ARHGAP17
Rho GTPase activating protein 17
Summary
RICH1 is a GTPase-activating protein (GAP). GAPs stimulate the intrinsic GTP hydrolysis of small G proteins, such as RHOA (MIM 165390), RAC1 (MIM 602048), and CDC42 (MIM 116952).[supplied by OMIM, Apr 2004]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1278750681 | 16:24,931,458 | G/A | — | uncertain significance |
| rs148385769 | 16:24,931,497 | C/T | — | likely benign |
| rs999318435 | 16:24,931,504 | G/A | — | uncertain significance |
| rs760135610 | 16:24,931,551 | C/T | — | uncertain significance |
| rs4788439 | 16:24,931,798 | C/A | coding sequence variant | — |
| rs4787655 | 16:24,931,894 | A/G | coding sequence variant | — |
| rs368479893 | 16:24,942,230 | G/T | — | uncertain significance |
| rs370125785 | 16:24,942,236 | G/A | — | uncertain significance |
| rs376036575 | 16:24,942,329 | G/A | — | uncertain significance |
| rs202032364 | 16:24,942,345 | T/C | — | uncertain significance |
| rs2507567988 | 16:24,942,357 | G/A | — | uncertain significance |
| rs569039543 | 16:24,942,364 | G/C | — | uncertain significance |
| rs2507572030 | 16:24,942,477 | G/A | — | uncertain significance |
| rs752563170 | 16:24,942,524 | C/T | — | uncertain significance |
| rs1331678570 | 16:24,942,584 | G/A | — | uncertain significance |
| rs370592030 | 16:24,942,713 | G/T | — | uncertain significance |
| rs771605905 | 16:24,942,723 | C/T | — | uncertain significance |
| rs577832914 | 16:24,946,796 | C/T | — | uncertain significance |
| rs1363589763 | 16:24,946,802 | G/A | — | uncertain significance |
| rs893277352 | 16:24,946,870 | C/G | — | uncertain significance |
| rs139744528 | 16:24,946,904 | T/C | — | likely benign |
| rs755242883 | 16:24,946,949 | G/A | — | uncertain significance |
| rs55954168 | 16:24,949,543 | G/C | intron variant | — |
| rs1230946195 | 16:24,950,710 | G/C | — | uncertain significance |
| rs2507698502 | 16:24,950,755 | T/C | — | uncertain significance |
| rs1253745769 | 16:24,950,767 | T/C | — | uncertain significance |
| rs956942077 | 16:24,950,769 | G/C | — | uncertain significance |
| rs368132068 | 16:24,950,772 | C/T | — | uncertain significance |
| rs757927930 | 16:24,950,776 | G/C | — | uncertain significance |
| rs1369197390 | 16:24,950,781 | G/C | — | uncertain significance |
| rs149025741 | 16:24,950,797 | C/T | — | uncertain significance |
| rs549344360 | 16:24,950,800 | G/A | — | uncertain significance |
| rs199828507 | 16:24,950,803 | C/T | — | uncertain significance |
| rs750090760 | 16:24,950,826 | G/A | — | uncertain significance |
| rs140685431 | 16:24,950,835 | G/A | — | uncertain significance |
| rs965697583 | 16:24,953,345 | T/C | — | uncertain significance |
| rs199829132 | 16:24,953,357 | G/A | — | uncertain significance |
| rs2507741009 | 16:24,953,378 | A/G | — | uncertain significance |
| rs2141189188 | 16:24,953,390 | T/G | — | uncertain significance |
| rs2051327718 | 16:24,953,392 | C/G | — | uncertain significance |
| rs111873081 | 16:24,955,577 | C/G | — | — |
| rs749151012 | 16:24,958,804 | C/T | — | uncertain significance |
| rs2507827591 | 16:24,958,823 | C/G | — | uncertain significance |
| rs2051508354 | 16:24,958,845 | G/A | — | uncertain significance |
| rs1030856729 | 16:24,958,854 | C/T | — | uncertain significance |
| rs2507829365 | 16:24,958,909 | T/A | — | uncertain significance |
| rs1285259763 | 16:24,964,297 | T/C | — | uncertain significance |
| rs762867053 | 16:24,971,003 | C/T | — | uncertain significance |
| rs370710220 | 16:24,975,537 | T/C | — | uncertain significance |
| rs763769060 | 16:24,979,709 | C/T | — | uncertain significance |
| rs4787294 | 16:25,002,350 | A/T | intron variant | — |
| rs9926667 | 16:25,002,707 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.