Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g28600 | A03 | 13267898 | C | T | missense_variant | MODERATE | c.1165C>T|p.Pro389Ser |
S66 |