NUP160

nucleoporin 160

Summary

A structural constituent of nuclear pore. Involved in mRNA export from nucleus and nephron development. Located in kinetochore and nuclear envelope. Part of nuclear pore outer ring. Implicated in nephrotic syndrome type 19. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants253 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1215002128	11:47,800,698	C/G	—	uncertain significance
rs980955283	11:47,800,702	T/G	—	uncertain significance
rs56962998	11:47,800,723	T/C	—	benign
rs201495092	11:47,800,749	A/G	—	uncertain significance
rs186321019	11:47,801,897	C/T	—	uncertain significance
rs1467327632	11:47,801,931	A/G	—	likely benign
rs1030016657	11:47,801,934	T/C	—	likely benign
rs62000434	11:47,801,951	T/C	—	uncertain significance
rs377383850	11:47,801,953	G/A	—	uncertain significance
rs149674516	11:47,801,958	G/A	—	likely benign
rs750659752	11:47,801,961	T/C	—	likely benign
rs147754476	11:47,801,975	T/C	—	uncertain significance
rs779427209	11:47,801,978	G/C	—	uncertain significance
rs185707803	11:47,804,611	T/C	—	likely benign
rs756620160	11:47,804,627	C/T	—	uncertain significance
rs2097662442	11:47,804,665	T/C	—	uncertain significance
rs771502743	11:47,804,693	C/T	—	uncertain significance
rs199762443	11:47,804,713	T/G	—	uncertain significance
rs2510178998	11:47,804,731	A/C	—	uncertain significance
rs1470894628	11:47,804,764	G/A	—	likely benign
rs35805829	11:47,805,478	T/C	intron variant	—
rs371080808	11:47,806,467	C/G	—	likely benign
rs200105376	11:47,806,468	G/A	—	uncertain significance
rs146411765	11:47,806,477	G/A	—	likely benign
rs373842346	11:47,806,506	G/T	—	uncertain significance
rs2510180307	11:47,806,541	T/C	—	uncertain significance
rs1256906901	11:47,806,549	C/A	—	uncertain significance
rs1366830653	11:47,806,573	C/T	—	likely benign
rs2510180386	11:47,806,587	A/G	—	uncertain significance
rs780453055	11:47,806,608	C/T	—	uncertain significance
rs1230522675	11:47,806,614	C/T	—	uncertain significance
rs1220659995	11:47,806,634	G/T	—	likely benign
rs2097663758	11:47,806,635	A/C	—	likely benign
rs554894200	11:47,806,657	A/T	intron variant	—
rs748229219	11:47,807,986	T/C	—	likely benign
rs2510181345	11:47,807,996	G/C	—	likely benign
rs771291784	11:47,808,012	C/T	—	uncertain significance
rs1381477206	11:47,808,034	G/T	—	likely benign
rs146457879	11:47,808,090	A/G	—	uncertain significance
rs748273136	11:47,808,102	T/C	—	uncertain significance
rs561686954	11:47,809,719	T/A	—	likely benign
rs535059681	11:47,809,761	G/A	—	uncertain significance
rs199893111	11:47,809,770	A/T	—	uncertain significance
rs761440602	11:47,809,794	A/G	—	uncertain significance
rs2135346265	11:47,809,804	C/G	—	uncertain significance
rs1382066574	11:47,809,824	A/C	—	uncertain significance
rs533558791	11:47,809,832	G/T	—	likely benign
rs2510183167	11:47,809,849	A/C	—	uncertain significance
rs2510183182	11:47,809,872	A/G	—	likely benign
rs145992472	11:47,810,059	C/G	—	uncertain significance
rs1213235579	11:47,810,063	A/C	—	likely benign
rs1334818725	11:47,810,070	G/A	—	uncertain significance
rs141812661	11:47,810,074	G/A	—	uncertain significance
rs202064082	11:47,810,108	C/G	—	uncertain significance
rs778756977	11:47,810,158	G/C	—	uncertain significance
rs749581419	11:47,810,167	T/C	—	likely benign
rs2125838	11:47,811,933	A/G	intron variant	—
rs777319816	11:47,813,484	G/C	—	uncertain significance
rs756729056	11:47,813,487	G/A	—	uncertain significance
rs745871321	11:47,813,521	G/A	—	uncertain significance
rs1329710562	11:47,813,532	G/A	—	uncertain significance
rs2097668610	11:47,814,361	C/A	—	uncertain significance
rs369156455	11:47,814,369	G/A	—	uncertain significance
rs753215206	11:47,814,381	C/T	—	uncertain significance
rs146186362	11:47,814,413	A/G	—	likely benign
rs751519690	11:47,814,414	T/A	—	uncertain significance
rs61755075	11:47,814,467	C/G	—	likely benign
rs2494712857	11:47,814,489	A/G	—	uncertain significance
rs140949934	11:47,819,322	A/G	—	likely benign
rs752680140	11:47,819,348	C/T	—	uncertain significance
rs551317169	11:47,819,349	G/A	—	uncertain significance
rs2494722150	11:47,819,386	G/T	—	uncertain significance
rs1337959392	11:47,819,426	A/G	—	uncertain significance
rs995816921	11:47,819,431	C/T	—	likely benign
rs2097671836	11:47,819,543	T/G	—	uncertain significance
rs1352439837	11:47,819,557	C/G	—	uncertain significance
rs898735293	11:47,819,562	C/G	—	uncertain significance
rs147712305	11:47,819,609	C/T	—	uncertain significance
rs936125416	11:47,819,727	A/T	—	uncertain significance
rs2097671966	11:47,819,736	T/C	—	uncertain significance
rs1307205029	11:47,819,753	T/C	—	uncertain significance
rs761860296	11:47,819,786	T/C	—	uncertain significance
rs774114700	11:47,819,903	T/G	—	likely benign
rs114776609	11:47,819,940	C/T	—	benign
rs558863897	11:47,819,948	G/A	—	uncertain significance
rs758931011	11:47,819,961	T/C	—	uncertain significance
rs2494723970	11:47,819,969	T/C	—	uncertain significance
rs751943060	11:47,819,971	A/C	—	uncertain significance
rs201369503	11:47,820,020	C/T	—	benign
rs548825905	11:47,822,231	C/T	—	—
rs369790346	11:47,823,347	C/T	—	likely benign
rs1230897717	11:47,823,349	A/G	—	likely benign
rs1477454818	11:47,823,385	G/C	—	uncertain significance
rs199886252	11:47,823,395	C/T	—	uncertain significance
rs1391312169	11:47,823,401	C/T	—	uncertain significance
rs745749003	11:47,823,415	C/T	—	uncertain significance
rs374918751	11:47,823,416	G/A	—	uncertain significance
rs942923988	11:47,823,424	C/T	—	uncertain significance
rs181012736	11:47,823,434	A/G	—	uncertain significance
rs557543573	11:47,824,980	T/C	—	likely benign

Showing 100 of 253 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.