Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22000 | A08 | 16602754 | C | T | synonymous_variant | LOW | c.573C>T|p.Asn191Asn |
S252 |
2 | BAA08g22000 | A08 | 16602956 | C | T | stop_gained | HIGH | c.688C>T|p.Arg230* |
S44 |
3 | BAA08g22000 | A08 | 16603206 | C | T | missense_variant | MODERATE | c.938C>T|p.Ser313Phe |
S17 |