TBC1D10A
TBC1 domain family member 10A
Summary
Enables PDZ domain binding activity. Involved in positive regulation of proteolysis and retrograde transport, endosome to Golgi. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs779296181 | 22:30,688,385 | C/G | — | uncertain significance |
| rs373742072 | 22:30,688,395 | G/A | — | uncertain significance |
| rs751666624 | 22:30,688,495 | G/T | — | uncertain significance |
| rs370014538 | 22:30,688,555 | C/T | — | uncertain significance |
| rs1029504465 | 22:30,688,623 | G/A | — | uncertain significance |
| rs4823086 | 22:30,688,659 | C/T | — | benign |
| rs775256563 | 22:30,688,740 | G/A | — | uncertain significance |
| rs772289218 | 22:30,688,747 | G/A | — | likely benign |
| rs1337756861 | 22:30,688,762 | C/T | — | uncertain significance |
| rs754413591 | 22:30,688,783 | G/A | — | uncertain significance |
| rs751133458 | 22:30,688,815 | C/T | — | uncertain significance |
| rs1469082897 | 22:30,689,642 | C/T | — | uncertain significance |
| rs2518139729 | 22:30,689,695 | T/A | — | uncertain significance |
| rs747908846 | 22:30,689,697 | G/C | — | uncertain significance |
| rs758161918 | 22:30,689,699 | T/C | — | uncertain significance |
| rs770050410 | 22:30,689,705 | C/T | — | uncertain significance |
| rs200927000 | 22:30,689,740 | G/A | — | uncertain significance |
| rs765107481 | 22:30,689,756 | T/G | — | uncertain significance |
| rs2518139831 | 22:30,689,759 | G/C | — | uncertain significance |
| rs758359779 | 22:30,689,993 | A/G | — | uncertain significance |
| rs149056616 | 22:30,690,805 | C/T | — | uncertain significance |
| rs143051895 | 22:30,690,945 | C/T | — | uncertain significance |
| rs148180975 | 22:30,690,990 | C/G | — | uncertain significance |
| rs373381826 | 22:30,690,995 | C/T | — | uncertain significance |
| rs749055989 | 22:30,691,027 | C/T | — | uncertain significance |
| rs768962153 | 22:30,691,772 | G/A | — | uncertain significance |
| rs929454 | 22:30,692,353 | A/C | — | — |
| rs748252342 | 22:30,695,494 | C/T | — | uncertain significance |
| rs201457560 | 22:30,695,519 | C/T | — | uncertain significance |
| rs2518144096 | 22:30,695,520 | C/A | — | uncertain significance |
| rs769649437 | 22:30,695,536 | C/T | — | uncertain significance |
| rs1930271266 | 22:30,700,533 | T/C | — | uncertain significance |
| rs1365195595 | 22:30,700,565 | G/T | — | uncertain significance |
| rs1930272444 | 22:30,700,570 | G/C | — | uncertain significance |
| rs2041200 | 22:30,709,531 | G/C | regulatory region variant | — |
| rs564057543 | 22:30,709,584 | G/T | — | — |
| rs28360656 | 22:30,717,739 | T/C | intron variant | — |
| rs370312386 | 22:30,722,771 | T/C | — | likely benign |
| rs758403562 | 22:30,722,812 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.