ARHGAP19
Rho GTPase activating protein 19
Summary
Members of the ARHGAP family, such as ARHGAP19, encode negative regulators of Rho GTPases (see RHOA; MIM 165390), which are involved in cell migration, proliferation, and differentiation, actin remodeling, and G1 cell cycle progression (Lv et al., 2007 [PubMed 17454002]).[supplied by OMIM, Mar 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs181614433 | 10:98,985,942 | T/C | intron variant | — |
| rs756846192 | 10:98,988,957 | G/A | — | uncertain significance |
| rs11189052 | 10:98,993,378 | A/C | — | — |
| rs559397638 | 10:98,995,006 | C/T | — | uncertain significance |
| rs368950765 | 10:98,995,038 | C/A | — | uncertain significance |
| rs11189058 | 10:99,001,258 | G/A | intron variant | — |
| rs11595634 | 10:99,001,779 | A/T | intron variant | — |
| rs111882812 | 10:99,003,732 | A/G | — | uncertain significance |
| rs778966332 | 10:99,003,772 | C/T | — | uncertain significance |
| rs141595671 | 10:99,003,804 | G/A | — | uncertain significance |
| rs1842527679 | 10:99,003,817 | T/C | — | uncertain significance |
| rs746359494 | 10:99,006,037 | C/A | — | uncertain significance |
| rs2493381223 | 10:99,006,062 | C/G | — | uncertain significance |
| rs10882880 | 10:99,008,068 | G/A | intron variant | — |
| rs762116671 | 10:99,016,080 | A/G | — | uncertain significance |
| rs147811749 | 10:99,019,280 | C/T | — | uncertain significance |
| rs755467381 | 10:99,019,332 | G/A | — | uncertain significance |
| rs1296582807 | 10:99,019,338 | T/C | — | uncertain significance |
| rs148938316 | 10:99,023,208 | A/C | — | uncertain significance |
| rs1183997541 | 10:99,023,244 | C/T | — | uncertain significance |
| rs141073658 | 10:99,023,318 | G/A | — | uncertain significance |
| rs1842859620 | 10:99,023,348 | T/C | — | uncertain significance |
| rs796980 | 10:99,024,154 | G/A | intron variant | — |
| rs777657178 | 10:99,024,600 | A/G | — | uncertain significance |
| rs2538861688 | 10:99,024,642 | G/A | — | uncertain significance |
| rs757185815 | 10:99,025,622 | C/T | — | uncertain significance |
| rs1192518173 | 10:99,025,670 | C/A | — | uncertain significance |
| rs1325378652 | 10:99,025,703 | A/G | — | uncertain significance |
| rs750201004 | 10:99,025,748 | T/C | — | uncertain significance |
| rs145373661 | 10:99,025,796 | T/G | — | uncertain significance |
| rs752107486 | 10:99,052,338 | G/C | — | uncertain significance |
| rs773297476 | 10:99,052,356 | T/G | — | uncertain significance |
| rs373969394 | 10:99,052,357 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.