TRIM56
tripartite motif containing 56
Summary
Enables ubiquitin protein ligase activity. Involved in defense response to virus; positive regulation of signal transduction; and protein monoubiquitination. Predicted to be located in cytoplasm. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113421429 | 7:100,729,247 | C/G | — | — |
| rs768593984 | 7:100,730,598 | T/A | — | uncertain significance |
| rs368094365 | 7:100,730,630 | G/A | — | uncertain significance |
| rs745789998 | 7:100,730,747 | G/A | — | likely benign |
| rs374149817 | 7:100,730,753 | G/A | — | likely benign |
| rs767709463 | 7:100,730,771 | C/T | — | uncertain significance |
| rs756425998 | 7:100,730,774 | G/A | — | uncertain significance |
| rs753231090 | 7:100,730,828 | G/A | — | uncertain significance |
| rs2116527678 | 7:100,730,873 | C/G | — | uncertain significance |
| rs772532404 | 7:100,730,922 | C/T | — | uncertain significance |
| rs779808128 | 7:100,730,961 | G/A | — | uncertain significance |
| rs36004695 | 7:100,730,992 | C/T | — | benign |
| rs200821663 | 7:100,731,027 | G/A | — | uncertain significance |
| rs374323876 | 7:100,731,077 | C/T | — | uncertain significance |
| rs145410552 | 7:100,731,112 | C/T | — | likely benign |
| rs755369296 | 7:100,731,222 | G/A | — | uncertain significance |
| rs781559092 | 7:100,731,228 | G/A | — | uncertain significance |
| rs771778501 | 7:100,731,254 | G/A | — | uncertain significance |
| rs775823952 | 7:100,731,291 | C/T | — | uncertain significance |
| rs1193925069 | 7:100,731,363 | A/G | — | uncertain significance |
| rs1050546199 | 7:100,731,374 | G/T | — | uncertain significance |
| rs1293218935 | 7:100,731,386 | G/A | — | uncertain significance |
| rs2485992629 | 7:100,731,400 | G/T | — | uncertain significance |
| rs372265809 | 7:100,731,458 | C/T | — | uncertain significance |
| rs754163311 | 7:100,731,512 | G/A | — | uncertain significance |
| rs1442901519 | 7:100,731,521 | C/T | — | uncertain significance |
| rs574536166 | 7:100,731,522 | G/A | — | uncertain significance |
| rs779987368 | 7:100,731,525 | G/A | — | uncertain significance |
| rs202076977 | 7:100,731,613 | G/C | — | uncertain significance |
| rs763535074 | 7:100,731,693 | G/A | — | likely benign |
| rs1795494878 | 7:100,731,717 | C/T | — | uncertain significance |
| rs80324038 | 7:100,731,776 | C/T | — | benign |
| rs200171638 | 7:100,731,777 | G/A | — | likely benign |
| rs371086359 | 7:100,731,797 | A/G | — | uncertain significance |
| rs1449723759 | 7:100,731,800 | G/A | — | uncertain significance |
| rs1167379619 | 7:100,731,808 | G/C | — | uncertain significance |
| rs200279454 | 7:100,731,872 | A/G | — | uncertain significance |
| rs762799398 | 7:100,732,008 | G/A | — | uncertain significance |
| rs879446871 | 7:100,732,047 | C/G | — | uncertain significance |
| rs759424639 | 7:100,732,089 | C/T | — | uncertain significance |
| rs755441953 | 7:100,732,203 | A/G | — | uncertain significance |
| rs756566787 | 7:100,732,208 | G/A | — | uncertain significance |
| rs192903356 | 7:100,732,223 | G/A | — | uncertain significance |
| rs200239788 | 7:100,732,262 | G/A | — | uncertain significance |
| rs368846650 | 7:100,732,275 | C/T | — | uncertain significance |
| rs995226252 | 7:100,732,325 | G/A | — | uncertain significance |
| rs200782863 | 7:100,732,370 | G/A | — | uncertain significance |
| rs374349123 | 7:100,732,377 | C/T | — | uncertain significance |
| rs776810486 | 7:100,732,391 | G/A | — | uncertain significance |
| rs200430251 | 7:100,732,424 | G/T | — | uncertain significance |
| rs911037236 | 7:100,732,437 | A/G | — | uncertain significance |
| rs370129810 | 7:100,732,496 | C/T | — | uncertain significance |
| rs201235744 | 7:100,732,598 | G/A | — | uncertain significance |
| rs1162980916 | 7:100,732,605 | A/C | — | uncertain significance |
| rs775579142 | 7:100,732,609 | G/C | — | uncertain significance |
| rs776810064 | 7:100,732,713 | C/T | — | uncertain significance |
| rs752394870 | 7:100,732,745 | G/C | — | uncertain significance |
| rs560489358 | 7:100,732,753 | C/A | — | uncertain significance |
| rs200686433 | 7:100,732,805 | G/A | — | uncertain significance |
| rs28709821 | 7:100,735,887 | G/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.