Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55990 | A09 | 55878156 | C | T | missense_variant | MODERATE | c.823G>A|p.Gly275Arg |
S17 |
2 | BAA09g55990 | A09 | 55878808 | G | A | synonymous_variant | LOW | c.171C>T|p.Leu57Leu |
S202 S246 |
3 | BAA09g55990 | A09 | 55880234 | C | T | upstream_gene_variant | MODIFIER | c.-937G>A| |
S61 |
4 | BAA09g55990 | A09 | 55880385 | G | A | upstream_gene_variant | MODIFIER | c.-1088C>T| |
S40 S49 |
5 | BAA09g55990 | A09 | 55883701 | C | T | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S191 |
6 | BAA09g55990 | A09 | 55883743 | C | T | upstream_gene_variant | MODIFIER | c.-4446G>A| |
S174 |