Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17490 | A02 | 8707286 | G | A | upstream_gene_variant | MODIFIER | c.-4842G>A| |
S132 S137 S138 S215 S237 S288 S89 |
2 | BAA02g17490 | A02 | 8708149 | G | A | upstream_gene_variant | MODIFIER | c.-3979G>A| |
S98 |
3 | BAA02g17490 | A02 | 8709422 | C | T | upstream_gene_variant | MODIFIER | c.-2706C>T| |
S219 |
4 | BAA02g17490 | A02 | 8711281 | G | A | upstream_gene_variant | MODIFIER | c.-847G>A| |
S197 |
5 | BAA02g17490 | A02 | 8711284 | G | A | upstream_gene_variant | MODIFIER | c.-844G>A| |
S59 |
6 | BAA02g17490 | A02 | 8713106 | C | T | synonymous_variant | LOW | c.567C>T|p.Leu189Leu |
S293 |
7 | BAA02g17490 | A02 | 8713375 | C | T | missense_variant | MODERATE | c.767C>T|p.Ala256Val |
S87 |
8 | BAA02g17490 | A02 | 8713610 | G | A | missense_variant | MODERATE | c.929G>A|p.Gly310Asp |
S95 |
9 | BAA02g17490 | A02 | 8714131 | C | T | synonymous_variant | LOW | c.1377C>T|p.Ile459Ile |
S156 S34 |
10 | BAA02g17490 | A02 | 8714277 | C | T | missense_variant | MODERATE | c.1523C>T|p.Ser508Phe |
S44 |
11 | BAA02g17490 | A02 | 8714773 | C | T | synonymous_variant | LOW | c.2019C>T|p.Ser673Ser |
S71 |