NCKAP5

NCK associated protein 5

Summary

Predicted to be involved in microtubule bundle formation and microtubule depolymerization. Predicted to be active in microtubule plus-end. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants161 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs746785063	2:133,483,209	C/T	—	uncertain significance
rs772960524	2:133,483,229	A/G	—	uncertain significance
rs199719142	2:133,486,397	C/T	—	uncertain significance
rs201952722	2:133,486,408	A/T	—	benign
rs201643159	2:133,486,432	G/A	—	uncertain significance
rs746477429	2:133,486,477	G/A	—	uncertain significance
rs768083355	2:133,486,478	T/C	—	uncertain significance
rs116732206	2:133,489,334	G/A	—	benign
rs761488484	2:133,489,394	T/C	—	uncertain significance
rs765563733	2:133,489,397	C/T	—	likely benign
rs777248110	2:133,489,418	C/T	—	likely benign
rs202128241	2:133,489,544	G/A	—	uncertain significance
rs760508642	2:133,489,564	G/A	—	uncertain significance
rs564109970	2:133,502,209	A/T	—	—
rs13033310	2:133,523,605	G/A	intron variant	—
rs372390578	2:133,531,390	T/C	—	uncertain significance
rs772240429	2:133,531,391	A/G	—	uncertain significance
rs747935901	2:133,531,400	C/T	—	uncertain significance
rs189199346	2:133,531,464	T/G	—	uncertain significance
rs758429982	2:133,538,632	T/A	—	uncertain significance
rs111861429	2:133,538,668	T/A	—	conflicting classifications of pathogenicity
rs61742426	2:133,538,703	G/A	—	benign
rs780758821	2:133,539,528	G/A	—	uncertain significance
rs77373192	2:133,539,546	G/A	—	conflicting classifications of pathogenicity
rs878945774	2:133,539,553	A/G	—	uncertain significance
rs1311162065	2:133,539,564	C/A	—	uncertain significance
rs2468087519	2:133,539,567	T/C	—	uncertain significance
rs201294911	2:133,539,582	T/C	—	uncertain significance
rs2468087796	2:133,539,586	T/C	—	uncertain significance
rs7607544	2:133,539,621	C/T	—	conflicting classifications of pathogenicity
rs760973428	2:133,539,643	C/T	—	uncertain significance
rs181883434	2:133,539,660	G/A	—	likely benign
rs147016733	2:133,539,679	T/A	—	uncertain significance
rs376182292	2:133,539,774	G/C	—	uncertain significance
rs186478619	2:133,539,970	T/C	—	uncertain significance
rs112873686	2:133,540,011	G/A	—	uncertain significance
rs1325431934	2:133,540,087	G/T	—	uncertain significance
rs756221410	2:133,540,093	T/C	—	uncertain significance
rs749495496	2:133,540,110	A/T	—	uncertain significance
rs906231370	2:133,540,135	T/G	—	uncertain significance
rs765989595	2:133,540,165	G/A	—	uncertain significance
rs2105030787	2:133,540,188	G/C	—	uncertain significance
rs968058109	2:133,540,318	C/T	—	uncertain significance
rs373110207	2:133,540,342	C/T	—	likely benign
rs757282426	2:133,540,413	T/C	—	likely benign
rs1189517691	2:133,540,431	G/A	—	uncertain significance
rs373549422	2:133,540,443	C/T	—	uncertain significance
rs538437785	2:133,540,455	T/C	—	uncertain significance
rs764718255	2:133,540,459	C/T	—	uncertain significance
rs545006757	2:133,540,491	C/T	—	uncertain significance
rs376373106	2:133,540,510	C/T	—	uncertain significance
rs749776982	2:133,540,552	A/G	—	uncertain significance
rs200887045	2:133,540,623	G/A	—	uncertain significance
rs74900692	2:133,540,634	G/C	—	benign
rs775482886	2:133,540,648	C/A	—	uncertain significance
rs1166884977	2:133,540,665	C/A	—	uncertain significance
rs1261780094	2:133,540,713	G/A	—	uncertain significance
rs72847214	2:133,540,714	G/A	—	benign
rs758870807	2:133,540,746	G/A	—	likely benign
rs72989583	2:133,540,754	T/C	—	benign
rs202180979	2:133,540,763	A/T	—	uncertain significance
rs200334792	2:133,540,776	G/A	—	uncertain significance
rs201602771	2:133,540,888	C/T	—	uncertain significance
rs1043761298	2:133,540,890	G/C	—	uncertain significance
rs2468113976	2:133,540,915	G/C	—	uncertain significance
rs1370141013	2:133,540,930	C/T	—	uncertain significance
rs201086054	2:133,541,129	A/G	—	likely benign
rs375896892	2:133,541,148	G/A	—	uncertain significance
rs775876157	2:133,541,223	A/G	—	uncertain significance
rs761369446	2:133,541,236	G/C	—	uncertain significance
rs780384987	2:133,541,319	G/A	—	uncertain significance
rs377381048	2:133,541,328	C/T	—	uncertain significance
rs760521196	2:133,541,367	G/T	—	uncertain significance
rs61746887	2:133,541,422	T/A	—	benign
rs368218260	2:133,541,469	G/A	—	uncertain significance
rs2468127126	2:133,541,523	G/C	—	uncertain significance
rs765119484	2:133,541,548	C/T	—	uncertain significance
rs749784294	2:133,541,579	C/A	—	uncertain significance
rs772271616	2:133,541,595	G/A	—	uncertain significance
rs752311759	2:133,541,625	G/A	—	uncertain significance
rs184979029	2:133,541,651	C/T	—	benign
rs749095227	2:133,541,680	C/T	—	uncertain significance
rs774183431	2:133,541,686	C/T	—	uncertain significance
rs779991490	2:133,541,766	G/A	—	uncertain significance
rs368192716	2:133,541,792	G/C	—	uncertain significance
rs1683339455	2:133,541,793	T/C	—	uncertain significance
rs144491492	2:133,541,805	C/T	—	likely benign
rs2468133475	2:133,541,833	C/T	—	uncertain significance
rs1206470319	2:133,541,971	G/A	—	uncertain significance
rs760081455	2:133,541,997	T/A	—	uncertain significance
rs767551538	2:133,541,998	G/T	—	uncertain significance
rs147993981	2:133,542,004	T/C	—	conflicting classifications of pathogenicity
rs200676700	2:133,542,010	T/C	—	conflicting classifications of pathogenicity
rs1370198994	2:133,542,013	G/A	—	likely benign
rs374385691	2:133,542,017	C/T	—	likely benign
rs368526094	2:133,542,100	T/C	—	uncertain significance
rs76227896	2:133,542,166	C/T	—	uncertain significance
rs1683387913	2:133,542,220	G/A	—	uncertain significance
rs777329197	2:133,542,231	G/T	—	uncertain significance
rs530244033	2:133,542,357	C/T	—	uncertain significance

Showing 100 of 161 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.