Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46980 | A02 | 38032561 | C | T | missense_variant | MODERATE | c.325C>T|p.Pro109Ser |
S4 |
2 | BAA02g46980 | A02 | 38032733 | C | T | missense_variant | MODERATE | c.497C>T|p.Pro166Leu |
S16 |
3 | BAA02g46980 | A02 | 38032818 | G | A | synonymous_variant | LOW | c.582G>A|p.Lys194Lys |
S41 |