| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 161151 | BAA02g08300 | A02 | 3555326 | C | T | downstream_gene_variant | MODIFIER | c.*2376C>T| |
S200 |
| 161152 | BAA02g08300 | A02 | 3555344 | A | T | downstream_gene_variant | MODIFIER | c.*2394A>T| |
S238 |
| 161153 | BAA02g08300 | A02 | 3555856 | G | A | downstream_gene_variant | MODIFIER | c.*2906G>A| |
S245 |
| 161154 | BAA02g08300 | A02 | 3556276 | C | T | downstream_gene_variant | MODIFIER | c.*3326C>T| |
S233 |
| 161155 | BAA02g08300 | A02 | 3557752 | G | A | downstream_gene_variant | MODIFIER | c.*4802G>A| |
S82 S92 |
| 161156 | BAA02g08320 | A02 | 3559274 | C | T | upstream_gene_variant | MODIFIER | c.-3673C>T| |
S200 |
| 161157 | BAA02g08310 | A02 | 3560601 | G | A | synonymous_variant | LOW | c.1320C>T|p.Phe440Phe |
S247 |
| 161158 | BAA02g08320 | A02 | 3561113 | G | A | upstream_gene_variant | MODIFIER | c.-1834G>A| |
S17 |
| 161159 | BAA02g08310 | A02 | 3562748 | T | A | upstream_gene_variant | MODIFIER | c.-35A>T| |
S156 |
| 161160 | BAA02g08320 | A02 | 3563704 | G | A | synonymous_variant | LOW | c.375G>A|p.Val125Val |
S164 |
| 161161 | BAA02g08320 | A02 | 3563933 | G | A | missense_variant | MODERATE | c.511G>A|p.Glu171Lys |
S98 |
| 161162 | BAA02g08320 | A02 | 3564187 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.562-1G>A| |
S74 |
| 161163 | BAA02g08320 | A02 | 3565276 | G | A | missense_variant | MODERATE | c.1123G>A|p.Gly375Arg |
S294 |
| 161164 | BAA02g08310 | A02 | 3565530 | C | T | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S111 |
| 161165 | BAA02g08310 | A02 | 3565620 | G | A | upstream_gene_variant | MODIFIER | c.-2907C>T| |
S13 S140 S168 S219 S279 S64 S72 |
| 161166 | BAA02g08330 | A02 | 3567872 | G | A | upstream_gene_variant | MODIFIER | c.-214G>A| |
S228 |
| 161167 | BAA02g08330 | A02 | 3568375 | G | A | missense_variant | MODERATE | c.290G>A|p.Arg97Lys |
S158 |
| 161168 | BAA02g08330 | A02 | 3568543 | C | T | missense_variant&splice_region_variant | MODERATE | c.458C>T|p.Ala153Val |
S202 |
| 161169 | BAA02g08340 | A02 | 3569831 | G | A | missense_variant | MODERATE | c.164C>T|p.Ala55Val |
S188 |
| 161170 | BAA02g08340 | A02 | 3570671 | C | T | upstream_gene_variant | MODIFIER | c.-677G>A| |
S54 |
| 161171 | BAA02g08340 | A02 | 3572577 | C | T | upstream_gene_variant | MODIFIER | c.-2583G>A| |
S136 |
| 161172 | BAA02g08350 | A02 | 3574985 | C | T | splice_region_variant&intron_variant | LOW | c.2475+5G>A| |
S159 S188 S276 S298 S299 |
| 161173 | BAA02g08350 | A02 | 3575064 | G | A | missense_variant | MODERATE | c.2401C>T|p.Arg801Trp |
S52 |
| 161174 | BAA02g08350 | A02 | 3575895 | G | A | synonymous_variant | LOW | c.1869C>T|p.Pro623Pro |
S260 |
| 161175 | BAA02g08350 | A02 | 3575913 | G | A | splice_region_variant&intron_variant | LOW | c.1856-5C>T| |
S127 |