| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 185301 | BAA02g23020 | A02 | 12509550 | C | T | downstream_gene_variant | MODIFIER | c.*176G>A| |
S32 |
| 185302 | BAA02g23020 | A02 | 12511314 | C | T | missense_variant | MODERATE | c.638G>A|p.Gly213Glu |
S180 |
| 185303 | BAA02g23020 | A02 | 12511489 | C | T | missense_variant | MODERATE | c.463G>A|p.Asp155Asn |
S240 |
| 185304 | BAA02g23020 | A02 | 12511623 | G | A | missense_variant | MODERATE | c.329C>T|p.Thr110Ile |
S17 |
| 185305 | BAA02g23020 | A02 | 12511862 | C | T | synonymous_variant | LOW | c.90G>A|p.Lys30Lys |
S84 S93 |
| 185306 | BAA02g23020 | A02 | 12513882 | G | A | upstream_gene_variant | MODIFIER | c.-1931C>T| |
S60 |
| 185307 | BAA02g23020 | A02 | 12514033 | C | T | upstream_gene_variant | MODIFIER | c.-2082G>A| |
S203 |
| 185308 | BAA02g23020 | A02 | 12516587 | G | A | upstream_gene_variant | MODIFIER | c.-4636C>T| |
S278 |
| 185309 | BAA02g23020 | A02 | 12516608 | G | A | upstream_gene_variant | MODIFIER | c.-4657C>T| |
S197 |
| 185310 | BAA02g23050 | A02 | 12521210 | G | A | missense_variant | MODERATE | c.251C>T|p.Ser84Phe |
S92 |
| 185311 | BAA02g23040 | A02 | 12523027 | G | A | upstream_gene_variant | MODIFIER | c.-3546C>T| |
S113 |
| 185312 | BAA02g23040 | A02 | 12524453 | C | T | upstream_gene_variant | MODIFIER | c.-4972G>A| |
S192 |
| 185313 | BAA02g23050 | A02 | 12525788 | C | T | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S183 S198 |
| 185314 | BAA02g23050 | A02 | 12525975 | C | T | upstream_gene_variant | MODIFIER | c.-4515G>A| |
S203 |
| 185315 | BAA02g23070 | A02 | 12526276 | G | A | synonymous_variant | LOW | c.849C>T|p.Phe283Phe |
S232 |
| 185316 | BAA02g23070 | A02 | 12526365 | G | A | missense_variant | MODERATE | c.760C>T|p.His254Tyr |
S269 |
| 185317 | BAA02g23070 | A02 | 12526520 | G | A | missense_variant | MODERATE | c.605C>T|p.Ser202Phe |
S100 |
| 185318 | BAA02g23070 | A02 | 12526953 | G | A | missense_variant | MODERATE | c.332C>T|p.Ala111Val |
S136 |
| 185319 | BAA02g23070 | A02 | 12527011 | C | T | missense_variant | MODERATE | c.274G>A|p.Gly92Arg |
S212 |
| 185320 | BAA02g23060 | A02 | 12527061 | G | A | downstream_gene_variant | MODIFIER | c.*1932G>A| |
S303 |
| 185321 | BAA02g23060 | A02 | 12527097 | C | T | downstream_gene_variant | MODIFIER | c.*1968C>T| |
S179 |
| 185322 | BAA02g23060 | A02 | 12527119 | G | A | downstream_gene_variant | MODIFIER | c.*1990G>A| |
S107 |
| 185323 | BAA02g23070 | A02 | 12527541 | C | T | upstream_gene_variant | MODIFIER | c.-82G>A| |
S252 |
| 185324 | BAA02g23070 | A02 | 12529080 | C | T | upstream_gene_variant | MODIFIER | c.-1621G>A| |
S40 S49 |
| 185325 | BAA02g23070 | A02 | 12529284 | C | T | upstream_gene_variant | MODIFIER | c.-1825G>A| |
S140 |