| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g27200 | A02 | 15252175 | C | T | downstream_gene_variant | MODIFIER | c.*3034G>A| |
S8 |
| 2 | BAA02g27200 | A02 | 15252557 | G | A | downstream_gene_variant | MODIFIER | c.*2652C>T| |
S302 |
| 3 | BAA02g27200 | A02 | 15253015 | G | A | downstream_gene_variant | MODIFIER | c.*2194C>T| |
S103 |
| 4 | BAA02g27200 | A02 | 15254101 | G | A | downstream_gene_variant | MODIFIER | c.*1108C>T| |
S184 |
| 5 | BAA02g27200 | A02 | 15254775 | G | A | downstream_gene_variant | MODIFIER | c.*434C>T| |
S25 |
| 6 | BAA02g27200 | A02 | 15254820 | G | A | downstream_gene_variant | MODIFIER | c.*389C>T| |
S155 S211 |
| 7 | BAA02g27200 | A02 | 15255370 | G | A | missense_variant | MODERATE | c.1774C>T|p.Pro592Ser |
S161 |
| 8 | BAA02g27200 | A02 | 15255750 | C | T | missense_variant | MODERATE | c.1394G>A|p.Arg465His |
S107 |
| 9 | BAA02g27200 | A02 | 15257000 | C | T | missense_variant | MODERATE | c.436G>A|p.Asp146Asn |
S139 |
| 10 | BAA02g27200 | A02 | 15257185 | G | A | missense_variant | MODERATE | c.251C>T|p.Ser84Phe |
S188 |
| 11 | BAA02g27200 | A02 | 15257930 | G | A | upstream_gene_variant | MODIFIER | c.-414C>T| |
S294 |
| 12 | BAA02g27200 | A02 | 15258270 | C | T | upstream_gene_variant | MODIFIER | c.-754G>A| |
S42 |
| 13 | BAA02g27200 | A02 | 15259232 | G | A | upstream_gene_variant | MODIFIER | c.-1716C>T| |
S239 |
| 14 | BAA02g27200 | A02 | 15259322 | G | A | upstream_gene_variant | MODIFIER | c.-1806C>T| |
S35 |
| 15 | BAA02g27200 | A02 | 15259833 | G | A | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S56 |
| 16 | BAA02g27200 | A02 | 15261264 | G | A | upstream_gene_variant | MODIFIER | c.-3748C>T| |
S139 |
| 17 | BAA02g27200 | A02 | 15261281 | G | A | upstream_gene_variant | MODIFIER | c.-3765C>T| |
S155 S211 |
| 18 | BAA02g27200 | A02 | 15261320 | C | T | upstream_gene_variant | MODIFIER | c.-3804G>A| |
S2 |
| 19 | BAA02g27200 | A02 | 15261584 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S179 |