Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47980 | A02 | 38643826 | G | A | synonymous_variant | LOW | c.54G>A|p.Arg18Arg |
S111 |
2 | BAA02g47980 | A02 | 38644028 | C | T | missense_variant | MODERATE | c.196C>T|p.Pro66Ser |
S121 |
3 | BAA02g47980 | A02 | 38644112 | C | T | synonymous_variant | LOW | c.280C>T|p.Leu94Leu |
S181 |