ALPK1

alpha kinase 1

Summary

This gene encodes an alpha kinase. Mice which were homozygous for disrupted copies of this gene exhibited coordination defects (PMID: 21208416). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

Known Variants545 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs556569191	4:113,246,506	T/C	—	—
rs150560693	4:113,279,681	G/A	coding sequence variant	—
rs73841009	4:113,298,428	C/A	intron variant	—
rs77273710	4:113,298,659	G/A	intron variant	—
rs762537510	4:113,298,956	C/A	—	uncertain significance
rs747314175	4:113,298,965	T/C	—	uncertain significance
rs759431854	4:113,298,973	T/C	—	uncertain significance
rs116018927	4:113,298,987	G/A	—	benign
rs199994656	4:113,298,988	G/A	—	uncertain significance
rs779112711	4:113,299,001	T/G	—	uncertain significance
rs2476390386	4:113,299,002	G/A	—	likely benign
rs2476390394	4:113,299,006	G/A	—	uncertain significance
rs369223684	4:113,299,007	C/T	—	uncertain significance
rs61747962	4:113,299,008	G/A	—	benign
rs780322472	4:113,299,017	G/A	—	likely benign
rs747393894	4:113,299,019	C/T	—	benign
rs202167520	4:113,299,020	G/C	—	likely benign
rs2476390454	4:113,299,025	A/C	—	uncertain significance
rs2476390469	4:113,299,032	G/T	—	uncertain significance
rs543243733	4:113,299,035	C/T	—	likely benign
rs779703332	4:113,299,036	G/A	—	conflicting classifications of pathogenicity
rs373809231	4:113,299,046	G/A	—	uncertain significance
rs1731738921	4:113,299,070	G/A	—	likely benign
rs1293661453	4:113,299,074	C/T	—	likely benign
rs1358216318	4:113,303,537	A/G	—	likely benign
rs1731960536	4:113,303,538	A/G	—	likely benign
rs375325807	4:113,303,562	C/T	—	uncertain significance
rs746785388	4:113,303,563	C/T	—	uncertain significance
rs182602784	4:113,303,567	C/T	—	likely benign
rs776572834	4:113,303,568	G/A	—	uncertain significance
rs2476401716	4:113,303,570	G/C	—	uncertain significance
rs369534780	4:113,303,576	G/A	—	likely benign
rs763029486	4:113,303,589	G/A	—	uncertain significance
rs751762758	4:113,303,592	G/A	—	uncertain significance
rs1179821884	4:113,303,606	G/A	—	likely benign
rs188866014	4:113,303,616	G/A	—	conflicting classifications of pathogenicity
rs33943680	4:113,303,632	A/G	—	likely benign
rs2476402037	4:113,303,655	G/A	—	uncertain significance
rs746624721	4:113,303,665	C/A	—	uncertain significance
rs2476402066	4:113,303,666	A/C	—	likely benign
rs2476402083	4:113,303,673	A/G	—	uncertain significance
rs2476402133	4:113,303,682	A/G	—	uncertain significance
rs773063913	4:113,303,688	G/C	—	uncertain significance
rs770990158	4:113,303,690	C/T	—	likely benign
rs148869813	4:113,303,691	G/A	—	likely benign
rs2476402246	4:113,303,706	C/T	—	likely benign
rs1044292289	4:113,303,708	G/C	—	likely benign
rs1374094746	4:113,303,710	T/C	—	uncertain significance
rs904457280	4:113,303,711	A/G	—	uncertain significance
rs377455823	4:113,303,723	A/G	—	likely benign
rs965012	4:113,310,635	C/G	—	—
rs4833407	4:113,311,790	C/G	—	—
rs57590313	4:113,323,430	C/G	—	—
rs6838440	4:113,328,078	C/T	intron variant	—
rs751091985	4:113,332,968	A/G	—	likely benign
rs1285016553	4:113,332,969	C/T	—	likely benign
rs1436623345	4:113,332,970	G/C	—	uncertain significance
rs375367633	4:113,332,984	C/T	—	uncertain significance
rs2476467700	4:113,332,986	T/C	—	uncertain significance
rs778659546	4:113,333,010	C/G	—	uncertain significance
rs772239630	4:113,333,011	G/A	—	uncertain significance
rs775879914	4:113,333,013	G/T	—	uncertain significance
rs376695615	4:113,333,021	G/A	—	likely benign
rs2476467919	4:113,333,034	A/C	—	uncertain significance
rs370872798	4:113,333,039	G/T	—	likely benign
rs767060999	4:113,333,046	G/C	—	benign
rs755828218	4:113,333,049	G/A	—	uncertain significance
rs778943984	4:113,333,061	T/C	—	uncertain significance
rs780322054	4:113,333,069	C/G	—	likely benign
rs1336343869	4:113,333,070	G/C	—	uncertain significance
rs942090186	4:113,333,080	G/T	—	uncertain significance
rs924445505	4:113,333,088	C/G	—	uncertain significance
rs2476468169	4:113,333,098	C/G	—	uncertain significance
rs776648904	4:113,333,104	G/A	—	uncertain significance
rs770001847	4:113,333,116	T/C	—	uncertain significance
rs367762485	4:113,333,117	G/T	—	uncertain significance
rs201002217	4:113,333,124	G/A	—	benign
rs1427050994	4:113,333,137	C/T	—	uncertain significance
rs2476468300	4:113,333,141	G/A	—	likely benign
rs374550552	4:113,333,155	G/C	—	uncertain significance
rs2476468400	4:113,333,163	C/G	—	uncertain significance
rs550191337	4:113,333,167	T/C	—	conflicting classifications of pathogenicity
rs2476468432	4:113,333,169	T/C	—	uncertain significance
rs146381479	4:113,333,171	C/T	—	likely benign
rs2476468494	4:113,333,185	T/A	—	uncertain significance
rs1488531927	4:113,333,186	G/A	—	uncertain significance
rs781497943	4:113,333,191	C/T	—	likely benign
rs2476468542	4:113,333,197	C/G	—	likely benign
rs201681617	4:113,345,092	C/T	—	likely benign
rs2476490932	4:113,345,102	A/C	—	uncertain significance
rs138427105	4:113,345,113	A/G	—	likely benign
rs2476490999	4:113,345,128	G/A	—	likely benign
rs6533616	4:113,345,147	A/G	—	uncertain significance
rs376769752	4:113,345,158	G/A	—	likely benign
rs767363240	4:113,345,172	A/G	—	likely benign
rs2476493225	4:113,346,803	T/G	—	likely benign
rs1264626670	4:113,346,815	T/C	—	likely benign
rs2476493282	4:113,346,831	G/A	—	likely benign
rs373046330	4:113,346,842	A/G	—	uncertain significance
rs138151334	4:113,346,846	T/G	—	likely benign

Showing 100 of 545 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.