PHRF1

PHD and ring finger domains 1

Summary

Predicted to enable RNA polymerase binding activity. Predicted to be involved in protein ubiquitination. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants207 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs56333810	11:575,408	C/T	—	—
rs201520162	11:581,522	G/A	—	uncertain significance
rs766073376	11:581,559	C/T	—	uncertain significance
rs749479153	11:581,597	G/A	—	likely benign
rs369756671	11:581,605	T/C	—	likely benign
rs1854232028	11:581,983	G/A	—	uncertain significance
rs202082756	11:581,994	G/C	—	uncertain significance
rs376068613	11:582,033	G/A	—	uncertain significance
rs189966372	11:583,293	C/T	intron variant	—
rs184621366	11:584,857	C/T	intron variant	—
rs759532390	11:587,266	G/T	—	uncertain significance
rs375337887	11:587,279	G/A	—	uncertain significance
rs374957305	11:587,327	G/A	—	uncertain significance
rs201641830	11:587,343	A/G	—	uncertain significance
rs201661078	11:587,352	A/G	—	uncertain significance
rs141010415	11:587,384	G/A	—	likely benign
rs188373855	11:587,385	C/T	—	uncertain significance
rs745882774	11:587,423	G/A	—	uncertain significance
rs916023226	11:587,447	A/G	—	uncertain significance
rs4963128	11:589,564	T/G	—	—
rs767027832	11:591,418	T/A	—	uncertain significance
rs1210504234	11:591,433	T/G	—	uncertain significance
rs374555031	11:591,446	T/A	—	uncertain significance
rs533670986	11:592,581	C/T	—	uncertain significance
rs2493510006	11:592,598	G/T	—	uncertain significance
rs200929014	11:592,602	C/T	—	uncertain significance
rs998184843	11:592,661	G/A	—	uncertain significance
rs1285318703	11:596,940	T/C	—	uncertain significance
rs375286479	11:596,985	C/T	—	uncertain significance
rs201614026	11:596,996	G/C	—	uncertain significance
rs757891068	11:597,006	T/G	—	uncertain significance
rs765534515	11:597,421	G/T	—	uncertain significance
rs1476739536	11:597,425	C/G	—	uncertain significance
rs375365360	11:597,451	A/G	—	uncertain significance
rs368253631	11:597,466	C/T	—	uncertain significance
rs375161703	11:597,473	G/A	—	uncertain significance
rs1279721147	11:597,542	A/T	—	uncertain significance
rs201679778	11:598,386	G/A	—	likely benign
rs765863584	11:598,395	C/A	—	uncertain significance
rs200204469	11:598,449	T/C	—	uncertain significance
rs746722170	11:598,475	A/G	—	likely benign
rs974559384	11:598,478	C/G	—	uncertain significance
rs1277938728	11:601,615	G/A	—	likely benign
rs551874512	11:601,624	G/A	—	uncertain significance
rs753441545	11:601,661	G/A	—	uncertain significance
rs1450608513	11:601,688	G/A	—	uncertain significance
rs2396545	11:601,785	T/C	intron variant	—
rs777599565	11:605,123	A/T	—	uncertain significance
rs764761550	11:605,148	G/A	—	likely benign
rs766421281	11:605,153	C/T	—	uncertain significance
rs1386579212	11:605,237	C/T	—	uncertain significance
rs372144693	11:605,711	G/A	—	likely benign
rs746584881	11:606,446	C/T	—	uncertain significance
rs2493705117	11:606,485	G/A	—	uncertain significance
rs1210839118	11:606,536	A/T	—	uncertain significance
rs375875310	11:606,567	G/A	—	uncertain significance
rs953756335	11:606,581	A/T	—	uncertain significance
rs748055751	11:607,119	T/A	—	uncertain significance
rs758396446	11:607,162	C/T	—	uncertain significance
rs2493719259	11:607,168	A/G	—	uncertain significance
rs1856003225	11:607,222	C/G	—	uncertain significance
rs372391732	11:607,224	C/T	—	likely benign
rs781036601	11:607,233	G/A	—	uncertain significance
rs200753321	11:607,237	G/A	—	uncertain significance
rs772002124	11:607,378	C/A	—	uncertain significance
rs138408584	11:607,394	G/C	—	likely benign
rs1479012529	11:607,405	C/T	—	uncertain significance
rs754289507	11:607,460	G/C	—	uncertain significance
rs367803474	11:607,477	C/T	—	uncertain significance
rs757963125	11:607,524	G/A	—	likely benign
rs375255487	11:607,537	G/A	—	likely benign
rs376249758	11:607,609	A/G	—	uncertain significance
rs912599241	11:607,620	C/A	—	uncertain significance
rs1856036233	11:607,657	G/A	—	uncertain significance
rs376556111	11:607,672	G/A	—	likely benign
rs113889171	11:607,680	G/A	—	benign
rs202005033	11:607,687	A/G	—	uncertain significance
rs759992846	11:607,690	C/T	—	uncertain significance
rs747280133	11:607,701	C/T	—	uncertain significance
rs372916162	11:607,702	G/A	—	uncertain significance
rs768113382	11:607,711	C/G	—	uncertain significance
rs767179863	11:607,737	C/T	—	uncertain significance
rs199939943	11:607,767	G/A	—	uncertain significance
rs746033686	11:607,789	G/A	—	uncertain significance
rs765284476	11:607,858	G/A	—	uncertain significance
rs907601999	11:607,867	A/C	—	uncertain significance
rs749408326	11:607,899	C/T	—	uncertain significance
rs754994881	11:607,902	C/G	—	uncertain significance
rs746676771	11:607,933	G/A	—	uncertain significance
rs766638984	11:607,956	G/A	—	uncertain significance
rs1387076403	11:607,960	C/G	—	uncertain significance
rs1017730860	11:607,964	C/T	—	likely benign
rs1351068237	11:607,978	G/C	—	uncertain significance
rs372016767	11:607,980	G/A	—	uncertain significance
rs776348620	11:607,995	C/G	—	uncertain significance
rs761645941	11:608,077	A/C	—	uncertain significance
rs527301822	11:608,104	C/T	—	uncertain significance
rs2493747961	11:608,127	G/C	—	uncertain significance
rs763075200	11:608,155	C/G	—	uncertain significance
rs2493749951	11:608,181	G/A	—	uncertain significance

Showing 100 of 207 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.