CNTLN

centlein

Summary

Enables protein domain specific binding activity; protein kinase binding activity; and protein-macromolecule adaptor activity. Involved in centriole-centriole cohesion and protein localization to organelle. Located in cytosol; microtubule organizing center; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants118 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs757057300	9:17,135,103	C/T	—	uncertain significance
rs1224252917	9:17,135,122	C/A	—	uncertain significance
rs775891673	9:17,135,149	C/T	—	uncertain significance
rs1296992017	9:17,135,179	C/T	—	uncertain significance
rs1258221815	9:17,135,231	C/G	—	uncertain significance
rs1563807017	9:17,135,244	G/A	—	uncertain significance
rs376268060	9:17,135,272	G/C	—	uncertain significance
rs1259640199	9:17,135,274	G/A	—	likely benign
rs1010581392	9:17,135,277	G/A	—	uncertain significance
rs1029571218	9:17,135,278	C/T	—	uncertain significance
rs1817625904	9:17,135,287	C/G	—	uncertain significance
rs181004987	9:17,135,298	C/G	—	uncertain significance
rs540988878	9:17,135,305	G/T	—	uncertain significance
rs200028190	9:17,135,315	G/T	—	uncertain significance
rs181512541	9:17,135,711	C/T	regulatory region variant	—
rs1160160161	9:17,143,290	A/T	—	uncertain significance
rs144902675	9:17,143,294	A/C	—	uncertain significance
rs2537506015	9:17,143,308	C/G	—	uncertain significance
rs2537506565	9:17,143,352	G/A	—	uncertain significance
rs10962908	9:17,214,938	A/T	intron variant	—
rs1229654584	9:17,235,666	T/C	—	uncertain significance
rs767419795	9:17,235,689	C/T	—	uncertain significance
rs528248591	9:17,235,698	C/T	—	uncertain significance
rs200513513	9:17,235,770	G/C	—	uncertain significance
rs910837260	9:17,236,560	A/C	—	uncertain significance
rs763714990	9:17,236,561	A/G	—	uncertain significance
rs190848809	9:17,259,201	A/G	intron variant	—
rs371678003	9:17,273,767	G/A	—	likely benign
rs61745833	9:17,273,794	G/T	—	benign
rs202140760	9:17,273,800	T/C	—	uncertain significance
rs606382	9:17,291,195	C/T	—	—
rs1278004499	9:17,298,224	G/C	—	uncertain significance
rs1818093918	9:17,298,292	A/G	—	uncertain significance
rs1818095430	9:17,298,307	A/G	—	uncertain significance
rs1436980697	9:17,298,336	A/G	—	uncertain significance
rs190047946	9:17,309,120	G/A	—	benign
rs747841488	9:17,309,141	A/G	—	uncertain significance
rs771915001	9:17,309,143	C/G	—	uncertain significance
rs764733054	9:17,309,159	A/G	—	uncertain significance
rs7031361	9:17,324,645	T/A	intron variant	—
rs12553068	9:17,328,928	C/T	intron variant	—
rs1420398059	9:17,330,631	T/A	—	uncertain significance
rs765685721	9:17,330,640	G/A	—	uncertain significance
rs751840154	9:17,330,651	T/C	—	uncertain significance
rs201214080	9:17,330,730	A/C	—	uncertain significance
rs1192540126	9:17,332,637	C/G	—	uncertain significance
rs374064354	9:17,332,696	A/G	—	uncertain significance
rs61735057	9:17,340,839	T/A	—	benign
rs764821839	9:17,340,865	G/A	—	uncertain significance
rs752938914	9:17,340,889	A/G	—	uncertain significance
rs1233735733	9:17,340,895	A/G	—	uncertain significance
rs1163343070	9:17,340,903	G/T	—	likely benign
rs768560996	9:17,340,943	G/A	—	uncertain significance
rs985503843	9:17,342,325	C/A	—	uncertain significance
rs200118767	9:17,342,376	A/T	—	uncertain significance
rs1328974391	9:17,342,390	T/A	—	uncertain significance
rs187296474	9:17,342,419	A/T	—	uncertain significance
rs769492076	9:17,366,649	G/A	—	uncertain significance
rs760952380	9:17,366,661	A/G	—	likely benign
rs77333912	9:17,366,694	T/A	—	uncertain significance
rs761885379	9:17,388,183	G/A	—	uncertain significance
rs201201728	9:17,388,195	A/G	—	uncertain significance
rs760569104	9:17,388,199	G/C	—	uncertain significance
rs2537758774	9:17,388,234	G/C	—	uncertain significance
rs1489873795	9:17,394,670	G/A	—	uncertain significance
rs2537818196	9:17,394,745	A/C	—	uncertain significance
rs138152539	9:17,394,802	T/C	—	benign
rs61730197	9:17,394,852	G/A	—	benign
rs369185770	9:17,394,853	T/C	—	uncertain significance
rs369975567	9:17,394,908	A/G	—	uncertain significance
rs202094174	9:17,394,950	C/T	—	uncertain significance
rs200206318	9:17,394,973	C/G	—	uncertain significance
rs776415018	9:17,394,974	G/A	—	uncertain significance
rs201062003	9:17,395,011	G/A	—	uncertain significance
rs1161685956	9:17,395,012	A/G	—	uncertain significance
rs1282217008	9:17,409,295	G/C	—	uncertain significance
rs375351490	9:17,409,320	C/G	—	uncertain significance
rs369583267	9:17,409,335	T/C	—	uncertain significance
rs761699777	9:17,409,365	C/T	—	uncertain significance
rs1453976041	9:17,409,431	T/G	—	uncertain significance
rs202121332	9:17,415,794	T/G	—	uncertain significance
rs2538003130	9:17,415,844	T/A	—	uncertain significance
rs1828184041	9:17,415,868	T/G	—	uncertain significance
rs200826065	9:17,415,873	A/G	—	uncertain significance
rs536923331	9:17,415,960	G/T	—	benign
rs907510647	9:17,415,985	A/G	—	uncertain significance
rs1280945022	9:17,415,997	A/C	—	uncertain significance
rs751605497	9:17,416,032	C/T	—	uncertain significance
rs775953389	9:17,416,091	A/C	—	uncertain significance
rs200769542	9:17,416,134	C/T	—	uncertain significance
rs374233404	9:17,416,143	C/G	—	uncertain significance
rs267602191	9:17,416,150	C/G	—	uncertain significance
rs10963108	9:17,457,513	A/T	—	benign
rs200594824	9:17,457,550	G/A	—	uncertain significance
rs769880889	9:17,457,681	T/A	—	uncertain significance
rs762648975	9:17,457,691	A/T	—	uncertain significance
rs10810790	9:17,458,872	C/G	—	—
rs748800287	9:17,464,544	G/A	—	uncertain significance
rs766597821	9:17,464,557	G/A	—	uncertain significance
rs773481332	9:17,466,078	C/A	—	uncertain significance

Showing 100 of 118 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.