Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45660 | A09 | 50790623 | G | A | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S36 |
2 | BAA09g45660 | A09 | 50791513 | C | T | upstream_gene_variant | MODIFIER | c.-3716C>T| |
S39 |
3 | BAA09g45660 | A09 | 50792054 | G | A | upstream_gene_variant | MODIFIER | c.-3175G>A| |
S283 |
4 | BAA09g45660 | A09 | 50792491 | G | A | upstream_gene_variant | MODIFIER | c.-2738G>A| |
S166 |
5 | BAA09g45660 | A09 | 50792507 | G | A | upstream_gene_variant | MODIFIER | c.-2722G>A| |
S185 |
6 | BAA09g45660 | A09 | 50792645 | G | A | upstream_gene_variant | MODIFIER | c.-2584G>A| |
S156 |
7 | BAA09g45660 | A09 | 50792803 | C | T | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S213 |
8 | BAA09g45660 | A09 | 50792854 | G | A | upstream_gene_variant | MODIFIER | c.-2375G>A| |
S107 |
9 | BAA09g45660 | A09 | 50795760 | C | T | missense_variant | MODERATE | c.532C>T|p.Leu178Phe |
S181 |
10 | BAA09g45660 | A09 | 50795790 | G | A | missense_variant | MODERATE | c.562G>A|p.Glu188Lys |
S280 |