RNF150
ring finger protein 150
Summary
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147587329 | 4:141,789,513 | T/G | — | uncertain significance |
| rs2546200620 | 4:141,789,525 | C/G | — | uncertain significance |
| rs2546200629 | 4:141,789,530 | T/G | — | uncertain significance |
| rs370169622 | 4:141,832,303 | G/A | — | uncertain significance |
| rs372029197 | 4:141,832,396 | A/G | — | uncertain significance |
| rs138178278 | 4:141,832,499 | C/T | — | uncertain significance |
| rs75303982 | 4:141,842,011 | G/T | — | — |
| rs546525624 | 4:141,850,789 | G/T | — | — |
| rs1310970883 | 4:141,868,830 | C/T | — | uncertain significance |
| rs1251404570 | 4:141,888,859 | A/G | — | uncertain significance |
| rs1396617699 | 4:141,888,987 | T/G | — | uncertain significance |
| rs10007052 | 4:142,005,573 | C/T | — | — |
| rs370749493 | 4:142,053,557 | A/G | — | uncertain significance |
| rs1002480174 | 4:142,053,561 | G/T | — | uncertain significance |
| rs777923551 | 4:142,053,570 | C/A | — | uncertain significance |
| rs773571878 | 4:142,053,631 | G/A | — | uncertain significance |
| rs2546506890 | 4:142,053,689 | T/A | — | uncertain significance |
| rs2546506912 | 4:142,053,700 | C/T | — | uncertain significance |
| rs748636212 | 4:142,053,742 | C/G | — | uncertain significance |
| rs1049131188 | 4:142,053,757 | G/C | — | uncertain significance |
| rs2546507245 | 4:142,053,832 | A/T | — | uncertain significance |
| rs759133138 | 4:142,053,895 | A/C | — | uncertain significance |
| rs199609830 | 4:142,053,908 | G/T | — | uncertain significance |
| rs1726935641 | 4:142,053,935 | A/G | — | likely benign |
| rs1550057 | 4:142,117,424 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.