Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00890 | A02 | 417795 | G | A | missense_variant | MODERATE | c.10G>A|p.Ala4Thr |
S286 |
2 | BAA02g00890 | A02 | 418151 | C | T | missense_variant | MODERATE | c.298C>T|p.Pro100Ser |
S97 |
3 | BAA02g00890 | A02 | 419052 | G | A | splice_donor_variant&intron_variant | HIGH | c.830+1G>A| |
S136 |