TRIM47
tripartite motif containing 47
Summary
Enables ubiquitin protein ligase activity. Involved in protein ubiquitination. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs777374029 | 17:73,870,739 | C/T | — | uncertain significance |
| rs200111313 | 17:73,870,745 | C/T | — | uncertain significance |
| rs1357229420 | 17:73,870,764 | G/A | — | uncertain significance |
| rs748329899 | 17:73,870,782 | C/G | — | uncertain significance |
| rs2143966202 | 17:73,870,785 | C/T | — | uncertain significance |
| rs753469319 | 17:73,870,818 | C/T | — | uncertain significance |
| rs142759674 | 17:73,870,902 | G/A | — | uncertain significance |
| rs1438488350 | 17:73,870,906 | A/T | — | uncertain significance |
| rs201795953 | 17:73,870,919 | C/T | — | uncertain significance |
| rs374555938 | 17:73,870,937 | C/T | — | uncertain significance |
| rs754803973 | 17:73,870,983 | C/T | — | uncertain significance |
| rs752505775 | 17:73,871,091 | G/A | — | uncertain significance |
| rs748897915 | 17:73,871,178 | C/T | — | uncertain significance |
| rs374357476 | 17:73,871,504 | G/A | — | uncertain significance |
| rs767591451 | 17:73,871,532 | C/T | — | uncertain significance |
| rs367558209 | 17:73,872,060 | C/T | — | uncertain significance |
| rs141224201 | 17:73,872,078 | C/T | — | uncertain significance |
| rs752319450 | 17:73,872,171 | C/A | — | uncertain significance |
| rs1270822032 | 17:73,872,350 | A/C | — | uncertain significance |
| rs554195809 | 17:73,872,407 | C/T | — | uncertain significance |
| rs750276447 | 17:73,872,417 | G/C | — | uncertain significance |
| rs1235287038 | 17:73,872,420 | C/G | — | uncertain significance |
| rs769937554 | 17:73,872,429 | G/C | — | uncertain significance |
| rs199950413 | 17:73,872,432 | G/A | — | uncertain significance |
| rs763668176 | 17:73,872,453 | C/G | — | uncertain significance |
| rs147455759 | 17:73,872,478 | G/A | — | likely benign |
| rs2546008319 | 17:73,872,492 | C/G | — | uncertain significance |
| rs1290180239 | 17:73,872,524 | G/C | — | uncertain significance |
| rs113622800 | 17:73,872,539 | C/T | — | likely benign |
| rs766166934 | 17:73,872,564 | C/T | — | uncertain significance |
| rs144258462 | 17:73,872,569 | G/A | — | uncertain significance |
| rs146809867 | 17:73,872,848 | T/C | — | uncertain significance |
| rs2546009093 | 17:73,872,889 | C/G | — | uncertain significance |
| rs201164040 | 17:73,872,894 | C/A | — | uncertain significance |
| rs1055129 | 17:73,872,948 | A/G | coding sequence variant | — |
| rs761109651 | 17:73,874,040 | C/A | — | uncertain significance |
| rs754261808 | 17:73,874,049 | C/A | — | uncertain significance |
| rs4600514 | 17:73,874,071 | G/A | missense variant | — |
| rs989273747 | 17:73,874,091 | C/G | — | uncertain significance |
| rs567457667 | 17:73,874,106 | C/A | — | uncertain significance |
| rs1349643705 | 17:73,874,124 | C/T | — | uncertain significance |
| rs556327620 | 17:73,874,157 | G/A | — | uncertain significance |
| rs914923454 | 17:73,874,181 | G/T | — | uncertain significance |
| rs922371907 | 17:73,874,197 | G/A | — | uncertain significance |
| rs2065147299 | 17:73,874,247 | C/A | — | uncertain significance |
| rs2065147355 | 17:73,874,248 | G/A | — | uncertain significance |
| rs908449895 | 17:73,874,250 | A/T | — | uncertain significance |
| rs1206115242 | 17:73,874,352 | G/A | — | uncertain significance |
| rs2546010931 | 17:73,874,386 | C/A | — | uncertain significance |
| rs762270260 | 17:73,874,479 | C/T | — | uncertain significance |
| rs1189441049 | 17:73,874,624 | G/C | — | uncertain significance |
| rs116044941 | 17:73,874,684 | G/T | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.