Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g13900 | A04 | 19165712 | C | T | missense_variant | MODERATE | c.1172C>T|p.Thr391Ile |
S168 |