Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55120 | A09 | 55411836 | G | A | upstream_gene_variant | MODIFIER | c.-4547G>A| |
S166 |
2 | BAA09g55120 | A09 | 55413759 | G | A | upstream_gene_variant | MODIFIER | c.-2624G>A| |
S308 |
3 | BAA09g55120 | A09 | 55416120 | C | T | upstream_gene_variant | MODIFIER | c.-263C>T| |
S269 |
4 | BAA09g55120 | A09 | 55416562 | C | T | synonymous_variant | LOW | c.180C>T|p.Leu60Leu |
S278 |
5 | BAA09g55120 | A09 | 55417358 | G | A | missense_variant | MODERATE | c.976G>A|p.Val326Met |
S113 |
6 | BAA09g55120 | A09 | 55417583 | C | T | synonymous_variant | LOW | c.1201C>T|p.Leu401Leu |
S140 |
7 | BAA09g55120 | A09 | 55421628 | C | T | downstream_gene_variant | MODIFIER | c.*2807C>T| |
S1 S20 S90 |
8 | BAA09g55120 | A09 | 55422035 | C | T | downstream_gene_variant | MODIFIER | c.*3214C>T| |
S41 |
9 | BAA09g55120 | A09 | 55422753 | C | T | downstream_gene_variant | MODIFIER | c.*3932C>T| |
S259 |