Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26280 | A02 | 14581785 | G | A | missense_variant | MODERATE | c.431C>T|p.Ala144Val |
S184 |
2 | BAA02g26280 | A02 | 14582190 | C | T | missense_variant | MODERATE | c.109G>A|p.Ala37Thr |
S54 |
3 | BAA02g26280 | A02 | 14584084 | G | A | upstream_gene_variant | MODIFIER | c.-1214C>T| |
S251 |
4 | BAA02g26280 | A02 | 14584175 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S181 |
5 | BAA02g26280 | A02 | 14584272 | C | T | upstream_gene_variant | MODIFIER | c.-1402G>A| |
S262 |
6 | BAA02g26280 | A02 | 14584853 | C | T | upstream_gene_variant | MODIFIER | c.-1983G>A| |
S203 |
7 | BAA02g26280 | A02 | 14586817 | G | A | upstream_gene_variant | MODIFIER | c.-3947C>T| |
S158 |