Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07590 | A02 | 3265661 | C | T | missense_variant | MODERATE | c.211G>A|p.Ala71Thr |
S117 |
2 | BAA02g07590 | A02 | 3266918 | C | T | upstream_gene_variant | MODIFIER | c.-1047G>A| |
S73 S91 |
3 | BAA02g07590 | A02 | 3268034 | G | A | upstream_gene_variant | MODIFIER | c.-2163C>T| |
S287 |
4 | BAA02g07590 | A02 | 3268378 | C | T | upstream_gene_variant | MODIFIER | c.-2507G>A| |
S167 |
5 | BAA02g07590 | A02 | 3268821 | C | T | upstream_gene_variant | MODIFIER | c.-2950G>A| |
S120 |
6 | BAA02g07590 | A02 | 3269277 | G | A | upstream_gene_variant | MODIFIER | c.-3406C>T| |
S265 |
7 | BAA02g07590 | A02 | 3270496 | G | A | upstream_gene_variant | MODIFIER | c.-4625C>T| |
S74 |
8 | BAA02g07590 | A02 | 3270546 | G | A | upstream_gene_variant | MODIFIER | c.-4675C>T| |
S197 |
9 | BAA02g07590 | A02 | 3270751 | C | T | upstream_gene_variant | MODIFIER | c.-4880G>A| |
S129 |
10 | BAA02g07590 | A02 | 3270763 | G | A | upstream_gene_variant | MODIFIER | c.-4892C>T| |
S23 |