| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157801 | BAA02g05430 | A02 | 2367289 | A | C | upstream_gene_variant | MODIFIER | c.-2424T>G| |
S107 S295 S42 |
| 157802 | BAA02g05430 | A02 | 2367291 | A | C | upstream_gene_variant | MODIFIER | c.-2426T>G| |
S107 S288 S295 S42 |
| 157803 | BAA02g05430 | A02 | 2367673 | C | T | upstream_gene_variant | MODIFIER | c.-2808G>A| |
S100 |
| 157804 | BAA02g05430 | A02 | 2368016 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S183 S198 |
| 157805 | BAA02g05450 | A02 | 2368469 | C | T | splice_donor_variant&intron_variant | HIGH | c.738+1G>A| |
S278 |
| 157806 | BAA02g05450 | A02 | 2368593 | G | A | synonymous_variant | LOW | c.615C>T|p.Leu205Leu |
S223 |
| 157807 | BAA02g05450 | A02 | 2368954 | C | T | synonymous_variant | LOW | c.333G>A|p.Arg111Arg |
S97 |
| 157808 | BAA02g05430 | A02 | 2369560 | C | T | upstream_gene_variant | MODIFIER | c.-4695G>A| |
S103 |
| 157809 | BAA02g05450 | A02 | 2369912 | G | A | upstream_gene_variant | MODIFIER | c.-626C>T| |
S263 |
| 157810 | BAA02g05450 | A02 | 2369934 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S169 |
| 157811 | BAA02g05450 | A02 | 2370040 | G | A | upstream_gene_variant | MODIFIER | c.-754C>T| |
S72 S78 |
| 157812 | BAA02g05450 | A02 | 2370048 | C | T | upstream_gene_variant | MODIFIER | c.-762G>A| |
S71 |
| 157813 | BAA02g05450 | A02 | 2370255 | G | A | upstream_gene_variant | MODIFIER | c.-969C>T| |
S232 |
| 157814 | BAA02g05450 | A02 | 2373358 | G | A | upstream_gene_variant | MODIFIER | c.-4072C>T| |
S223 |
| 157815 | BAA02g05470 | A02 | 2375062 | G | A | upstream_gene_variant | MODIFIER | c.-664G>A| |
S266 |
| 157816 | BAA02g05470 | A02 | 2375226 | C | T | upstream_gene_variant | MODIFIER | c.-500C>T| |
S87 |
| 157817 | BAA02g05480 | A02 | 2376780 | C | T | upstream_gene_variant | MODIFIER | c.-704C>T| |
S200 |
| 157818 | BAA02g05480 | A02 | 2377862 | G | A | missense_variant | MODERATE | c.172G>A|p.Val58Ile |
S163 |
| 157819 | BAA02g05480 | A02 | 2377868 | C | T | missense_variant | MODERATE | c.178C>T|p.Arg60Cys |
S165 S296 |
| 157820 | BAA02g05490 | A02 | 2380239 | G | A | missense_variant | MODERATE | c.499G>A|p.Val167Ile |
S17 |
| 157821 | BAA02g05490 | A02 | 2380719 | G | A | missense_variant | MODERATE | c.979G>A|p.Val327Met |
S244 |
| 157822 | BAA02g05500 | A02 | 2382867 | C | T | upstream_gene_variant | MODIFIER | c.-197C>T| |
S255 |
| 157823 | BAA02g05500 | A02 | 2383575 | C | A | stop_gained | HIGH | c.512C>A|p.Ser171* |
S279 |
| 157824 | BAA02g05490 | A02 | 2385024 | C | T | downstream_gene_variant | MODIFIER | c.*3116C>T| |
S207 |
| 157825 | BAA02g05490 | A02 | 2385093 | G | A | downstream_gene_variant | MODIFIER | c.*3185G>A| |
S7 |