Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21920 | A02 | 11802500 | C | T | missense_variant | MODERATE | c.545C>T|p.Ala182Val |
S16 |
2 | BAA02g21920 | A02 | 11802513 | G | A | synonymous_variant | LOW | c.558G>A|p.Ala186Ala |
S232 |
3 | BAA02g21920 | A02 | 11802563 | G | A | missense_variant | MODERATE | c.608G>A|p.Gly203Glu |
S235 |