Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00090 | A05 | 44136 | C | T | missense_variant | MODERATE | c.593G>A|p.Gly198Glu |
S261 |
2 | BAA05g00090 | A05 | 48305 | G | A | upstream_gene_variant | MODIFIER | c.-3428C>T| |
S277 |
3 | BAA05g00090 | A05 | 49442 | C | T | upstream_gene_variant | MODIFIER | c.-4565G>A| |
S221 |