Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g37690 | A09 | 45784088 | C | T | missense_variant | MODERATE | c.919G>A|p.Asp307Asn |
S139 |
2 | BAA09g37690 | A09 | 45789328 | A | T | upstream_gene_variant | MODIFIER | c.-4322T>A| |
S184 |
3 | BAA09g37690 | A09 | 45789369 | G | A | upstream_gene_variant | MODIFIER | c.-4363C>T| |
S81 S85 |