CCDC141

coiled-coil domain containing 141

Summary

Predicted to be involved in brain development. Predicted to act upstream of or within centrosome localization and cerebral cortex radially oriented cell migration. Predicted to be located in centrosome and cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants304 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1844334	2:179,681,330	T/C	intron variant	—
rs10497527	2:179,698,596	A/G	—	benign
rs78585114	2:179,698,844	G/A	—	benign
rs1684376115	2:179,698,907	G/C	—	uncertain significance
rs16866554	2:179,698,945	A/G	—	benign
rs1324936014	2:179,698,954	G/A	—	likely benign
rs199532854	2:179,698,994	C/A	—	uncertain significance
rs2535076375	2:179,698,996	T/C	—	uncertain significance
rs780755107	2:179,698,997	G/C	—	uncertain significance
rs994534626	2:179,699,007	G/A	—	uncertain significance
rs199670476	2:179,699,031	C/T	—	benign
rs2154365508	2:179,699,033	C/T	—	uncertain significance
rs375249342	2:179,699,049	G/A	—	uncertain significance
rs539116633	2:179,699,056	A/C	—	uncertain significance
rs760885419	2:179,699,067	C/T	—	uncertain significance
rs1373488677	2:179,699,082	C/T	—	uncertain significance
rs866780379	2:179,699,104	C/A	—	uncertain significance
rs934941192	2:179,699,109	T/A	—	uncertain significance
rs2535078876	2:179,699,110	C/T	—	likely benign
rs145610810	2:179,699,124	C/T	—	likely benign
rs572250404	2:179,699,142	C/G	—	uncertain significance
rs917442110	2:179,699,146	C/A	—	uncertain significance
rs62175451	2:179,699,384	A/G	—	benign
rs1684498900	2:179,701,634	G/A	—	uncertain significance
rs2535105265	2:179,701,651	A/T	—	uncertain significance
rs1575112506	2:179,701,686	G/T	—	likely benign
rs2535105917	2:179,701,690	G/A	—	uncertain significance
rs999347387	2:179,701,703	G/C	—	uncertain significance
rs1250111685	2:179,701,709	T/C	—	uncertain significance
rs376103810	2:179,701,745	C/T	—	likely benign
rs1275066432	2:179,701,772	T/A	—	uncertain significance
rs368802405	2:179,701,780	C/T	—	likely benign
rs148579179	2:179,701,786	A/G	—	conflicting classifications of pathogenicity
rs1369562881	2:179,701,813	G/A	—	uncertain significance
rs13031147	2:179,701,839	G/A	—	likely benign
rs375212636	2:179,701,858	T/C	—	uncertain significance
rs2535110594	2:179,701,891	T/A	—	uncertain significance
rs2535111168	2:179,701,928	C/T	—	uncertain significance
rs754465185	2:179,701,935	C/G	—	uncertain significance
rs143659554	2:179,701,998	A/C	—	uncertain significance
rs369418999	2:179,702,067	C/T	—	likely benign
rs2154365792	2:179,702,096	A/T	—	uncertain significance
rs200623862	2:179,702,124	A/T	—	uncertain significance
rs1326629479	2:179,702,125	T/A	—	uncertain significance
rs1212530049	2:179,702,159	C/G	—	uncertain significance
rs150447553	2:179,702,164	G/A	—	uncertain significance
rs185286713	2:179,702,193	C/T	—	likely benign
rs888332352	2:179,702,195	C/A	—	uncertain significance
rs1260988210	2:179,702,237	G/T	—	uncertain significance
rs1032283	2:179,702,268	A/G	—	benign
rs150972468	2:179,702,316	T/C	—	likely benign
rs990151073	2:179,702,319	G/A	—	likely benign
rs778933944	2:179,702,345	G/C	—	uncertain significance
rs745596115	2:179,702,348	T/C	—	uncertain significance
rs370699879	2:179,702,375	C/T	—	uncertain significance
rs761023328	2:179,702,419	C/T	—	conflicting classifications of pathogenicity
rs143765782	2:179,702,420	G/A	—	uncertain significance
rs13419085	2:179,702,437	T/C	—	benign
rs746635252	2:179,702,441	T/C	—	likely benign
rs139096421	2:179,702,446	A/T	—	likely benign
rs2078403	2:179,702,610	T/C	—	benign
rs777389777	2:179,710,336	T/G	—	likely benign
rs143948587	2:179,710,378	G/T	—	uncertain significance
rs1476012042	2:179,710,381	T/G	—	uncertain significance
rs17453403	2:179,710,550	C/G	—	benign
rs6433738	2:179,710,706	A/G	—	benign
rs4894055	2:179,714,675	C/T	—	benign
rs369890692	2:179,714,830	A/G	—	likely benign
rs9808576	2:179,714,896	G/A	—	benign
rs1170263217	2:179,714,897	G/C	—	likely benign
rs13033688	2:179,718,133	T/A	—	benign
rs777571122	2:179,718,214	T/C	—	likely benign
rs151235903	2:179,718,220	C/T	—	likely benign
rs150440298	2:179,718,221	G/A	—	conflicting classifications of pathogenicity
rs2535286418	2:179,718,284	T/C	—	uncertain significance
rs1685257420	2:179,718,286	G/A	—	likely benign
rs762557906	2:179,718,287	C/T	—	uncertain significance
rs149198764	2:179,718,301	T/A	—	likely benign
rs952664164	2:179,718,308	A/T	—	uncertain significance
rs139365189	2:179,718,336	C/T	—	conflicting classifications of pathogenicity
rs370006865	2:179,718,337	G/A	—	likely benign
rs1872203	2:179,719,966	A/T	—	benign
rs368755845	2:179,720,055	C/A	—	likely benign
rs2535306319	2:179,720,155	A/T	—	uncertain significance
rs778418261	2:179,720,170	C/G	—	uncertain significance
rs774941644	2:179,720,186	A/G	—	uncertain significance
rs2535307530	2:179,720,232	T/C	—	uncertain significance
rs367973013	2:179,720,971	A/G	—	likely benign
rs146231973	2:179,720,987	C/A	—	uncertain significance
rs757178613	2:179,720,988	A/G	—	uncertain significance
rs12464157	2:179,721,032	C/T	—	benign
rs142773032	2:179,721,045	C/T	—	uncertain significance
rs17362588	2:179,721,046	G/A	missense variant	benign
rs529109294	2:179,721,050	T/C	—	likely benign
rs775840947	2:179,721,069	T/C	—	uncertain significance
rs150493199	2:179,721,072	T/A	—	uncertain significance
rs768794326	2:179,721,083	A/G	—	likely benign
rs966608278	2:179,721,104	A/G	—	likely benign
rs148586284	2:179,721,354	C/T	—	benign
rs73973173	2:179,730,268	A/G	—	benign

Showing 100 of 304 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.