Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03770 | A02 | 1660757 | G | A | missense_variant | MODERATE | c.464G>A|p.Arg155Lys |
S206 S26 |
2 | BAA02g03770 | A02 | 1661881 | G | A | missense_variant | MODERATE | c.1168G>A|p.Ala390Thr |
S110 |
3 | BAA02g03770 | A02 | 1662028 | C | T | missense_variant | MODERATE | c.1237C>T|p.Pro413Ser |
S242 |