Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16120 | A05 | 8873155 | C | T | synonymous_variant | LOW | c.627G>A|p.Val209Val |
S45 |
2 | BAA05g16120 | A05 | 8874615 | C | T | upstream_gene_variant | MODIFIER | c.-154G>A| |
S7 |
3 | BAA05g16120 | A05 | 8874834 | G | A | upstream_gene_variant | MODIFIER | c.-373C>T| |
S187 |
4 | BAA05g16120 | A05 | 8875150 | T | A | upstream_gene_variant | MODIFIER | c.-689A>T| |
S115 S68 |
5 | BAA05g16120 | A05 | 8875497 | A | T | upstream_gene_variant | MODIFIER | c.-1036T>A| |
S250 |
6 | BAA05g16120 | A05 | 8875950 | C | T | upstream_gene_variant | MODIFIER | c.-1489G>A| |
S89 |
7 | BAA05g16120 | A05 | 8876168 | G | A | upstream_gene_variant | MODIFIER | c.-1707C>T| |
S7 |
8 | BAA05g16120 | A05 | 8876574 | C | T | upstream_gene_variant | MODIFIER | c.-2113G>A| |
S59 |
9 | BAA05g16120 | A05 | 8877418 | C | T | upstream_gene_variant | MODIFIER | c.-2957G>A| |
S13 |
10 | BAA05g16120 | A05 | 8878329 | G | A | upstream_gene_variant | MODIFIER | c.-3868C>T| |
S298 |