Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g34660 | A10 | 24295578 | C | T | missense_variant | MODERATE | c.16C>T|p.Pro6Ser |
S13 |