ACAP1
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1
Summary
Predicted to enable GTPase activator activity and zinc ion binding activity. Predicted to be involved in protein transport. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs760803287 | 17:7,240,057 | A/T | — | uncertain significance |
| rs374103329 | 17:7,240,066 | C/G | — | uncertain significance |
| rs147825679 | 17:7,240,100 | G/A | — | uncertain significance |
| rs150346841 | 17:7,245,267 | C/G | — | uncertain significance |
| rs370473529 | 17:7,245,303 | C/T | — | uncertain significance |
| rs370190619 | 17:7,245,328 | C/A | — | uncertain significance |
| rs145850889 | 17:7,245,383 | G/A | — | uncertain significance |
| rs781574569 | 17:7,245,627 | C/T | — | uncertain significance |
| rs201609564 | 17:7,245,786 | G/A | — | uncertain significance |
| rs150661712 | 17:7,246,705 | C/G | — | uncertain significance |
| rs746768465 | 17:7,246,727 | G/T | — | uncertain significance |
| rs762155212 | 17:7,246,792 | C/T | — | uncertain significance |
| rs538307560 | 17:7,247,187 | G/A | — | uncertain significance |
| rs373061856 | 17:7,247,239 | C/G | — | uncertain significance |
| rs772458780 | 17:7,247,268 | G/C | — | uncertain significance |
| rs1318820640 | 17:7,247,407 | G/A | — | uncertain significance |
| rs549313700 | 17:7,247,873 | G/A | — | uncertain significance |
| rs148480413 | 17:7,247,946 | A/G | — | uncertain significance |
| rs756756826 | 17:7,250,191 | A/T | — | uncertain significance |
| rs143239962 | 17:7,250,218 | C/T | — | uncertain significance |
| rs140256517 | 17:7,250,423 | G/C | — | uncertain significance |
| rs145239336 | 17:7,250,428 | G/C | — | uncertain significance |
| rs767344218 | 17:7,250,431 | G/A | — | uncertain significance |
| rs144821659 | 17:7,250,437 | G/A | — | uncertain significance |
| rs753865344 | 17:7,250,438 | T/C | — | uncertain significance |
| rs1034152904 | 17:7,250,471 | C/A | — | uncertain significance |
| rs376167360 | 17:7,250,551 | G/A | — | uncertain significance |
| rs143351258 | 17:7,251,257 | T/C | — | uncertain significance |
| rs2073363692 | 17:7,251,279 | C/T | — | uncertain significance |
| rs760063972 | 17:7,251,764 | C/T | — | uncertain significance |
| rs760206336 | 17:7,251,767 | C/T | — | uncertain significance |
| rs2508790000 | 17:7,252,322 | T/A | — | uncertain significance |
| rs751510898 | 17:7,252,346 | C/T | — | uncertain significance |
| rs1463950587 | 17:7,252,376 | C/T | — | uncertain significance |
| rs2073377410 | 17:7,252,426 | T/G | — | uncertain significance |
| rs762488840 | 17:7,252,446 | G/A | — | uncertain significance |
| rs769289872 | 17:7,253,282 | G/A | — | uncertain significance |
| rs762534928 | 17:7,253,300 | G/C | — | uncertain significance |
| rs760636497 | 17:7,253,450 | G/T | — | uncertain significance |
| rs1297832674 | 17:7,253,510 | C/G | — | uncertain significance |
| rs1170730852 | 17:7,253,528 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.