| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155351 | BAA02g03470 | A02 | 1538890 | C | T | downstream_gene_variant | MODIFIER | c.*3713C>T| |
S252 |
| 155352 | BAA02g03470 | A02 | 1539176 | G | A | downstream_gene_variant | MODIFIER | c.*3999G>A| |
S155 S211 |
| 155353 | BAA02g03490 | A02 | 1539460 | C | T | missense_variant&splice_region_variant | MODERATE | c.611C>T|p.Ala204Val |
S216 |
| 155354 | BAA02g03490 | A02 | 1540990 | G | A | missense_variant | MODERATE | c.1126G>A|p.Glu376Lys |
S180 |
| 155355 | BAA02g03480 | A02 | 1541223 | C | T | downstream_gene_variant | MODIFIER | c.*3686C>T| |
S124 |
| 155356 | BAA02g03480 | A02 | 1541647 | G | A | downstream_gene_variant | MODIFIER | c.*4110G>A| |
S70 |
| 155357 | BAA02g03480 | A02 | 1541682 | G | A | downstream_gene_variant | MODIFIER | c.*4145G>A| |
S62 |
| 155358 | BAA02g03500 | A02 | 1544655 | C | T | upstream_gene_variant | MODIFIER | c.-918G>A| |
S281 |
| 155359 | BAA02g03500 | A02 | 1547282 | G | A | upstream_gene_variant | MODIFIER | c.-3545C>T| |
S187 |
| 155360 | BAA02g03500 | A02 | 1547315 | C | T | upstream_gene_variant | MODIFIER | c.-3578G>A| |
S159 |
| 155361 | BAA02g03520 | A02 | 1551921 | C | T | missense_variant | MODERATE | c.377G>A|p.Arg126Lys |
S111 |
| 155362 | BAA02g03510 | A02 | 1552564 | C | T | downstream_gene_variant | MODIFIER | c.*2848C>T| |
S103 |
| 155363 | BAA02g03510 | A02 | 1552800 | G | A | downstream_gene_variant | MODIFIER | c.*3084G>A| |
S118 |
| 155364 | BAA02g03520 | A02 | 1553014 | G | A | synonymous_variant | LOW | c.204C>T|p.Leu68Leu |
S78 |
| 155365 | BAA02g03520 | A02 | 1553662 | G | A | upstream_gene_variant | MODIFIER | c.-335C>T| |
S162 |
| 155366 | BAA02g03520 | A02 | 1557778 | C | T | upstream_gene_variant | MODIFIER | c.-4451G>A| |
S157 |
| 155367 | BAA02g03520 | A02 | 1558311 | G | A | upstream_gene_variant | MODIFIER | c.-4984C>T| |
S191 |
| 155368 | BAA02g03550 | A02 | 1563533 | C | T | downstream_gene_variant | MODIFIER | c.*1561G>A| |
S130 |
| 155369 | BAA02g03540 | A02 | 1563859 | C | T | missense_variant | MODERATE | c.856C>T|p.His286Tyr |
S233 |
| 155370 | BAA02g03540 | A02 | 1564912 | C | T | downstream_gene_variant | MODIFIER | c.*343C>T| |
S200 |
| 155371 | BAA02g03540 | A02 | 1565056 | G | A | downstream_gene_variant | MODIFIER | c.*487G>A| |
S50 |
| 155372 | BAA02g03550 | A02 | 1566409 | G | T | upstream_gene_variant | MODIFIER | c.-464C>A| |
S294 |
| 155373 | BAA02g03550 | A02 | 1566548 | C | T | upstream_gene_variant | MODIFIER | c.-603G>A| |
S267 |
| 155374 | BAA02g03550 | A02 | 1567233 | C | T | upstream_gene_variant | MODIFIER | c.-1288G>A| |
S178 S196 |
| 155375 | BAA02g03550 | A02 | 1567690 | G | A | upstream_gene_variant | MODIFIER | c.-1745C>T| |
S190 |