Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20600 | A02 | 10921004 | C | T | missense_variant | MODERATE | c.566C>T|p.Ser189Phe |
S180 |
2 | BAA02g20600 | A02 | 10925356 | C | T | downstream_gene_variant | MODIFIER | c.*3486C>T| |
S127 |
3 | BAA02g20600 | A02 | 10925712 | G | A | downstream_gene_variant | MODIFIER | c.*3842G>A| |
S156 |