| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 29101 | BAA01g20530 | A01 | 10130857 | G | A | upstream_gene_variant | MODIFIER | c.-473G>A| |
S155 |
| 29102 | BAA01g20530 | A01 | 10131876 | G | A | missense_variant | MODERATE | c.236G>A|p.Gly79Asp |
S293 |
| 29103 | BAA01g20530 | A01 | 10132253 | C | T | synonymous_variant | LOW | c.411C>T|p.Asn137Asn |
S175 S226 S250 S291 |
| 29104 | BAA01g20530 | A01 | 10132960 | C | T | intron_variant | MODIFIER | c.743+11C>T| |
S151 |
| 29105 | BAA01g20530 | A01 | 10133841 | C | T | downstream_gene_variant | MODIFIER | c.*682C>T| |
S159 S243 |
| 29106 | BAA01g20540 | A01 | 10134903 | G | A | upstream_gene_variant | MODIFIER | c.-4842G>A| |
S237 |
| 29107 | BAA01g20540 | A01 | 10134986 | G | A | upstream_gene_variant | MODIFIER | c.-4759G>A| |
S116 |
| 29108 | BAA01g20540 | A01 | 10135229 | G | A | upstream_gene_variant | MODIFIER | c.-4516G>A| |
S173 |
| 29109 | BAA01g20540 | A01 | 10135347 | C | T | upstream_gene_variant | MODIFIER | c.-4398C>T| |
S70 |
| 29110 | BAA01g20540 | A01 | 10136651 | C | T | upstream_gene_variant | MODIFIER | c.-3094C>T| |
S291 |
| 29111 | BAA01g20540 | A01 | 10137835 | C | T | upstream_gene_variant | MODIFIER | c.-1910C>T| |
S179 |
| 29112 | BAA01g20540 | A01 | 10138017 | C | T | upstream_gene_variant | MODIFIER | c.-1728C>T| |
S166 |
| 29113 | BAA01g20540 | A01 | 10139302 | G | A | upstream_gene_variant | MODIFIER | c.-443G>A| |
S175 |
| 29114 | BAA01g20540 | A01 | 10139979 | C | T | missense_variant | MODERATE | c.235C>T|p.Leu79Phe |
S177 |
| 29115 | BAA01g20540 | A01 | 10140110 | C | T | synonymous_variant | LOW | c.366C>T|p.His122His |
S54 |
| 29116 | BAA01g20540 | A01 | 10140903 | C | T | missense_variant | MODERATE | c.1159C>T|p.Pro387Ser |
S179 |
| 29117 | BAA01g20550 | A01 | 10141545 | G | A | upstream_gene_variant | MODIFIER | c.-314G>A| |
S142 |
| 29118 | BAA01g20550 | A01 | 10143617 | C | T | synonymous_variant | LOW | c.819C>T|p.Tyr273Tyr |
S265 |
| 29119 | BAA01g20550 | A01 | 10143642 | C | T | missense_variant | MODERATE | c.844C>T|p.Leu282Phe |
S11 |
| 29120 | BAA01g20540 | A01 | 10143994 | C | T | downstream_gene_variant | MODIFIER | c.*2717C>T| |
S270 |
| 29121 | BAA01g20540 | A01 | 10144007 | G | A | downstream_gene_variant | MODIFIER | c.*2730G>A| |
S239 |
| 29122 | BAA01g20540 | A01 | 10145056 | G | A | downstream_gene_variant | MODIFIER | c.*3779G>A| |
S244 |
| 29123 | BAA01g20560 | A01 | 10145846 | A | G | synonymous_variant | LOW | c.1059T>C|p.Ser353Ser |
S176 |
| 29124 | BAA01g20560 | A01 | 10146118 | G | A | missense_variant | MODERATE | c.787C>T|p.Pro263Ser |
S229 |
| 29125 | BAA01g20560 | A01 | 10146346 | G | A | missense_variant | MODERATE | c.559C>T|p.Pro187Ser |
S73 S91 |