ANO7

anoctamin 7

Summary

This prostate-specific gene encodes a cytoplasmic protein, as well as a polytopic membrane protein which may serve as a target in prostate cancer diagnosis and immunotherapy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2011]

Known Variants173 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs199544347	2:242,128,090	G/A	—	uncertain significance
rs148609049	2:242,128,114	C/T	—	benign
rs150946357	2:242,128,115	G/A	—	likely benign
rs756508348	2:242,128,129	G/A	—	uncertain significance
rs150079713	2:242,128,153	G/A	—	uncertain significance
rs11694278	2:242,128,416	G/A	—	benign
rs11694282	2:242,128,447	A/G	—	benign
rs11683690	2:242,129,266	T/C	—	benign
rs2302053	2:242,129,445	A/G	—	benign
rs11695874	2:242,129,487	G/T	—	benign
rs2302054	2:242,129,515	G/A	—	benign
rs150023062	2:242,129,553	G/C	—	likely benign
rs543636867	2:242,129,563	G/A	—	uncertain significance
rs61749471	2:242,129,583	G/A	—	benign
rs1342836441	2:242,129,584	G/A	—	uncertain significance
rs4675985	2:242,129,769	G/T	—	benign
rs4675826	2:242,129,831	A/G	—	benign
rs763477706	2:242,130,619	A/C	—	uncertain significance
rs199899635	2:242,130,624	G/A	—	uncertain significance
rs2531571695	2:242,130,631	C/T	—	uncertain significance
rs2531571857	2:242,130,640	C/G	—	uncertain significance
rs138809031	2:242,130,660	C/T	—	uncertain significance
rs141913177	2:242,130,661	G/A	—	uncertain significance
rs2074837	2:242,130,939	T/A	—	benign
rs12998792	2:242,134,857	A/G	—	benign
rs12694996	2:242,135,017	C/A	—	benign
rs763097219	2:242,135,207	T/C	—	uncertain significance
rs150352902	2:242,135,235	G/A	—	uncertain significance
rs543656184	2:242,135,247	T/C	—	uncertain significance
rs78972598	2:242,135,257	C/A	—	benign
rs77559646	2:242,135,265	G/A	splice region variant	—
rs11674264	2:242,138,490	A/G	—	benign
rs777601769	2:242,138,746	G/A	—	uncertain significance
rs141499501	2:242,138,767	G/A	—	uncertain significance
rs765577295	2:242,138,806	G/T	—	uncertain significance
rs775131941	2:242,138,830	C/T	—	uncertain significance
rs34107209	2:242,138,912	T/C	—	benign
rs35554938	2:242,139,052	G/A	—	benign
rs2013250	2:242,139,491	T/C	—	benign
rs201908062	2:242,139,532	C/T	—	uncertain significance
rs373524213	2:242,139,537	G/A	—	uncertain significance
rs150195342	2:242,139,572	G/T	—	benign
rs150865579	2:242,139,591	G/A	—	uncertain significance
rs77482050	2:242,139,600	G/A	—	benign
rs76538371	2:242,139,853	C/A	—	benign
rs2074839	2:242,139,879	C/T	—	benign
rs2011792	2:242,140,427	C/A	—	benign
rs2531795040	2:242,140,764	C/A	—	uncertain significance
rs78154103	2:242,140,785	C/G	—	benign
rs4675823	2:242,141,312	C/T	—	benign
rs111236002	2:242,141,513	C/T	—	benign
rs766009434	2:242,141,613	T/C	—	uncertain significance
rs368389233	2:242,141,637	A/T	—	uncertain significance
rs144282712	2:242,141,641	C/G	—	benign
rs145225314	2:242,141,645	G/A	—	uncertain significance
rs1448282490	2:242,141,672	C/G	—	uncertain significance
rs776216582	2:242,141,702	G/A	—	uncertain significance
rs2074840	2:242,141,719	T/C	—	benign
rs2074841	2:242,141,926	C/T	—	benign
rs2074842	2:242,142,508	G/A	—	benign
rs1179530	2:242,142,737	T/C	—	benign
rs374614039	2:242,142,761	C/T	—	uncertain significance
rs755290927	2:242,142,763	C/A	—	uncertain significance
rs150246596	2:242,142,800	G/A	—	uncertain significance
rs1054241858	2:242,142,808	C/A	—	uncertain significance
rs565229836	2:242,142,864	C/T	—	likely benign
rs748837286	2:242,142,865	G/A	—	uncertain significance
rs201506858	2:242,142,869	G/A	—	uncertain significance
rs761832893	2:242,142,904	G/A	—	uncertain significance
rs77640154	2:242,142,921	C/T	—	benign
rs59218195	2:242,143,050	C/T	—	benign
rs13410224	2:242,143,169	G/A	—	benign
rs113870213	2:242,144,009	A/G	—	benign
rs2531887988	2:242,144,283	T/G	—	uncertain significance
rs111978925	2:242,144,307	C/T	—	likely benign
rs745909935	2:242,146,997	T/C	—	uncertain significance
rs147733698	2:242,147,020	G/A	—	uncertain significance
rs145388383	2:242,147,036	G/A	—	likely benign
rs137878201	2:242,147,068	G/A	—	uncertain significance
rs78218749	2:242,147,095	G/A	—	benign
rs114496336	2:242,147,158	C/A	—	benign
rs9679681	2:242,147,264	C/A	—	benign
rs11674804	2:242,148,380	C/T	—	benign
rs4675983	2:242,148,390	T/C	—	benign
rs566270205	2:242,148,391	C/T	—	benign
rs13021863	2:242,148,404	A/G	—	benign
rs772860631	2:242,148,703	G/A	—	uncertain significance
rs753977406	2:242,148,721	G/A	—	uncertain significance
rs141888987	2:242,148,730	G/A	—	uncertain significance
rs927123726	2:242,148,752	C/T	—	uncertain significance
rs4675982	2:242,148,764	T/A	—	benign
rs2068667248	2:242,148,803	T/C	—	uncertain significance
rs777662566	2:242,148,811	C/T	—	uncertain significance
rs560238171	2:242,148,959	C/T	—	likely benign
rs147198890	2:242,148,972	G/A	—	likely benign
rs1194319748	2:242,148,990	C/T	—	likely benign
rs57677160	2:242,149,010	C/T	—	benign
rs757887974	2:242,149,015	C/T	—	uncertain significance
rs201707610	2:242,149,016	G/A	—	uncertain significance
rs748178998	2:242,149,042	G/C	—	likely benign

Showing 100 of 173 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.