FRMD8
FERM domain containing 8
Summary
Involved in positive regulation of tumor necrosis factor production. Located in several cellular components, including centriolar satellite; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34400381 | 11:65,143,892 | G/A | missense variant | — |
| rs624307 | 11:65,144,075 | T/C | missense variant | — |
| rs78829599 | 11:65,147,013 | C/T | missense variant | — |
| rs115561468 | 11:65,147,581 | C/T | downstream gene variant | — |
| rs201038206 | 11:65,149,323 | A/G | regulatory region variant | — |
| rs569323385 | 11:65,154,563 | G/A | — | uncertain significance |
| rs144532045 | 11:65,154,621 | C/T | — | likely benign |
| rs142184687 | 11:65,156,839 | C/T | — | likely benign |
| rs190868663 | 11:65,156,871 | T/C | — | uncertain significance |
| rs2495567147 | 11:65,156,894 | C/T | — | uncertain significance |
| rs149665891 | 11:65,161,085 | C/T | — | uncertain significance |
| rs771500950 | 11:65,161,142 | A/G | — | uncertain significance |
| rs184521656 | 11:65,161,450 | C/T | intron variant | — |
| rs774674530 | 11:65,161,730 | A/T | — | uncertain significance |
| rs1384757947 | 11:65,161,794 | G/A | — | uncertain significance |
| rs1049110052 | 11:65,161,799 | C/G | — | uncertain significance |
| rs756643091 | 11:65,161,800 | C/T | — | uncertain significance |
| rs776360172 | 11:65,161,820 | G/A | — | uncertain significance |
| rs150610909 | 11:65,161,845 | G/A | — | uncertain significance |
| rs199560325 | 11:65,161,874 | C/T | — | uncertain significance |
| rs574296783 | 11:65,161,875 | G/A | — | likely benign |
| rs12417665 | 11:65,164,357 | C/T | synonymous variant | — |
| rs763409317 | 11:65,164,384 | C/A | — | uncertain significance |
| rs1321142675 | 11:65,164,397 | G/C | — | uncertain significance |
| rs186475050 | 11:65,164,418 | G/A | missense variant | — |
| rs562393260 | 11:65,164,421 | G/A | — | uncertain significance |
| rs947555369 | 11:65,164,482 | C/T | — | uncertain significance |
| rs2495598300 | 11:65,167,221 | A/C | — | uncertain significance |
| rs779110878 | 11:65,167,268 | C/T | — | uncertain significance |
| rs569673889 | 11:65,167,269 | G/A | — | uncertain significance |
| rs770076651 | 11:65,167,304 | G/A | — | uncertain significance |
| rs569914571 | 11:65,168,244 | C/G | — | uncertain significance |
| rs145735901 | 11:65,168,285 | G/A | — | uncertain significance |
| rs764735918 | 11:65,168,294 | G/A | — | uncertain significance |
| rs10128627 | 11:65,170,600 | T/C | intron variant | — |
| rs780987499 | 11:65,172,384 | C/T | — | likely benign |
| rs139552682 | 11:65,172,423 | C/T | — | uncertain significance |
| rs150215273 | 11:65,172,429 | C/T | — | uncertain significance |
| rs2495615188 | 11:65,172,489 | T/A | — | uncertain significance |
| rs777008508 | 11:65,172,501 | G/A | — | uncertain significance |
| rs138836971 | 11:65,172,530 | G/A | — | uncertain significance |
| rs1311818663 | 11:65,178,785 | G/A | — | uncertain significance |
| rs780232791 | 11:65,178,805 | C/A | — | uncertain significance |
| rs61755084 | 11:65,178,810 | T/C | — | likely benign |
| rs512715 | 11:65,191,208 | C/G | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.