Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67690 | A09 | 61209415 | C | T | missense_variant | MODERATE | c.781C>T|p.Pro261Ser |
S267 |