Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59480 | A03 | 29809248 | C | T | downstream_gene_variant | MODIFIER | c.*847G>A| |
S120 |
2 | BAA03g59480 | A03 | 29809349 | C | T | downstream_gene_variant | MODIFIER | c.*746G>A| |
S256 |
3 | BAA03g59480 | A03 | 29813186 | G | A | synonymous_variant | LOW | c.1875C>T|p.Val625Val |
S51 |
4 | BAA03g59480 | A03 | 29815213 | C | T | intron_variant | MODIFIER | c.1434+48G>A| |
S158 |
5 | BAA03g59480 | A03 | 29815493 | C | T | missense_variant | MODERATE | c.1285G>A|p.Ala429Thr |
S120 |
6 | BAA03g59480 | A03 | 29815709 | G | A | intron_variant | MODIFIER | c.1258-189C>T| |
S9 |
7 | BAA03g59480 | A03 | 29816084 | C | T | missense_variant | MODERATE | c.1213G>A|p.Glu405Lys |
S9 |
8 | BAA03g59480 | A03 | 29816176 | G | A | missense_variant | MODERATE | c.1121C>T|p.Ser374Leu |
S282 |
9 | BAA03g59480 | A03 | 29817085 | C | T | missense_variant | MODERATE | c.401G>A|p.Arg134Lys |
S113 |
10 | BAA03g59480 | A03 | 29817095 | C | T | missense_variant | MODERATE | c.391G>A|p.Val131Ile |
S139 |
11 | BAA03g59480 | A03 | 29817431 | G | A | missense_variant | MODERATE | c.55C>T|p.Pro19Ser |
S247 |
12 | BAA03g59480 | A03 | 29819129 | C | T | upstream_gene_variant | MODIFIER | c.-1644G>A| |
S11 |
13 | BAA03g59480 | A03 | 29821026 | C | T | upstream_gene_variant | MODIFIER | c.-3541G>A| |
S25 |
14 | BAA03g59480 | A03 | 29822132 | G | A | upstream_gene_variant | MODIFIER | c.-4647C>T| |
S73 S91 |