Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27990 | A01 | 17077667 | G | A | downstream_gene_variant | MODIFIER | c.*1401C>T| |
S1 S90 |
2 | BAA01g27990 | A01 | 17079919 | G | A | missense_variant | MODERATE | c.1618C>T|p.Arg540Cys |
S209 |
3 | BAA01g27990 | A01 | 17080028 | G | A | synonymous_variant | LOW | c.1509C>T|p.His503His |
S36 |
4 | BAA01g27990 | A01 | 17080060 | C | T | missense_variant | MODERATE | c.1477G>A|p.Ala493Thr |
S128 |
5 | BAA01g27990 | A01 | 17080075 | C | T | missense_variant | MODERATE | c.1462G>A|p.Ala488Thr |
S136 |
6 | BAA01g27990 | A01 | 17080151 | G | A | synonymous_variant | LOW | c.1386C>T|p.Arg462Arg |
S195 |