Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65770 | A09 | 60423165 | G | A | missense_variant | MODERATE | c.956G>A|p.Arg319Lys |
S275 |
2 | BAA09g65770 | A09 | 60423263 | G | A | missense_variant | MODERATE | c.1054G>A|p.Gly352Ser |
S32 |
3 | BAA09g65770 | A09 | 60423439 | C | T | synonymous_variant | LOW | c.1230C>T|p.Ile410Ile |
S204 |
4 | BAA09g65770 | A09 | 60423444 | G | A | missense_variant | MODERATE | c.1235G>A|p.Cys412Tyr |
S178 |
5 | BAA09g65770 | A09 | 60424376 | C | T | downstream_gene_variant | MODIFIER | c.*700C>T| |
S237 |
6 | BAA09g65770 | A09 | 60425241 | C | T | downstream_gene_variant | MODIFIER | c.*1565C>T| |
S199 |
7 | BAA09g65770 | A09 | 60426637 | C | T | downstream_gene_variant | MODIFIER | c.*2961C>T| |
S208 S219 |
8 | BAA09g65770 | A09 | 60426942 | G | A | downstream_gene_variant | MODIFIER | c.*3266G>A| |
S172 S217 |
9 | BAA09g65770 | A09 | 60427981 | C | T | downstream_gene_variant | MODIFIER | c.*4305C>T| |
S239 |