Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17770 | A02 | 8840886 | G | A | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S166 |
2 | BAA02g17770 | A02 | 8841273 | C | T | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S121 |
3 | BAA02g17770 | A02 | 8841863 | C | T | upstream_gene_variant | MODIFIER | c.-438C>T| |
S228 |
4 | BAA02g17770 | A02 | 8842315 | C | T | synonymous_variant | LOW | c.15C>T|p.Ala5Ala |
S208 S219 |
5 | BAA02g17770 | A02 | 8842991 | G | A | missense_variant | MODERATE | c.380G>A|p.Arg127Gln |
S263 |
6 | BAA02g17770 | A02 | 8843357 | C | T | splice_region_variant&intron_variant | LOW | c.579+6C>T| |
S292 |