| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 59251 | BAA01g31770 | A01 | 20773268 | C | T | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S255 |
| 59252 | BAA01g31770 | A01 | 20773457 | G | A | upstream_gene_variant | MODIFIER | c.-2539C>T| |
S174 S216 |
| 59253 | BAA01g31770 | A01 | 20773535 | C | T | upstream_gene_variant | MODIFIER | c.-2617G>A| |
S28 |
| 59254 | BAA01g31770-BAA01g31780 | A01 | 20777509 | G | A | intergenic_region | MODIFIER | n.20777509G>A| |
S174 S27 |
| 59255 | BAA01g31770-BAA01g31780 | A01 | 20780304 | C | T | intergenic_region | MODIFIER | n.20780304C>T| |
S125 |
| 59256 | BAA01g31780 | A01 | 20786669 | G | A | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S99 |
| 59257 | BAA01g31780 | A01 | 20786886 | G | A | upstream_gene_variant | MODIFIER | c.-2312G>A| |
S302 |
| 59258 | BAA01g31780 | A01 | 20787391 | G | A | upstream_gene_variant | MODIFIER | c.-1807G>A| |
S61 |
| 59259 | BAA01g31780 | A01 | 20787429 | C | T | upstream_gene_variant | MODIFIER | c.-1769C>T| |
S177 |
| 59260 | BAA01g31780 | A01 | 20787768 | C | T | upstream_gene_variant | MODIFIER | c.-1430C>T| |
S46 |
| 59261 | BAA01g31780 | A01 | 20788016 | G | A | upstream_gene_variant | MODIFIER | c.-1182G>A| |
S196 S25 |
| 59262 | BAA01g31780 | A01 | 20788320 | C | T | upstream_gene_variant | MODIFIER | c.-878C>T| |
S270 |
| 59263 | BAA01g31780 | A01 | 20788386 | G | A | upstream_gene_variant | MODIFIER | c.-812G>A| |
S218 |
| 59264 | BAA01g31780 | A01 | 20788583 | G | A | upstream_gene_variant | MODIFIER | c.-615G>A| |
S155 S211 S280 |
| 59265 | BAA01g31780 | A01 | 20788859 | C | T | upstream_gene_variant | MODIFIER | c.-339C>T| |
S305 |
| 59266 | BAA01g31780 | A01 | 20789986 | G | A | synonymous_variant | LOW | c.690G>A|p.Lys230Lys |
S5 |
| 59267 | BAA01g31790 | A01 | 20790501 | C | G | synonymous_variant | LOW | c.1848G>C|p.Val616Val |
S179 |
| 59268 | BAA01g31780 | A01 | 20791037 | C | T | downstream_gene_variant | MODIFIER | c.*994C>T| |
S183 S198 |
| 59269 | BAA01g31780 | A01 | 20791647 | G | A | downstream_gene_variant | MODIFIER | c.*1604G>A| |
S38 |
| 59270 | BAA01g31780 | A01 | 20791693 | C | T | downstream_gene_variant | MODIFIER | c.*1650C>T| |
S266 |
| 59271 | BAA01g31780 | A01 | 20792044 | G | A | downstream_gene_variant | MODIFIER | c.*2001G>A| |
S84 |
| 59272 | BAA01g31790 | A01 | 20792308 | C | T | missense_variant | MODERATE | c.1310G>A|p.Arg437His |
S126 |
| 59273 | BAA01g31790 | A01 | 20792548 | C | T | missense_variant | MODERATE | c.1159G>A|p.Glu387Lys |
S162 |
| 59274 | BAA01g31780 | A01 | 20793160 | G | A | downstream_gene_variant | MODIFIER | c.*3117G>A| |
S212 |
| 59275 | BAA01g31790 | A01 | 20793438 | C | T | missense_variant | MODERATE | c.553G>A|p.Glu185Lys |
S81 S85 |