Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05220 | A02 | 2290065 | C | T | synonymous_variant | LOW | c.114C>T|p.Pro38Pro |
S15 S3 |
2 | BAA02g05220 | A02 | 2290151 | C | T | missense_variant | MODERATE | c.200C>T|p.Thr67Ile |
S46 |
3 | BAA02g05220 | A02 | 2293396 | C | T | downstream_gene_variant | MODIFIER | c.*2977C>T| |
S182 |