| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 104451 | BAA10g07980-BAA10g07990 | A10 | 5091877 | G | A | intergenic_region | MODIFIER | n.5091877G>A| |
S99 |
| 104452 | BAA10g07990 | A10 | 5092873 | G | A | downstream_gene_variant | MODIFIER | c.*4578C>T| |
S85 |
| 104453 | BAA10g07990 | A10 | 5093346 | G | A | downstream_gene_variant | MODIFIER | c.*4105C>T| |
S69 |
| 104454 | BAA10g07990 | A10 | 5094370 | G | A | downstream_gene_variant | MODIFIER | c.*3081C>T| |
S174 S216 S241 S27 S39 |
| 104455 | BAA10g07990 | A10 | 5096474 | G | A | downstream_gene_variant | MODIFIER | c.*977C>T| |
S245 |
| 104456 | BAA10g07990 | A10 | 5096635 | G | A | downstream_gene_variant | MODIFIER | c.*816C>T| |
S148 S30 S31 |
| 104457 | BAA10g07990 | A10 | 5096783 | G | A | downstream_gene_variant | MODIFIER | c.*668C>T| |
S230 |
| 104458 | BAA10g07990 | A10 | 5097065 | G | A | downstream_gene_variant | MODIFIER | c.*386C>T| |
S295 |
| 104459 | BAA10g07990 | A10 | 5098877 | C | T | upstream_gene_variant | MODIFIER | c.-1085G>A| |
S87 |
| 104460 | BAA10g07990 | A10 | 5098902 | C | T | upstream_gene_variant | MODIFIER | c.-1110G>A| |
S142 |
| 104461 | BAA10g07990 | A10 | 5099859 | C | T | upstream_gene_variant | MODIFIER | c.-2067G>A| |
S9 |
| 104462 | BAA10g07990 | A10 | 5100037 | G | A | upstream_gene_variant | MODIFIER | c.-2245C>T| |
S264 |
| 104463 | BAA10g07990 | A10 | 5100039 | T | A | upstream_gene_variant | MODIFIER | c.-2247A>T| |
S247 |
| 104464 | BAA10g07990 | A10 | 5100514 | C | T | upstream_gene_variant | MODIFIER | c.-2722G>A| |
S117 |
| 104465 | BAA10g07990 | A10 | 5101833 | G | A | upstream_gene_variant | MODIFIER | c.-4041C>T| |
S261 |
| 104466 | BAA10g07990 | A10 | 5102093 | C | T | upstream_gene_variant | MODIFIER | c.-4301G>A| |
S149 |
| 104467 | BAA10g07990 | A10 | 5102353 | C | T | upstream_gene_variant | MODIFIER | c.-4561G>A| |
S169 |
| 104468 | BAA10g07990-BAA10g08000 | A10 | 5103540 | C | T | intergenic_region | MODIFIER | n.5103540C>T| |
S155 S211 |
| 104469 | BAA10g07990-BAA10g08000 | A10 | 5103677 | C | T | intergenic_region | MODIFIER | n.5103677C>T| |
S10 |
| 104470 | BAA10g08000 | A10 | 5110394 | C | T | downstream_gene_variant | MODIFIER | c.*1271G>A| |
S195 |
| 104471 | BAA10g08000 | A10 | 5110652 | G | A | downstream_gene_variant | MODIFIER | c.*1013C>T| |
S161 |
| 104472 | BAA10g08000 | A10 | 5111204 | G | A | downstream_gene_variant | MODIFIER | c.*461C>T| |
S125 |
| 104473 | BAA10g08000 | A10 | 5112450 | G | A | synonymous_variant | LOW | c.946C>T|p.Leu316Leu |
S201 |
| 104474 | BAA10g08000 | A10 | 5112640 | C | T | synonymous_variant | LOW | c.756G>A|p.Gly252Gly |
S92 |
| 104475 | BAA10g08000 | A10 | 5112689 | G | A | missense_variant | MODERATE | c.707C>T|p.Ser236Leu |
S18 |