Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19920 | A02 | 10459777 | C | A | upstream_gene_variant | MODIFIER | c.-633C>A| |
S209 |
2 | BAA02g19920 | A02 | 10461274 | G | A | splice_region_variant&intron_variant | LOW | c.481+6G>A| |
S263 |
3 | BAA02g19920 | A02 | 10461461 | G | A | missense_variant | MODERATE | c.569G>A|p.Arg190Lys |
S247 |