| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 38051 | BAA01g24570 | A01 | 13074171 | G | A | downstream_gene_variant | MODIFIER | c.*818G>A| |
S280 |
| 38052 | BAA01g24580 | A01 | 13079302 | C | T | downstream_gene_variant | MODIFIER | c.*1282G>A| |
S130 |
| 38053 | BAA01g24580 | A01 | 13079497 | G | A | downstream_gene_variant | MODIFIER | c.*1087C>T| |
S172 S217 |
| 38054 | BAA01g24580 | A01 | 13080608 | G | A | synonymous_variant | LOW | c.300C>T|p.Arg100Arg |
S203 |
| 38055 | BAA01g24580 | A01 | 13080661 | C | T | missense_variant | MODERATE | c.247G>A|p.Asp83Asn |
S107 |
| 38056 | BAA01g24580 | A01 | 13080881 | C | T | synonymous_variant | LOW | c.93G>A|p.Lys31Lys |
S4 |
| 38057 | BAA01g24580 | A01 | 13081296 | C | T | upstream_gene_variant | MODIFIER | c.-323G>A| |
S270 |
| 38058 | BAA01g24580 | A01 | 13081602 | G | A | upstream_gene_variant | MODIFIER | c.-629C>T| |
S187 |
| 38059 | BAA01g24580 | A01 | 13083645 | G | A | upstream_gene_variant | MODIFIER | c.-2672C>T| |
S249 |
| 38060 | BAA01g24590 | A01 | 13084718 | C | T | missense_variant | MODERATE | c.334G>A|p.Asp112Asn |
S41 |
| 38061 | BAA01g24590 | A01 | 13084771 | C | T | missense_variant | MODERATE | c.281G>A|p.Gly94Asp |
S210 S225 |
| 38062 | BAA01g24580 | A01 | 13085179 | G | A | upstream_gene_variant | MODIFIER | c.-4206C>T| |
S23 |
| 38063 | BAA01g24590 | A01 | 13086379 | C | T | upstream_gene_variant | MODIFIER | c.-1328G>A| |
S20 |
| 38064 | BAA01g24590 | A01 | 13088421 | G | A | upstream_gene_variant | MODIFIER | c.-3370C>T| |
S56 |
| 38065 | BAA01g24590 | A01 | 13088951 | T | G | upstream_gene_variant | MODIFIER | c.-3900A>C| |
S163 |
| 38066 | BAA01g24590 | A01 | 13089093 | C | T | upstream_gene_variant | MODIFIER | c.-4042G>A| |
S256 |
| 38067 | BAA01g24590 | A01 | 13089586 | G | A | upstream_gene_variant | MODIFIER | c.-4535C>T| |
S138 |
| 38068 | BAA01g24600 | A01 | 13089868 | C | T | missense_variant | MODERATE | c.202C>T|p.His68Tyr |
S57 |
| 38069 | BAA01g24600 | A01 | 13090521 | C | T | missense_variant | MODERATE | c.308C>T|p.Pro103Leu |
S4 |
| 38070 | BAA01g24610 | A01 | 13090604 | G | A | downstream_gene_variant | MODIFIER | c.*4013C>T| |
S63 |
| 38071 | BAA01g24610 | A01 | 13090720 | C | T | downstream_gene_variant | MODIFIER | c.*3897G>A| |
S47 |
| 38072 | BAA01g24600 | A01 | 13091545 | G | A | downstream_gene_variant | MODIFIER | c.*515G>A| |
S261 |
| 38073 | BAA01g24600 | A01 | 13091561 | G | A | downstream_gene_variant | MODIFIER | c.*531G>A| |
S124 |
| 38074 | BAA01g24600 | A01 | 13091908 | C | T | downstream_gene_variant | MODIFIER | c.*878C>T| |
S53 |
| 38075 | BAA01g24600 | A01 | 13093984 | C | T | downstream_gene_variant | MODIFIER | c.*2954C>T| |
S305 |