Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g07440 | A09 | 4134409 | C | T | upstream_gene_variant | MODIFIER | c.-1566C>T| |
S239 |
2 | BAA09g07440 | A09 | 4134690 | G | A | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S185 |
3 | BAA09g07440 | A09 | 4134695 | G | A | upstream_gene_variant | MODIFIER | c.-1280G>A| |
S78 |
4 | BAA09g07440 | A09 | 4135042 | C | T | upstream_gene_variant | MODIFIER | c.-933C>T| |
S161 |
5 | BAA09g07440 | A09 | 4135695 | G | A | upstream_gene_variant | MODIFIER | c.-280G>A| |
S139 |
6 | BAA09g07440 | A09 | 4135974 | G | A | upstream_gene_variant | MODIFIER | c.-1G>A| |
S289 S290 |
7 | BAA09g07440 | A09 | 4138032 | G | A | synonymous_variant | LOW | c.1317G>A|p.Arg439Arg |
S260 |
8 | BAA09g07440 | A09 | 4138601 | C | T | downstream_gene_variant | MODIFIER | c.*353C>T| |
S168 |
9 | BAA09g07440 | A09 | 4138734 | C | T | downstream_gene_variant | MODIFIER | c.*486C>T| |
S208 S219 |