IQGAP2
IQ motif containing GTPase activating protein 2
Summary
This gene encodes a member of the IQGAP family. The encoded protein contains three IQ domains, one calponin homology domain, one Ras-GAP domain and one WW domain. This protein interacts with components of the cytoskeleton, with cell adhesion molecules, and with several signaling molecules to regulate cell morphology and motility. It also acts as a tumor suppressor and has been found to play a role in regulating innate antiviral responses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]
Known Variants113 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13357820 | 5:75,698,761 | G/C | — | — |
| rs747881615 | 5:75,699,390 | C/A | — | uncertain significance |
| rs569312379 | 5:75,699,404 | C/A | — | benign |
| rs9293684 | 5:75,705,131 | A/T | — | — |
| rs10065322 | 5:75,709,413 | G/A | intron variant | — |
| rs10043040 | 5:75,720,006 | T/C | intron variant | — |
| rs7706078 | 5:75,740,199 | C/G | — | — |
| rs372040696 | 5:75,757,405 | C/T | — | likely benign |
| rs2531918290 | 5:75,757,437 | A/G | — | uncertain significance |
| rs760630948 | 5:75,757,463 | G/A | — | uncertain significance |
| rs72775777 | 5:75,768,011 | C/T | — | — |
| rs2478644158 | 5:75,858,247 | A/T | — | uncertain significance |
| rs1034084718 | 5:75,858,262 | C/T | — | uncertain significance |
| rs369077131 | 5:75,858,283 | G/A | — | uncertain significance |
| rs779912911 | 5:75,858,295 | A/T | — | uncertain significance |
| rs1461180566 | 5:75,858,343 | A/T | — | uncertain significance |
| rs376517879 | 5:75,858,369 | C/T | — | uncertain significance |
| rs192694811 | 5:75,866,423 | C/T | — | uncertain significance |
| rs2478714624 | 5:75,866,430 | C/T | — | uncertain significance |
| rs778273441 | 5:75,866,441 | G/A | — | uncertain significance |
| rs2478714933 | 5:75,866,459 | A/C | — | uncertain significance |
| rs1224673865 | 5:75,871,527 | C/G | — | uncertain significance |
| rs2478758486 | 5:75,871,555 | A/G | — | uncertain significance |
| rs905162 | 5:75,878,994 | G/A | intron variant | — |
| rs1131232 | 5:75,884,734 | G/A | — | benign |
| rs1015904819 | 5:75,884,739 | T/A | — | uncertain significance |
| rs202016097 | 5:75,884,759 | C/A | — | uncertain significance |
| rs752998022 | 5:75,884,765 | A/G | — | uncertain significance |
| rs147531108 | 5:75,886,292 | G/A | — | benign |
| rs1397729527 | 5:75,886,298 | A/T | — | uncertain significance |
| rs1680352862 | 5:75,886,302 | T/C | — | uncertain significance |
| rs1264875033 | 5:75,888,748 | A/C | — | uncertain significance |
| rs371271172 | 5:75,893,288 | A/G | — | uncertain significance |
| rs137915513 | 5:75,893,293 | G/C | — | uncertain significance |
| rs566526969 | 5:75,893,348 | C/T | — | uncertain significance |
| rs1277944586 | 5:75,893,378 | C/T | — | uncertain significance |
| rs1235472592 | 5:75,896,692 | C/A | — | uncertain significance |
| rs138552758 | 5:75,896,757 | G/A | — | likely benign |
| rs761045939 | 5:75,896,773 | A/G | — | uncertain significance |
| rs2478981860 | 5:75,896,781 | A/C | — | uncertain significance |
| rs766791151 | 5:75,896,796 | C/T | — | uncertain significance |
| rs17652394 | 5:75,898,196 | C/T | regulatory region variant | — |
| rs2479030740 | 5:75,902,092 | G/A | — | uncertain significance |
| rs768240974 | 5:75,902,096 | T/C | — | uncertain significance |
| rs3822530 | 5:75,906,923 | C/A | — | benign |
| rs998409885 | 5:75,906,947 | A/G | — | uncertain significance |
