Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10000 | A02 | 4416628 | C | T | upstream_gene_variant | MODIFIER | c.-2010C>T| |
S15 S3 |
2 | BAA02g10000 | A02 | 4417756 | C | T | upstream_gene_variant | MODIFIER | c.-882C>T| |
S251 |
3 | BAA02g10000 | A02 | 4418899 | C | T | missense_variant | MODERATE | c.262C>T|p.Arg88Cys |
S233 |