| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 163401 | BAA02g10150 | A02 | 4493631 | C | T | downstream_gene_variant | MODIFIER | c.*2301G>A| |
S270 |
| 163402 | BAA02g10150 | A02 | 4494136 | C | T | downstream_gene_variant | MODIFIER | c.*1796G>A| |
S138 |
| 163403 | BAA02g10150 | A02 | 4494453 | C | T | downstream_gene_variant | MODIFIER | c.*1479G>A| |
S121 |
| 163404 | BAA02g10150 | A02 | 4494698 | G | A | downstream_gene_variant | MODIFIER | c.*1234C>T| |
S169 |
| 163405 | BAA02g10150 | A02 | 4494735 | C | T | downstream_gene_variant | MODIFIER | c.*1197G>A| |
S267 |
| 163406 | BAA02g10150 | A02 | 4494827 | C | T | downstream_gene_variant | MODIFIER | c.*1105G>A| |
S257 |
| 163407 | BAA02g10150 | A02 | 4494872 | C | T | downstream_gene_variant | MODIFIER | c.*1060G>A| |
S135 |
| 163408 | BAA02g10150 | A02 | 4494960 | C | T | downstream_gene_variant | MODIFIER | c.*972G>A| |
S157 |
| 163409 | BAA02g10150 | A02 | 4496534 | C | T | splice_donor_variant&intron_variant | HIGH | c.833+1G>A| |
S65 S67 |
| 163410 | BAA02g10150 | A02 | 4496849 | G | A | synonymous_variant | LOW | c.519C>T|p.Tyr173Tyr |
S173 |
| 163411 | BAA02g10150 | A02 | 4497923 | C | T | upstream_gene_variant | MODIFIER | c.-556G>A| |
S216 |
| 163412 | BAA02g10150 | A02 | 4498183 | C | T | upstream_gene_variant | MODIFIER | c.-816G>A| |
S234 |
| 163413 | BAA02g10150 | A02 | 4498389 | C | T | upstream_gene_variant | MODIFIER | c.-1022G>A| |
S58 |
| 163414 | BAA02g10150 | A02 | 4499913 | G | A | upstream_gene_variant | MODIFIER | c.-2546C>T| |
S23 |
| 163415 | BAA02g10150 | A02 | 4501547 | C | T | upstream_gene_variant | MODIFIER | c.-4180G>A| |
S178 |
| 163416 | BAA02g10150 | A02 | 4502167 | G | A | upstream_gene_variant | MODIFIER | c.-4800C>T| |
S173 |
| 163417 | BAA02g10150-BAA02g10160 | A02 | 4502711 | G | A | intergenic_region | MODIFIER | n.4502711G>A| |
S45 |
| 163418 | BAA02g10160 | A02 | 4503726 | C | A | upstream_gene_variant | MODIFIER | c.-4772C>A| |
S262 |
| 163419 | BAA02g10160 | A02 | 4504012 | G | A | upstream_gene_variant | MODIFIER | c.-4486G>A| |
S282 |
| 163420 | BAA02g10160 | A02 | 4504063 | C | T | upstream_gene_variant | MODIFIER | c.-4435C>T| |
S289 S290 |
| 163421 | BAA02g10160 | A02 | 4504677 | G | A | upstream_gene_variant | MODIFIER | c.-3821G>A| |
S203 |
| 163422 | BAA02g10160 | A02 | 4505849 | C | T | upstream_gene_variant | MODIFIER | c.-2649C>T| |
S263 |
| 163423 | BAA02g10160 | A02 | 4506395 | G | A | upstream_gene_variant | MODIFIER | c.-2103G>A| |
S168 |
| 163424 | BAA02g10160 | A02 | 4508634 | C | T | missense_variant | MODERATE | c.137C>T|p.Thr46Ile |
S242 |
| 163425 | BAA02g10160 | A02 | 4509130 | G | A | stop_gained | HIGH | c.633G>A|p.Trp211* |
S263 |