| rs36087650 | 5:75,906,957 | T/C | — | benign |
| rs145465543 | 5:75,923,289 | G/A | — | likely benign |
| rs764047209 | 5:75,927,810 | A/G | — | uncertain significance |
| rs10037254 | 5:75,930,640 | G/A | intron variant | — |
| rs771181771 | 5:75,932,870 | G/A | — | uncertain significance |
| rs1751193095 | 5:75,932,886 | T/G | — | uncertain significance |
| rs530310707 | 5:75,932,910 | A/G | — | uncertain significance |
| rs768691178 | 5:75,932,999 | G/A | — | uncertain significance |
| rs35544895 | 5:75,936,773 | G/C | — | benign |
| rs766715473 | 5:75,936,791 | C/T | — | uncertain significance |
| rs752667143 | 5:75,936,805 | G/T | — | uncertain significance |
| rs749100595 | 5:75,936,830 | C/T | — | uncertain significance |
| rs754159279 | 5:75,936,854 | C/A | — | uncertain significance |
| rs1258279165 | 5:75,936,864 | G/A | — | uncertain significance |
| rs530993260 | 5:75,936,911 | A/T | — | uncertain significance |
| rs752542403 | 5:75,950,036 | G/C | — | uncertain significance |
| rs558998741 | 5:75,950,067 | C/T | — | uncertain significance |
| rs769297993 | 5:75,950,081 | G/T | — | uncertain significance |
| rs371448195 | 5:75,950,797 | G/A | — | likely benign |
| rs776511510 | 5:75,950,810 | G/A | — | uncertain significance |
| rs745980959 | 5:75,950,812 | T/G | — | uncertain significance |
| rs534842328 | 5:75,954,316 | C/T | — | uncertain significance |
| rs759325601 | 5:75,954,317 | G/A | — | uncertain significance |
| rs34968964 | 5:75,960,968 | G/C | missense variant | — |
| rs779784878 | 5:75,960,992 | C/T | — | uncertain significance |
| rs2150476828 | 5:75,964,591 | T/C | — | uncertain significance |
| rs201385729 | 5:75,964,594 | A/G | — | uncertain significance |
| rs2479648016 | 5:75,964,623 | T/A | — | uncertain significance |
| rs1022204712 | 5:75,967,659 | A/C | — | uncertain significance |
| rs138211969 | 5:75,967,720 | G/A | — | uncertain significance |
| rs76979655 | 5:75,967,722 | T/C | — | benign |
| rs773126027 | 5:75,967,742 | A/G | — | uncertain significance |
| rs962206317 | 5:75,969,341 | G/T | — | uncertain significance |
| rs2287932 | 5:75,969,360 | G/T | — | benign |
| rs139792880 | 5:75,969,389 | A/G | — | uncertain significance |
| rs145178581 | 5:75,969,801 | A/G | — | benign |
| rs2479708370 | 5:75,969,821 | A/T | — | uncertain significance |
| rs2479715081 | 5:75,970,318 | T/A | — | uncertain significance |
| rs2479715427 | 5:75,970,332 | A/C | — | uncertain significance |
| rs140188703 | 5:75,970,383 | G/A | — | uncertain significance |
| rs1744646338 | 5:75,970,473 | G/A | — | uncertain significance |
| rs201262213 | 5:75,970,486 | A/T | — | uncertain significance |
| rs2303161 | 5:75,972,881 | C/A | intron variant | — |
| rs563043798 | 5:75,977,918 | G/A | — | — |
| rs1323563457 | 5:75,978,958 | G/T | — | uncertain significance |
| rs34076951 | 5:75,979,008 | G/A | — | benign |
| rs185223948 | 5:75,979,027 | G/A | — | uncertain significance |
| rs376614167 | 5:75,979,708 | G/A | — | uncertain significance |
| rs73127565 | 5:75,988,003 | A/G | regulatory region variant | — |
| rs373730789 | 5:75,989,208 | C/T | — | uncertain significance |
| rs192621142 | 5:75,989,244 | G/C | — | uncertain significance |
| rs1746637917 | 5:75,991,287 | C/A | — | uncertain significance |
| rs377308848 | 5:75,991,289 | A/G | — | uncertain significance |
| rs2479873029 | 5:75,991,300 | A/T | — | uncertain significance |
Showing 100 of 113 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.