| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 12851 | BAA01g10170 | A01 | 4609604 | G | A | missense_variant | MODERATE | c.895G>A|p.Val299Met |
S239 |
| 12852 | BAA01g10170 | A01 | 4609766 | G | A | intron_variant | MODIFIER | c.1030+27G>A| |
S56 |
| 12853 | BAA01g10180 | A01 | 4610318 | C | T | downstream_gene_variant | MODIFIER | c.*4997G>A| |
S206 |
| 12854 | BAA01g10180 | A01 | 4610963 | G | A | downstream_gene_variant | MODIFIER | c.*4352C>T| |
S153 |
| 12855 | BAA01g10180 | A01 | 4611691 | C | T | downstream_gene_variant | MODIFIER | c.*3624G>A| |
S202 |
| 12856 | BAA01g10170 | A01 | 4612224 | G | A | missense_variant | MODERATE | c.1200G>A|p.Met400Ile |
S165 |
| 12857 | BAA01g10180 | A01 | 4612655 | C | T | downstream_gene_variant | MODIFIER | c.*2660G>A| |
S50 |
| 12858 | BAA01g10170 | A01 | 4613377 | C | T | synonymous_variant | LOW | c.1743C>T|p.Ile581Ile |
S202 |
| 12859 | BAA01g10170 | A01 | 4613483 | G | A | missense_variant | MODERATE | c.1849G>A|p.Val617Ile |
S80 |
| 12860 | BAA01g10170 | A01 | 4613631 | C | T | missense_variant | MODERATE | c.1997C>T|p.Ala666Val |
S233 |
| 12861 | BAA01g10170 | A01 | 4615927 | C | T | downstream_gene_variant | MODIFIER | c.*1686C>T| |
S44 |
| 12862 | BAA01g10170 | A01 | 4617032 | G | A | downstream_gene_variant | MODIFIER | c.*2791G>A| |
S208 S219 |
| 12863 | BAA01g10180 | A01 | 4620660 | C | T | upstream_gene_variant | MODIFIER | c.-2748G>A| |
S100 |
| 12864 | BAA01g10180 | A01 | 4621452 | C | T | upstream_gene_variant | MODIFIER | c.-3540G>A| |
S71 |
| 12865 | BAA01g10180 | A01 | 4621648 | C | T | upstream_gene_variant | MODIFIER | c.-3736G>A| |
S120 |
| 12866 | BAA01g10180 | A01 | 4622394 | G | A | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S251 |
| 12867 | BAA01g10190 | A01 | 4622970 | C | T | downstream_gene_variant | MODIFIER | c.*3357G>A| |
S100 |
| 12868 | BAA01g10190 | A01 | 4623122 | C | T | downstream_gene_variant | MODIFIER | c.*3205G>A| |
S244 |
| 12869 | BAA01g10200 | A01 | 4623807 | C | T | upstream_gene_variant | MODIFIER | c.-4996C>T| |
S166 |
| 12870 | BAA01g10200 | A01 | 4625047 | G | A | upstream_gene_variant | MODIFIER | c.-3756G>A| |
S301 S304 |
| 12871 | BAA01g10200 | A01 | 4626125 | G | A | upstream_gene_variant | MODIFIER | c.-2678G>A| |
S256 |
| 12872 | BAA01g10190 | A01 | 4626353 | G | A | missense_variant | MODERATE | c.892C>T|p.Pro298Ser |
S10 |
| 12873 | BAA01g10190 | A01 | 4626394 | G | A | missense_variant | MODERATE | c.851C>T|p.Ser284Phe |
S292 |
| 12874 | BAA01g10190 | A01 | 4626778 | G | A | missense_variant | MODERATE | c.467C>T|p.Thr156Ile |
S92 |
| 12875 | BAA01g10190 | A01 | 4626882 | G | A | synonymous_variant | LOW | c.363C>T|p.Leu121Leu |
S193 |