Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17790 | A02 | 8847816 | G | A | synonymous_variant | LOW | c.1536C>T|p.Asn512Asn |
S35 |
2 | BAA02g17790 | A02 | 8850964 | G | A | intron_variant | MODIFIER | c.643-13C>T| |
S259 |
3 | BAA02g17790 | A02 | 8851260 | G | A | intron_variant | MODIFIER | c.470-40C>T| |
S289 S290 |
4 | BAA02g17790 | A02 | 8852864 | C | T | upstream_gene_variant | MODIFIER | c.-733G>A| |
S44 |
5 | BAA02g17790 | A02 | 8853114 | C | T | upstream_gene_variant | MODIFIER | c.-983G>A| |
S218 |
6 | BAA02g17790 | A02 | 8853223 | C | T | upstream_gene_variant | MODIFIER | c.-1092G>A| |
S8 |
7 | BAA02g17790 | A02 | 8854450 | C | T | upstream_gene_variant | MODIFIER | c.-2319G>A| |
S71 |
8 | BAA02g17790 | A02 | 8854744 | C | T | upstream_gene_variant | MODIFIER | c.-2613G>A| |
S138 |
9 | BAA02g17790 | A02 | 8854847 | C | T | upstream_gene_variant | MODIFIER | c.-2716G>A| |
S182 |