Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45460 | A09 | 50659060 | C | T | upstream_gene_variant | MODIFIER | c.-718C>T| |
S206 S26 |
2 | BAA09g45460 | A09 | 50659425 | C | T | upstream_gene_variant | MODIFIER | c.-353C>T| |
S293 |
3 | BAA09g45460 | A09 | 50659874 | G | A | missense_variant | MODERATE | c.97G>A|p.Val33Met |
S86 |
4 | BAA09g45460 | A09 | 50663646 | C | T | downstream_gene_variant | MODIFIER | c.*3701C>T| |
S261 |
5 | BAA09g45460 | A09 | 50663660 | C | T | downstream_gene_variant | MODIFIER | c.*3715C>T| |
S278 |
6 | BAA09g45460 | A09 | 50663901 | G | A | downstream_gene_variant | MODIFIER | c.*3956G>A| |
S88 |
7 | BAA09g45460 | A09 | 50664361 | C | T | downstream_gene_variant | MODIFIER | c.*4416C>T| |
S18 |