| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 180301 | BAA02g20300 | A02 | 10722136 | C | T | upstream_gene_variant | MODIFIER | c.-1875C>T| |
S139 |
| 180302 | BAA02g20300 | A02 | 10722236 | G | A | upstream_gene_variant | MODIFIER | c.-1775G>A| |
S59 |
| 180303 | BAA02g20300 | A02 | 10724002 | G | A | upstream_gene_variant | MODIFIER | c.-9G>A| |
S281 |
| 180304 | BAA02g20300 | A02 | 10725814 | C | T | synonymous_variant | LOW | c.1144C>T|p.Leu382Leu |
S189 |
| 180305 | BAA02g20310 | A02 | 10726557 | C | T | upstream_gene_variant | MODIFIER | c.-2711C>T| |
S140 |
| 180306 | BAA02g20300 | A02 | 10729767 | T | A | downstream_gene_variant | MODIFIER | c.*3723T>A| |
S273 |
| 180307 | BAA02g20310-BAA02g20320 | A02 | 10737312 | C | T | intergenic_region | MODIFIER | n.10737312C>T| |
S77 S82 |
| 180308 | BAA02g20310-BAA02g20320 | A02 | 10738595 | C | T | intergenic_region | MODIFIER | n.10738595C>T| |
S166 |
| 180309 | BAA02g20310-BAA02g20320 | A02 | 10738695 | G | A | intergenic_region | MODIFIER | n.10738695G>A| |
S109 |
| 180310 | BAA02g20310-BAA02g20320 | A02 | 10741083 | G | A | intergenic_region | MODIFIER | n.10741083G>A| |
S176 |
| 180311 | BAA02g20320 | A02 | 10745464 | G | A | downstream_gene_variant | MODIFIER | c.*1536C>T| |
S225 |
| 180312 | BAA02g20320 | A02 | 10746227 | G | A | downstream_gene_variant | MODIFIER | c.*773C>T| |
S37 |
| 180313 | BAA02g20320 | A02 | 10746432 | G | A | downstream_gene_variant | MODIFIER | c.*568C>T| |
S204 |
| 180314 | BAA02g20320 | A02 | 10747439 | C | T | missense_variant | MODERATE | c.2326G>A|p.Glu776Lys |
S255 |
| 180315 | BAA02g20320 | A02 | 10749282 | G | A | synonymous_variant | LOW | c.948C>T|p.Ile316Ile |
S70 |
| 180316 | BAA02g20320 | A02 | 10749905 | C | T | synonymous_variant | LOW | c.585G>A|p.Lys195Lys |
S181 |
| 180317 | BAA02g20320 | A02 | 10750135 | G | A | intron_variant | MODIFIER | c.499+23C>T| |
S303 |
| 180318 | BAA02g20320 | A02 | 10750221 | C | T | missense_variant | MODERATE | c.436G>A|p.Asp146Asn |
S189 |
| 180319 | BAA02g20320 | A02 | 10750738 | C | T | upstream_gene_variant | MODIFIER | c.-7G>A| |
S255 |
| 180320 | BAA02g20320 | A02 | 10750760 | G | A | upstream_gene_variant | MODIFIER | c.-29C>T| |
S259 |
| 180321 | BAA02g20320 | A02 | 10750902 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S47 |
| 180322 | BAA02g20320 | A02 | 10751400 | C | T | upstream_gene_variant | MODIFIER | c.-669G>A| |
S62 |
| 180323 | BAA02g20320 | A02 | 10751472 | G | A | upstream_gene_variant | MODIFIER | c.-741C>T| |
S247 |
| 180324 | BAA02g20320 | A02 | 10752129 | G | A | upstream_gene_variant | MODIFIER | c.-1398C>T| |
S1 S90 |
| 180325 | BAA02g20320 | A02 | 10752496 | C | T | upstream_gene_variant | MODIFIER | c.-1765G>A| |
S77 S82 |