| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 44351 | BAA01g26920 | A01 | 15209265 | C | T | upstream_gene_variant | MODIFIER | c.-672G>A| |
S135 |
| 44352 | BAA01g26920 | A01 | 15209396 | G | A | upstream_gene_variant | MODIFIER | c.-803C>T| |
S274 |
| 44353 | BAA01g26920 | A01 | 15209579 | C | T | upstream_gene_variant | MODIFIER | c.-986G>A| |
S176 |
| 44354 | BAA01g26920 | A01 | 15209644 | G | A | upstream_gene_variant | MODIFIER | c.-1051C>T| |
S207 |
| 44355 | BAA01g26920 | A01 | 15209724 | G | A | upstream_gene_variant | MODIFIER | c.-1131C>T| |
S263 |
| 44356 | BAA01g26920 | A01 | 15209839 | C | T | upstream_gene_variant | MODIFIER | c.-1246G>A| |
S286 |
| 44357 | BAA01g26920 | A01 | 15209951 | C | T | upstream_gene_variant | MODIFIER | c.-1358G>A| |
S177 |
| 44358 | BAA01g26920 | A01 | 15210107 | G | A | upstream_gene_variant | MODIFIER | c.-1514C>T| |
S161 |
| 44359 | BAA01g26920 | A01 | 15210961 | C | T | upstream_gene_variant | MODIFIER | c.-2368G>A| |
S82 S92 |
| 44360 | BAA01g26920 | A01 | 15212309 | C | T | upstream_gene_variant | MODIFIER | c.-3716G>A| |
S279 |
| 44361 | BAA01g26920 | A01 | 15212731 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S139 |
| 44362 | BAA01g26920 | A01 | 15213024 | G | A | upstream_gene_variant | MODIFIER | c.-4431C>T| |
S174 S27 |
| 44363 | BAA01g26920 | A01 | 15213095 | C | T | upstream_gene_variant | MODIFIER | c.-4502G>A| |
S242 |
| 44364 | BAA01g26930 | A01 | 15214003 | G | A | upstream_gene_variant | MODIFIER | c.-4727G>A| |
S103 |
| 44365 | BAA01g26930 | A01 | 15215027 | G | A | upstream_gene_variant | MODIFIER | c.-3703G>A| |
S163 |
| 44366 | BAA01g26930 | A01 | 15215147 | C | T | upstream_gene_variant | MODIFIER | c.-3583C>T| |
S155 S211 |
| 44367 | BAA01g26930 | A01 | 15215530 | G | A | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S229 |
| 44368 | BAA01g26930 | A01 | 15216479 | C | T | upstream_gene_variant | MODIFIER | c.-2251C>T| |
S177 |
| 44369 | BAA01g26930 | A01 | 15216601 | G | A | upstream_gene_variant | MODIFIER | c.-2129G>A| |
S266 |
| 44370 | BAA01g26930 | A01 | 15216873 | C | T | upstream_gene_variant | MODIFIER | c.-1857C>T| |
S183 |
| 44371 | BAA01g26930 | A01 | 15217729 | G | A | upstream_gene_variant | MODIFIER | c.-1001G>A| |
S70 |
| 44372 | BAA01g26930 | A01 | 15217825 | G | A | upstream_gene_variant | MODIFIER | c.-905G>A| |
S13 |
| 44373 | BAA01g26930 | A01 | 15218047 | G | A | upstream_gene_variant | MODIFIER | c.-683G>A| |
S157 |
| 44374 | BAA01g26930 | A01 | 15219063 | C | T | missense_variant | MODERATE | c.272C>T|p.Thr91Ile |
S10 |
| 44375 | BAA01g26930 | A01 | 15219180 | C | T | splice_region_variant&intron_variant | LOW | c.322-5C>T| |
S44 |