Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g33870 | A07 | 32592002 | C | T | missense_variant | MODERATE | c.437C>T|p.Ala146Val |
S174 |