TRIM49C
tripartite motif containing 49C
Summary
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in innate immune response and regulation of gene expression. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1950718196 | 11:89,768,470 | G/A | — | uncertain significance |
| rs201947848 | 11:89,768,558 | A/G | — | uncertain significance |
| rs200407947 | 11:89,768,564 | T/G | — | likely benign |
| rs745546443 | 11:89,768,591 | A/G | — | uncertain significance |
| rs1950721361 | 11:89,768,653 | A/C | — | uncertain significance |
| rs755859963 | 11:89,768,698 | G/A | — | uncertain significance |
| rs199600157 | 11:89,768,707 | C/A | — | uncertain significance |
| rs773959976 | 11:89,768,735 | A/T | — | uncertain significance |
| rs747531769 | 11:89,768,743 | C/T | — | uncertain significance |
| rs1332255499 | 11:89,768,788 | C/T | — | uncertain significance |
| rs781776418 | 11:89,769,068 | C/A | — | likely benign |
| rs775664696 | 11:89,769,144 | G/T | — | uncertain significance |
| rs551502938 | 11:89,771,111 | C/G | — | likely benign |
| rs1238912021 | 11:89,771,112 | G/A | — | uncertain significance |
| rs1950744830 | 11:89,771,862 | C/G | — | likely benign |
| rs917438655 | 11:89,773,055 | A/G | — | uncertain significance |
| rs749686485 | 11:89,773,056 | T/C | — | uncertain significance |
| rs1044492870 | 11:89,773,094 | A/T | — | uncertain significance |
| rs780486250 | 11:89,774,237 | A/G | — | uncertain significance |
| rs2496418444 | 11:89,774,246 | C/A | — | uncertain significance |
| rs776471601 | 11:89,774,286 | G/A | — | uncertain significance |
| rs754334278 | 11:89,774,339 | G/T | — | uncertain significance |
| rs567763263 | 11:89,774,381 | A/G | — | uncertain significance |
| rs202068848 | 11:89,774,403 | G/T | — | likely benign |
| rs542193285 | 11:89,774,582 | G/A | — | uncertain significance |
| rs1204281097 | 11:89,774,642 | G/C | — | uncertain significance |
| rs539658069 | 11:89,804,751 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.