| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 173501 | BAA02g16790 | A02 | 8289762 | C | T | upstream_gene_variant | MODIFIER | c.-3982G>A| |
S276 |
| 173502 | BAA02g16790 | A02 | 8290090 | G | A | upstream_gene_variant | MODIFIER | c.-4310C>T| |
S247 |
| 173503 | BAA02g16790 | A02 | 8290688 | C | T | upstream_gene_variant | MODIFIER | c.-4908G>A| |
S171 |
| 173504 | BAA02g16800 | A02 | 8292073 | C | T | upstream_gene_variant | MODIFIER | c.-2838G>A| |
S117 |
| 173505 | BAA02g16800 | A02 | 8292095 | G | A | upstream_gene_variant | MODIFIER | c.-2860C>T| |
S289 S290 |
| 173506 | BAA02g16800 | A02 | 8293098 | G | A | upstream_gene_variant | MODIFIER | c.-3863C>T| |
S122 |
| 173507 | BAA02g16800 | A02 | 8293871 | G | A | upstream_gene_variant | MODIFIER | c.-4636C>T| |
S265 |
| 173508 | BAA02g16810 | A02 | 8294779 | C | T | downstream_gene_variant | MODIFIER | c.*2237G>A| |
S127 |
| 173509 | BAA02g16810 | A02 | 8294816 | C | T | downstream_gene_variant | MODIFIER | c.*2200G>A| |
S293 |
| 173510 | BAA02g16810 | A02 | 8294992 | G | A | downstream_gene_variant | MODIFIER | c.*2024C>T| |
S193 |
| 173511 | BAA02g16810 | A02 | 8295241 | C | T | downstream_gene_variant | MODIFIER | c.*1775G>A| |
S5 |
| 173512 | BAA02g16810 | A02 | 8296287 | C | T | downstream_gene_variant | MODIFIER | c.*729G>A| |
S244 S79 |
| 173513 | BAA02g16810 | A02 | 8296341 | G | A | downstream_gene_variant | MODIFIER | c.*675C>T| |
S203 |
| 173514 | BAA02g16810 | A02 | 8297346 | C | T | missense_variant | MODERATE | c.4117G>A|p.Asp1373Asn |
S257 |
| 173515 | BAA02g16810 | A02 | 8297544 | G | A | missense_variant | MODERATE | c.3919C>T|p.Leu1307Phe |
S287 |
| 173516 | BAA02g16810 | A02 | 8298048 | C | T | missense_variant | MODERATE | c.3637G>A|p.Gly1213Ser |
S71 |
| 173517 | BAA02g16810 | A02 | 8298243 | G | A | intron_variant | MODIFIER | c.3510+17C>T| |
S166 |
| 173518 | BAA02g16810 | A02 | 8298607 | G | A | missense_variant | MODERATE | c.3329C>T|p.Pro1110Leu |
S51 |
| 173519 | BAA02g16810 | A02 | 8301491 | G | A | missense_variant | MODERATE | c.1769C>T|p.Ser590Phe |
S173 |
| 173520 | BAA02g16810 | A02 | 8301609 | C | T | intron_variant | MODIFIER | c.1720-69G>A| |
S66 |
| 173521 | BAA02g16810 | A02 | 8301687 | C | T | intron_variant | MODIFIER | c.1720-147G>A| |
S121 |
| 173522 | BAA02g16810 | A02 | 8302513 | C | T | intron_variant | MODIFIER | c.1512+53G>A| |
S174 S27 |
| 173523 | BAA02g16810 | A02 | 8302795 | G | A | missense_variant | MODERATE | c.1364C>T|p.Pro455Leu |
S288 |
| 173524 | BAA02g16810 | A02 | 8302807 | G | A | missense_variant | MODERATE | c.1352C>T|p.Ala451Val |
S298 |
| 173525 | BAA02g16810 | A02 | 8304110 | G | A | synonymous_variant | LOW | c.864C>T|p.Cys288Cys |
S34 |