Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25960 | A02 | 14390241 | C | T | missense_variant | MODERATE | c.191C>T|p.Ala64Val |
S9 |
2 | BAA02g25960 | A02 | 14390547 | C | T | missense_variant | MODERATE | c.338C>T|p.Pro113Leu |
S183 S198 |
3 | BAA02g25960 | A02 | 14390588 | C | T | missense_variant | MODERATE | c.379C>T|p.His127Tyr |
S242 |