Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16790 | A09 | 9923432 | G | A | upstream_gene_variant | MODIFIER | c.-4871G>A| |
S165 |
2 | BAA09g16790 | A09 | 9924103 | C | T | upstream_gene_variant | MODIFIER | c.-4200C>T| |
S35 |
3 | BAA09g16790 | A09 | 9925106 | C | T | upstream_gene_variant | MODIFIER | c.-3197C>T| |
S137 S215 |
4 | BAA09g16790 | A09 | 9925979 | C | T | upstream_gene_variant | MODIFIER | c.-2324C>T| |
S148 |
5 | BAA09g16790 | A09 | 9926039 | G | A | upstream_gene_variant | MODIFIER | c.-2264G>A| |
S72 S78 |
6 | BAA09g16790 | A09 | 9926426 | G | A | upstream_gene_variant | MODIFIER | c.-1877G>A| |
S13 |
7 | BAA09g16790 | A09 | 9926883 | G | A | upstream_gene_variant | MODIFIER | c.-1420G>A| |
S271 |
8 | BAA09g16790 | A09 | 9926979 | C | T | upstream_gene_variant | MODIFIER | c.-1324C>T| |
S97 |
9 | BAA09g16790 | A09 | 9929384 | G | A | missense_variant | MODERATE | c.589G>A|p.Glu197Lys |
S42 |
10 | BAA09g16790 | A09 | 9929389 | C | T | synonymous_variant | LOW | c.594C>T|p.Leu198Leu |
S176 |
11 | BAA09g16790 | A09 | 9932723 | G | A | downstream_gene_variant | MODIFIER | c.*1539G>A| |
S66 |
12 | BAA09g16790 | A09 | 9935007 | C | A | downstream_gene_variant | MODIFIER | c.*3823C>A| |
S5 |