| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 172101 | BAA02g15970 | A02 | 7784543 | G | A | downstream_gene_variant | MODIFIER | c.*1086G>A| |
S59 |
| 172102 | BAA02g15970 | A02 | 7784658 | G | A | downstream_gene_variant | MODIFIER | c.*1201G>A| |
S210 |
| 172103 | BAA02g15970 | A02 | 7785113 | G | A | downstream_gene_variant | MODIFIER | c.*1656G>A| |
S229 |
| 172104 | BAA02g15970 | A02 | 7785303 | C | T | downstream_gene_variant | MODIFIER | c.*1846C>T| |
S200 |
| 172105 | BAA02g15970 | A02 | 7785825 | C | T | downstream_gene_variant | MODIFIER | c.*2368C>T| |
S299 |
| 172106 | BAA02g15970 | A02 | 7786026 | G | A | downstream_gene_variant | MODIFIER | c.*2569G>A| |
S289 S290 |
| 172107 | BAA02g15970 | A02 | 7786673 | G | A | downstream_gene_variant | MODIFIER | c.*3216G>A| |
S28 |
| 172108 | BAA02g15980 | A02 | 7787970 | C | T | upstream_gene_variant | MODIFIER | c.-552G>A| |
S34 |
| 172109 | BAA02g15980 | A02 | 7788225 | G | A | upstream_gene_variant | MODIFIER | c.-807C>T| |
S288 |
| 172110 | BAA02g15980 | A02 | 7788638 | G | A | upstream_gene_variant | MODIFIER | c.-1220C>T| |
S156 |
| 172111 | BAA02g15980 | A02 | 7788679 | G | A | upstream_gene_variant | MODIFIER | c.-1261C>T| |
S139 |
| 172112 | BAA02g15990 | A02 | 7795025 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S191 |
| 172113 | BAA02g16000 | A02 | 7795122 | C | T | downstream_gene_variant | MODIFIER | c.*1766G>A| |
S244 |
| 172114 | BAA02g16000 | A02 | 7795962 | C | T | downstream_gene_variant | MODIFIER | c.*926G>A| |
S38 |
| 172115 | BAA02g16000 | A02 | 7796270 | C | T | downstream_gene_variant | MODIFIER | c.*618G>A| |
S182 |
| 172116 | BAA02g16000 | A02 | 7796401 | G | A | downstream_gene_variant | MODIFIER | c.*487C>T| |
S11 |
| 172117 | BAA02g16000 | A02 | 7797302 | C | T | synonymous_variant | LOW | c.354G>A|p.Glu118Glu |
S42 |
| 172118 | BAA02g16000 | A02 | 7797307 | C | T | missense_variant | MODERATE | c.349G>A|p.Ala117Thr |
S182 |
| 172119 | BAA02g16000 | A02 | 7798496 | G | A | upstream_gene_variant | MODIFIER | c.-841C>T| |
S59 |
| 172120 | BAA02g16000 | A02 | 7799803 | C | T | upstream_gene_variant | MODIFIER | c.-2148G>A| |
S195 |
| 172121 | BAA02g16000 | A02 | 7800584 | G | A | upstream_gene_variant | MODIFIER | c.-2929C>T| |
S61 |
| 172122 | BAA02g16000 | A02 | 7801118 | C | T | upstream_gene_variant | MODIFIER | c.-3463G>A| |
S200 |
| 172123 | BAA02g16000 | A02 | 7801211 | A | G | upstream_gene_variant | MODIFIER | c.-3556T>C| |
S268 |
| 172124 | BAA02g16000 | A02 | 7801416 | C | T | upstream_gene_variant | MODIFIER | c.-3761G>A| |
S276 |
| 172125 | BAA02g16000 | A02 | 7801607 | C | T | upstream_gene_variant | MODIFIER | c.-3952G>A| |
S167 |