ZC3H4

zinc finger CCCH-type containing 4

Summary

This gene encodes a member of a family of CCCH (C-x8-C-x5-C-x3-H type) zinc finger domain-containing proteins. These zinc finger domains, which coordinate zinc finger binding and are characterized by three cysteine residues and one histidine residue, are nucleic acid-binding. Other family members are known to function in post-transcriptional regulation. [provided by RefSeq, Aug 2011]

Known Variants135 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs3810291	19:47,569,003	G/C	—	—
rs2514352320	19:47,569,620	C/T	—	uncertain significance
rs2514352425	19:47,569,626	G/C	—	uncertain significance
rs142249528	19:47,569,691	G/A	—	benign
rs535312702	19:47,569,756	C/T	—	uncertain significance
rs377724718	19:47,569,779	T/C	—	uncertain significance
rs780166090	19:47,569,825	C/T	—	uncertain significance
rs3810292	19:47,569,826	G/A	—	benign
rs770492026	19:47,569,837	C/T	—	likely benign
rs748827850	19:47,569,840	G/A	—	uncertain significance
rs309195	19:47,569,842	G/C	—	benign
rs201679707	19:47,569,867	G/A	—	uncertain significance
rs766356116	19:47,569,900	C/T	—	uncertain significance
rs147880083	19:47,569,913	G/A	—	benign
rs779715995	19:47,569,954	C/T	—	uncertain significance
rs1335870709	19:47,570,023	C/T	—	uncertain significance
rs200843141	19:47,570,025	G/A	—	likely benign
rs546413565	19:47,570,057	C/T	—	likely benign
rs184799751	19:47,570,132	C/G	—	benign
rs202213560	19:47,570,199	G/A	—	benign
rs200501790	19:47,570,206	C/T	—	likely benign
rs757124661	19:47,570,218	G/A	—	likely benign
rs758335179	19:47,570,220	G/A	—	uncertain significance
rs746350746	19:47,570,240	G/A	—	likely benign
rs377045786	19:47,570,247	C/T	—	uncertain significance
rs775865015	19:47,570,329	C/T	—	uncertain significance
rs768270228	19:47,570,337	C/G	—	uncertain significance
rs141514527	19:47,570,343	A/G	—	benign
rs764124666	19:47,570,352	G/A	—	uncertain significance
rs200138538	19:47,570,354	G/A	—	likely benign
rs1213360717	19:47,570,369	T/C	—	likely benign
rs368809461	19:47,570,433	G/A	—	uncertain significance
rs759357646	19:47,570,455	G/A	—	uncertain significance
rs771929582	19:47,570,458	C/T	—	uncertain significance
rs201967618	19:47,570,459	G/A	—	benign
rs546975609	19:47,570,466	G/A	—	uncertain significance
rs748848632	19:47,570,494	G/A	—	uncertain significance
rs756816889	19:47,570,511	A/G	—	uncertain significance
rs746919580	19:47,570,527	C/T	—	uncertain significance
rs764689178	19:47,570,560	T/G	—	uncertain significance
rs771032970	19:47,570,601	C/T	—	uncertain significance
rs777854150	19:47,570,728	G/A	—	uncertain significance
rs772264154	19:47,570,736	C/T	—	uncertain significance
rs375563795	19:47,570,757	G/A	—	uncertain significance
rs770220818	19:47,570,764	G/A	—	uncertain significance
rs371749033	19:47,570,766	G/A	—	uncertain significance
rs1160737383	19:47,570,767	G/A	—	uncertain significance
rs148102372	19:47,570,842	C/T	—	likely benign
rs201437060	19:47,570,861	G/A	—	likely benign
rs200034595	19:47,570,871	G/A	—	uncertain significance
rs751591118	19:47,570,881	G/T	—	uncertain significance
rs1186433676	19:47,570,923	G/A	—	uncertain significance
rs200363812	19:47,570,953	G/A	—	uncertain significance
rs754139171	19:47,570,982	C/T	—	uncertain significance
rs201540357	19:47,570,985	G/C	—	uncertain significance
rs553465405	19:47,570,998	C/G	—	uncertain significance
rs761586146	19:47,571,033	C/G	—	uncertain significance
rs769473208	19:47,571,036	C/G	—	uncertain significance
rs896149481	19:47,571,042	G/A	—	uncertain significance
rs141967234	19:47,571,088	C/T	—	uncertain significance
rs1532127	19:47,571,938	G/C	—	—
rs1568529861	19:47,572,370	G/C	—	uncertain significance
rs373440831	19:47,572,390	C/T	—	uncertain significance
rs202116030	19:47,572,395	C/T	—	likely benign
rs554387468	19:47,572,526	C/G	—	likely benign
rs764776440	19:47,572,528	G/T	—	uncertain significance
rs62136856	19:47,573,527	A/G	intron variant	—
rs1220123542	19:47,575,068	T/C	—	uncertain significance
rs137920489	19:47,575,122	G/A	—	uncertain significance
rs116366877	19:47,575,144	G/A	—	benign
rs372115183	19:47,575,158	C/T	—	uncertain significance
rs753009395	19:47,575,170	T/C	—	uncertain significance
rs1045107056	19:47,575,184	G/C	—	uncertain significance
rs1185234258	19:47,575,217	C/A	—	uncertain significance
rs375487722	19:47,575,219	C/T	—	uncertain significance
rs148480867	19:47,575,223	G/A	—	uncertain significance
rs569170414	19:47,575,272	G/A	—	uncertain significance
rs76187449	19:47,575,279	G/C	—	likely benign
rs1425222570	19:47,575,284	G/A	—	uncertain significance
rs2514413582	19:47,575,290	C/A	—	uncertain significance
rs79459609	19:47,575,291	A/G	—	benign
rs78020601	19:47,575,294	A/G	—	benign
rs374529527	19:47,575,299	T/C	—	uncertain significance
rs2514414775	19:47,575,348	T/G	—	likely benign
rs759032521	19:47,575,356	G/T	—	uncertain significance
rs1383493003	19:47,575,652	C/T	—	uncertain significance
rs1337333122	19:47,575,680	G/C	—	uncertain significance
rs368259473	19:47,575,704	C/G	—	uncertain significance
rs3745618	19:47,575,716	C/T	synonymous variant	—
rs1374276705	19:47,575,786	G/A	—	uncertain significance
rs1470864552	19:47,575,796	C/T	—	uncertain significance
rs551623720	19:47,575,834	G/A	—	uncertain significance
rs143699469	19:47,575,881	C/T	—	benign
rs201967193	19:47,575,975	G/A	—	benign
rs4804023	19:47,579,613	T/A	upstream gene variant	—
rs11667244	19:47,580,185	A/G	upstream gene variant	—
rs75022794	19:47,584,761	G/A	—	benign
rs73943616	19:47,584,869	C/T	—	benign
rs7250850	19:47,585,517	C/G	—	benign
rs376326334	19:47,585,547	G/C	—	uncertain significance

Showing 100 of 135 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.