Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21700 | A08 | 16412275 | C | T | downstream_gene_variant | MODIFIER | c.*1053G>A| |
S28 |
2 | BAA08g21700 | A08 | 16413562 | G | A | synonymous_variant | LOW | c.1230C>T|p.Ser410Ser |
S282 |
3 | BAA08g21700 | A08 | 16413869 | C | T | missense_variant | MODERATE | c.1000G>A|p.Glu334Lys |
S183 S198 |
4 | BAA08g21700 | A08 | 16414112 | G | A | splice_region_variant&intron_variant | LOW | c.833+5C>T| |
S84 S93 |
5 | BAA08g21700 | A08 | 16414372 | G | A | missense_variant | MODERATE | c.668C>T|p.Thr223Ile |
S1 S161 S244 S289 S290 S90 |
6 | BAA08g21700 | A08 | 16414835 | G | A | missense_variant | MODERATE | c.428C>T|p.Thr143Ile |
S11 |
7 | BAA08g21700 | A08 | 16415186 | G | A | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S58 |
8 | BAA08g21700 | A08 | 16419801 | C | T | upstream_gene_variant | MODIFIER | c.-4440G>A| |
S122 |