TBC1D8
TBC1 domain family member 8
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in blood circulation and positive regulation of cell population proliferation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs749419550 | 2:101,624,323 | C/T | — | uncertain significance |
| rs1460224050 | 2:101,624,328 | T/G | — | uncertain significance |
| rs1364127385 | 2:101,624,378 | A/G | — | uncertain significance |
| rs201882166 | 2:101,624,509 | G/C | — | uncertain significance |
| rs370459788 | 2:101,624,561 | G/A | — | uncertain significance |
| rs752796494 | 2:101,624,596 | G/A | — | uncertain significance |
| rs371112222 | 2:101,624,647 | A/G | — | uncertain significance |
| rs2466900449 | 2:101,627,428 | T/C | — | uncertain significance |
| rs200716618 | 2:101,627,915 | T/C | — | uncertain significance |
| rs751146917 | 2:101,627,918 | G/T | — | uncertain significance |
| rs1062062 | 2:101,627,925 | C/T | — | benign |
| rs748358702 | 2:101,627,951 | A/G | — | uncertain significance |
| rs11886914 | 2:101,637,515 | T/G | downstream gene variant | — |
| rs183633494 | 2:101,638,199 | T/C | — | uncertain significance |
| rs201583665 | 2:101,638,778 | T/G | — | uncertain significance |
| rs200848642 | 2:101,638,808 | G/A | — | uncertain significance |
| rs372757533 | 2:101,638,839 | C/T | — | uncertain significance |
| rs368734566 | 2:101,638,892 | A/G | — | uncertain significance |
| rs764066990 | 2:101,638,893 | T/C | — | uncertain significance |
| rs1306256823 | 2:101,638,910 | T/C | — | uncertain significance |
| rs779401993 | 2:101,638,916 | C/T | — | uncertain significance |
| rs1680098420 | 2:101,638,967 | C/T | — | uncertain significance |
| rs139953660 | 2:101,643,856 | C/T | — | uncertain significance |
| rs746727869 | 2:101,643,913 | G/C | — | uncertain significance |
| rs376791505 | 2:101,644,526 | G/A | — | uncertain significance |
| rs199616962 | 2:101,644,779 | G/C | — | uncertain significance |
| rs755006747 | 2:101,644,821 | C/T | — | uncertain significance |
| rs758001242 | 2:101,644,824 | C/T | — | uncertain significance |
| rs759365632 | 2:101,644,893 | A/T | — | uncertain significance |
| rs1447061102 | 2:101,645,971 | G/T | — | uncertain significance |
| rs564042549 | 2:101,646,088 | G/A | — | uncertain significance |
| rs186711956 | 2:101,646,143 | C/T | — | likely benign |
| rs55771809 | 2:101,647,894 | G/A | intron variant | — |
| rs2466961781 | 2:101,648,748 | A/G | — | uncertain significance |
| rs755195520 | 2:101,648,766 | G/A | — | uncertain significance |
| rs868459830 | 2:101,649,425 | A/G | — | — |
| rs200825898 | 2:101,650,092 | C/T | — | uncertain significance |
| rs376930921 | 2:101,650,166 | T/G | — | uncertain significance |
| rs1398703515 | 2:101,650,193 | G/C | — | uncertain significance |
| rs2466976290 | 2:101,654,019 | C/A | — | uncertain significance |
| rs979365033 | 2:101,654,041 | C/T | — | likely benign |
| rs760839882 | 2:101,654,085 | T/C | — | uncertain significance |
| rs201011787 | 2:101,654,089 | C/T | — | uncertain significance |
| rs368634804 | 2:101,654,106 | A/G | — | uncertain significance |
| rs189907725 | 2:101,654,525 | A/T | intron variant | — |
| rs535403545 | 2:101,654,933 | T/A | — | uncertain significance |
| rs751447886 | 2:101,654,934 | C/T | — | uncertain significance |
| rs763921122 | 2:101,654,942 | G/A | — | uncertain significance |
| rs1322611837 | 2:101,654,948 | T/C | — | uncertain significance |
| rs781370079 | 2:101,654,959 | G/C | — | uncertain significance |
| rs767524342 | 2:101,654,991 | G/A | — | uncertain significance |
| rs752283302 | 2:101,655,020 | C/T | — | uncertain significance |
| rs202111685 | 2:101,655,021 | G/A | — | uncertain significance |
| rs371898061 | 2:101,655,099 | T/C | — | uncertain significance |
| rs376684318 | 2:101,656,680 | C/T | — | likely benign |
| rs373113146 | 2:101,656,719 | C/T | — | uncertain significance |
| rs34425369 | 2:101,656,748 | C/T | — | benign |
| rs370330869 | 2:101,656,749 | G/A | — | uncertain significance |
| rs1003818142 | 2:101,656,813 | G/A | — | uncertain significance |
| rs1278984647 | 2:101,656,836 | G/A | — | uncertain significance |
| rs1573938281 | 2:101,666,887 | T/C | — | uncertain significance |
| rs754985690 | 2:101,666,917 | T/G | — | uncertain significance |
| rs1211500827 | 2:101,666,945 | C/T | — | uncertain significance |
| rs369454665 | 2:101,667,019 | G/A | — | uncertain significance |
| rs568388681 | 2:101,667,028 | C/T | — | uncertain significance |
| rs372928611 | 2:101,667,052 | T/C | — | uncertain significance |
| rs2278729 | 2:101,668,857 | G/A | intron variant | — |
| rs2467012992 | 2:101,670,612 | T/C | — | uncertain significance |
| rs750144028 | 2:101,670,621 | A/G | — | uncertain significance |
| rs759875939 | 2:101,670,635 | C/T | — | uncertain significance |
| rs78556703 | 2:101,670,676 | G/A | — | benign |
| rs1005998201 | 2:101,670,691 | C/G | — | uncertain significance |
| rs747535253 | 2:101,670,693 | C/T | — | uncertain significance |
| rs1051291220 | 2:101,670,744 | C/T | — | uncertain significance |
| rs368740197 | 2:101,675,956 | T/C | — | uncertain significance |
| rs13032971 | 2:101,689,726 | T/G | downstream gene variant | — |
| rs1422122794 | 2:101,706,749 | G/C | — | uncertain significance |
| rs2919691 | 2:101,734,933 | T/A | — | — |
| rs796056 | 2:101,735,276 | A/T | — | — |
| rs2309996 | 2:101,735,838 | T/C | — | — |
| rs118129147 | 2:101,756,135 | T/A | intron variant | — |
| rs1275308341 | 2:101,767,671 | C/A | — | uncertain significance |
| rs928201850 | 2:101,767,705 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.