Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13860 | A02 | 6470986 | C | T | missense_variant | MODERATE | c.779C>T|p.Ser260Phe |
S115 |