| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 18251 | BAA01g13630 | A01 | 6484069 | G | A | downstream_gene_variant | MODIFIER | c.*4879C>T| |
S238 |
| 18252 | BAA01g13630 | A01 | 6484439 | G | A | downstream_gene_variant | MODIFIER | c.*4509C>T| |
S208 S219 |
| 18253 | BAA01g13630 | A01 | 6484466 | G | A | downstream_gene_variant | MODIFIER | c.*4482C>T| |
S67 |
| 18254 | BAA01g13630 | A01 | 6484506 | C | T | downstream_gene_variant | MODIFIER | c.*4442G>A| |
S44 |
| 18255 | BAA01g13630 | A01 | 6485273 | G | A | downstream_gene_variant | MODIFIER | c.*3675C>T| |
S131 |
| 18256 | BAA01g13630 | A01 | 6485508 | C | T | downstream_gene_variant | MODIFIER | c.*3440G>A| |
S18 |
| 18257 | BAA01g13630 | A01 | 6485621 | G | A | downstream_gene_variant | MODIFIER | c.*3327C>T| |
S256 |
| 18258 | BAA01g13630 | A01 | 6488792 | A | C | downstream_gene_variant | MODIFIER | c.*156T>G| |
S272 S275 S73 |
| 18259 | BAA01g13630 | A01 | 6488834 | C | T | downstream_gene_variant | MODIFIER | c.*114G>A| |
S2 |
| 18260 | BAA01g13630 | A01 | 6489535 | G | A | upstream_gene_variant | MODIFIER | c.-99C>T| |
S259 |
| 18261 | BAA01g13630 | A01 | 6494430 | C | T | upstream_gene_variant | MODIFIER | c.-4994G>A| |
S247 |
| 18262 | BAA01g13640 | A01 | 6494516 | C | T | upstream_gene_variant | MODIFIER | c.-575C>T| |
S118 |
| 18263 | BAA01g13650 | A01 | 6496601 | G | A | upstream_gene_variant | MODIFIER | c.-1479G>A| |
S156 |
| 18264 | BAA01g13650 | A01 | 6498510 | C | T | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S61 |
| 18265 | BAA01g13650 | A01 | 6498772 | G | A | missense_variant | MODERATE | c.409G>A|p.Asp137Asn |
S149 |
| 18266 | BAA01g13650 | A01 | 6498790 | C | T | missense_variant | MODERATE | c.427C>T|p.Leu143Phe |
S291 |
| 18267 | BAA01g13650 | A01 | 6498866 | C | T | missense_variant | MODERATE | c.503C>T|p.Ser168Leu |
S16 |
| 18268 | BAA01g13650 | A01 | 6499118 | G | A | missense_variant | MODERATE | c.679G>A|p.Glu227Lys |
S172 S217 |
| 18269 | BAA01g13670 | A01 | 6499754 | C | T | upstream_gene_variant | MODIFIER | c.-3109C>T| |
S144 |
| 18270 | BAA01g13660 | A01 | 6502028 | G | A | upstream_gene_variant | MODIFIER | c.-392C>T| |
S162 |
| 18271 | BAA01g13670 | A01 | 6503086 | C | T | missense_variant | MODERATE | c.224C>T|p.Ser75Phe |
S69 |
| 18272 | BAA01g13670 | A01 | 6503437 | C | T | missense_variant | MODERATE | c.575C>T|p.Thr192Met |
S176 |
| 18273 | BAA01g13660 | A01 | 6506304 | G | A | upstream_gene_variant | MODIFIER | c.-4668C>T| |
S279 |
| 18274 | BAA01g13680 | A01 | 6506664 | C | T | downstream_gene_variant | MODIFIER | c.*3623G>A| |
S153 |
| 18275 | BAA01g13670 | A01 | 6506810 | G | A | missense_variant | MODERATE | c.2416G>A|p.Val806Ile |
S259 |