| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 162351 | BAA02g09270 | A02 | 4097515 | C | T | missense_variant | MODERATE | c.481C>T|p.Leu161Phe |
S112 |
| 162352 | BAA02g09260 | A02 | 4098583 | C | T | upstream_gene_variant | MODIFIER | c.-4991G>A| |
S226 |
| 162353 | BAA02g09280 | A02 | 4098662 | C | T | upstream_gene_variant | MODIFIER | c.-620C>T| |
S108 |
| 162354 | BAA02g09280 | A02 | 4099224 | G | A | upstream_gene_variant | MODIFIER | c.-58G>A| |
S110 |
| 162355 | BAA02g09280 | A02 | 4099300 | G | A | missense_variant | MODERATE | c.19G>A|p.Ala7Thr |
S159 S243 |
| 162356 | BAA02g09290 | A02 | 4099706 | C | T | upstream_gene_variant | MODIFIER | c.-2222C>T| |
S278 |
| 162357 | BAA02g09290 | A02 | 4101418 | C | T | upstream_gene_variant | MODIFIER | c.-510C>T| |
S241 |
| 162358 | BAA02g09290 | A02 | 4101979 | C | T | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S118 |
| 162359 | BAA02g09270 | A02 | 4102459 | C | T | downstream_gene_variant | MODIFIER | c.*4072C>T| |
S64 |
| 162360 | BAA02g09290 | A02 | 4103032 | G | A | missense_variant | MODERATE | c.878G>A|p.Gly293Glu |
S173 |
| 162361 | BAA02g09270 | A02 | 4103101 | C | T | downstream_gene_variant | MODIFIER | c.*4714C>T| |
S94 |
| 162362 | BAA02g09280 | A02 | 4103464 | C | T | downstream_gene_variant | MODIFIER | c.*2575C>T| |
S276 |
| 162363 | BAA02g09280 | A02 | 4103533 | C | T | downstream_gene_variant | MODIFIER | c.*2644C>T| |
S274 |
| 162364 | BAA02g09280 | A02 | 4103639 | G | A | downstream_gene_variant | MODIFIER | c.*2750G>A| |
S166 |
| 162365 | BAA02g09280 | A02 | 4103779 | G | A | downstream_gene_variant | MODIFIER | c.*2890G>A| |
S237 |
| 162366 | BAA02g09280 | A02 | 4104276 | G | A | downstream_gene_variant | MODIFIER | c.*3387G>A| |
S295 |
| 162367 | BAA02g09300 | A02 | 4105138 | G | A | missense_variant | MODERATE | c.137C>T|p.Ser46Phe |
S176 |
| 162368 | BAA02g09300 | A02 | 4105273 | G | A | missense_variant&splice_region_variant | MODERATE | c.98C>T|p.Ala33Val |
S293 |
| 162369 | BAA02g09300 | A02 | 4105364 | C | T | missense_variant | MODERATE | c.7G>A|p.Ala3Thr |
S185 |
| 162370 | BAA02g09300 | A02 | 4106773 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S80 |
| 162371 | BAA02g09300 | A02 | 4107064 | C | T | upstream_gene_variant | MODIFIER | c.-1694G>A| |
S16 |
| 162372 | BAA02g09300 | A02 | 4107489 | G | A | upstream_gene_variant | MODIFIER | c.-2119C>T| |
S289 S290 |
| 162373 | BAA02g09310 | A02 | 4108481 | C | T | synonymous_variant | LOW | c.225G>A|p.Glu75Glu |
S255 |
| 162374 | BAA02g09300 | A02 | 4109416 | C | T | upstream_gene_variant | MODIFIER | c.-4046G>A| |
S251 |
| 162375 | BAA02g09300 | A02 | 4109525 | C | T | upstream_gene_variant | MODIFIER | c.-4155G>A| |
S202 |