SPHKAP

SPHK1 interactor, AKAP domain containing

Summary

Enables protein kinase A binding activity. Predicted to be located in Z disc. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants131 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs148966662	2:228,846,486	C/T	—	uncertain significance
rs147820842	2:228,846,548	C/T	—	likely benign
rs61755300	2:228,846,564	C/G	—	likely benign
rs2469414881	2:228,846,567	C/A	—	uncertain significance
rs143649393	2:228,855,759	G/T	—	uncertain significance
rs746889542	2:228,855,765	C/A	—	uncertain significance
rs2469439071	2:228,855,786	C/T	—	uncertain significance
rs764818556	2:228,855,832	G/C	—	uncertain significance
rs61752221	2:228,855,993	C/T	—	benign
rs79492600	2:228,858,241	G/T	—	benign
rs2469447264	2:228,858,265	G/T	—	uncertain significance
rs2469447589	2:228,858,316	G/A	—	uncertain significance
rs776554607	2:228,860,334	G/T	—	uncertain significance
rs1693611400	2:228,860,343	C/T	—	uncertain significance
rs141675542	2:228,860,405	C/T	—	uncertain significance
rs758260088	2:228,881,125	T/C	—	uncertain significance
rs776724748	2:228,881,222	T/C	—	uncertain significance
rs370848705	2:228,881,250	A/C	—	likely benign
rs760739252	2:228,881,302	G/A	—	uncertain significance
rs190144340	2:228,881,318	T/C	—	uncertain significance
rs759122353	2:228,881,404	T/C	—	uncertain significance
rs913204735	2:228,881,447	A/G	—	uncertain significance
rs1244370075	2:228,881,516	C/G	—	uncertain significance
rs1235292719	2:228,881,524	T/C	—	uncertain significance
rs370472666	2:228,881,558	C/G	—	uncertain significance
rs763870430	2:228,881,564	C/T	—	uncertain significance
rs61752223	2:228,881,588	C/T	—	likely benign
rs200923997	2:228,881,644	G/A	—	uncertain significance
rs146255336	2:228,881,675	C/G	—	uncertain significance
rs763134458	2:228,881,677	G/T	—	uncertain significance
rs776850489	2:228,881,731	G/A	—	uncertain significance
rs764243029	2:228,881,743	G/A	—	uncertain significance
rs750948775	2:228,881,762	C/G	—	uncertain significance
rs1195536945	2:228,881,894	G/A	—	uncertain significance
rs780995075	2:228,881,929	C/T	—	uncertain significance
rs137869603	2:228,881,941	G/T	—	uncertain significance
rs1213889932	2:228,881,945	T/C	—	likely benign
rs1475864522	2:228,881,955	G/C	—	likely benign
rs760142985	2:228,881,963	C/T	—	uncertain significance
rs765555224	2:228,881,966	T/C	—	uncertain significance
rs200357217	2:228,882,040	C/T	—	uncertain significance
rs751157752	2:228,882,065	G/A	—	uncertain significance
rs780150576	2:228,882,070	G/A	—	uncertain significance
rs2469524766	2:228,882,083	C/T	—	uncertain significance
rs756170282	2:228,882,244	G/A	—	uncertain significance
rs2469525698	2:228,882,277	T/C	—	uncertain significance
rs181336336	2:228,882,290	T/C	—	uncertain significance
rs749393045	2:228,882,340	C/T	—	uncertain significance
rs748667861	2:228,882,347	A/C	—	uncertain significance
rs2469526452	2:228,882,361	A/G	—	uncertain significance
rs778910801	2:228,882,388	G/A	—	uncertain significance
rs769323258	2:228,882,421	G/A	—	uncertain significance
rs2469526871	2:228,882,426	G/C	—	uncertain significance
rs147925248	2:228,882,431	T/C	—	uncertain significance
rs1375464722	2:228,882,505	A/G	—	uncertain significance
rs1694667159	2:228,882,509	C/T	—	uncertain significance
rs752182241	2:228,882,550	G/A	—	uncertain significance
rs374937865	2:228,882,574	C/T	—	uncertain significance
rs373462091	2:228,882,826	G/A	—	likely benign
rs766620177	2:228,882,869	G/T	—	uncertain significance
rs779273312	2:228,882,931	T/C	—	uncertain significance
rs758635656	2:228,882,939	C/G	—	likely benign
rs374779308	2:228,883,006	G/C	—	uncertain significance
rs116336001	2:228,883,043	T/C	—	uncertain significance
rs1005317700	2:228,883,117	T/C	—	uncertain significance
rs201425414	2:228,883,123	C/T	—	likely benign
rs2469531053	2:228,883,127	A/T	—	uncertain significance
rs1201164918	2:228,883,132	T/A	—	uncertain significance
rs1694696430	2:228,883,148	G/C	—	uncertain significance
rs757308335	2:228,883,162	C/A	—	uncertain significance
rs186338171	2:228,883,231	G/T	—	uncertain significance
rs144775838	2:228,883,264	G/A	—	uncertain significance
rs540293771	2:228,883,297	G/A	—	uncertain significance
rs1694710187	2:228,883,388	C/T	—	uncertain significance
rs779285113	2:228,883,411	G/A	—	uncertain significance
rs202062274	2:228,883,497	G/T	—	uncertain significance
rs140179852	2:228,883,564	T/C	—	uncertain significance
rs544987045	2:228,883,602	G/C	—	likely benign
rs1394113706	2:228,883,639	T/C	—	uncertain significance
rs142236970	2:228,883,735	T/C	—	uncertain significance
rs112738851	2:228,883,801	G/A	—	likely benign
rs145506918	2:228,883,976	T/C	—	likely benign
rs760510406	2:228,883,993	G/A	—	uncertain significance
rs762515585	2:228,884,042	T/G	—	uncertain significance
rs767368345	2:228,884,059	G/T	—	uncertain significance
rs865967990	2:228,884,068	G/C	—	uncertain significance
rs763615196	2:228,884,117	C/T	—	uncertain significance
rs370738563	2:228,884,162	A/G	—	uncertain significance
rs761353940	2:228,884,183	G/A	—	uncertain significance
rs1296817245	2:228,884,284	A/G	—	uncertain significance
rs776408173	2:228,884,441	C/T	—	uncertain significance
rs761969914	2:228,884,452	T/C	—	likely benign
rs1270434757	2:228,884,500	C/T	—	uncertain significance
rs1161273820	2:228,884,536	T/A	—	uncertain significance
rs2469539745	2:228,884,644	T/A	—	uncertain significance
rs139197816	2:228,884,650	T/G	—	uncertain significance
rs61752226	2:228,884,686	G/C	—	uncertain significance
rs149176310	2:228,884,740	G/T	—	likely benign
rs72973340	2:228,884,750	T/C	—	uncertain significance
rs772823521	2:228,884,834	T/C	—	uncertain significance

Showing 100 of 131 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.