| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167351 | BAA02g13120 | A02 | 5901279 | G | A | upstream_gene_variant | MODIFIER | c.-2969G>A| |
S213 |
| 167352 | BAA02g13120 | A02 | 5901449 | G | A | upstream_gene_variant | MODIFIER | c.-2799G>A| |
S162 |
| 167353 | BAA02g13120 | A02 | 5901987 | G | A | upstream_gene_variant | MODIFIER | c.-2261G>A| |
S302 |
| 167354 | BAA02g13120 | A02 | 5902500 | C | T | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S261 |
| 167355 | BAA02g13120 | A02 | 5904044 | G | A | upstream_gene_variant | MODIFIER | c.-204G>A| |
S153 S213 |
| 167356 | BAA02g13120 | A02 | 5905100 | G | A | missense_variant | MODERATE | c.389G>A|p.Arg130His |
S166 |
| 167357 | BAA02g13120 | A02 | 5905364 | C | T | missense_variant | MODERATE | c.653C>T|p.Ala218Val |
S206 S26 |
| 167358 | BAA02g13120 | A02 | 5906218 | C | T | missense_variant | MODERATE | c.1262C>T|p.Thr421Ile |
S120 |
| 167359 | BAA02g13120 | A02 | 5906863 | G | A | missense_variant | MODERATE | c.1825G>A|p.Ala609Thr |
S36 |
| 167360 | BAA02g13120 | A02 | 5907398 | G | A | downstream_gene_variant | MODIFIER | c.*482G>A| |
S17 |
| 167361 | BAA02g13120 | A02 | 5907660 | G | A | downstream_gene_variant | MODIFIER | c.*744G>A| |
S68 |
| 167362 | BAA02g13120 | A02 | 5907939 | G | A | downstream_gene_variant | MODIFIER | c.*1023G>A| |
S106 |
| 167363 | BAA02g13120 | A02 | 5908276 | G | A | downstream_gene_variant | MODIFIER | c.*1360G>A| |
S187 |
| 167364 | BAA02g13120 | A02 | 5908733 | G | A | downstream_gene_variant | MODIFIER | c.*1817G>A| |
S268 |
| 167365 | BAA02g13120 | A02 | 5910447 | C | T | downstream_gene_variant | MODIFIER | c.*3531C>T| |
S120 |
| 167366 | BAA02g13120 | A02 | 5911527 | G | A | downstream_gene_variant | MODIFIER | c.*4611G>A| |
S50 |
| 167367 | BAA02g13130 | A02 | 5918107 | G | A | upstream_gene_variant | MODIFIER | c.-4504G>A| |
S56 |
| 167368 | BAA02g13130 | A02 | 5918665 | C | T | upstream_gene_variant | MODIFIER | c.-3946C>T| |
S78 |
| 167369 | BAA02g13130 | A02 | 5919313 | G | A | upstream_gene_variant | MODIFIER | c.-3298G>A| |
S302 |
| 167370 | BAA02g13130 | A02 | 5920953 | C | T | upstream_gene_variant | MODIFIER | c.-1658C>T| |
S167 |
| 167371 | BAA02g13130 | A02 | 5923263 | C | T | downstream_gene_variant | MODIFIER | c.*248C>T| |
S99 |
| 167372 | BAA02g13140 | A02 | 5924248 | C | T | stop_gained | HIGH | c.666G>A|p.Trp222* |
S216 |
| 167373 | BAA02g13140 | A02 | 5924588 | G | A | missense_variant | MODERATE | c.410C>T|p.Thr137Ile |
S153 S213 |
| 167374 | BAA02g13140 | A02 | 5925123 | G | A | upstream_gene_variant | MODIFIER | c.-34C>T| |
S140 S219 S278 S64 S72 |
| 167375 | BAA02g13140 | A02 | 5928042 | G | A | upstream_gene_variant | MODIFIER | c.-2953C>T| |
S251 |