| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 196551 | BAA02g28960-BAA02g28970 | A02 | 16446663 | G | A | intergenic_region | MODIFIER | n.16446663G>A| |
S249 S36 |
| 196552 | BAA02g28960-BAA02g28970 | A02 | 16446999 | C | T | intergenic_region | MODIFIER | n.16446999C>T| |
S264 |
| 196553 | BAA02g28960-BAA02g28970 | A02 | 16447304 | C | T | intergenic_region | MODIFIER | n.16447304C>T| |
S107 |
| 196554 | BAA02g28960-BAA02g28970 | A02 | 16447874 | C | T | intergenic_region | MODIFIER | n.16447874C>T| |
S78 S83 |
| 196555 | BAA02g28970 | A02 | 16448668 | C | T | downstream_gene_variant | MODIFIER | c.*4686G>A| |
S308 |
| 196556 | BAA02g28970 | A02 | 16449342 | C | T | downstream_gene_variant | MODIFIER | c.*4012G>A| |
S10 S275 |
| 196557 | BAA02g28970 | A02 | 16449846 | C | T | downstream_gene_variant | MODIFIER | c.*3508G>A| |
S170 |
| 196558 | BAA02g28970 | A02 | 16450181 | G | A | downstream_gene_variant | MODIFIER | c.*3173C>T| |
S133 |
| 196559 | BAA02g28970 | A02 | 16450976 | C | T | downstream_gene_variant | MODIFIER | c.*2378G>A| |
S299 |
| 196560 | BAA02g28970 | A02 | 16451100 | C | T | downstream_gene_variant | MODIFIER | c.*2254G>A| |
S162 |
| 196561 | BAA02g28970 | A02 | 16451149 | C | T | downstream_gene_variant | MODIFIER | c.*2205G>A| |
S94 |
| 196562 | BAA02g28970 | A02 | 16451499 | C | T | downstream_gene_variant | MODIFIER | c.*1855G>A| |
S62 |
| 196563 | BAA02g28970 | A02 | 16451942 | C | T | downstream_gene_variant | MODIFIER | c.*1412G>A| |
S216 |
| 196564 | BAA02g28970 | A02 | 16452801 | C | T | downstream_gene_variant | MODIFIER | c.*553G>A| |
S224 |
| 196565 | BAA02g28970 | A02 | 16454670 | C | T | missense_variant | MODERATE | c.994G>A|p.Asp332Asn |
S1 S161 S228 S244 S289 S290 S90 |
| 196566 | BAA02g28970 | A02 | 16454740 | G | A | synonymous_variant | LOW | c.924C>T|p.Pro308Pro |
S36 |
| 196567 | BAA02g28970 | A02 | 16455032 | G | A | missense_variant | MODERATE | c.632C>T|p.Ala211Val |
S47 |
| 196568 | BAA02g28970 | A02 | 16455254 | C | T | missense_variant | MODERATE | c.410G>A|p.Arg137Lys |
S266 |
| 196569 | BAA02g28970 | A02 | 16456082 | G | A | upstream_gene_variant | MODIFIER | c.-419C>T| |
S126 |
| 196570 | BAA02g28970 | A02 | 16456709 | G | A | upstream_gene_variant | MODIFIER | c.-1046C>T| |
S17 |
| 196571 | BAA02g28970 | A02 | 16456937 | G | A | upstream_gene_variant | MODIFIER | c.-1274C>T| |
S241 |
| 196572 | BAA02g28970 | A02 | 16457474 | G | A | upstream_gene_variant | MODIFIER | c.-1811C>T| |
S302 |
| 196573 | BAA02g28970 | A02 | 16457604 | C | T | upstream_gene_variant | MODIFIER | c.-1941G>A| |
S305 |
| 196574 | BAA02g28970 | A02 | 16457999 | G | A | upstream_gene_variant | MODIFIER | c.-2336C>T| |
S249 |
| 196575 | BAA02g28970 | A02 | 16458621 | G | A | upstream_gene_variant | MODIFIER | c.-2958C>T| |
S263 |