Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11300 | A02 | 5105186 | C | T | missense_variant | MODERATE | c.89C>T|p.Ser30Phe |
S162 |
2 | BAA02g11300 | A02 | 5109950 | G | A | downstream_gene_variant | MODIFIER | c.*4290G>A| |
S79 S91 |
3 | BAA02g11300 | A02 | 5110470 | G | A | downstream_gene_variant | MODIFIER | c.*4810G>A| |
S82 S92 |