Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51390 | A09 | 53766584 | C | T | missense_variant | MODERATE | c.118C>T|p.Pro40Ser |
S7 |