| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 124051 | BAA10g13780 | A10 | 14736203 | C | T | upstream_gene_variant | MODIFIER | c.-260C>T| |
S44 |
| 124052 | BAA10g13780 | A10 | 14736337 | G | T | upstream_gene_variant | MODIFIER | c.-126G>T| |
S292 |
| 124053 | BAA10g13790 | A10 | 14736670 | C | T | upstream_gene_variant | MODIFIER | c.-775C>T| |
S275 |
| 124054 | BAA10g13790 | A10 | 14737158 | G | A | upstream_gene_variant | MODIFIER | c.-287G>A| |
S223 |
| 124055 | BAA10g13790 | A10 | 14737495 | G | A | stop_gained | HIGH | c.51G>A|p.Trp17* |
S69 |
| 124056 | BAA10g13770 | A10 | 14739083 | C | T | downstream_gene_variant | MODIFIER | c.*3266C>T| |
S297 |
| 124057 | BAA10g13770 | A10 | 14739259 | C | T | downstream_gene_variant | MODIFIER | c.*3442C>T| |
S204 |
| 124058 | BAA10g13770 | A10 | 14740431 | G | A | downstream_gene_variant | MODIFIER | c.*4614G>A| |
S292 |
| 124059 | BAA10g13770 | A10 | 14740599 | G | A | downstream_gene_variant | MODIFIER | c.*4782G>A| |
S69 |
| 124060 | BAA10g13780 | A10 | 14740964 | A | T | downstream_gene_variant | MODIFIER | c.*4319A>T| |
S230 |
| 124061 | BAA10g13780 | A10 | 14741426 | C | T | downstream_gene_variant | MODIFIER | c.*4781C>T| |
S233 |
| 124062 | BAA10g13790 | A10 | 14742971 | C | T | downstream_gene_variant | MODIFIER | c.*4042C>T| |
S188 |
| 124063 | BAA10g13800 | A10 | 14744941 | G | A | downstream_gene_variant | MODIFIER | c.*1923C>T| |
S159 S243 |
| 124064 | BAA10g13810 | A10 | 14745959 | C | T | upstream_gene_variant | MODIFIER | c.-4295C>T| |
S23 |
| 124065 | BAA10g13810 | A10 | 14746648 | C | T | upstream_gene_variant | MODIFIER | c.-3606C>T| |
S133 |
| 124066 | BAA10g13810 | A10 | 14747474 | G | A | upstream_gene_variant | MODIFIER | c.-2780G>A| |
S163 |
| 124067 | BAA10g13800 | A10 | 14748662 | G | A | upstream_gene_variant | MODIFIER | c.-596C>T| |
S43 |
| 124068 | BAA10g13800 | A10 | 14748984 | G | A | upstream_gene_variant | MODIFIER | c.-918C>T| |
S95 |
| 124069 | BAA10g13810 | A10 | 14750379 | C | T | missense_variant | MODERATE | c.98C>T|p.Pro33Leu |
S168 |
| 124070 | BAA10g13810 | A10 | 14750713 | G | A | missense_variant | MODERATE | c.334G>A|p.Ala112Thr |
S78 S83 |
| 124071 | BAA10g13810 | A10 | 14750726 | G | A | missense_variant | MODERATE | c.347G>A|p.Gly116Glu |
S34 |
| 124072 | BAA10g13800 | A10 | 14750782 | G | A | upstream_gene_variant | MODIFIER | c.-2716C>T| |
S79 |
| 124073 | BAA10g13800 | A10 | 14751536 | G | A | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S129 |
| 124074 | BAA10g13800 | A10 | 14752807 | G | A | upstream_gene_variant | MODIFIER | c.-4741C>T| |
S125 |
| 124075 | BAA10g13830 | A10 | 14753255 | C | T | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S136 |