ARHGAP25
Rho GTPase activating protein 25
Summary
ARHGAPs, such as ARHGAP25, encode negative regulators of Rho GTPases (see ARHA; MIM 165390), which are implicated in actin remodeling, cell polarity, and cell migration (Katoh and Katoh, 2004 [PubMed 15254788]).[supplied by OMIM, Mar 2008]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4854494 | 2:68,938,815 | C/A | — | — |
| rs4854446 | 2:68,939,684 | C/A | intron variant | — |
| rs144263620 | 2:68,952,433 | G/A | intron variant | — |
| rs2280243 | 2:68,979,331 | G/T | regulatory region variant | — |
| rs551816260 | 2:69,002,391 | G/A | — | uncertain significance |
| rs369807257 | 2:69,002,404 | C/T | — | uncertain significance |
| rs766366901 | 2:69,002,520 | T/C | — | uncertain significance |
| rs1293246856 | 2:69,009,380 | C/G | — | uncertain significance |
| rs756666210 | 2:69,009,404 | G/A | — | uncertain significance |
| rs530704143 | 2:69,026,028 | C/G | — | — |
| rs115522963 | 2:69,033,583 | C/T | regulatory region variant | — |
| rs142788069 | 2:69,034,420 | G/A | — | uncertain significance |
| rs1363842271 | 2:69,034,482 | G/A | — | uncertain significance |
| rs958078986 | 2:69,034,596 | C/T | — | uncertain significance |
| rs114063280 | 2:69,040,411 | T/C | — | benign |
| rs2466648527 | 2:69,040,480 | C/T | — | uncertain significance |
| rs61758703 | 2:69,040,504 | G/A | missense variant | Likely benign |
| rs779296785 | 2:69,040,507 | G/A | — | uncertain significance |
| rs774311887 | 2:69,040,545 | G/C | — | uncertain significance |
| rs201905093 | 2:69,043,451 | A/G | — | uncertain significance |
| rs770908301 | 2:69,043,461 | G/A | — | uncertain significance |
| rs143413666 | 2:69,046,285 | T/G | — | uncertain significance |
| rs149839883 | 2:69,046,332 | C/A | — | uncertain significance |
| rs757436657 | 2:69,046,370 | A/T | — | uncertain significance |
| rs143476860 | 2:69,049,522 | G/A | — | benign |
| rs150901180 | 2:69,049,538 | A/G | — | uncertain significance |
| rs199776517 | 2:69,049,686 | C/T | — | uncertain significance |
| rs143665378 | 2:69,049,729 | G/A | — | benign |
| rs910432799 | 2:69,049,758 | A/T | — | uncertain significance |
| rs140413752 | 2:69,049,766 | C/T | — | uncertain significance |
| rs781613158 | 2:69,049,767 | G/A | — | uncertain significance |
| rs140111652 | 2:69,049,871 | A/C | — | uncertain significance |
| rs370768048 | 2:69,049,890 | G/A | — | uncertain significance |
| rs751934453 | 2:69,049,905 | A/G | — | uncertain significance |
| rs768309526 | 2:69,049,973 | C/G | — | uncertain significance |
| rs942770478 | 2:69,053,219 | C/T | — | uncertain significance |
| rs374053151 | 2:69,053,220 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.