ATCAY

ATCAY kinesin light chain interacting caytaxin

Summary

This gene encodes a neuron-restricted protein that contains a CRAL-TRIO motif common to proteins that bind small lipophilic molecules. Mutations in this gene are associated with cerebellar ataxia, Cayman type. [provided by RefSeq, Jul 2008]

Known Variants183 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs186140929	19:3,880,650	C/A	—	likely benign
rs140876148	19:3,880,658	A/G	—	benign
rs886054373	19:3,880,673	G/T	—	uncertain significance
rs376727951	19:3,880,807	C/T	—	benign
rs553381633	19:3,880,850	C/G	—	uncertain significance
rs911941440	19:3,880,872	C/T	—	uncertain significance
rs1034699695	19:3,880,878	C/A	—	uncertain significance
rs140772342	19:3,884,703	G/A	—	uncertain significance
rs529428286	19:3,885,712	G/A	—	uncertain significance
rs937126056	19:3,885,776	C/T	—	uncertain significance
rs368213837	19:3,885,801	C/T	—	conflicting classifications of pathogenicity
rs2512114312	19:3,885,824	A/T	—	uncertain significance
rs769474716	19:3,902,502	C/T	—	uncertain significance
rs200614118	19:3,902,503	G/A	—	likely benign
rs763273815	19:3,902,504	G/A	—	uncertain significance
rs147031440	19:3,902,505	G/A	—	conflicting classifications of pathogenicity
rs73919387	19:3,905,421	T/C	—	likely benign
rs373392142	19:3,905,457	C/T	—	conflicting classifications of pathogenicity
rs772361307	19:3,905,496	G/A	—	likely benign
rs549326005	19:3,905,577	C/T	—	likely benign
rs1381590154	19:3,905,578	G/A	—	uncertain significance
rs201501328	19:3,905,590	G/A	—	uncertain significance
rs753594529	19:3,907,718	C/T	—	uncertain significance
rs758678492	19:3,907,733	C/T	—	likely benign
rs371914915	19:3,907,734	G/A	—	uncertain significance
rs147684273	19:3,907,743	G/A	—	uncertain significance
rs368675084	19:3,907,747	C/T	—	uncertain significance
rs756591751	19:3,907,752	G/A	—	uncertain significance
rs200734663	19:3,907,767	G/A	—	uncertain significance
rs372829245	19:3,907,770	G/A	—	uncertain significance
rs564040857	19:3,907,775	C/T	—	uncertain significance
rs202077180	19:3,907,778	G/A	—	conflicting classifications of pathogenicity
rs548256146	19:3,907,793	C/T	—	uncertain significance
rs373080859	19:3,907,799	G/A	—	likely benign
rs781683142	19:3,907,802	G/A	—	likely benign
rs200021943	19:3,907,815	G/A	—	uncertain significance
rs199529579	19:3,907,818	G/A	—	uncertain significance
rs756194762	19:3,907,824	G/A	—	uncertain significance
rs375699107	19:3,907,837	G/A	—	uncertain significance
rs374611192	19:3,907,851	G/A	—	uncertain significance
rs2038878624	19:3,907,905	G/A	—	uncertain significance
rs3810373	19:3,908,201	C/T	—	benign
rs370662253	19:3,908,258	C/T	—	likely benign
rs929406456	19:3,908,273	C/G	—	uncertain significance
rs367736161	19:3,908,276	C/A	—	uncertain significance
rs763717373	19:3,908,277	G/A	—	uncertain significance
rs781251468	19:3,908,281	G/C	—	uncertain significance
rs537155754	19:3,908,289	G/A	—	uncertain significance
rs946719341	19:3,908,292	A/G	—	uncertain significance
rs777360536	19:3,908,298	G/A	—	uncertain significance
rs748957456	19:3,908,304	G/A	—	uncertain significance
rs1349281740	19:3,908,334	C/T	—	uncertain significance
rs112563476	19:3,908,336	C/A	—	likely benign
rs368644309	19:3,908,337	G/A	—	uncertain significance
rs181866005	19:3,908,378	C/T	—	likely benign
rs755568668	19:3,908,382	C/T	—	uncertain significance
rs117167523	19:3,908,383	G/A	—	uncertain significance
rs186430171	19:3,908,385	G/A	—	benign
rs756838654	19:3,909,475	C/T	—	likely benign
rs750121820	19:3,909,478	G/C	—	likely benign
rs886054415	19:3,909,514	G/A	—	uncertain significance
rs377568098	19:3,909,528	T/C	—	uncertain significance
rs2512134600	19:3,909,539	C/A	—	uncertain significance
rs138571070	19:3,909,541	G/C	—	uncertain significance
rs1300743591	19:3,909,545	G/A	—	uncertain significance
rs768556456	19:3,909,553	G/A	—	conflicting classifications of pathogenicity
rs2038904766	19:3,909,557	C/T	—	uncertain significance
rs1005319363	19:3,909,578	G/A	—	uncertain significance
rs2512134658	19:3,909,580	C/T	—	likely benign
rs1599290979	19:3,909,593	T/A	—	uncertain significance
rs755437219	19:3,909,612	G/A	—	uncertain significance
rs61746441	19:3,910,831	C/T	—	benign
rs372306459	19:3,910,843	G/A	—	likely benign
rs753930037	19:3,910,880	T/G	—	uncertain significance
rs116660680	19:3,910,893	A/G	—	benign
rs140799527	19:3,910,894	C/T	—	likely benign
rs746110322	19:3,910,895	G/A	—	likely benign
rs375049279	19:3,910,897	G/A	—	likely benign
rs1485447287	19:3,913,787	C/T	—	uncertain significance
rs2145256501	19:3,913,792	C/G	—	pathogenic
rs370680121	19:3,913,846	C/T	—	uncertain significance
rs2038943096	19:3,913,857	G/T	—	pathogenic
rs200905154	19:3,913,864	C/A	—	likely benign
rs2512141992	19:3,917,745	A/G	—	uncertain significance
rs947725462	19:3,917,766	G/A	—	uncertain significance
rs767813874	19:3,918,804	C/T	—	uncertain significance
rs1199162322	19:3,918,818	C/T	—	uncertain significance
rs200965736	19:3,918,819	G/A	—	likely benign
rs1362233598	19:3,918,845	A/G	—	uncertain significance
rs369876142	19:3,918,855	G/A	—	conflicting classifications of pathogenicity
rs756401076	19:3,918,862	C/T	—	uncertain significance
rs10420591	19:3,920,750	T/C	—	benign
rs199991972	19:3,920,806	A/T	—	conflicting classifications of pathogenicity
rs60814801	19:3,924,597	G/A	—	benign
rs190923267	19:3,924,616	T/C	—	likely benign
rs537298270	19:3,924,733	G/A	—	uncertain significance
rs764132493	19:3,924,802	C/T	—	uncertain significance
rs867087852	19:3,924,856	C/T	—	uncertain significance
rs541933098	19:3,924,899	C/T	—	likely benign
rs141455019	19:3,924,903	G/A	—	likely benign

Showing 100 of 183 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.