Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g49660 | A03 | 23894672 | G | A | missense_variant | MODERATE | c.263C>T|p.Ala88Val |
S294 |
2 | BAA03g49660 | A03 | 23895385 | C | T | upstream_gene_variant | MODIFIER | c.-361G>A| |
S205 |
3 | BAA03g49660 | A03 | 23896089 | C | A | upstream_gene_variant | MODIFIER | c.-1065G>T| |
S252 |