Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46420 | A09 | 51172478 | C | T | missense_variant | MODERATE | c.34C>T|p.Leu12Phe |
S136 |