WDR59
WD repeat domain 59
Summary
Predicted to enable signaling adaptor activity. Involved in cellular response to amino acid starvation and positive regulation of TORC1 signaling. Located in cytosol and lysosomal membrane. Part of GATOR2 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61733724 | 16:74,908,146 | G/A | — | benign |
| rs201095907 | 16:74,908,213 | G/T | — | uncertain significance |
| rs199693877 | 16:74,908,226 | T/C | — | uncertain significance |
| rs776566274 | 16:74,908,231 | G/A | — | uncertain significance |
| rs368951096 | 16:74,908,285 | A/G | — | uncertain significance |
| rs147565383 | 16:74,908,297 | G/A | — | uncertain significance |
| rs144948949 | 16:74,908,315 | C/T | — | uncertain significance |
| rs112782182 | 16:74,918,674 | T/G | — | — |
| rs756003450 | 16:74,919,557 | C/G | — | uncertain significance |
| rs2507137444 | 16:74,919,575 | G/A | — | uncertain significance |
| rs759083994 | 16:74,920,205 | G/A | — | uncertain significance |
| rs61733726 | 16:74,921,593 | C/A | — | benign |
| rs761933462 | 16:74,922,101 | C/T | — | uncertain significance |
| rs767610772 | 16:74,922,102 | G/A | — | uncertain significance |
| rs9940422 | 16:74,922,106 | A/G | — | benign |
| rs767371477 | 16:74,922,194 | C/T | — | uncertain significance |
| rs761154451 | 16:74,922,195 | G/A | — | uncertain significance |
| rs144238663 | 16:74,922,200 | C/T | — | likely benign |
| rs755993642 | 16:74,922,206 | T/C | — | uncertain significance |
| rs149156771 | 16:74,923,697 | G/A | — | uncertain significance |
| rs751221419 | 16:74,923,706 | G/A | — | uncertain significance |
| rs145041449 | 16:74,926,406 | G/A | — | likely benign |
| rs778203835 | 16:74,927,595 | G/A | — | uncertain significance |
| rs922620822 | 16:74,927,600 | G/C | — | uncertain significance |
| rs775251469 | 16:74,927,635 | T/C | — | uncertain significance |
| rs779078769 | 16:74,927,661 | C/T | — | uncertain significance |
| rs376086980 | 16:74,927,685 | C/T | — | uncertain significance |
| rs145664758 | 16:74,927,691 | C/T | — | uncertain significance |
| rs201234819 | 16:74,937,942 | C/T | — | uncertain significance |
| rs1965686322 | 16:74,937,958 | C/T | — | uncertain significance |
| rs201965155 | 16:74,942,828 | A/G | — | uncertain significance |
| rs766144636 | 16:74,942,833 | G/A | — | uncertain significance |
| rs753696504 | 16:74,942,836 | C/T | — | uncertain significance |
| rs544155248 | 16:74,942,837 | G/A | — | uncertain significance |
| rs147993698 | 16:74,942,844 | T/C | — | likely benign |
| rs61734551 | 16:74,943,471 | T/C | — | benign |
| rs753169846 | 16:74,943,492 | G/A | — | uncertain significance |
| rs2507161720 | 16:74,943,549 | C/T | — | uncertain significance |
| rs772480957 | 16:74,943,734 | G/A | — | uncertain significance |
| rs1460756718 | 16:74,946,158 | G/T | — | uncertain significance |
| rs375654496 | 16:74,946,214 | T/C | — | uncertain significance |
| rs1384976643 | 16:74,949,876 | G/A | — | likely benign |
| rs61734553 | 16:74,949,890 | G/C | — | benign |
| rs2507207696 | 16:74,950,059 | A/T | — | uncertain significance |
| rs760823907 | 16:74,950,129 | A/G | — | uncertain significance |
| rs539179981 | 16:74,950,148 | T/G | — | uncertain significance |
| rs1454651235 | 16:74,951,834 | A/G | — | uncertain significance |
| rs371525112 | 16:74,951,864 | G/C | — | uncertain significance |
| rs948167361 | 16:74,951,882 | G/A | — | uncertain significance |
| rs201897171 | 16:74,955,905 | G/C | — | uncertain significance |
| rs116230305 | 16:74,955,911 | G/C | — | benign |
| rs751731132 | 16:74,957,876 | T/C | — | uncertain significance |
| rs142760193 | 16:74,957,879 | C/G | — | uncertain significance |
| rs2030524834 | 16:74,957,896 | C/A | — | uncertain significance |
| rs778499534 | 16:74,972,055 | G/A | — | uncertain significance |
| rs2032332304 | 16:74,976,655 | A/C | — | uncertain significance |
| rs201155431 | 16:74,976,680 | G/C | — | uncertain significance |
| rs2042415 | 16:74,978,618 | G/A | intron variant | — |
| rs147831394 | 16:74,982,420 | C/T | — | uncertain significance |
| rs772939841 | 16:74,982,434 | A/T | — | uncertain significance |
| rs143754167 | 16:74,983,639 | G/A | — | likely benign |
| rs2507367960 | 16:74,985,396 | C/T | — | uncertain significance |
| rs1484585471 | 16:74,990,468 | C/T | — | uncertain significance |
| rs747872806 | 16:74,999,704 | A/G | — | uncertain significance |
| rs77985639 | 16:74,999,712 | C/T | — | benign |
| rs371150311 | 16:74,999,713 | G/A | — | uncertain significance |
| rs2507416896 | 16:74,999,719 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.