| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170451 | BAA02g15080 | A02 | 7204275 | C | T | upstream_gene_variant | MODIFIER | c.-3782G>A| |
S284 |
| 170452 | BAA02g15080 | A02 | 7204736 | C | T | upstream_gene_variant | MODIFIER | c.-4243G>A| |
S255 |
| 170453 | BAA02g15080-BAA02g15090 | A02 | 7206867 | C | T | intergenic_region | MODIFIER | n.7206867C>T| |
S284 |
| 170454 | BAA02g15080-BAA02g15090 | A02 | 7206882 | C | T | intergenic_region | MODIFIER | n.7206882C>T| |
S180 |
| 170455 | BAA02g15090 | A02 | 7207187 | G | A | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S87 |
| 170456 | BAA02g15090 | A02 | 7207704 | C | T | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S267 |
| 170457 | BAA02g15090 | A02 | 7207711 | G | A | upstream_gene_variant | MODIFIER | c.-4289G>A| |
S125 |
| 170458 | BAA02g15090 | A02 | 7208006 | C | T | upstream_gene_variant | MODIFIER | c.-3994C>T| |
S38 |
| 170459 | BAA02g15090 | A02 | 7208886 | G | A | upstream_gene_variant | MODIFIER | c.-3114G>A| |
S203 |
| 170460 | BAA02g15090 | A02 | 7209457 | G | A | upstream_gene_variant | MODIFIER | c.-2543G>A| |
S297 |
| 170461 | BAA02g15090 | A02 | 7210197 | C | T | upstream_gene_variant | MODIFIER | c.-1803C>T| |
S63 |
| 170462 | BAA02g15090 | A02 | 7211847 | C | T | upstream_gene_variant | MODIFIER | c.-153C>T| |
S71 |
| 170463 | BAA02g15090 | A02 | 7212298 | G | A | missense_variant | MODERATE | c.299G>A|p.Arg100Lys |
S190 |
| 170464 | BAA02g15090 | A02 | 7213832 | G | A | intron_variant | MODIFIER | c.400-36G>A| |
S23 |
| 170465 | BAA02g15090 | A02 | 7213851 | C | T | intron_variant | MODIFIER | c.400-17C>T| |
S289 S290 |
| 170466 | BAA02g15090 | A02 | 7213994 | G | A | missense_variant | MODERATE | c.526G>A|p.Ala176Thr |
S33 |
| 170467 | BAA02g15090 | A02 | 7214512 | G | A | synonymous_variant | LOW | c.1044G>A|p.Lys348Lys |
S204 |
| 170468 | BAA02g15090 | A02 | 7214707 | C | T | synonymous_variant | LOW | c.1239C>T|p.Leu413Leu |
S66 |
| 170469 | BAA02g15090 | A02 | 7215020 | G | A | intron_variant | MODIFIER | c.1403-101G>A| |
S79 S91 |
| 170470 | BAA02g15100 | A02 | 7220332 | C | T | upstream_gene_variant | MODIFIER | c.-4502C>T| |
S1 S90 |
| 170471 | BAA02g15100 | A02 | 7220515 | C | T | upstream_gene_variant | MODIFIER | c.-4319C>T| |
S47 |
| 170472 | BAA02g15100 | A02 | 7220994 | G | A | upstream_gene_variant | MODIFIER | c.-3840G>A| |
S2 |
| 170473 | BAA02g15100 | A02 | 7221197 | C | T | upstream_gene_variant | MODIFIER | c.-3637C>T| |
S179 |
| 170474 | BAA02g15100 | A02 | 7221363 | G | A | upstream_gene_variant | MODIFIER | c.-3471G>A| |
S67 |
| 170475 | BAA02g15100 | A02 | 7222084 | C | T | upstream_gene_variant | MODIFIER | c.-2750C>T| |
S199 |