Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42590 | A02 | 35448072 | C | T | upstream_gene_variant | MODIFIER | c.-4003C>T| |
S158 |
2 | BAA02g42590 | A02 | 35449503 | C | T | upstream_gene_variant | MODIFIER | c.-2572C>T| |
S118 |
3 | BAA02g42590 | A02 | 35452301 | C | T | missense_variant | MODERATE | c.148C>T|p.Leu50Phe |
S257 |