Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40490 | A01 | 26823884 | C | T | missense_variant | MODERATE | c.422C>T|p.Pro141Leu |
S210 |