Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39600 | A02 | 33617856 | G | A | missense_variant | MODERATE | c.607G>A|p.Asp203Asn |
S38 |
2 | BAA02g39600 | A02 | 33617880 | G | A | missense_variant | MODERATE | c.631G>A|p.Asp211Asn |
S279 |
3 | BAA02g39600 | A02 | 33621058 | C | T | downstream_gene_variant | MODIFIER | c.*2975C>T| |
S249 |