Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32690 | A02 | 27913784 | C | T | missense_variant | MODERATE | c.403C>T|p.His135Tyr |
S299 |
2 | BAA02g32690 | A02 | 27914552 | G | A | synonymous_variant | LOW | c.1044G>A|p.Gln348Gln |
S12 |
3 | BAA02g32690 | A02 | 27914853 | C | T | missense_variant | MODERATE | c.1256C>T|p.Ser419Phe |
S301 S304 |
4 | BAA02g32690 | A02 | 27915429 | G | A | missense_variant | MODERATE | c.1585G>A|p.Asp529Asn |
S256 |
5 | BAA02g32690 | A02 | 27915678 | C | T | missense_variant | MODERATE | c.1834C>T|p.Arg612Trp |
S123 |