| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 114451 | BAA10g09300 | A10 | 11294683 | G | A | downstream_gene_variant | MODIFIER | c.*2846C>T| |
S283 |
| 114452 | BAA10g09300 | A10 | 11294848 | G | A | downstream_gene_variant | MODIFIER | c.*2681C>T| |
S295 |
| 114453 | BAA10g09300 | A10 | 11295084 | C | T | downstream_gene_variant | MODIFIER | c.*2445G>A| |
S126 |
| 114454 | BAA10g09300 | A10 | 11295136 | C | T | downstream_gene_variant | MODIFIER | c.*2393G>A| |
S81 S85 |
| 114455 | BAA10g09300 | A10 | 11295163 | C | T | downstream_gene_variant | MODIFIER | c.*2366G>A| |
S28 S30 |
| 114456 | BAA10g09300 | A10 | 11295175 | C | T | downstream_gene_variant | MODIFIER | c.*2354G>A| |
S200 |
| 114457 | BAA10g09300 | A10 | 11295771 | C | T | downstream_gene_variant | MODIFIER | c.*1758G>A| |
S20 |
| 114458 | BAA10g09300 | A10 | 11296164 | C | T | downstream_gene_variant | MODIFIER | c.*1365G>A| |
S269 |
| 114459 | BAA10g09300 | A10 | 11296212 | C | T | downstream_gene_variant | MODIFIER | c.*1317G>A| |
S237 |
| 114460 | BAA10g09300 | A10 | 11296229 | C | T | downstream_gene_variant | MODIFIER | c.*1300G>A| |
S98 |
| 114461 | BAA10g09300 | A10 | 11296475 | C | T | downstream_gene_variant | MODIFIER | c.*1054G>A| |
S225 |
| 114462 | BAA10g09300 | A10 | 11296592 | C | T | downstream_gene_variant | MODIFIER | c.*937G>A| |
S270 |
| 114463 | BAA10g09300 | A10 | 11296862 | C | T | downstream_gene_variant | MODIFIER | c.*667G>A| |
S278 |
| 114464 | BAA10g09300 | A10 | 11297083 | G | A | downstream_gene_variant | MODIFIER | c.*446C>T| |
S289 |
| 114465 | BAA10g09300 | A10 | 11297094 | C | T | downstream_gene_variant | MODIFIER | c.*435G>A| |
S244 |
| 114466 | BAA10g09300 | A10 | 11297623 | G | A | missense_variant | MODERATE | c.2126C>T|p.Ser709Leu |
S205 |
| 114467 | BAA10g09300 | A10 | 11298530 | G | A | synonymous_variant | LOW | c.1293C>T|p.Ile431Ile |
S100 |
| 114468 | BAA10g09300 | A10 | 11299404 | C | T | stop_gained | HIGH | c.716G>A|p.Trp239* |
S86 |
| 114469 | BAA10g09300 | A10 | 11299429 | G | A | missense_variant | MODERATE | c.691C>T|p.Pro231Ser |
S95 |
| 114470 | BAA10g09300 | A10 | 11300875 | C | T | upstream_gene_variant | MODIFIER | c.-248G>A| |
S225 S73 |
| 114471 | BAA10g09300 | A10 | 11301172 | C | T | upstream_gene_variant | MODIFIER | c.-545G>A| |
S268 |
| 114472 | BAA10g09300 | A10 | 11301914 | C | T | upstream_gene_variant | MODIFIER | c.-1287G>A| |
S143 |
| 114473 | BAA10g09300 | A10 | 11301977 | C | T | upstream_gene_variant | MODIFIER | c.-1350G>A| |
S144 |
| 114474 | BAA10g09300 | A10 | 11303632 | G | A | upstream_gene_variant | MODIFIER | c.-3005C>T| |
S172 |
| 114475 | BAA10g09300 | A10 | 11303840 | C | T | upstream_gene_variant | MODIFIER | c.-3213G>A| |
S235 |