Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02360 | A02 | 1052598 | C | T | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S18 |
2 | BAA02g02360 | A02 | 1052784 | G | A | missense_variant | MODERATE | c.238G>A|p.Ala80Thr |
S263 |
3 | BAA02g02360 | A02 | 1052849 | C | T | synonymous_variant | LOW | c.303C>T|p.Arg101Arg |
S193 |