Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03770 | A01 | 1708298 | G | A | missense_variant | MODERATE | c.337G>A|p.Val113Ile |
S263 |
2 | BAA01g03770 | A01 | 1710161 | G | A | missense_variant&splice_region_variant | MODERATE | c.1759G>A|p.Glu587Lys |
S156 |
3 | BAA01g03770 | A01 | 1710640 | G | A | missense_variant | MODERATE | c.1986G>A|p.Met662Ile |
S118 |
4 | BAA01g03770 | A01 | 1711774 | G | A | synonymous_variant | LOW | c.2514G>A|p.Glu838Glu |
S34 |
5 | BAA01g03770 | A01 | 1711782 | C | T | missense_variant | MODERATE | c.2522C>T|p.Thr841Ile |
S43 |
6 | BAA01g03770 | A01 | 1711997 | C | T | missense_variant | MODERATE | c.2641C>T|p.Pro881Ser |
S81 S85 |
7 | BAA01g03770 | A01 | 1713279 | C | T | missense_variant | MODERATE | c.3193C>T|p.Pro1065Ser |
S47 |
8 | BAA01g03770 | A01 | 1713771 | G | A | downstream_gene_variant | MODIFIER | c.*122G>A| |
S230 |