| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 168851 | BAA02g14000 | A02 | 6585727 | G | A | upstream_gene_variant | MODIFIER | c.-1770C>T| |
S23 |
| 168852 | BAA02g14000 | A02 | 6586600 | G | A | upstream_gene_variant | MODIFIER | c.-2643C>T| |
S148 S210 |
| 168853 | BAA02g14000 | A02 | 6587755 | C | T | upstream_gene_variant | MODIFIER | c.-3798G>A| |
S165 |
| 168854 | BAA02g14020 | A02 | 6589653 | G | A | upstream_gene_variant | MODIFIER | c.-299C>T| |
S256 |
| 168855 | BAA02g14020 | A02 | 6590070 | G | A | upstream_gene_variant | MODIFIER | c.-716C>T| |
S232 |
| 168856 | BAA02g14020 | A02 | 6590463 | C | T | upstream_gene_variant | MODIFIER | c.-1109G>A| |
S16 S56 |
| 168857 | BAA02g14020 | A02 | 6591482 | C | T | upstream_gene_variant | MODIFIER | c.-2128G>A| |
S234 |
| 168858 | BAA02g14030 | A02 | 6591671 | C | T | missense_variant | MODERATE | c.253G>A|p.Asp85Asn |
S142 |
| 168859 | BAA02g14020 | A02 | 6592066 | C | T | upstream_gene_variant | MODIFIER | c.-2712G>A| |
S179 |
| 168860 | BAA02g14020 | A02 | 6593763 | G | A | upstream_gene_variant | MODIFIER | c.-4409C>T| |
S126 |
| 168861 | BAA02g14030 | A02 | 6594647 | C | T | upstream_gene_variant | MODIFIER | c.-2271G>A| |
S277 |
| 168862 | BAA02g14030 | A02 | 6595779 | T | G | upstream_gene_variant | MODIFIER | c.-3403A>C| |
S28 |
| 168863 | BAA02g14050 | A02 | 6595943 | G | A | synonymous_variant | LOW | c.918C>T|p.Asp306Asp |
S289 S290 |
| 168864 | BAA02g14040 | A02 | 6597551 | C | T | upstream_gene_variant | MODIFIER | c.-3318G>A| |
S32 |
| 168865 | BAA02g14040 | A02 | 6597954 | C | T | upstream_gene_variant | MODIFIER | c.-3721G>A| |
S226 |
| 168866 | BAA02g14040 | A02 | 6598787 | C | T | upstream_gene_variant | MODIFIER | c.-4554G>A| |
S289 S290 |
| 168867 | BAA02g14050 | A02 | 6600023 | C | T | upstream_gene_variant | MODIFIER | c.-2479G>A| |
S164 |
| 168868 | BAA02g14050 | A02 | 6600959 | C | T | upstream_gene_variant | MODIFIER | c.-3415G>A| |
S112 |
| 168869 | BAA02g14050 | A02 | 6601168 | G | A | upstream_gene_variant | MODIFIER | c.-3624C>T| |
S153 S213 |
| 168870 | BAA02g14050 | A02 | 6601428 | A | C | upstream_gene_variant | MODIFIER | c.-3884T>G| |
S41 S9 |
| 168871 | BAA02g14050 | A02 | 6602092 | G | A | upstream_gene_variant | MODIFIER | c.-4548C>T| |
S303 |
| 168872 | BAA02g14060 | A02 | 6602695 | C | T | upstream_gene_variant | MODIFIER | c.-2853G>A| |
S87 |
| 168873 | BAA02g14060 | A02 | 6602703 | C | T | upstream_gene_variant | MODIFIER | c.-2861G>A| |
S186 |
| 168874 | BAA02g14060 | A02 | 6602854 | G | A | upstream_gene_variant | MODIFIER | c.-3012C>T| |
S10 |
| 168875 | BAA02g14070 | A02 | 6604223 | G | A | missense_variant | MODERATE | c.743G>A|p.Cys248Tyr |
S231 |