Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11000 | A02 | 4955854 | C | T | upstream_gene_variant | MODIFIER | c.-4205C>T| |
S1 S90 |
2 | BAA02g11000 | A02 | 4956686 | C | T | upstream_gene_variant | MODIFIER | c.-3373C>T| |
S185 |
3 | BAA02g11000 | A02 | 4958230 | C | T | upstream_gene_variant | MODIFIER | c.-1829C>T| |
S81 |
4 | BAA02g11000 | A02 | 4958315 | C | T | upstream_gene_variant | MODIFIER | c.-1744C>T| |
S192 |
5 | BAA02g11000 | A02 | 4958332 | C | T | upstream_gene_variant | MODIFIER | c.-1727C>T| |
S44 |
6 | BAA02g11000 | A02 | 4958366 | C | T | upstream_gene_variant | MODIFIER | c.-1693C>T| |
S138 |
7 | BAA02g11000 | A02 | 4959993 | C | T | upstream_gene_variant | MODIFIER | c.-66C>T| |
S195 |
8 | BAA02g11000 | A02 | 4960078 | G | A | missense_variant | MODERATE | c.20G>A|p.Ser7Asn |
S190 |