Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66490 | A09 | 60744643 | C | T | missense_variant | MODERATE | c.13C>T|p.Leu5Phe |
S242 |
2 | BAA09g66490 | A09 | 60744648 | G | A | synonymous_variant | LOW | c.18G>A|p.Arg6Arg |
S174 |
3 | BAA09g66490 | A09 | 60744822 | G | A | synonymous_variant | LOW | c.192G>A|p.Glu64Glu |
S81 S85 |