ZNF638

zinc finger protein 638

Summary

The protein encoded by this gene is a nucleoplasmic protein. It binds cytidine-rich sequences in double-stranded DNA. This protein has three types of domains: MH1, MH2 (repeated three times) and MH3. It is associated with packaging, transferring, or processing transcripts. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]

Known Variants128 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2287326	2:71,559,107	T/G	regulatory region variant	—
rs3771381	2:71,560,665	A/T	regulatory region variant	—
rs6746731	2:71,572,917	T/G	intron variant	—
rs779079673	2:71,576,238	C/T	—	uncertain significance
rs2104173475	2:71,576,298	C/G	—	uncertain significance
rs755317686	2:71,576,301	G/A	—	uncertain significance
rs1387360454	2:71,576,373	G/C	—	uncertain significance
rs2078904672	2:71,576,473	A/G	—	uncertain significance
rs368733519	2:71,576,485	G/A	—	uncertain significance
rs150249098	2:71,576,559	C/T	—	uncertain significance
rs778708515	2:71,576,563	A/T	—	uncertain significance
rs554209501	2:71,576,638	G/A	—	uncertain significance
rs572307441	2:71,576,679	C/T	—	uncertain significance
rs2466469365	2:71,576,682	G/A	—	uncertain significance
rs1241453324	2:71,576,791	A/T	—	uncertain significance
rs748817770	2:71,576,799	G/A	—	likely benign
rs2466470396	2:71,576,880	G/A	—	uncertain significance
rs150990011	2:71,576,922	A/G	—	uncertain significance
rs776893707	2:71,576,929	G/A	—	likely benign
rs767193378	2:71,576,947	A/G	—	uncertain significance
rs1573030247	2:71,577,012	T/A	—	uncertain significance
rs143329395	2:71,577,015	G/A	—	uncertain significance
rs750256713	2:71,577,019	A/G	—	likely benign
rs777449446	2:71,577,070	C/T	—	uncertain significance
rs201306909	2:71,577,097	C/T	—	uncertain significance
rs200383884	2:71,577,100	C/T	—	uncertain significance
rs774301789	2:71,577,133	G/A	—	uncertain significance
rs746908881	2:71,577,135	A/G	—	uncertain significance
rs1558834379	2:71,577,186	G/A	—	uncertain significance
rs190073602	2:71,577,267	A/G	—	uncertain significance
rs141088778	2:71,577,295	T/G	—	uncertain significance
rs12986712	2:71,582,308	G/T	—	—
rs763281468	2:71,582,903	C/A	—	uncertain significance
rs6726122	2:71,583,924	A/G	—	—
rs56408212	2:71,584,201	C/T	intron variant	—
rs7568069	2:71,584,485	G/A	intron variant	—
rs558811434	2:71,591,149	G/A	—	likely benign
rs143227391	2:71,591,171	T/A	—	uncertain significance
rs764018085	2:71,591,199	A/G	—	likely benign
rs368420709	2:71,591,200	T/C	—	uncertain significance
rs1573052548	2:71,591,223	A/C	—	uncertain significance
rs747199568	2:71,591,248	G/A	—	uncertain significance
rs142061376	2:71,591,296	G/A	—	uncertain significance
rs150230256	2:71,591,355	A/G	—	uncertain significance
rs748059432	2:71,591,368	C/T	—	uncertain significance
rs2104278830	2:71,592,619	A/C	—	uncertain significance
rs200872776	2:71,592,675	A/T	—	uncertain significance
rs2466547438	2:71,592,738	G/A	—	uncertain significance
rs2419076	2:71,594,906	G/T	—	—
rs41285973	2:71,595,602	T/G	—	likely benign
rs6740645	2:71,596,041	C/T	intron variant	—
rs751190634	2:71,597,073	A/G	—	uncertain significance
rs146178620	2:71,597,083	C/T	—	likely benign
rs748345539	2:71,607,377	T/C	—	likely benign
rs773523527	2:71,607,392	T/C	—	uncertain significance
rs369140345	2:71,607,681	C/T	—	uncertain significance
rs6745907	2:71,609,073	A/C	—	—
rs12478953	2:71,618,599	T/A	—	—
rs151000390	2:71,623,315	T/C	—	uncertain significance
rs150135565	2:71,625,840	C/G	—	uncertain significance
rs767761139	2:71,627,248	C/G	—	uncertain significance
rs766374468	2:71,627,256	A/G	—	uncertain significance
rs571966370	2:71,627,287	A/C	—	uncertain significance
rs766768102	2:71,627,610	G/T	—	uncertain significance
rs1389527070	2:71,629,131	A/G	—	uncertain significance
rs750155443	2:71,629,150	A/T	—	uncertain significance
rs745367329	2:71,629,156	A/G	—	likely benign
rs757637845	2:71,631,025	C/G	—	uncertain significance
rs377545571	2:71,631,042	A/G	—	uncertain significance
rs969390854	2:71,631,111	A/G	—	uncertain significance
rs4852256	2:71,631,345	A/T	intron variant	—
rs3732233	2:71,633,275	T/C	—	benign
rs201827229	2:71,633,283	G/A	—	uncertain significance
rs2466715304	2:71,633,319	T/C	—	uncertain significance
rs6714975	2:71,633,389	C/T	—	benign
rs371946968	2:71,635,294	T/C	—	uncertain significance
rs780559545	2:71,635,295	A/G	—	uncertain significance
rs775999084	2:71,635,324	A/G	—	uncertain significance
rs12474072	2:71,636,036	A/G	intron variant	—
rs146127214	2:71,637,553	C/T	intron variant	—
rs551406637	2:71,644,092	C/T	—	—
rs4852785	2:71,647,809	C/G	—	—
rs185703288	2:71,650,047	A/G	—	uncertain significance
rs372732229	2:71,650,080	C/T	—	uncertain significance
rs369766558	2:71,650,131	G/C	—	uncertain significance
rs748933753	2:71,650,230	G/A	—	uncertain significance
rs1371071681	2:71,650,234	A/G	—	uncertain significance
rs761034610	2:71,650,263	A/G	—	uncertain significance
rs1249936405	2:71,650,293	A/G	—	uncertain significance
rs2466778724	2:71,650,443	A/G	—	uncertain significance
rs1261036152	2:71,650,458	T/A	—	uncertain significance
rs749709808	2:71,650,594	C/T	—	uncertain significance
rs554155463	2:71,650,660	A/T	—	likely benign
rs144170489	2:71,650,689	A/G	—	likely benign
rs2080477137	2:71,650,823	C/G	—	uncertain significance
rs201371403	2:71,650,824	A/G	—	uncertain significance
rs748409176	2:71,650,837	T/C	—	uncertain significance
rs542517256	2:71,650,894	T/A	—	uncertain significance
rs2080479305	2:71,650,934	G/C	—	uncertain significance
rs2080480950	2:71,651,031	C/T	—	uncertain significance

Showing 100 of 128 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.