| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 152451 | BAA02g01070 | A02 | 489222 | G | A | missense_variant | MODERATE | c.422G>A|p.Gly141Glu |
S286 |
| 152452 | BAA02g01070 | A02 | 489853 | G | A | missense_variant | MODERATE | c.784G>A|p.Asp262Asn |
S68 |
| 152453 | BAA02g01070 | A02 | 490000 | C | T | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S246 |
| 152454 | BAA02g01070 | A02 | 490261 | G | A | missense_variant | MODERATE | c.1100G>A|p.Gly367Asp |
S5 |
| 152455 | BAA02g01070 | A02 | 490292 | C | T | synonymous_variant | LOW | c.1131C>T|p.Asp377Asp |
S177 |
| 152456 | BAA02g01070 | A02 | 490937 | C | T | synonymous_variant | LOW | c.1542C>T|p.Tyr514Tyr |
S2 |
| 152457 | BAA02g01070 | A02 | 491446 | C | T | stop_gained | HIGH | c.1969C>T|p.Gln657* |
S19 |
| 152458 | BAA02g01060 | A02 | 492056 | C | T | downstream_gene_variant | MODIFIER | c.*3931C>T| |
S178 |
| 152459 | BAA02g01070 | A02 | 494322 | G | A | downstream_gene_variant | MODIFIER | c.*2577G>A| |
S50 |
| 152460 | BAA02g01070-BAA02g01080 | A02 | 497686 | G | A | intergenic_region | MODIFIER | n.497686G>A| |
S156 |
| 152461 | BAA02g01070-BAA02g01080 | A02 | 497967 | G | A | intergenic_region | MODIFIER | n.497967G>A| |
S23 |
| 152462 | BAA02g01070-BAA02g01080 | A02 | 498026 | C | T | intergenic_region | MODIFIER | n.498026C>T| |
S8 |
| 152463 | BAA02g01070-BAA02g01080 | A02 | 498751 | C | T | intergenic_region | MODIFIER | n.498751C>T| |
S1 S90 |
| 152464 | BAA02g01070-BAA02g01080 | A02 | 499112 | G | A | intergenic_region | MODIFIER | n.499112G>A| |
S173 |
| 152465 | BAA02g01070-BAA02g01080 | A02 | 499125 | C | T | intergenic_region | MODIFIER | n.499125C>T| |
S200 |
| 152466 | BAA02g01070-BAA02g01080 | A02 | 499605 | G | A | intergenic_region | MODIFIER | n.499605G>A| |
S282 |
| 152467 | BAA02g01080 | A02 | 500076 | C | T | upstream_gene_variant | MODIFIER | c.-4746C>T| |
S201 |
| 152468 | BAA02g01080 | A02 | 500486 | G | A | upstream_gene_variant | MODIFIER | c.-4336G>A| |
S289 S290 |
| 152469 | BAA02g01080 | A02 | 501003 | C | T | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S15 S3 |
| 152470 | BAA02g01080 | A02 | 502179 | G | A | upstream_gene_variant | MODIFIER | c.-2643G>A| |
S122 |
| 152471 | BAA02g01080 | A02 | 502423 | C | T | upstream_gene_variant | MODIFIER | c.-2399C>T| |
S243 S299 |
| 152472 | BAA02g01080 | A02 | 504876 | G | A | missense_variant | MODERATE | c.55G>A|p.Gly19Ser |
S202 |
| 152473 | BAA02g01080 | A02 | 505016 | G | A | synonymous_variant | LOW | c.195G>A|p.Gln65Gln |
S221 |
| 152474 | BAA02g01080 | A02 | 507149 | G | A | missense_variant | MODERATE | c.1186G>A|p.Gly396Ser |
S148 S210 S30 S31 |
| 152475 | BAA02g01080 | A02 | 507602 | C | T | synonymous_variant | LOW | c.1639C>T|p.Leu547Leu |
S172 S217 |