RHPN1
rhophilin Rho GTPase binding protein 1
Summary
Predicted to be involved in negative regulation of stress fiber assembly. Predicted to act upstream of or within several processes, including focal adhesion assembly; glomerular filtration; and renal albumin absorption. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs771346133 | 8:144,451,174 | G/A | — | uncertain significance |
| rs991931060 | 8:144,451,175 | G/C | — | uncertain significance |
| rs184179564 | 8:144,456,879 | C/T | regulatory region variant | — |
| rs745874856 | 8:144,457,769 | G/T | — | uncertain significance |
| rs200629468 | 8:144,457,793 | T/C | — | uncertain significance |
| rs144295575 | 8:144,457,821 | C/T | — | likely benign |
| rs764387997 | 8:144,457,822 | G/A | — | uncertain significance |
| rs377309042 | 8:144,457,837 | A/G | — | uncertain significance |
| rs1818353936 | 8:144,459,566 | C/T | — | uncertain significance |
| rs905784139 | 8:144,460,439 | G/A | — | uncertain significance |
| rs759454447 | 8:144,460,472 | G/A | — | likely benign |
| rs527948233 | 8:144,460,883 | C/G | — | uncertain significance |
| rs549702946 | 8:144,460,894 | C/T | — | uncertain significance |
| rs369639862 | 8:144,460,947 | C/T | — | uncertain significance |
| rs1442034169 | 8:144,460,974 | G/A | — | uncertain significance |
| rs781526277 | 8:144,460,988 | C/G | — | uncertain significance |
| rs776018449 | 8:144,461,105 | C/T | — | uncertain significance |
| rs377125823 | 8:144,461,116 | C/T | — | uncertain significance |
| rs757250054 | 8:144,461,117 | G/A | — | uncertain significance |
| rs1357188037 | 8:144,461,156 | T/C | — | uncertain significance |
| rs368252881 | 8:144,461,185 | C/T | — | uncertain significance |
| rs757952646 | 8:144,461,204 | C/G | — | uncertain significance |
| rs759609324 | 8:144,461,524 | C/G | — | uncertain significance |
| rs756087813 | 8:144,461,541 | G/A | — | uncertain significance |
| rs771562036 | 8:144,461,556 | G/A | — | uncertain significance |
| rs750285691 | 8:144,461,605 | G/A | — | uncertain significance |
| rs866899720 | 8:144,461,656 | G/A | — | likely benign |
| rs772366178 | 8:144,462,008 | G/A | — | uncertain significance |
| rs374320170 | 8:144,462,035 | G/A | — | uncertain significance |
| rs749778767 | 8:144,462,059 | G/A | — | likely benign |
| rs554965312 | 8:144,462,128 | G/A | — | uncertain significance |
| rs766683293 | 8:144,462,132 | C/G | — | uncertain significance |
| rs371467725 | 8:144,462,149 | G/A | — | likely benign |
| rs903014871 | 8:144,462,243 | G/A | — | uncertain significance |
| rs1029873497 | 8:144,462,316 | C/T | — | uncertain significance |
| rs1004411994 | 8:144,462,334 | G/A | — | uncertain significance |
| rs2537612934 | 8:144,462,789 | G/A | — | uncertain significance |
| rs117282246 | 8:144,462,841 | A/G | — | likely benign |
| rs562688370 | 8:144,462,855 | C/T | — | uncertain significance |
| rs371230736 | 8:144,462,870 | C/T | — | uncertain significance |
| rs760715263 | 8:144,462,878 | C/T | — | uncertain significance |
| rs1408244996 | 8:144,462,892 | G/C | — | uncertain significance |
| rs780984814 | 8:144,462,897 | C/T | — | uncertain significance |
| rs779347633 | 8:144,462,924 | G/A | — | uncertain significance |
| rs1232776210 | 8:144,462,933 | C/T | — | uncertain significance |
| rs932007771 | 8:144,463,459 | A/G | — | uncertain significance |
| rs202062863 | 8:144,463,510 | G/A | — | uncertain significance |
| rs1191079253 | 8:144,463,745 | C/T | — | uncertain significance |
| rs1818734946 | 8:144,463,764 | C/G | — | uncertain significance |
| rs779834813 | 8:144,463,978 | C/T | — | uncertain significance |
| rs373058084 | 8:144,464,025 | C/T | — | uncertain significance |
| rs2537619371 | 8:144,464,055 | G/A | — | uncertain significance |
| rs774554008 | 8:144,464,083 | C/T | — | uncertain significance |
| rs376102578 | 8:144,464,616 | G/A | — | uncertain significance |
| rs1437513844 | 8:144,464,618 | C/T | — | uncertain significance |
| rs368945775 | 8:144,464,621 | G/A | — | uncertain significance |
| rs1473921673 | 8:144,464,625 | T/C | — | uncertain significance |
| rs371349813 | 8:144,464,678 | C/T | — | uncertain significance |
| rs371512488 | 8:144,464,702 | C/T | — | uncertain significance |
| rs746096284 | 8:144,464,703 | G/C | — | uncertain significance |
| rs758787319 | 8:144,464,787 | C/T | — | likely benign |
| rs200767805 | 8:144,464,795 | T/A | — | uncertain significance |
| rs754713735 | 8:144,465,704 | A/G | — | — |
| rs73365860 | 8:144,466,737 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.