Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g30120 | A03 | 14095482 | G | A | intron_variant | MODIFIER | c.263+23G>A| |
S236 |
2 | BAA03g30120 | A03 | 14095603 | A | T | splice_region_variant&intron_variant | LOW | c.342+3A>T| |
S124 |
3 | BAA03g30120 | A03 | 14095629 | C | T | intron_variant | MODIFIER | c.342+29C>T| |
S165 |
4 | BAA03g30120 | A03 | 14095680 | C | T | missense_variant | MODERATE | c.355C>T|p.Pro119Ser |
S156 |
5 | BAA03g30120 | A03 | 14095901 | G | A | missense_variant | MODERATE | c.508G>A|p.Gly170Arg |
S119 |
6 | BAA03g30120 | A03 | 14097786 | C | T | missense_variant | MODERATE | c.1325C>T|p.Ala442Val |
S85 |
7 | BAA03g30120 | A03 | 14099475 | G | A | missense_variant&splice_region_variant | MODERATE | c.2413G>A|p.Gly805Arg |
S286 |
8 | BAA03g30120 | A03 | 14100018 | G | A | missense_variant | MODERATE | c.2605G>A|p.Asp869Asn |
S272 |
9 | BAA03g30120 | A03 | 14100875 | C | T | downstream_gene_variant | MODIFIER | c.*825C>T| |
S19 |