Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02110 | A09 | 1430198 | C | T | missense_variant | MODERATE | c.562G>A|p.Asp188Asn |
S152 |
2 | BAA09g02110 | A09 | 1434291 | C | T | upstream_gene_variant | MODIFIER | c.-3001G>A| |
S118 S272 |
3 | BAA09g02110 | A09 | 1434689 | G | A | upstream_gene_variant | MODIFIER | c.-3399C>T| |
S209 |