Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66350 | A09 | 60699345 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S176 |