| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 191301 | BAA02g26390 | A02 | 14663106 | G | A | upstream_gene_variant | MODIFIER | c.-4551G>A| |
S70 |
| 191302 | BAA02g26390 | A02 | 14663454 | C | T | upstream_gene_variant | MODIFIER | c.-4203C>T| |
S185 |
| 191303 | BAA02g26390 | A02 | 14663709 | C | T | upstream_gene_variant | MODIFIER | c.-3948C>T| |
S280 |
| 191304 | BAA02g26390 | A02 | 14665005 | C | T | upstream_gene_variant | MODIFIER | c.-2652C>T| |
S178 |
| 191305 | BAA02g26390 | A02 | 14666113 | G | A | upstream_gene_variant | MODIFIER | c.-1544G>A| |
S36 |
| 191306 | BAA02g26390 | A02 | 14666169 | G | A | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S158 |
| 191307 | BAA02g26390 | A02 | 14666459 | C | T | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S139 |
| 191308 | BAA02g26390 | A02 | 14667010 | A | T | upstream_gene_variant | MODIFIER | c.-647A>T| |
S186 |
| 191309 | BAA02g26390 | A02 | 14668178 | G | A | intron_variant | MODIFIER | c.368-26G>A| |
S293 |
| 191310 | BAA02g26390 | A02 | 14668483 | G | A | missense_variant | MODERATE | c.580G>A|p.Gly194Arg |
S125 |
| 191311 | BAA02g26390 | A02 | 14668507 | C | T | missense_variant | MODERATE | c.604C>T|p.His202Tyr |
S192 |
| 191312 | BAA02g26390 | A02 | 14669889 | A | T | intron_variant | MODIFIER | c.1461+40A>T| |
S58 |
| 191313 | BAA02g26390 | A02 | 14670718 | C | T | missense_variant | MODERATE | c.1928C>T|p.Ala643Val |
S6 |
| 191314 | BAA02g26390 | A02 | 14671110 | G | A | downstream_gene_variant | MODIFIER | c.*361G>A| |
S237 |
| 191315 | BAA02g26390 | A02 | 14672449 | C | T | downstream_gene_variant | MODIFIER | c.*1700C>T| |
S163 |
| 191316 | BAA02g26390 | A02 | 14675058 | G | A | downstream_gene_variant | MODIFIER | c.*4309G>A| |
S230 |
| 191317 | BAA02g26390 | A02 | 14675126 | C | T | downstream_gene_variant | MODIFIER | c.*4377C>T| |
S38 |
| 191318 | BAA02g26400 | A02 | 14676653 | G | A | upstream_gene_variant | MODIFIER | c.-588C>T| |
S166 |
| 191319 | BAA02g26400 | A02 | 14676657 | G | A | upstream_gene_variant | MODIFIER | c.-592C>T| |
S150 |
| 191320 | BAA02g26400 | A02 | 14677486 | C | T | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S183 S198 S54 |
| 191321 | BAA02g26400 | A02 | 14677755 | G | A | upstream_gene_variant | MODIFIER | c.-1690C>T| |
S133 |
| 191322 | BAA02g26400 | A02 | 14678220 | C | T | upstream_gene_variant | MODIFIER | c.-2155G>A| |
S18 |
| 191323 | BAA02g26400 | A02 | 14678505 | C | T | upstream_gene_variant | MODIFIER | c.-2440G>A| |
S183 S198 |
| 191324 | BAA02g26400 | A02 | 14680793 | G | A | upstream_gene_variant | MODIFIER | c.-4728C>T| |
S203 |
| 191325 | BAA02g26410 | A02 | 14681614 | G | A | upstream_gene_variant | MODIFIER | c.-1020G>A| |
S228 |