| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 45251 | BAA01g27140-BAA01g27150 | A01 | 15544776 | C | T | intergenic_region | MODIFIER | n.15544776C>T| |
S260 |
| 45252 | BAA01g27140-BAA01g27150 | A01 | 15545218 | C | T | intergenic_region | MODIFIER | n.15545218C>T| |
S120 |
| 45253 | BAA01g27140-BAA01g27150 | A01 | 15546319 | G | A | intergenic_region | MODIFIER | n.15546319G>A| |
S247 |
| 45254 | BAA01g27140-BAA01g27150 | A01 | 15547979 | G | A | intergenic_region | MODIFIER | n.15547979G>A| |
S162 |
| 45255 | BAA01g27140-BAA01g27150 | A01 | 15548179 | G | A | intergenic_region | MODIFIER | n.15548179G>A| |
S263 |
| 45256 | BAA01g27150 | A01 | 15548939 | C | T | upstream_gene_variant | MODIFIER | c.-4312C>T| |
S192 |
| 45257 | BAA01g27150 | A01 | 15552338 | G | A | upstream_gene_variant | MODIFIER | c.-913G>A| |
S123 |
| 45258 | BAA01g27150 | A01 | 15553440 | C | T | missense_variant | MODERATE | c.190C>T|p.Leu64Phe |
S85 |
| 45259 | BAA01g27150 | A01 | 15553706 | C | T | synonymous_variant | LOW | c.456C>T|p.Phe152Phe |
S166 |
| 45260 | BAA01g27150 | A01 | 15554460 | G | A | missense_variant | MODERATE | c.1112G>A|p.Gly371Glu |
S180 |
| 45261 | BAA01g27150 | A01 | 15554779 | C | T | synonymous_variant | LOW | c.1431C>T|p.Phe477Phe |
S198 |
| 45262 | BAA01g27150 | A01 | 15556146 | C | T | downstream_gene_variant | MODIFIER | c.*1172C>T| |
S210 S225 |
| 45263 | BAA01g27160 | A01 | 15557247 | C | T | upstream_gene_variant | MODIFIER | c.-988G>A| |
S293 |
| 45264 | BAA01g27160 | A01 | 15557552 | G | A | upstream_gene_variant | MODIFIER | c.-1293C>T| |
S110 |
| 45265 | BAA01g27160 | A01 | 15557686 | G | A | upstream_gene_variant | MODIFIER | c.-1427C>T| |
S278 |
| 45266 | BAA01g27160 | A01 | 15559648 | C | T | upstream_gene_variant | MODIFIER | c.-3389G>A| |
S184 |
| 45267 | BAA01g27170 | A01 | 15561596 | C | T | upstream_gene_variant | MODIFIER | c.-977C>T| |
S284 |
| 45268 | BAA01g27170 | A01 | 15563192 | C | T | missense_variant | MODERATE | c.488C>T|p.Ser163Phe |
S20 |
| 45269 | BAA01g27170 | A01 | 15563859 | G | A | missense_variant | MODERATE | c.851G>A|p.Gly284Glu |
S110 |
| 45270 | BAA01g27170 | A01 | 15564047 | C | T | intron_variant | MODIFIER | c.978-38C>T| |
S151 |
| 45271 | BAA01g27170 | A01 | 15564525 | G | A | missense_variant | MODERATE | c.1256G>A|p.Gly419Glu |
S251 |
| 45272 | BAA01g27170 | A01 | 15565924 | G | A | downstream_gene_variant | MODIFIER | c.*687G>A| |
S287 |
| 45273 | BAA01g27170 | A01 | 15566920 | C | T | downstream_gene_variant | MODIFIER | c.*1683C>T| |
S242 |
| 45274 | BAA01g27180 | A01 | 15572753 | G | A | downstream_gene_variant | MODIFIER | c.*1055C>T| |
S85 |
| 45275 | BAA01g27180 | A01 | 15573068 | C | T | downstream_gene_variant | MODIFIER | c.*740G>A| |
S88 |