ARHGAP10
Rho GTPase activating protein 10
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in cytoskeleton organization and negative regulation of apoptotic process. Located in cytosol and endosome membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1380582093 | 4:148,653,586 | A/G | — | uncertain significance |
| rs964170 | 4:148,695,956 | G/C | — | — |
| rs2530982851 | 4:148,743,892 | C/A | — | uncertain significance |
| rs748951462 | 4:148,743,920 | A/G | — | uncertain significance |
| rs185914335 | 4:148,744,044 | C/T | — | likely benign |
| rs776619814 | 4:148,768,311 | G/A | — | uncertain significance |
| rs761673846 | 4:148,768,317 | G/A | — | uncertain significance |
| rs2531051644 | 4:148,768,337 | G/T | — | uncertain significance |
| rs775350718 | 4:148,786,021 | C/T | — | uncertain significance |
| rs1734491693 | 4:148,786,106 | C/T | — | uncertain significance |
| rs1734583211 | 4:148,787,929 | A/G | — | uncertain significance |
| rs145720035 | 4:148,787,930 | A/G | — | uncertain significance |
| rs759498019 | 4:148,796,182 | G/T | — | uncertain significance |
| rs483352827 | 4:148,796,185 | T/A | — | not provided |
| rs113611599 | 4:148,796,198 | G/A | — | benign |
| rs483352830 | 4:148,796,291 | C/T | — | not provided |
| rs749982137 | 4:148,800,409 | G/A | — | uncertain significance |
| rs146827185 | 4:148,800,431 | G/A | — | uncertain significance |
| rs762494538 | 4:148,800,485 | A/T | — | uncertain significance |
| rs138388284 | 4:148,802,995 | G/A | — | uncertain significance |
| rs61758694 | 4:148,803,027 | G/A | — | likely benign |
| rs769655337 | 4:148,803,044 | T/C | — | uncertain significance |
| rs540570241 | 4:148,827,793 | G/A | — | uncertain significance |
| rs61748165 | 4:148,827,795 | C/T | — | likely benign |
| rs756616736 | 4:148,827,796 | G/A | — | uncertain significance |
| rs938338038 | 4:148,827,823 | G/A | — | uncertain significance |
| rs1479359567 | 4:148,827,839 | A/G | — | uncertain significance |
| rs148015211 | 4:148,827,850 | G/A | — | uncertain significance |
| rs483352831 | 4:148,827,891 | A/G | — | not provided |
| rs774458424 | 4:148,830,902 | C/T | — | uncertain significance |
| rs548299896 | 4:148,830,907 | A/G | — | uncertain significance |
| rs373428584 | 4:148,834,254 | A/G | — | uncertain significance |
| rs147640829 | 4:148,834,256 | T/G | — | uncertain significance |
| rs140550063 | 4:148,834,277 | C/T | — | benign |
| rs2531330702 | 4:148,867,793 | C/A | — | uncertain significance |
| rs2531352704 | 4:148,876,486 | A/G | — | uncertain significance |
| rs7658486 | 4:148,884,189 | C/T | intron variant | — |
| rs17024215 | 4:148,886,185 | C/T | — | benign |
| rs483352828 | 4:148,886,192 | T/C | — | not provided |
| rs755998386 | 4:148,886,196 | G/C | — | uncertain significance |
| rs10213171 | 4:148,937,537 | C/G | intron variant | — |
| rs201271675 | 4:148,944,420 | C/T | — | uncertain significance |
| rs372199389 | 4:148,944,421 | G/A | — | uncertain significance |
| rs758356862 | 4:148,944,474 | C/A | — | uncertain significance |
| rs779982536 | 4:148,944,477 | A/T | — | uncertain significance |
| rs752960515 | 4:148,944,508 | G/A | — | uncertain significance |
| rs115152490 | 4:148,944,539 | C/T | — | benign |
| rs10027347 | 4:148,946,690 | G/T | intron variant | — |
| rs61659434 | 4:148,950,193 | G/A | intron variant | — |
| rs6839459 | 4:148,952,982 | A/G | intron variant | — |
| rs1297542169 | 4:148,968,051 | C/A | — | uncertain significance |
| rs377561565 | 4:148,968,123 | G/C | — | uncertain significance |
| rs558149671 | 4:148,968,187 | A/G | — | uncertain significance |
| rs74523651 | 4:148,968,201 | A/G | — | likely benign |
| rs6845865 | 4:148,974,602 | T/C | intron variant | — |
| rs10027275 | 4:148,981,496 | G/T | — | — |
| rs6853741 | 4:148,982,559 | G/A | intron variant | — |
| rs11099674 | 4:148,982,916 | G/T | — | — |
| rs771126748 | 4:148,984,316 | C/G | — | uncertain significance |
| rs368707168 | 4:148,984,393 | G/C | — | uncertain significance |
| rs572568347 | 4:148,984,414 | T/A | — | uncertain significance |
| rs541506840 | 4:148,984,415 | C/T | — | uncertain significance |
| rs747898571 | 4:148,985,569 | T/A | — | uncertain significance |
| rs200388255 | 4:148,985,577 | C/T | — | uncertain significance |
| rs146780598 | 4:148,985,592 | G/A | — | uncertain significance |
| rs141244949 | 4:148,985,599 | C/T | — | uncertain significance |
| rs483352829 | 4:148,985,614 | A/G | — | not provided |
| rs12649972 | 4:148,987,061 | C/G | — | — |
| rs917678428 | 4:148,993,192 | A/C | — | uncertain significance |
| rs547309760 | 4:148,993,218 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.