAA02g05980 | A02 | 2540529 | C | T | upstream_gene_variant | MODIFIER | c.-4005G>A| |
S249 |
6 | BAA02g05980 | A02 | 2540547 | C | T | upstream_gene_variant | MODIFIER | c.-4023G>A| |
S221 |