Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46460 | A02 | 37758350 | C | T | downstream_gene_variant | MODIFIER | c.*4277G>A| |
S208 S93 |
2 | BAA02g46460 | A02 | 37763149 | C | T | missense_variant | MODERATE | c.632G>A|p.Gly211Glu |
S95 |
3 | BAA02g46460 | A02 | 37764402 | C | T | upstream_gene_variant | MODIFIER | c.-317G>A| |
S241 |
4 | BAA02g46460 | A02 | 37764752 | C | T | upstream_gene_variant | MODIFIER | c.-667G>A| |
S182 |
5 | BAA02g46460 | A02 | 37765024 | C | T | upstream_gene_variant | MODIFIER | c.-939G>A| |
S301 S304 |
6 | BAA02g46460 | A02 | 37765557 | C | T | upstream_gene_variant | MODIFIER | c.-1472G>A| |
S242 |
7 | BAA02g46460 | A02 | 37767685 | C | T | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S105 S106 |