Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17850 | A02 | 8926126 | C | T | upstream_gene_variant | MODIFIER | c.-609C>T| |
S177 |
2 | BAA02g17850 | A02 | 8926642 | G | A | upstream_gene_variant | MODIFIER | c.-93G>A| |
S129 |
3 | BAA02g17850 | A02 | 8926817 | C | T | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S130 |
4 | BAA02g17850 | A02 | 8927770 | C | T | downstream_gene_variant | MODIFIER | c.*394C>T| |
S124 |
5 | BAA02g17850 | A02 | 8927775 | T | G | downstream_gene_variant | MODIFIER | c.*399T>G| |
S127 S129 S152 S236 S62 |
6 | BAA02g17850 | A02 | 8928347 | G | A | downstream_gene_variant | MODIFIER | c.*971G>A| |
S240 |