Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g17890 | A03 | 7871249 | C | T | upstream_gene_variant | MODIFIER | c.-2254C>T| |
S303 |
2 | BAA03g17890 | A03 | 7874924 | G | A | splice_region_variant&intron_variant | LOW | c.666+7G>A| |
S297 |
3 | BAA03g17890 | A03 | 7875145 | C | T | synonymous_variant | LOW | c.741C>T|p.Leu247Leu |
S139 |
4 | BAA03g17890 | A03 | 7875221 | G | A | missense_variant&splice_region_variant | MODERATE | c.817G>A|p.Gly273Arg |
S267 |
5 | BAA03g17890 | A03 | 7875894 | C | T | synonymous_variant | LOW | c.987C>T|p.Phe329Phe |
S19 |
6 | BAA03g17890 | A03 | 7876778 | G | A | missense_variant | MODERATE | c.1333G>A|p.Glu445Lys |
S160 |
7 | BAA03g17890 | A03 | 7877391 | G | A | downstream_gene_variant | MODIFIER | c.*206G>A| |
S118 |
8 | BAA03g17890 | A03 | 7878108 | G | A | downstream_gene_variant | MODIFIER | c.*923G>A| |
S185 |
9 | BAA03g17890 | A03 | 7878521 | C | T | downstream_gene_variant | MODIFIER | c.*1336C>T| |
S28 |