Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00240 | A01 | 117466 | C | T | missense_variant | MODERATE | c.161C>T|p.Ala54Val |
S76 |
2 | BAA01g00240 | A01 | 117581 | C | T | synonymous_variant | LOW | c.276C>T|p.Phe92Phe |
S273 |
3 | BAA01g00240 | A01 | 117899 | C | T | synonymous_variant | LOW | c.594C>T|p.Asp198Asp |
S126 |