Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39860 | A02 | 33749969 | A | C | missense_variant | MODERATE | c.260A>C|p.Tyr87Ser |
S103 S120 S183 S184 S196 S206 S30 S64 S91 |
2 | BAA02g39860 | A02 | 33750550 | C | T | downstream_gene_variant | MODIFIER | c.*199C>T| |
S165 S278 |