Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12390 | A10 | 13833467 | C | T | missense_variant | MODERATE | c.830C>T|p.Ala277Val |
S19 |