TBC1D16
TBC1 domain family member 16
Summary
Enables GTPase activator activity. Involved in regulation of receptor recycling. Located in cytosol and early endosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12450069 | 17:77,908,321 | G/A | downstream gene variant | — |
| rs7214378 | 17:77,909,085 | C/T | regulatory region variant | — |
| rs56014161 | 17:77,910,740 | C/T | — | — |
| rs367785113 | 17:77,914,672 | C/T | — | uncertain significance |
| rs374603858 | 17:77,914,686 | G/A | — | uncertain significance |
| rs1718893598 | 17:77,914,735 | T/C | — | uncertain significance |
| rs759469164 | 17:77,914,750 | C/T | — | uncertain significance |
| rs756894540 | 17:77,914,771 | C/T | — | uncertain significance |
| rs755414026 | 17:77,914,782 | C/T | — | uncertain significance |
| rs759693304 | 17:77,914,797 | G/T | — | uncertain significance |
| rs778148705 | 17:77,914,849 | C/T | — | uncertain significance |
| rs746141447 | 17:77,914,865 | G/C | — | uncertain significance |
| rs772249685 | 17:77,914,869 | C/T | — | uncertain significance |
| rs141943473 | 17:77,915,863 | C/T | — | uncertain significance |
| rs200514216 | 17:77,915,864 | G/A | — | uncertain significance |
| rs747993015 | 17:77,915,876 | C/G | — | uncertain significance |
| rs1278973760 | 17:77,915,879 | C/T | — | uncertain significance |
| rs770778543 | 17:77,915,903 | C/T | — | uncertain significance |
| rs377148307 | 17:77,915,926 | G/A | — | uncertain significance |
| rs144060365 | 17:77,915,949 | G/A | — | likely benign |
| rs145969761 | 17:77,915,970 | G/A | — | benign |
| rs368445644 | 17:77,916,004 | G/A | — | uncertain significance |
| rs2509880852 | 17:77,918,757 | G/A | — | uncertain significance |
| rs760829629 | 17:77,918,790 | G/A | — | uncertain significance |
| rs2032390185 | 17:77,918,803 | C/A | — | uncertain significance |
| rs1226225126 | 17:77,918,810 | A/G | — | uncertain significance |
| rs142146072 | 17:77,918,858 | G/A | — | uncertain significance |
| rs1017275591 | 17:77,918,874 | C/T | — | uncertain significance |
| rs993990631 | 17:77,918,876 | C/T | — | uncertain significance |
| rs747368486 | 17:77,918,877 | G/A | — | uncertain significance |
| rs147673750 | 17:77,921,287 | C/T | regulatory region variant | — |
| rs2509911822 | 17:77,922,675 | T/C | — | uncertain significance |
| rs181752232 | 17:77,922,704 | C/G | — | uncertain significance |
| rs2509913227 | 17:77,922,750 | C/T | — | uncertain significance |
| rs2509921724 | 17:77,923,542 | C/A | — | uncertain significance |
| rs144489628 | 17:77,924,245 | G/T | — | uncertain significance |
| rs767395568 | 17:77,924,292 | A/G | — | uncertain significance |
| rs762333584 | 17:77,925,296 | C/T | — | uncertain significance |
| rs754925270 | 17:77,925,320 | C/T | — | uncertain significance |
| rs1469230085 | 17:77,925,358 | C/T | — | uncertain significance |
| rs757938163 | 17:77,926,468 | C/T | — | uncertain significance |
| rs147640226 | 17:77,926,508 | C/T | — | uncertain significance |
| rs762764896 | 17:77,926,510 | C/T | — | uncertain significance |
| rs765065786 | 17:77,926,553 | G/A | — | uncertain significance |
| rs746228874 | 17:77,926,580 | C/T | — | uncertain significance |
| rs370095669 | 17:77,926,588 | C/T | — | uncertain significance |
| rs776784994 | 17:77,926,589 | G/A | — | uncertain significance |
| rs773835984 | 17:77,926,601 | C/T | — | uncertain significance |
| rs760338893 | 17:77,983,989 | C/T | — | uncertain significance |
| rs140663983 | 17:77,984,004 | G/A | — | uncertain significance |
| rs761192599 | 17:77,984,089 | C/G | — | uncertain significance |
| rs148590391 | 17:77,984,122 | C/T | — | uncertain significance |
| rs746792976 | 17:77,984,130 | C/T | — | uncertain significance |
| rs370285162 | 17:77,984,131 | G/A | — | uncertain significance |
| rs747788377 | 17:77,984,133 | G/A | — | likely benign |
| rs35393459 | 17:77,984,168 | G/A | — | benign |
| rs747537940 | 17:77,984,193 | C/T | — | uncertain significance |
| rs201402527 | 17:77,984,208 | G/A | — | uncertain significance |
| rs543310279 | 17:77,984,244 | G/A | — | uncertain significance |
| rs1169381990 | 17:77,984,313 | A/G | — | uncertain significance |
| rs1320162763 | 17:77,984,334 | G/A | — | likely benign |
| rs778214302 | 17:77,984,347 | G/A | — | uncertain significance |
| rs759593097 | 17:77,984,358 | G/T | — | uncertain significance |
| rs1413218666 | 17:77,984,371 | G/A | — | uncertain significance |
| rs1360049202 | 17:77,984,377 | C/T | — | uncertain significance |
| rs548841668 | 17:77,984,389 | G/A | — | uncertain significance |
| rs755651950 | 17:77,984,391 | G/A | — | uncertain significance |
| rs748684793 | 17:77,984,407 | G/A | — | uncertain significance |
| rs747087052 | 17:77,984,454 | A/G | — | uncertain significance |
| rs2144669660 | 17:77,984,523 | A/G | — | uncertain significance |
| rs35564207 | 17:77,987,281 | G/T | — | benign |
| rs1008121720 | 17:77,987,289 | G/A | — | uncertain significance |
| rs747760676 | 17:77,987,321 | C/A | — | uncertain significance |
| rs1003195224 | 17:77,987,324 | C/T | — | uncertain significance |
| rs62074525 | 17:77,992,033 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.