Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g56930 | A03 | 28210642 | C | T | missense_variant | MODERATE | c.10C>T|p.Pro4Ser |
S129 |
2 | BAA03g56930 | A03 | 28212331 | C | T | synonymous_variant | LOW | c.648C>T|p.Phe216Phe |
S142 |
3 | BAA03g56930 | A03 | 28212785 | G | A | synonymous_variant | LOW | c.933G>A|p.Ala311Ala |
S297 |