| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 190901 | BAA02g26140 | A02 | 14482307 | C | T | upstream_gene_variant | MODIFIER | c.-24G>A| |
S142 |
| 190902 | BAA02g26140 | A02 | 14482627 | G | A | upstream_gene_variant | MODIFIER | c.-344C>T| |
S189 |
| 190903 | BAA02g26140 | A02 | 14482779 | G | A | upstream_gene_variant | MODIFIER | c.-496C>T| |
S150 |
| 190904 | BAA02g26140 | A02 | 14482819 | G | A | upstream_gene_variant | MODIFIER | c.-536C>T| |
S103 |
| 190905 | BAA02g26140 | A02 | 14483418 | G | A | upstream_gene_variant | MODIFIER | c.-1135C>T| |
S255 |
| 190906 | BAA02g26140 | A02 | 14485199 | C | T | upstream_gene_variant | MODIFIER | c.-2916G>A| |
S179 |
| 190907 | BAA02g26140 | A02 | 14485403 | G | A | upstream_gene_variant | MODIFIER | c.-3120C>T| |
S278 |
| 190908 | BAA02g26140 | A02 | 14486106 | C | T | upstream_gene_variant | MODIFIER | c.-3823G>A| |
S181 |
| 190909 | BAA02g26140 | A02 | 14486253 | C | T | upstream_gene_variant | MODIFIER | c.-3970G>A| |
S127 |
| 190910 | BAA02g26140 | A02 | 14486528 | C | T | upstream_gene_variant | MODIFIER | c.-4245G>A| |
S118 |
| 190911 | BAA02g26140 | A02 | 14486787 | G | A | upstream_gene_variant | MODIFIER | c.-4504C>T| |
S187 |
| 190912 | BAA02g26140 | A02 | 14486970 | C | T | upstream_gene_variant | MODIFIER | c.-4687G>A| |
S51 |
| 190913 | BAA02g26140 | A02 | 14487126 | G | A | upstream_gene_variant | MODIFIER | c.-4843C>T| |
S71 |
| 190914 | BAA02g26150 | A02 | 14488135 | C | T | downstream_gene_variant | MODIFIER | c.*433G>A| |
S116 |
| 190915 | BAA02g26150 | A02 | 14489129 | C | T | intron_variant | MODIFIER | c.2631+32G>A| |
S226 |
| 190916 | BAA02g26150 | A02 | 14489355 | G | A | missense_variant | MODERATE | c.2437C>T|p.His813Tyr |
S297 |
| 190917 | BAA02g26150 | A02 | 14489838 | G | A | missense_variant | MODERATE | c.1954C>T|p.Leu652Phe |
S85 |
| 190918 | BAA02g26150 | A02 | 14490172 | G | A | synonymous_variant | LOW | c.1620C>T|p.Phe540Phe |
S202 |
| 190919 | BAA02g26150 | A02 | 14491085 | G | A | missense_variant | MODERATE | c.707C>T|p.Ala236Val |
S259 |
| 190920 | BAA02g26150 | A02 | 14491473 | G | A | intron_variant | MODIFIER | c.481-38C>T| |
S153 S213 |
| 190921 | BAA02g26150 | A02 | 14491637 | C | T | intron_variant | MODIFIER | c.426+17G>A| |
S174 |
| 190922 | BAA02g26150 | A02 | 14491796 | G | A | missense_variant | MODERATE | c.284C>T|p.Ser95Phe |
S62 |
| 190923 | BAA02g26150 | A02 | 14492083 | G | A | stop_gained | HIGH | c.103C>T|p.Arg35* |
S251 |
| 190924 | BAA02g26150 | A02 | 14492555 | G | A | upstream_gene_variant | MODIFIER | c.-370C>T| |
S157 |
| 190925 | BAA02g26150 | A02 | 14492687 | G | A | upstream_gene_variant | MODIFIER | c.-502C>T| |
S62 |