CAPN15

calpain 15

Summary

This gene encodes a protein containing zinc-finger-like repeats and a calpain-like protease domain. The encoded protein may function as a transcription factor, RNA-binding protein, or in protein-protein interactions during visual system development. [provided by RefSeq, Jul 2008]

Known Variants195 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2266928	16:580,124	C/G	—	—
rs141885650	16:583,753	C/T	regulatory region variant	—
rs140928636	16:585,836	C/G	—	—
rs113355794	16:586,144	T/C	—	—
rs771093418	16:596,851	G/A	—	uncertain significance
rs753200597	16:596,888	C/T	—	uncertain significance
rs2071923	16:596,893	G/T	—	uncertain significance
rs375530346	16:596,957	G/A	—	uncertain significance
rs2505820310	16:596,960	T/G	—	uncertain significance
rs372023253	16:596,972	A/G	—	uncertain significance
rs369295076	16:596,989	G/T	—	uncertain significance
rs778754950	16:596,992	C/T	—	uncertain significance
rs1487254124	16:596,993	G/T	—	uncertain significance
rs775059866	16:597,030	C/T	—	likely benign
rs141227716	16:597,059	C/T	—	likely benign
rs768909338	16:597,080	C/G	—	uncertain significance
rs1236101518	16:597,094	G/C	—	uncertain significance
rs773799955	16:597,112	G/A	—	likely benign
rs74003979	16:597,150	A/G	—	benign
rs371030677	16:597,171	G/A	—	likely benign
rs1262506281	16:597,206	G/T	—	uncertain significance
rs1043275133	16:597,213	C/A	—	likely benign
rs1050165104	16:597,222	G/C	—	uncertain significance
rs199656743	16:597,229	A/G	—	likely benign
rs1008564197	16:597,247	G/A	—	uncertain significance
rs200344224	16:597,250	G/A	—	likely benign
rs145595428	16:597,258	G/A	—	likely benign
rs200574929	16:597,260	C/A	—	uncertain significance
rs112599163	16:597,266	C/G	—	benign
rs369178350	16:597,309	G/A	—	likely benign
rs746365723	16:597,331	G/A	—	uncertain significance
rs747547391	16:597,390	C/A	—	likely benign
rs766317408	16:597,401	T/C	—	uncertain significance
rs572003179	16:597,408	G/C	—	likely benign
rs371770669	16:597,411	C/T	—	likely benign
rs576084802	16:597,420	C/T	—	likely benign
rs543476764	16:597,421	G/A	—	uncertain significance
rs369551311	16:597,423	C/T	—	likely benign
rs368827959	16:597,424	G/A	—	uncertain significance
rs377457205	16:597,435	G/A	—	likely benign
rs770941673	16:597,437	C/A	—	uncertain significance
rs759184846	16:597,448	C/T	—	uncertain significance
rs141612773	16:597,453	C/T	—	likely benign
rs779315114	16:597,469	G/A	—	uncertain significance
rs759755087	16:597,521	G/A	—	uncertain significance
rs1409319312	16:597,548	C/T	—	uncertain significance
rs765439225	16:597,568	G/A	—	uncertain significance
rs749018970	16:597,581	G/A	—	uncertain significance
rs770957213	16:597,586	G/A	—	uncertain significance
rs912104078	16:597,625	G/T	—	uncertain significance
rs2034690198	16:597,667	G/A	—	uncertain significance
rs149179728	16:597,745	A/G	—	likely benign
rs143354752	16:597,746	C/T	—	likely benign
rs760213854	16:597,763	C/T	—	uncertain significance
rs140736836	16:597,772	G/C	—	uncertain significance
rs1250535838	16:597,776	G/A	—	uncertain significance
rs199791667	16:597,814	G/A	—	uncertain significance
rs748581792	16:597,815	G/T	—	uncertain significance
rs2034702714	16:597,821	C/T	—	uncertain significance
rs759112599	16:597,832	A/C	—	uncertain significance
rs1370056393	16:597,874	T/C	—	uncertain significance
rs1189841860	16:597,887	C/T	—	uncertain significance
rs763878383	16:597,921	G/A	—	likely benign
rs149502771	16:597,924	C/T	—	likely benign
rs144052786	16:597,925	T/C	—	uncertain significance
rs755212538	16:597,941	T/C	—	uncertain significance
rs1033847763	16:597,947	G/A	—	uncertain significance
rs1292144935	16:597,977	A/G	—	likely benign
rs753452010	16:598,030	C/T	—	uncertain significance
rs199911780	16:598,041	G/A	—	benign
rs1429988760	16:598,073	G/A	—	uncertain significance
rs748950993	16:598,076	C/T	—	uncertain significance
rs202055221	16:598,121	G/A	—	likely benign
rs202224861	16:598,135	G/A	—	uncertain significance
rs765231833	16:598,138	G/A	—	uncertain significance
rs746941603	16:598,172	G/A	—	uncertain significance
rs373024243	16:598,183	G/A	—	likely benign
rs376305319	16:598,185	G/A	—	likely benign
rs370414323	16:598,212	C/T	—	likely benign
rs374456445	16:598,242	C/T	—	likely benign
rs1024736307	16:598,283	G/A	—	uncertain significance
rs200359206	16:598,295	G/A	—	likely benign
rs549175319	16:598,689	G/A	—	—
rs145573740	16:598,989	G/A	—	benign
rs748393081	16:599,008	G/T	—	uncertain significance
rs2505842019	16:599,023	C/T	—	uncertain significance
rs148686276	16:599,028	C/T	—	likely benign
rs535269157	16:599,029	G/A	—	uncertain significance
rs139411778	16:599,116	G/A	—	uncertain significance
rs545798516	16:599,136	C/T	—	likely benign
rs147318382	16:599,297	C/T	—	likely benign
rs1176553372	16:599,306	G/A	—	likely benign
rs1022265639	16:599,314	C/T	—	uncertain significance
rs548702059	16:599,338	G/A	—	uncertain significance
rs149821359	16:599,399	C/T	—	benign
rs1239978070	16:599,451	G/A	—	uncertain significance
rs374949685	16:599,467	C/T	—	uncertain significance
rs759766924	16:599,475	G/C	—	likely benign
rs1228386819	16:599,615	G/T	—	uncertain significance
rs1402180871	16:599,647	C/G	—	uncertain significance

Showing 100 of 195 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.