Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44760 | A09 | 50280756 | C | T | missense_variant | MODERATE | c.554C>T|p.Thr185Ile |
S278 |
2 | BAA09g44760 | A09 | 50280854 | C | T | synonymous_variant | LOW | c.652C>T|p.Leu218Leu |
S99 |
3 | BAA09g44760 | A09 | 50280923 | C | T | missense_variant | MODERATE | c.721C>T|p.Pro241Ser |
S153 |
4 | BAA09g44760 | A09 | 50281024 | G | A | stop_gained | HIGH | c.822G>A|p.Trp274* |
S132 S137 S215 S89 |