NAV3

neuron navigator 3

Summary

This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]

Known Variants128 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs696451	12:77,980,345	G/A	intergenic variant	—
rs698153	12:78,023,777	A/G	intergenic variant	—
rs10745592	12:78,146,255	G/A	intergenic variant	—
rs112130810	12:78,149,439	A/C	—	—
rs939459	12:78,151,064	T/A	—	—
rs5019250	12:78,154,606	C/A	—	—
rs2887597	12:78,154,834	G/T	—	—
rs2090767	12:78,155,338	G/T	—	—
rs1520736	12:78,157,077	C/A	—	—
rs1113600	12:78,175,361	C/G	—	—
rs12811685	12:78,222,363	C/A	—	—
rs1163802650	12:78,225,277	G/A	—	likely benign
rs10735309	12:78,225,374	A/G	—	benign
rs2542145107	12:78,225,377	G/C	—	uncertain significance
rs1233829772	12:78,225,380	A/G	—	uncertain significance
rs747682850	12:78,225,416	A/C	—	uncertain significance
rs200146862	12:78,225,435	G/T	—	uncertain significance
rs753946153	12:78,225,473	G/C	—	uncertain significance
rs528385235	12:78,334,201	A/G	—	uncertain significance
rs1489620264	12:78,360,009	A/T	—	uncertain significance
rs118149283	12:78,360,089	G/A	—	likely benign
rs2137992263	12:78,362,406	C/T	—	uncertain significance
rs771641910	12:78,362,416	G/A	—	uncertain significance
rs775001284	12:78,362,431	C/T	—	uncertain significance
rs2137995042	12:78,362,454	G/A	—	uncertain significance
rs2137996023	12:78,362,475	C/T	—	uncertain significance
rs373504958	12:78,392,139	C/A	—	uncertain significance
rs746256657	12:78,392,233	A/G	—	uncertain significance
rs772446522	12:78,392,238	G/A	—	uncertain significance
rs755422149	12:78,400,243	G/A	—	likely benign
rs2136557787	12:78,400,294	C/G	—	uncertain significance
rs2136558008	12:78,400,298	G/C	—	uncertain significance
rs764756369	12:78,400,309	C/A	—	uncertain significance
rs201482142	12:78,400,356	C/G	—	benign
rs368953799	12:78,400,395	C/A	—	likely benign
rs779255279	12:78,400,450	C/A	—	uncertain significance
rs748769258	12:78,400,496	C/G	—	uncertain significance
rs184775230	12:78,400,499	G/C	—	uncertain significance
rs201438479	12:78,400,514	C/T	—	uncertain significance
rs1874301122	12:78,400,555	G/A	—	uncertain significance
rs114303302	12:78,400,566	C/T	—	benign
rs773789932	12:78,400,592	G/C	—	uncertain significance
rs778139901	12:78,400,691	A/C	—	uncertain significance
rs2542015737	12:78,400,714	A/G	—	uncertain significance
rs778799852	12:78,400,779	G/C	—	uncertain significance
rs370427296	12:78,400,820	A/G	—	uncertain significance
rs200981782	12:78,400,832	T/G	—	uncertain significance
rs533952691	12:78,400,939	A/G	—	likely benign
rs781577801	12:78,400,955	C/T	—	uncertain significance
rs750800578	12:78,401,060	C/A	—	uncertain significance
rs575710290	12:78,401,065	T/G	—	uncertain significance
rs372709335	12:78,415,552	G/A	—	uncertain significance
rs779043567	12:78,415,574	G/A	—	uncertain significance
rs1205484794	12:78,415,580	G/A	—	uncertain significance
rs918913417	12:78,443,823	T/A	—	uncertain significance
rs774502348	12:78,443,860	G/A	—	uncertain significance
rs781027432	12:78,444,627	C/G	—	uncertain significance
rs760819848	12:78,444,669	C/T	—	uncertain significance
rs61754794	12:78,444,690	G/A	—	uncertain significance
rs558608455	12:78,444,816	G/C	—	uncertain significance
rs2137405236	12:78,452,798	A/C	—	uncertain significance
rs374085687	12:78,452,823	G/A	—	uncertain significance
rs371471672	12:78,452,847	G/A	—	uncertain significance
rs751418701	12:78,452,873	G/A	—	uncertain significance
rs300489	12:78,485,994	G/T	—	—
rs763162312	12:78,510,668	C/G	—	uncertain significance
rs377644039	12:78,511,829	G/C	—	uncertain significance
rs1186177839	12:78,511,838	C/T	—	uncertain significance
rs2138565092	12:78,511,865	A/T	—	uncertain significance
rs781411104	12:78,511,876	C/A	—	likely benign
rs138798588	12:78,511,977	C/G	—	benign
rs757265301	12:78,511,979	T/C	—	uncertain significance
rs746054151	12:78,511,993	A/G	—	uncertain significance
rs762988858	12:78,512,025	A/T	—	uncertain significance
rs370297366	12:78,512,038	T/C	—	uncertain significance
rs2138577447	12:78,512,075	C/A	—	uncertain significance
rs374428675	12:78,513,037	G/A	—	uncertain significance
rs745825519	12:78,513,041	C/A	—	uncertain significance
rs372332757	12:78,513,080	A/G	—	uncertain significance
rs763341796	12:78,513,167	C/A	—	uncertain significance
rs766945766	12:78,513,172	G/A	—	uncertain significance
rs1017428269	12:78,513,224	G/C	—	uncertain significance
rs747734145	12:78,513,336	G/C	—	uncertain significance
rs772696173	12:78,513,493	G/T	—	uncertain significance
rs747478055	12:78,513,499	A/G	—	uncertain significance
rs2138628813	12:78,513,506	A/G	—	uncertain significance
rs774128541	12:78,513,539	G/A	—	uncertain significance
rs199936979	12:78,513,584	A/T	—	uncertain significance
rs1338079552	12:78,513,685	G/A	—	uncertain significance
rs140781984	12:78,515,886	G/A	—	uncertain significance
rs750554053	12:78,516,033	G/A	—	uncertain significance
rs1955947099	12:78,520,973	C/T	—	uncertain significance
rs374767030	12:78,522,491	C/A	—	uncertain significance
rs919658437	12:78,522,512	A/C	—	uncertain significance
rs747945999	12:78,522,520	G/C	—	uncertain significance
rs115472476	12:78,530,986	C/A	—	benign
rs61754236	12:78,530,991	T/C	—	benign
rs770042276	12:78,531,007	C/T	—	uncertain significance
rs200005671	12:78,531,043	G/A	—	uncertain significance
rs2544019206	12:78,531,115	T/G	—	uncertain significance

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

Gene information from NCBI Gene. Variant classifications from ClinVar.