| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 162501 | BAA02g09430 | A02 | 4151696 | G | A | missense_variant | MODERATE | c.1865C>T|p.Ser622Phe |
S146 |
| 162502 | BAA02g09430 | A02 | 4151867 | G | A | missense_variant | MODERATE | c.1777C>T|p.Pro593Ser |
S302 |
| 162503 | BAA02g09430 | A02 | 4152906 | C | T | missense_variant | MODERATE | c.1375G>A|p.Asp459Asn |
S130 |
| 162504 | BAA02g09430 | A02 | 4153787 | C | T | missense_variant | MODERATE | c.718G>A|p.Glu240Lys |
S179 |
| 162505 | BAA02g09440 | A02 | 4153985 | G | A | downstream_gene_variant | MODIFIER | c.*4482C>T| |
S51 |
| 162506 | BAA02g09430 | A02 | 4155593 | G | A | upstream_gene_variant | MODIFIER | c.-269C>T| |
S92 |
| 162507 | BAA02g09430 | A02 | 4156556 | C | T | upstream_gene_variant | MODIFIER | c.-1232G>A| |
S13 |
| 162508 | BAA02g09430 | A02 | 4157004 | G | A | upstream_gene_variant | MODIFIER | c.-1680C>T| |
S166 |
| 162509 | BAA02g09430 | A02 | 4157376 | G | A | upstream_gene_variant | MODIFIER | c.-2052C>T| |
S260 |
| 162510 | BAA02g09430 | A02 | 4157684 | G | A | upstream_gene_variant | MODIFIER | c.-2360C>T| |
S125 |
| 162511 | BAA02g09430 | A02 | 4157726 | G | A | upstream_gene_variant | MODIFIER | c.-2402C>T| |
S150 |
| 162512 | BAA02g09430 | A02 | 4157891 | G | A | upstream_gene_variant | MODIFIER | c.-2567C>T| |
S68 |
| 162513 | BAA02g09430 | A02 | 4158122 | G | A | upstream_gene_variant | MODIFIER | c.-2798C>T| |
S303 |
| 162514 | BAA02g09430 | A02 | 4158878 | G | A | upstream_gene_variant | MODIFIER | c.-3554C>T| |
S189 |
| 162515 | BAA02g09440 | A02 | 4161742 | G | A | upstream_gene_variant | MODIFIER | c.-2038C>T| |
S158 |
| 162516 | BAA02g09440 | A02 | 4163989 | G | A | upstream_gene_variant | MODIFIER | c.-4285C>T| |
S159 S243 |
| 162517 | BAA02g09450 | A02 | 4164503 | C | T | stop_gained | HIGH | c.801G>A|p.Trp267* |
S33 |
| 162518 | BAA02g09450 | A02 | 4166888 | C | T | upstream_gene_variant | MODIFIER | c.-1490G>A| |
S178 |
| 162519 | BAA02g09460 | A02 | 4168125 | C | T | missense_variant | MODERATE | c.184C>T|p.Arg62Cys |
S138 |
| 162520 | BAA02g09460 | A02 | 4168209 | G | A | missense_variant | MODERATE | c.268G>A|p.Asp90Asn |
S225 S73 |
| 162521 | BAA02g09460 | A02 | 4168368 | C | T | missense_variant | MODERATE | c.427C>T|p.Leu143Phe |
S116 |
| 162522 | BAA02g09460 | A02 | 4168476 | C | T | stop_gained | HIGH | c.535C>T|p.Gln179* |
S256 |
| 162523 | BAA02g09450 | A02 | 4169420 | C | T | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S121 |
| 162524 | BAA02g09460 | A02 | 4170620 | C | T | downstream_gene_variant | MODIFIER | c.*1647C>T| |
S71 |
| 162525 | BAA02g09470 | A02 | 4171045 | C | A | synonymous_variant | LOW | c.474C>A|p.Pro158Pro |
S224 |