Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49250 | A09 | 52690236 | G | C | downstream_gene_variant | MODIFIER | c.*4330C>G| |
S213 |
2 | BAA09g49250 | A09 | 52695294 | G | A | missense_variant | MODERATE | c.635C>T|p.Thr212Ile |
S274 |
3 | BAA09g49250 | A09 | 52697648 | G | A | upstream_gene_variant | MODIFIER | c.-1299C>T| |
S284 |
4 | BAA09g49250 | A09 | 52697718 | G | A | upstream_gene_variant | MODIFIER | c.-1369C>T| |
S90 |
5 | BAA09g49250 | A09 | 52700269 | G | A | upstream_gene_variant | MODIFIER | c.-3920C>T| |
S189 |
6 | BAA09g49250 | A09 | 52700327 | C | T | upstream_gene_variant | MODIFIER | c.-3978G>A| |
S64 |
7 | BAA09g49250 | A09 | 52700919 | C | T | upstream_gene_variant | MODIFIER | c.-4570G>A| |
S302 |