Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00950 | A01 | 417515 | C | T | missense_variant | MODERATE | c.1711C>T|p.Leu571Phe |
S276 |
2 | BAA01g00950 | A01 | 417686 | G | A | missense_variant | MODERATE | c.1882G>A|p.Glu628Lys |
S293 |
3 | BAA01g00950 | A01 | 417781 | C | T | synonymous_variant | LOW | c.1977C>T|p.Phe659Phe |
S97 |
4 | BAA01g00950 | A01 | 418104 | G | A | missense_variant | MODERATE | c.2300G>A|p.Gly767Glu |
S15 S3 |