Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08770 | A04 | 6060385 | C | T | upstream_gene_variant | MODIFIER | c.-4855C>T| |
S25 S264 |
2 | BAA04g08770 | A04 | 6060605 | C | T | upstream_gene_variant | MODIFIER | c.-4635C>T| |
S192 |
3 | BAA04g08770 | A04 | 6060615 | G | A | upstream_gene_variant | MODIFIER | c.-4625G>A| |
S286 |
4 | BAA04g08770 | A04 | 6060668 | C | T | upstream_gene_variant | MODIFIER | c.-4572C>T| |
S192 |
5 | BAA04g08770 | A04 | 6062377 | C | T | upstream_gene_variant | MODIFIER | c.-2863C>T| |
S257 |
6 | BAA04g08770 | A04 | 6062753 | G | A | upstream_gene_variant | MODIFIER | c.-2487G>A| |
S136 |
7 | BAA04g08770 | A04 | 6064513 | G | A | upstream_gene_variant | MODIFIER | c.-727G>A| |
S12 |
8 | BAA04g08770 | A04 | 6065000 | G | A | upstream_gene_variant | MODIFIER | c.-240G>A| |
S126 |
9 | BAA04g08770 | A04 | 6065465 | C | T | missense_variant | MODERATE | c.226C>T|p.Leu76Phe |
S130 |