PCGF3
polycomb group ring finger 3
Summary
The protein encoded by this gene contains a C3HC4 type RING finger, which is a motif known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. [provided by RefSeq, Jul 2008]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138807284 | 4:701,274 | C/T | intron variant | — |
| rs142708984 | 4:701,327 | C/A | — | — |
| rs73219293 | 4:702,169 | G/A | intron variant | — |
| rs11734460 | 4:705,074 | C/T | intron variant | — |
| rs73221104 | 4:707,135 | T/G | — | — |
| rs13126245 | 4:709,145 | T/A | — | — |
| rs4690295 | 4:719,715 | A/G | upstream gene variant | — |
| rs73221116 | 4:720,681 | G/A | regulatory region variant | — |
| rs11735280 | 4:724,061 | G/C | intron variant | — |
| rs56121601 | 4:725,109 | G/T | regulatory region variant | — |
| rs73221123 | 4:726,202 | C/G | — | — |
| rs780392365 | 4:727,521 | C/T | — | uncertain significance |
| rs73221128 | 4:728,111 | C/G | — | — |
| rs79713586 | 4:729,655 | A/T | intron variant | — |
| rs73221131 | 4:731,512 | C/T | intron variant | — |
| rs4234853 | 4:735,150 | G/A | intron variant | — |
| rs201716638 | 4:737,321 | A/C | — | uncertain significance |
| rs34993692 | 4:737,364 | A/G | — | uncertain significance |
| rs201838189 | 4:738,448 | A/G | — | uncertain significance |
| rs2474804421 | 4:738,475 | A/G | — | uncertain significance |
| rs17721766 | 4:744,538 | C/T | intron variant | — |
| rs142971131 | 4:748,124 | G/A | downstream gene variant | — |
| rs6856650 | 4:753,708 | C/G | regulatory region variant | — |
| rs1246980678 | 4:755,104 | G/A | — | uncertain significance |
| rs141712126 | 4:755,144 | G/A | — | benign |
| rs34100269 | 4:755,186 | C/T | — | benign |
| rs150203285 | 4:756,713 | C/T | regulatory region variant | — |
| rs1745284197 | 4:758,811 | C/T | — | uncertain significance |
| rs768601750 | 4:759,824 | C/T | — | uncertain significance |
| rs115135810 | 4:760,696 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.