Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43900 | A02 | 36266453 | C | T | missense_variant | MODERATE | c.656C>T|p.Pro219Leu |
S202 |