| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g09660 | A05 | 4894519 | C | T | synonymous_variant | LOW | c.1326G>A|p.Lys442Lys |
S211 S227 |
| 2 | BAA05g09660 | A05 | 4894623 | C | T | synonymous_variant | LOW | c.1302G>A|p.Thr434Thr |
S167 |
| 3 | BAA05g09660 | A05 | 4894884 | A | G | synonymous_variant | LOW | c.1041T>C|p.Cys347Cys |
S206 S26 |
| 4 | BAA05g09660 | A05 | 4895015 | C | T | missense_variant | MODERATE | c.910G>A|p.Val304Met |
S50 |
| 5 | BAA05g09660 | A05 | 4895108 | C | T | missense_variant | MODERATE | c.817G>A|p.Glu273Lys |
S105 S106 |
| 6 | BAA05g09660 | A05 | 4898342 | C | T | upstream_gene_variant | MODIFIER | c.-1804G>A| |
S287 |
| 7 | BAA05g09660 | A05 | 4899197 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S189 |
| 8 | BAA05g09660 | A05 | 4900297 | C | T | upstream_gene_variant | MODIFIER | c.-3759G>A| |
S36 |
| 9 | BAA05g09660 | A05 | 4900676 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S288 |
| 10 | BAA05g09660 | A05 | 4900866 | C | T | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S61 |
| 11 | BAA05g09660 | A05 | 4901090 | C | T | upstream_gene_variant | MODIFIER | c.-4552G>A| |
S19 |