Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46840 | A02 | 37959205 | C | T | missense_variant | MODERATE | c.208C>T|p.Pro70Ser |
S117 |