CLMN

calmin

Summary

Predicted to enable actin filament binding activity. Predicted to be involved in negative regulation of cell population proliferation. Predicted to act upstream of or within neuron projection development. Predicted to be located in membrane. Predicted to be part of meiotic nuclear membrane microtubule tethering complex. Predicted to be active in cytoplasm and nuclear outer membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants102 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs144887816	14:95,657,918	C/T	—	uncertain significance
rs370913265	14:95,657,969	T/A	—	uncertain significance
rs1463660110	14:95,657,990	G/T	—	uncertain significance
rs10149705	14:95,658,022	G/A	—	benign
rs768809029	14:95,658,028	T/C	—	uncertain significance
rs200929274	14:95,658,061	T/C	—	uncertain significance
rs149684020	14:95,660,182	C/T	—	benign
rs1128468	14:95,660,242	A/G	—	benign
rs148831726	14:95,660,243	T/C	—	likely benign
rs191962411	14:95,660,880	G/A	—	likely benign
rs61750771	14:95,662,845	T/A	—	benign
rs746570921	14:95,662,854	C/T	—	uncertain significance
rs367811329	14:95,662,889	A/G	—	uncertain significance
rs1896723747	14:95,662,991	A/G	—	uncertain significance
rs773234474	14:95,662,993	G/A	—	likely benign
rs138747415	14:95,663,003	A/C	—	uncertain significance
rs138296892	14:95,669,165	G/A	—	benign
rs150763369	14:95,669,187	C/T	—	uncertain significance
rs1271310285	14:95,669,231	G/A	—	uncertain significance
rs2543890654	14:95,669,261	G/A	—	uncertain significance
rs759681484	14:95,669,263	G/A	—	uncertain significance
rs199989778	14:95,669,300	G/T	—	uncertain significance
rs12147696	14:95,669,334	C/T	—	benign
rs147963787	14:95,669,374	T/G	—	likely benign
rs746046813	14:95,669,428	T/C	—	uncertain significance
rs753470058	14:95,669,450	C/T	—	uncertain significance
rs182859603	14:95,669,455	A/G	—	likely benign
rs114143013	14:95,669,487	C/T	—	benign
rs754960856	14:95,669,525	C/T	—	uncertain significance
rs745661185	14:95,669,549	A/G	—	uncertain significance
rs140199156	14:95,669,566	C/A	—	uncertain significance
rs140829875	14:95,669,574	G/A	—	likely benign
rs766644944	14:95,669,584	C/G	—	uncertain significance
rs2543892306	14:95,669,612	T/C	—	uncertain significance
rs1896941277	14:95,669,627	A/G	—	likely benign
rs2543892589	14:95,669,665	C/T	—	uncertain significance
rs149317388	14:95,669,683	G/A	—	uncertain significance
rs190623772	14:95,669,686	C/T	—	uncertain significance
rs201319473	14:95,669,897	C/A	—	uncertain significance
rs144975674	14:95,669,910	G/C	—	uncertain significance
rs529950009	14:95,669,962	G/C	—	uncertain significance
rs2543893894	14:95,669,969	A/C	—	uncertain significance
rs186980388	14:95,670,026	C/T	—	uncertain significance
rs143034500	14:95,670,080	C/T	—	uncertain significance
rs369150193	14:95,670,085	A/G	—	uncertain significance
rs10131338	14:95,670,132	G/A	—	benign
rs78561092	14:95,670,136	C/T	—	benign
rs373571746	14:95,670,148	T/G	—	uncertain significance
rs754274028	14:95,670,184	T/C	—	likely benign
rs1000450405	14:95,670,209	T/A	—	uncertain significance
rs116654567	14:95,670,221	C/A	—	benign
rs201041933	14:95,670,249	C/T	—	likely benign
rs1896968049	14:95,670,328	G/C	—	uncertain significance
rs2543895593	14:95,670,337	G/A	—	uncertain significance
rs751769788	14:95,670,349	A/C	—	uncertain significance
rs1318780873	14:95,670,391	G/A	—	uncertain significance
rs2543895902	14:95,670,405	G/T	—	uncertain significance
rs201300248	14:95,670,424	G/A	—	uncertain significance
rs1896971591	14:95,670,432	G/C	—	uncertain significance
rs750543097	14:95,670,557	T/C	—	uncertain significance
rs146464693	14:95,670,574	G/A	—	uncertain significance
rs757003520	14:95,670,583	G/C	—	uncertain significance
rs35010297	14:95,670,617	C/T	—	benign
rs140399405	14:95,670,649	G/C	—	uncertain significance
rs745676142	14:95,670,669	G/C	—	uncertain significance
rs201448932	14:95,670,676	G/T	—	uncertain significance
rs368900284	14:95,670,707	C/T	—	uncertain significance
rs116066710	14:95,670,747	G/C	—	likely benign
rs1217048564	14:95,670,804	C/A	—	likely benign
rs1187614	14:95,671,871	G/T	intron variant	—
rs118150470	14:95,675,791	C/T	—	likely benign
rs780456472	14:95,677,042	G/C	—	likely benign
rs755276214	14:95,677,049	T/C	—	uncertain significance
rs766956868	14:95,677,082	T/C	—	uncertain significance
rs150700470	14:95,677,156	C/T	—	likely benign
rs150401399	14:95,677,157	G/C	—	uncertain significance
rs1280192532	14:95,677,166	G/A	—	uncertain significance
rs139868659	14:95,677,204	C/T	—	likely benign
rs780050094	14:95,677,209	C/T	—	uncertain significance
rs749122559	14:95,677,210	G/A	—	likely benign
rs374580429	14:95,679,549	G/A	—	likely benign
rs145508613	14:95,679,580	G/A	—	uncertain significance
rs1239605624	14:95,679,596	T/C	—	uncertain significance
rs2543920351	14:95,679,668	C/T	—	uncertain significance
rs151018579	14:95,682,025	G/C	—	likely benign
rs142235299	14:95,682,062	C/A	—	benign
rs117326550	14:95,688,059	G/A	—	uncertain significance
rs138779390	14:95,688,060	C/T	—	uncertain significance
rs368293776	14:95,688,083	C/T	—	uncertain significance
rs112023847	14:95,688,084	G/A	—	uncertain significance
rs756412157	14:95,688,093	A/C	—	uncertain significance
rs2543942128	14:95,688,102	A/G	—	uncertain significance
rs1897623865	14:95,690,154	A/C	—	uncertain significance
rs752907924	14:95,690,182	G/C	—	uncertain significance
rs962477618	14:95,690,185	G/C	—	uncertain significance
rs758679603	14:95,690,188	T/G	—	uncertain significance
rs138831842	14:95,696,401	G/A	—	likely benign
rs116124564	14:95,696,436	T/C	—	likely benign
rs8014194	14:95,720,678	T/A	intron variant	—
rs115102486	14:95,764,564	A/G	intron variant	—

Showing 100 of 102 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.