Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12480 | A02 | 5608011 | C | T | upstream_gene_variant | MODIFIER | c.-2165C>T| |
S216 |
2 | BAA02g12480 | A02 | 5608676 | G | A | upstream_gene_variant | MODIFIER | c.-1500G>A| |
S136 |
3 | BAA02g12480 | A02 | 5608713 | G | A | upstream_gene_variant | MODIFIER | c.-1463G>A| |
S274 |
4 | BAA02g12480 | A02 | 5608919 | G | A | upstream_gene_variant | MODIFIER | c.-1257G>A| |
S149 |
5 | BAA02g12480 | A02 | 5609054 | C | T | upstream_gene_variant | MODIFIER | c.-1122C>T| |
S79 S84 |
6 | BAA02g12480 | A02 | 5609171 | G | A | upstream_gene_variant | MODIFIER | c.-1005G>A| |
S238 |
7 | BAA02g12480 | A02 | 5609387 | C | T | upstream_gene_variant | MODIFIER | c.-789C>T| |
S293 |
8 | BAA02g12480 | A02 | 5611199 | G | A | missense_variant | MODERATE | c.1024G>A|p.Ala342Thr |
S202 |
9 | BAA02g12480 | A02 | 5611394 | C | T | missense_variant | MODERATE | c.1219C>T|p.Leu407Phe |
S234 |