Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10250 | A02 | 4558688 | G | A | missense_variant | MODERATE | c.41G>A|p.Gly14Glu |
S238 |
2 | BAA02g10250 | A02 | 4563101 | C | T | downstream_gene_variant | MODIFIER | c.*2223C>T| |
S18 |
3 | BAA02g10250 | A02 | 4563123 | G | A | downstream_gene_variant | MODIFIER | c.*2245G>A| |
S206 S26 |