Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40190 | A01 | 26712993 | C | T | missense_variant | MODERATE | c.1052C>T|p.Ala351Val |
S303 |