Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27850 | A09 | 18269219 | C | T | synonymous_variant | LOW | c.276C>T|p.Phe92Phe |
S92 |
2 | BAA09g27850 | A09 | 18270100 | A | T | missense_variant | MODERATE | c.1001A>T|p.Asp334Val |
S205 S240 |
3 | BAA09g27850 | A09 | 18270795 | G | A | missense_variant | MODERATE | c.1441G>A|p.Val481Met |
S125 |
4 | BAA09g27850 | A09 | 18271393 | G | A | missense_variant | MODERATE | c.1831G>A|p.Glu611Lys |
S271 |
5 | BAA09g27850 | A09 | 18271663 | G | A | missense_variant | MODERATE | c.2026G>A|p.Glu676Lys |
S65 |
6 | BAA09g27850 | A09 | 18272686 | C | T | missense_variant | MODERATE | c.2777C>T|p.Pro926Leu |
S32 |
7 | BAA09g27850 | A09 | 18273081 | C | T | downstream_gene_variant | MODIFIER | c.*265C>T| |
S208 |
8 | BAA09g27850 | A09 | 18273252 | G | A | downstream_gene_variant | MODIFIER | c.*436G>A| |
S172 S217 |
9 | BAA09g27850 | A09 | 18274152 | G | A | downstream_gene_variant | MODIFIER | c.*1336G>A| |
S138 |