Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00160 | A04 | 52132 | G | A | missense_variant | MODERATE | c.257C>T|p.Ala86Val |
S278 |
2 | BAA04g00160 | A04 | 52729 | C | T | upstream_gene_variant | MODIFIER | c.-230G>A| |
S98 |
3 | BAA04g00160 | A04 | 52747 | C | T | upstream_gene_variant | MODIFIER | c.-248G>A| |
S189 |
4 | BAA04g00160 | A04 | 53461 | G | A | upstream_gene_variant | MODIFIER | c.-962C>T| |
S64 |
5 | BAA04g00160 | A04 | 53581 | G | A | upstream_gene_variant | MODIFIER | c.-1082C>T| |
S239 |
6 | BAA04g00160 | A04 | 55158 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S115 |
7 | BAA04g00160 | A04 | 55612 | C | T | upstream_gene_variant | MODIFIER | c.-3113G>A| |
S55 |
8 | BAA04g00160 | A04 | 55907 | G | A | upstream_gene_variant | MODIFIER | c.-3408C>T| |
S182 |
9 | BAA04g00160 | A04 | 56512 | C | T | upstream_gene_variant | MODIFIER | c.-4013G>A| |
S115 |