Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66050 | A03 | 40340554 | C | T | upstream_gene_variant | MODIFIER | c.-2361C>T| |
S179 |
2 | BAA03g66050 | A03 | 40341145 | G | A | upstream_gene_variant | MODIFIER | c.-1770G>A| |
S275 |
3 | BAA03g66050 | A03 | 40341436 | C | T | upstream_gene_variant | MODIFIER | c.-1479C>T| |
S136 |
4 | BAA03g66050 | A03 | 40342204 | C | T | upstream_gene_variant | MODIFIER | c.-711C>T| |
S8 |
5 | BAA03g66050 | A03 | 40342207 | G | A | upstream_gene_variant | MODIFIER | c.-708G>A| |
S247 |
6 | BAA03g66050 | A03 | 40342251 | C | T | upstream_gene_variant | MODIFIER | c.-664C>T| |
S246 |
7 | BAA03g66050 | A03 | 40342552 | G | A | upstream_gene_variant | MODIFIER | c.-363G>A| |
S153 S213 |
8 | BAA03g66050 | A03 | 40343192 | C | T | missense_variant | MODERATE | c.278C>T|p.Thr93Ile |
S208 |
9 | BAA03g66050 | A03 | 40343777 | T | A | missense_variant | MODERATE | c.599T>A|p.Ile200Asn |
S281 |
10 | BAA03g66050 | A03 | 40344264 | C | T | synonymous_variant | LOW | c.840C>T|p.Tyr280Tyr |
S195 |
11 | BAA03g66050 | A03 | 40350499 | C | T | downstream_gene_variant | MODIFIER | c.*4812C>T| |
S187 |