Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21050 | A02 | 11270363 | C | T | downstream_gene_variant | MODIFIER | c.*2002G>A| |
S99 |
2 | BAA02g21050 | A02 | 11270996 | G | A | downstream_gene_variant | MODIFIER | c.*1369C>T| |
S251 S258 |
3 | BAA02g21050 | A02 | 11271797 | G | A | downstream_gene_variant | MODIFIER | c.*568C>T| |
S134 |
4 | BAA02g21050 | A02 | 11271922 | G | A | downstream_gene_variant | MODIFIER | c.*443C>T| |
S223 |
5 | BAA02g21050 | A02 | 11272456 | G | A | missense_variant | MODERATE | c.614C>T|p.Ser205Leu |
S134 |
6 | BAA02g21050 | A02 | 11272672 | G | A | missense_variant | MODERATE | c.398C>T|p.Ala133Val |
S12 |
7 | BAA02g21050 | A02 | 11273105 | G | A | synonymous_variant | LOW | c.39C>T|p.His13His |
S132 S137 S215 |
8 | BAA02g21050 | A02 | 11273132 | G | A | synonymous_variant | LOW | c.12C>T|p.Ser4Ser |
S149 |
9 | BAA02g21050 | A02 | 11273405 | G | A | upstream_gene_variant | MODIFIER | c.-262C>T| |
S282 |
10 | BAA02g21050 | A02 | 11273565 | G | A | upstream_gene_variant | MODIFIER | c.-422C>T| |
S28 |