Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00350 | A09 | 430863 | T | C | missense_variant | MODERATE | c.761A>G|p.Asp254Gly |
S298 |
2 | BAA09g00350 | A09 | 431132 | C | T | missense_variant | MODERATE | c.599G>A|p.Arg200Lys |
S292 |
3 | BAA09g00350 | A09 | 431197 | G | A | synonymous_variant | LOW | c.534C>T|p.Leu178Leu |
S104 |
4 | BAA09g00350 | A09 | 435941 | C | T | upstream_gene_variant | MODIFIER | c.-4044G>A| |
S59 |