Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17200 | A02 | 8561759 | C | T | missense_variant | MODERATE | c.949G>A|p.Asp317Asn |
S255 |
2 | BAA02g17200 | A02 | 8562062 | C | T | missense_variant | MODERATE | c.646G>A|p.Asp216Asn |
S65 |
3 | BAA02g17200 | A02 | 8562948 | G | A | missense_variant | MODERATE | c.115C>T|p.Pro39Ser |
S162 |
4 | BAA02g17200 | A02 | 8563039 | C | T | synonymous_variant | LOW | c.24G>A|p.Thr8Thr |
S130 |
5 | BAA02g17200 | A02 | 8564724 | G | A | upstream_gene_variant | MODIFIER | c.-1662C>T| |
S294 |
6 | BAA02g17200 | A02 | 8564977 | G | A | upstream_gene_variant | MODIFIER | c.-1915C>T| |
S291 |
7 | BAA02g17200 | A02 | 8566630 | C | T | upstream_gene_variant | MODIFIER | c.-3568G>A| |
S25 |
8 | BAA02g17200 | A02 | 8567668 | C | T | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S292 |