Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17160 | A02 | 8542269 | C | T | upstream_gene_variant | MODIFIER | c.-4675C>T| |
S64 |
2 | BAA02g17160 | A02 | 8547158 | C | T | synonymous_variant | LOW | c.96C>T|p.Leu32Leu |
S282 |
3 | BAA02g17160 | A02 | 8547159 | C | T | missense_variant | MODERATE | c.97C>T|p.Pro33Ser |
S34 |
4 | BAA02g17160 | A02 | 8548191 | G | A | synonymous_variant | LOW | c.1041G>A|p.Val347Val |
S197 |
5 | BAA02g17160 | A02 | 8548345 | G | A | missense_variant | MODERATE | c.1195G>A|p.Glu399Lys |
S202 |
6 | BAA02g17160 | A02 | 8548506 | G | A | synonymous_variant | LOW | c.1356G>A|p.Gly452Gly |
S4 |
7 | BAA02g17160 | A02 | 8549130 | C | T | missense_variant | MODERATE | c.1789C>T|p.His597Tyr |
S127 |
8 | BAA02g17160 | A02 | 8549203 | C | T | missense_variant | MODERATE | c.1862C>T|p.Ser621Phe |
S255 |
9 | BAA02g17160 | A02 | 8549232 | C | T | missense_variant | MODERATE | c.1891C>T|p.Arg631Cys |
S18 |
10 | BAA02g17160 | A02 | 8549318 | C | T | synonymous_variant | LOW | c.1977C>T|p.Leu659Leu |
S223 |
11 | BAA02g17160 | A02 | 8549361 | C | T | missense_variant | MODERATE | c.2020C>T|p.Pro674Ser |
S302 |
12 | BAA02g17160 | A02 | 8550533 | C | T | synonymous_variant | LOW | c.2838C>T|p.Leu946Leu |
S194 |
13 | BAA02g17160 | A02 | 8550783 | G | A | missense_variant | MODERATE | c.3088G>A|p.Asp1030Asn |
S69 |
14 | BAA02g17160 | A02 | 8552085 | G | A | downstream_gene_variant | MODIFIER | c.*1174G>A| |
S289 S290 |
15 | BAA02g17160 | A02 | 8552365 | G | A | downstream_gene_variant | MODIFIER | c.*1454G>A| |
S136 |