Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00270 | A09 | 371174 | C | T | missense_variant | MODERATE | c.229C>T|p.His77Tyr |
S136 |