| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 166251 | BAA02g12340 | A02 | 5555665 | G | A | missense_variant | MODERATE | c.554G>A|p.Gly185Glu |
S89 |
| 166252 | BAA02g12340 | A02 | 5555911 | G | A | missense_variant | MODERATE | c.800G>A|p.Gly267Glu |
S166 |
| 166253 | BAA02g12360 | A02 | 5557520 | G | A | upstream_gene_variant | MODIFIER | c.-1296G>A| |
S165 |
| 166254 | BAA02g12360 | A02 | 5558394 | C | T | upstream_gene_variant | MODIFIER | c.-422C>T| |
S157 S163 |
| 166255 | BAA02g12360 | A02 | 5559736 | G | A | missense_variant | MODERATE | c.659G>A|p.Gly220Glu |
S168 |
| 166256 | BAA02g12360 | A02 | 5560331 | G | A | missense_variant | MODERATE | c.1010G>A|p.Gly337Glu |
S236 |
| 166257 | BAA02g12340 | A02 | 5560711 | C | T | downstream_gene_variant | MODIFIER | c.*4538C>T| |
S54 |
| 166258 | BAA02g12340 | A02 | 5560972 | C | T | downstream_gene_variant | MODIFIER | c.*4799C>T| |
S144 |
| 166259 | BAA02g12360 | A02 | 5561275 | G | A | missense_variant | MODERATE | c.1648G>A|p.Ala550Thr |
S271 |
| 166260 | BAA02g12350 | A02 | 5562042 | C | T | downstream_gene_variant | MODIFIER | c.*4603C>T| |
S135 |
| 166261 | BAA02g12380 | A02 | 5565457 | C | T | upstream_gene_variant | MODIFIER | c.-2781C>T| |
S172 S217 |
| 166262 | BAA02g12370 | A02 | 5565972 | C | T | missense_variant | MODERATE | c.379G>A|p.Ala127Thr |
S183 S198 |
| 166263 | BAA02g12370 | A02 | 5565997 | C | T | synonymous_variant | LOW | c.354G>A|p.Leu118Leu |
S283 |
| 166264 | BAA02g12370 | A02 | 5566155 | G | A | missense_variant | MODERATE | c.196C>T|p.His66Tyr |
S25 |
| 166265 | BAA02g12370 | A02 | 5566177 | C | T | stop_gained | HIGH | c.174G>A|p.Trp58* |
S257 |
| 166266 | BAA02g12380 | A02 | 5568404 | C | T | missense_variant | MODERATE | c.167C>T|p.Ala56Val |
S123 |
| 166267 | BAA02g12380 | A02 | 5568422 | G | A | missense_variant | MODERATE | c.185G>A|p.Arg62Lys |
S207 |
| 166268 | BAA02g12380 | A02 | 5568598 | G | A | missense_variant&splice_region_variant | MODERATE | c.361G>A|p.Glu121Lys |
S260 |
| 166269 | BAA02g12380 | A02 | 5568964 | C | T | synonymous_variant | LOW | c.637C>T|p.Leu213Leu |
S165 |
| 166270 | BAA02g12390 | A02 | 5571409 | C | T | missense_variant | MODERATE | c.509G>A|p.Gly170Glu |
S219 S72 |
| 166271 | BAA02g12390 | A02 | 5571849 | G | A | synonymous_variant | LOW | c.69C>T|p.Ser23Ser |
S17 |
| 166272 | BAA02g12390 | A02 | 5572558 | C | T | upstream_gene_variant | MODIFIER | c.-641G>A| |
S196 |
| 166273 | BAA02g12390 | A02 | 5572741 | C | T | upstream_gene_variant | MODIFIER | c.-824G>A| |
S246 |
| 166274 | BAA02g12390 | A02 | 5572761 | G | A | upstream_gene_variant | MODIFIER | c.-844C>T| |
S11 |
| 166275 | BAA02g12400 | A02 | 5573134 | G | A | missense_variant | MODERATE | c.244G>A|p.Ala82Thr |
S170 |