RASIP1
Ras interacting protein 1
Summary
Enables GTPase binding activity and protein homodimerization activity. Involved in several processes, including negative regulation of Rho protein signal transduction; negative regulation of metabolic process; and positive regulation of integrin activation. Located in cell-cell junction. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs947188410 | 19:49,224,075 | G/A | — | uncertain significance |
| rs140266474 | 19:49,224,105 | C/T | — | uncertain significance |
| rs142687046 | 19:49,224,107 | T/C | — | uncertain significance |
| rs2514005804 | 19:49,224,114 | C/T | — | uncertain significance |
| rs34800326 | 19:49,224,120 | C/T | — | likely benign |
| rs747036652 | 19:49,224,134 | C/T | — | uncertain significance |
| rs773516310 | 19:49,224,154 | G/T | — | uncertain significance |
| rs142588540 | 19:49,224,164 | T/C | — | uncertain significance |
| rs1446175729 | 19:49,224,252 | C/T | — | uncertain significance |
| rs763904617 | 19:49,225,120 | C/T | — | uncertain significance |
| rs369508351 | 19:49,225,167 | C/A | — | likely benign |
| rs2514007695 | 19:49,225,182 | T/C | — | uncertain significance |
| rs368997285 | 19:49,225,207 | G/T | — | uncertain significance |
| rs374430911 | 19:49,225,213 | C/T | — | uncertain significance |
| rs144844138 | 19:49,225,521 | C/A | upstream gene variant | — |
| rs11666792 | 19:49,227,043 | G/A | upstream gene variant | — |
| rs12979891 | 19:49,227,256 | C/T | upstream gene variant | — |
| rs11878908 | 19:49,227,443 | C/T | upstream gene variant | — |
| rs144734317 | 19:49,227,611 | G/A | — | likely benign |
| rs2514010113 | 19:49,227,617 | C/T | — | uncertain significance |
| rs2514010126 | 19:49,227,631 | A/G | — | uncertain significance |
| rs146642647 | 19:49,227,704 | C/T | — | uncertain significance |
| rs760469367 | 19:49,227,707 | G/A | — | uncertain significance |
| rs749820608 | 19:49,227,758 | G/A | — | uncertain significance |
| rs753452522 | 19:49,227,978 | T/A | — | uncertain significance |
| rs764758039 | 19:49,228,096 | A/G | — | uncertain significance |
| rs201454840 | 19:49,228,118 | C/T | — | uncertain significance |
| rs1265887441 | 19:49,228,141 | G/A | — | uncertain significance |
| rs202046985 | 19:49,228,142 | C/T | — | uncertain significance |
| rs777014384 | 19:49,228,151 | C/G | — | uncertain significance |
| rs899828449 | 19:49,228,166 | C/A | — | uncertain significance |
| rs375784788 | 19:49,228,171 | G/A | — | uncertain significance |
| rs754613166 | 19:49,228,204 | G/C | — | uncertain significance |
| rs2287921 | 19:49,228,272 | T/C | regulatory region variant | — |
| rs36108383 | 19:49,228,604 | C/T | regulatory region variant | — |
| rs146711212 | 19:49,229,870 | G/A | regulatory region variant | — |
| rs370059711 | 19:49,230,356 | C/T | — | uncertain significance |
| rs774923735 | 19:49,230,357 | G/A | — | uncertain significance |
| rs910870943 | 19:49,230,372 | C/T | — | uncertain significance |
| rs141745994 | 19:49,230,374 | G/A | — | uncertain significance |
| rs761314944 | 19:49,230,662 | C/T | — | uncertain significance |
| rs762726040 | 19:49,232,249 | C/T | — | uncertain significance |
| rs774281964 | 19:49,232,276 | T/C | — | uncertain significance |
| rs547402858 | 19:49,232,341 | G/A | — | likely benign |
| rs2033398149 | 19:49,232,377 | G/T | — | likely benign |
| rs1362365549 | 19:49,232,390 | C/G | — | uncertain significance |
| rs2033400141 | 19:49,232,453 | C/T | — | uncertain significance |
| rs1205113282 | 19:49,232,465 | C/T | — | uncertain significance |
| rs1172416469 | 19:49,232,583 | G/C | — | uncertain significance |
| rs1190606303 | 19:49,232,687 | G/A | — | uncertain significance |
| rs554071195 | 19:49,232,703 | C/T | — | uncertain significance |
| rs763085115 | 19:49,232,759 | T/C | — | uncertain significance |
| rs774939039 | 19:49,232,765 | G/T | — | uncertain significance |
| rs1178228161 | 19:49,232,786 | G/A | — | uncertain significance |
| rs1298593215 | 19:49,232,810 | A/G | — | uncertain significance |
| rs750017717 | 19:49,232,812 | G/T | — | uncertain significance |
| rs1479932309 | 19:49,232,826 | T/G | — | uncertain significance |
| rs768602596 | 19:49,232,831 | A/C | — | uncertain significance |
| rs281408 | 19:49,233,406 | C/T | — | — |
| rs77512339 | 19:49,236,557 | C/T | intron variant | — |
| rs12979144 | 19:49,237,547 | G/T | — | — |
| rs34050136 | 19:49,237,822 | G/A | intron variant | — |
| rs779241127 | 19:49,238,494 | G/T | — | uncertain significance |
| rs1467874828 | 19:49,238,601 | T/G | — | uncertain significance |
| rs776912733 | 19:49,238,694 | C/A | — | uncertain significance |
| rs543403071 | 19:49,238,727 | G/A | — | uncertain significance |
| rs774182562 | 19:49,238,772 | C/T | — | uncertain significance |
| rs1231281 | 19:49,239,200 | G/A | downstream gene variant | — |
| rs574469216 | 19:49,240,270 | G/C | — | — |
| rs427248 | 19:49,241,015 | C/T | regulatory region variant | — |
| rs867521650 | 19:49,242,224 | G/C | — | uncertain significance |
| rs2514023878 | 19:49,242,266 | C/T | — | likely benign |
| rs1253087830 | 19:49,242,276 | C/T | — | uncertain significance |
| rs2033625676 | 19:49,242,396 | C/G | — | uncertain significance |
| rs2514024136 | 19:49,242,411 | C/A | — | uncertain significance |
| rs766583933 | 19:49,242,463 | G/A | — | uncertain significance |
| rs1190229764 | 19:49,242,534 | C/T | — | uncertain significance |
| rs2033628889 | 19:49,242,615 | G/T | — | uncertain significance |
| rs760154453 | 19:49,242,643 | G/C | — | uncertain significance |
| rs980140144 | 19:49,242,645 | G/T | — | uncertain significance |
| rs1047517477 | 19:49,242,732 | G/A | — | uncertain significance |
| rs2514024827 | 19:49,242,820 | C/G | — | uncertain significance |
| rs2514024846 | 19:49,242,835 | G/C | — | uncertain significance |
| rs1202970542 | 19:49,243,427 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.