RASSF4
Ras association domain family member 4
Summary
The function of this gene has not yet been determined but may involve a role in tumor suppression. Alternative splicing of this gene results in several transcript variants; however, most of the variants have not been fully described. [provided by RefSeq, Jul 2008]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778343371 | 10:45,465,663 | T/A | — | uncertain significance |
| rs749561755 | 10:45,465,670 | C/T | — | uncertain significance |
| rs771764864 | 10:45,465,671 | G/A | — | likely benign |
| rs1454040910 | 10:45,465,682 | T/C | — | uncertain significance |
| rs773274560 | 10:45,467,291 | C/T | — | uncertain significance |
| rs200202697 | 10:45,478,015 | G/A | — | uncertain significance |
| rs148901129 | 10:45,478,024 | G/A | — | uncertain significance |
| rs202059965 | 10:45,478,033 | G/A | — | uncertain significance |
| rs142846160 | 10:45,478,043 | G/A | — | likely benign |
| rs151066058 | 10:45,478,044 | C/G | — | uncertain significance |
| rs201540828 | 10:45,478,053 | C/T | — | uncertain significance |
| rs139687864 | 10:45,478,054 | G/A | — | uncertain significance |
| rs145855403 | 10:45,478,096 | G/A | — | likely benign |
| rs79857424 | 10:45,479,476 | G/T | — | benign |
| rs1382797163 | 10:45,479,477 | C/T | — | uncertain significance |
| rs760088998 | 10:45,479,518 | C/A | — | uncertain significance |
| rs763261638 | 10:45,479,550 | C/T | — | uncertain significance |
| rs146592420 | 10:45,479,552 | G/A | — | uncertain significance |
| rs540078906 | 10:45,480,336 | G/C | — | uncertain significance |
| rs35924448 | 10:45,480,350 | G/A | — | benign |
| rs140069760 | 10:45,480,356 | G/A | — | likely benign |
| rs35672435 | 10:45,480,361 | G/C | — | benign |
| rs114276493 | 10:45,480,369 | G/A | — | benign |
| rs771576465 | 10:45,480,375 | G/A | — | uncertain significance |
| rs765083486 | 10:45,480,392 | A/G | — | uncertain significance |
| rs200905503 | 10:45,484,741 | C/A | — | uncertain significance |
| rs779431849 | 10:45,484,774 | G/A | — | uncertain significance |
| rs11540204 | 10:45,485,153 | C/G | — | uncertain significance |
| rs139516622 | 10:45,486,483 | T/C | — | uncertain significance |
| rs554573808 | 10:45,486,500 | G/A | — | uncertain significance |
| rs369965316 | 10:45,488,748 | C/T | — | uncertain significance |
| rs144038389 | 10:45,491,063 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.