Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43970 | A09 | 49880151 | C | T | upstream_gene_variant | MODIFIER | c.-912C>T| |
S135 |
2 | BAA09g43970 | A09 | 49883007 | C | T | synonymous_variant | LOW | c.897C>T|p.Phe299Phe |
S183 |
3 | BAA09g43970 | A09 | 49883785 | A | G | missense_variant | MODERATE | c.1342A>G|p.Asn448Asp |
S196 |