Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28430 | A10 | 21775788 | C | T | upstream_gene_variant | MODIFIER | c.-829C>T| |
S68 |
2 | BAA10g28430 | A10 | 21776002 | C | T | upstream_gene_variant | MODIFIER | c.-615C>T| |
S2 |
3 | BAA10g28430 | A10 | 21776702 | C | T | missense_variant | MODERATE | c.86C>T|p.Ala29Val |
S259 |