ADAP1
ArfGAP with dual PH domains 1
Summary
Enables GTPase activator activity. Predicted to be involved in cell surface receptor signaling pathway. Located in cytosol; nucleus; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1258238111 | 7:938,775 | C/T | — | uncertain significance |
| rs61995731 | 7:938,845 | C/T | — | benign |
| rs1329528728 | 7:938,870 | A/G | — | uncertain significance |
| rs3779613 | 7:939,369 | C/T | regulatory region variant | — |
| rs1319817873 | 7:940,175 | C/T | — | uncertain significance |
| rs370538517 | 7:943,843 | C/T | — | uncertain significance |
| rs2483114000 | 7:943,888 | T/C | — | uncertain significance |
| rs558466458 | 7:944,707 | T/C | — | uncertain significance |
| rs561202230 | 7:944,752 | C/T | — | uncertain significance |
| rs760068363 | 7:944,783 | G/A | — | uncertain significance |
| rs145005339 | 7:944,804 | G/A | — | uncertain significance |
| rs150718412 | 7:944,817 | G/C | — | benign |
| rs1431657025 | 7:959,613 | T/G | — | uncertain significance |
| rs769371283 | 7:959,616 | G/A | — | uncertain significance |
| rs748807680 | 7:959,687 | C/G | — | uncertain significance |
| rs1881117 | 7:961,700 | C/G | — | — |
| rs13230191 | 7:964,180 | T/C | intron variant | — |
| rs148979654 | 7:966,210 | C/T | — | uncertain significance |
| rs376277744 | 7:966,252 | G/A | — | uncertain significance |
| rs770303688 | 7:966,259 | C/T | — | uncertain significance |
| rs142995759 | 7:966,260 | G/A | — | likely benign |
| rs10480059 | 7:970,035 | C/A | — | — |
| rs10480060 | 7:970,039 | C/G | — | — |
| rs78582080 | 7:970,041 | C/A | — | — |
| rs2483279776 | 7:975,016 | C/T | — | uncertain significance |
| rs865869561 | 7:975,112 | C/T | — | uncertain significance |
| rs6969773 | 7:980,566 | T/C | intron variant | — |
| rs948350289 | 7:994,037 | G/A | — | uncertain significance |
| rs74601708 | 7:995,724 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.