Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11790 | A02 | 5326955 | C | T | upstream_gene_variant | MODIFIER | c.-982C>T| |
S50 |
2 | BAA02g11790 | A02 | 5328164 | C | T | synonymous_variant | LOW | c.228C>T|p.Ser76Ser |
S308 |
3 | BAA02g11790 | A02 | 5328262 | G | A | missense_variant | MODERATE | c.326G>A|p.Arg109Lys |
S168 |
4 | BAA02g11790 | A02 | 5328350 | G | A | missense_variant | MODERATE | c.414G>A|p.Met138Ile |
S4 |
5 | BAA02g11790 | A02 | 5328422 | C | T | synonymous_variant | LOW | c.486C>T|p.Ser162Ser |
S182 |
6 | BAA02g11790 | A02 | 5334069 | G | A | downstream_gene_variant | MODIFIER | c.*4960G>A| |
S245 |