Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51690 | A09 | 53894743 | C | T | missense_variant | MODERATE | c.449C>T|p.Ser150Phe |
S50 |
2 | BAA09g51690 | A09 | 53895427 | G | A | missense_variant | MODERATE | c.983G>A|p.Arg328Lys |
S55 |
3 | BAA09g51690 | A09 | 53895617 | C | T | synonymous_variant | LOW | c.1098C>T|p.Leu366Leu |
S60 |