Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19660 | A08 | 15425819 | C | T | missense_variant | MODERATE | c.952G>A|p.Ala318Thr |
S113 |
2 | BAA08g19660 | A08 | 15426259 | C | T | synonymous_variant | LOW | c.669G>A|p.Lys223Lys |
S293 |
3 | BAA08g19660 | A08 | 15426748 | C | T | synonymous_variant | LOW | c.342G>A|p.Lys114Lys |
S250 |
4 | BAA08g19660 | A08 | 15426816 | C | T | missense_variant | MODERATE | c.274G>A|p.Val92Ile |
S189 |
5 | BAA08g19660 | A08 | 15430363 | G | A | upstream_gene_variant | MODIFIER | c.-3274C>T| |
S126 |
6 | BAA08g19660 | A08 | 15430877 | G | A | upstream_gene_variant | MODIFIER | c.-3788C>T| |
S20 |
7 | BAA08g19660 | A08 | 15431940 | G | A | upstream_gene_variant | MODIFIER | c.-4851C>T| |
S219 |