| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 193451 | BAA02g27390 | A02 | 15404792 | C | T | intron_variant | MODIFIER | c.2716+118C>T| |
S171 |
| 193452 | BAA02g27390 | A02 | 15404925 | G | A | intron_variant | MODIFIER | c.2716+251G>A| |
S113 |
| 193453 | BAA02g27390 | A02 | 15405477 | G | A | intron_variant | MODIFIER | c.2716+803G>A| |
S10 |
| 193454 | BAA02g27390 | A02 | 15406646 | G | A | intron_variant | MODIFIER | c.2716+1972G>A| |
S293 |
| 193455 | BAA02g27390 | A02 | 15406836 | G | A | intron_variant | MODIFIER | c.2716+2162G>A| |
S10 |
| 193456 | BAA02g27390 | A02 | 15409033 | G | A | intron_variant | MODIFIER | c.2717-462G>A| |
S196 |
| 193457 | BAA02g27390 | A02 | 15409155 | C | T | intron_variant | MODIFIER | c.2717-340C>T| |
S100 |
| 193458 | BAA02g27390 | A02 | 15411343 | G | A | downstream_gene_variant | MODIFIER | c.*121G>A| |
S150 |
| 193459 | BAA02g27390 | A02 | 15412543 | G | A | downstream_gene_variant | MODIFIER | c.*1321G>A| |
S229 |
| 193460 | BAA02g27390 | A02 | 15413186 | C | T | downstream_gene_variant | MODIFIER | c.*1964C>T| |
S282 |
| 193461 | BAA02g27390 | A02 | 15413715 | G | A | downstream_gene_variant | MODIFIER | c.*2493G>A| |
S155 |
| 193462 | BAA02g27390 | A02 | 15414145 | G | A | downstream_gene_variant | MODIFIER | c.*2923G>A| |
S256 |
| 193463 | BAA02g27390 | A02 | 15414542 | G | A | downstream_gene_variant | MODIFIER | c.*3320G>A| |
S272 |
| 193464 | BAA02g27390 | A02 | 15414863 | G | T | downstream_gene_variant | MODIFIER | c.*3641G>T| |
S270 |
| 193465 | BAA02g27390 | A02 | 15415614 | C | T | downstream_gene_variant | MODIFIER | c.*4392C>T| |
S299 |
| 193466 | BAA02g27390 | A02 | 15415942 | C | T | downstream_gene_variant | MODIFIER | c.*4720C>T| |
S120 |
| 193467 | BAA02g27400 | A02 | 15416883 | C | T | missense_variant | MODERATE | c.964G>A|p.Gly322Ser |
S183 S198 |
| 193468 | BAA02g27400 | A02 | 15416970 | C | T | missense_variant | MODERATE | c.877G>A|p.Asp293Asn |
S81 S85 |
| 193469 | BAA02g27400 | A02 | 15416974 | G | A | synonymous_variant | LOW | c.873C>T|p.Ile291Ile |
S119 |
| 193470 | BAA02g27400 | A02 | 15417021 | C | T | intron_variant | MODIFIER | c.853-27G>A| |
S124 S15 |
| 193471 | BAA02g27400 | A02 | 15417163 | G | A | missense_variant | MODERATE | c.752C>T|p.Ala251Val |
S10 |
| 193472 | BAA02g27400 | A02 | 15417179 | C | T | missense_variant | MODERATE | c.736G>A|p.Asp246Asn |
S78 S83 |
| 193473 | BAA02g27400 | A02 | 15417699 | G | A | synonymous_variant | LOW | c.216C>T|p.Thr72Thr |
S70 |
| 193474 | BAA02g27410 | A02 | 15418220 | G | A | upstream_gene_variant | MODIFIER | c.-4385G>A| |
S238 |
| 193475 | BAA02g27400 | A02 | 15418370 | G | A | synonymous_variant | LOW | c.57C>T|p.Ser19Ser |
S91 |