ARHGAP45
Rho GTPase activating protein 45
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in negative regulation of small GTPase mediated signal transduction. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs73505251 | 19:1,068,095 | T/A | regulatory region variant | — |
| rs377283752 | 19:1,068,452 | G/A | — | uncertain significance |
| rs756372104 | 19:1,068,472 | C/T | — | likely benign |
| rs751570740 | 19:1,068,651 | C/T | — | uncertain significance |
| rs3764653 | 19:1,068,734 | C/T | — | benign |
| rs1801284 | 19:1,068,738 | G/A | — | benign |
| rs4807506 | 19:1,071,312 | T/C | — | benign |
| rs145027652 | 19:1,073,565 | C/T | — | uncertain significance |
| rs12974537 | 19:1,074,315 | C/T | intron variant | — |
| rs749157208 | 19:1,074,852 | G/A | — | uncertain significance |
| rs1174064437 | 19:1,077,934 | C/T | — | uncertain significance |
| rs75236288 | 19:1,077,947 | C/T | — | benign |
| rs758250463 | 19:1,077,974 | C/T | — | likely benign |
| rs35140707 | 19:1,078,297 | C/T | intron variant | — |
| rs35532684 | 19:1,078,303 | T/C | intron variant | — |
| rs2043386726 | 19:1,080,113 | G/A | — | uncertain significance |
| rs368248990 | 19:1,081,650 | C/T | — | likely benign |
| rs115889781 | 19:1,081,858 | G/A | — | benign |
| rs11878920 | 19:1,082,266 | G/C | regulatory region variant | — |
| rs113986255 | 19:1,082,835 | G/A | — | benign |
| rs745543210 | 19:1,082,988 | T/G | — | likely benign |
| rs904436394 | 19:1,083,230 | G/A | — | uncertain significance |
| rs371532691 | 19:1,083,342 | C/G | — | uncertain significance |
| rs35124413 | 19:1,084,314 | G/C | — | benign |
| rs146827391 | 19:1,084,321 | G/C | — | likely benign |
| rs112975635 | 19:1,084,336 | G/A | — | likely benign |
| rs149960692 | 19:1,085,690 | G/A | — | benign |
| rs760355452 | 19:1,085,856 | G/A | — | uncertain significance |
| rs61734935 | 19:1,085,863 | A/G | — | benign |
| rs759168052 | 19:1,085,888 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.