Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46900 | A02 | 37986203 | C | T | missense_variant | MODERATE | c.637C>T|p.His213Tyr |
S170 |
2 | BAA02g46900 | A02 | 37986734 | G | A | missense_variant | MODERATE | c.950G>A|p.Gly317Glu |
S224 S261 |
3 | BAA02g46900 | A02 | 37986860 | G | A | missense_variant | MODERATE | c.1000G>A|p.Gly334Ser |
S278 |
4 | BAA02g46900 | A02 | 37987358 | C | T | missense_variant | MODERATE | c.1187C>T|p.Thr396Ile |
S173 |
5 | BAA02g46900 | A02 | 37987787 | G | A | missense_variant | MODERATE | c.1327G>A|p.Val443Met |
S25 |
6 | BAA02g46900 | A02 | 37988269 | C | T | missense_variant | MODERATE | c.1565C>T|p.Pro522Leu |
S160 |
7 | BAA02g46900 | A02 | 37992790 | G | A | downstream_gene_variant | MODIFIER | c.*3937G>A| |
S54 |
8 | BAA02g46900 | A02 | 37992850 | G | A | downstream_gene_variant | MODIFIER | c.*3997G>A| |
S103 |
9 | BAA02g46900 | A02 | 37992908 | G | A | downstream_gene_variant | MODIFIER | c.*4055G>A| |
S272 |
10 | BAA02g46900 | A02 | 37993145 | G | A | downstream_gene_variant | MODIFIER | c.*4292G>A| |
S302 |