Clmn Variant Search Result - Rat Genome Database

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146 records found for search term Clmn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405287709	CV3208041	single nucleotide variant	NM_024734.4(CLMN):c.608+7C>T	CLMN-related disorder [RCV003924560]	likely benign	14	95213212	95213212	Human		name , trait , alternate_id
15196857	CV760141	single nucleotide variant	NM_024734.4(CLMN):c.144+8C>T	not provided [RCV000911814]	likely benign	14	95230064	95230064	Human		name
15147420	CV779649	single nucleotide variant	NM_024734.4(CLMN):c.886-4G>T	not provided [RCV000967336]	likely benign	14	95204467	95204467	Human		name
15135377	CV779648	single nucleotide variant	NM_024734.4(CLMN):c.2840+4G>A	CLMN-related disorder [RCV003960765]\|not provided [RCV000965278]	benign	14	95193845	95193845	Human		name , trait , alternate_id
15109342	CV779912	single nucleotide variant	NM_024734.4(CLMN):c.2511+10C>T	not provided [RCV000960678]	benign	14	95202828	95202828	Human		name
8584150	CV118722	single nucleotide variant	NM_024734.3(CLMN):c.83-41047C>T	Lung cancer [RCV000099242]	uncertain significance	14	95271180	95271180	Human		name
405288214	CV3200584	single nucleotide variant	NM_024734.4(CLMN):c.15G>A (p.Glu5=)	CLMN-related disorder [RCV003982297]	benign	14	95319778	95319778	Human		name , trait , alternate_id
15167455	CV779915	duplication	NM_024734.4(CLMN):c.886-13_886-12dup	CLMN-related disorder [RCV003928511]\|not provided [RCV000971404]	benign	14	95204467	95204468	Human		name , trait , alternate_id
401902248	CV2807213	single nucleotide variant	NM_024734.4(CLMN):c.117A>G (p.Thr39=)	not provided [RCV003393592]	likely benign	14	95230099	95230099	Human		name
407463041	CV3429243	single nucleotide variant	NM_024734.4(CLMN):c.22T>C (p.Trp8Arg)	not specified [RCV004613097]	uncertain significance	14	95319771	95319771	Human		name
156012087	CV2358846	single nucleotide variant	NM_024734.4(CLMN):c.46G>A (p.Gly16Arg)	not specified [RCV004212193]	uncertain significance	14	95319747	95319747	Human		name
401902245	CV2807211	single nucleotide variant	NM_024734.4(CLMN):c.669G>A (p.Ala223=)	not provided [RCV003393590]	likely benign	14	95210819	95210819	Human		name
401902247	CV2807212	single nucleotide variant	NM_024734.4(CLMN):c.615C>T (p.Gly205=)	not provided [RCV003393591]	likely benign	14	95210873	95210873	Human		name
405280264	CV3191713	single nucleotide variant	NM_024734.4(CLMN):c.939C>G (p.Arg313=)	CLMN-related disorder [RCV003919847]	likely benign	14	95204410	95204410	Human		name , trait , alternate_id
405275933	CV3199516	single nucleotide variant	NM_024734.4(CLMN):c.621G>A (p.Ala207=)	CLMN-related disorder [RCV003916915]	likely benign	14	95210867	95210867	Human		name , trait , alternate_id
405289691	CV3220976	single nucleotide variant	NM_024734.4(CLMN):c.783C>G (p.Pro261=)	CLMN-related disorder [RCV003961873]	likely benign	14	95210705	95210705	Human		name , trait , alternate_id
408367344	CV3510913	single nucleotide variant	NM_024734.4(CLMN):c.462C>T (p.Ser154=)	CLMN-related disorder [RCV004758395]	likely benign	14	95213365	95213365	Human		name , trait , alternate_id
408367514	CV3516776	single nucleotide variant	NM_024734.4(CLMN):c.735A>G (p.Glu245=)	CLMN-related disorder [RCV004758565]	likely benign	14	95210753	95210753	Human		name , trait , alternate_id
598244499	CV3944765	single nucleotide variant	NM_024734.4(CLMN):c.98T>G (p.Val33Gly)	not specified [RCV005322057]	uncertain significance	14	95230118	95230118	Human		name
15109348	CV714291	single nucleotide variant	NM_024734.4(CLMN):c.333G>T (p.Leu111=)	CLMN-related disorder [RCV003905822]\|not provided [RCV000960679]	benign	14	95215725	95215725	Human		name , trait , alternate_id
156258851	CV2204691	single nucleotide variant	NM_024734.4(CLMN):c.268C>T (p.Arg90Cys)	not specified [RCV004081794]	uncertain significance	14	95221747	95221747	Human		name
156384351	CV2231058	single nucleotide variant	NM_024734.4(CLMN):c.292G>A (p.Ala98Thr)	not specified [RCV004094289]	uncertain significance	14	95221723	95221723	Human		name
156033503	CV2256441	single nucleotide variant	NM_024734.4(CLMN):c.250T>C (p.Tyr84His)	not specified [RCV004118657]	uncertain significance	14	95221765	95221765	Human		name
156080128	CV2259317	single nucleotide variant	NM_024734.4(CLMN):c.269G>A (p.Arg90His)	not specified [RCV004122328]	uncertain significance	14	95221746	95221746	Human		name
156046980	CV2268721	single nucleotide variant	NM_024734.4(CLMN):c.293C>T (p.Ala98Val)	not specified [RCV004124120]	uncertain significance	14	95221722	95221722	Human		name
155993888	CV2377338	single nucleotide variant	NM_024734.4(CLMN):c.259T>G (p.Ser87Ala)	not specified [RCV004225519]	uncertain significance	14	95221756	95221756	Human		name
401758859	CV2694317	single nucleotide variant	NM_024734.4(CLMN):c.149A>C (p.Asn50Thr)	not specified [RCV004304513]	uncertain significance	14	95223851	95223851	Human		name
405284896	CV3190904	single nucleotide variant	NM_024734.4(CLMN):c.2550C>T (p.Pro850=)	CLMN-related disorder [RCV003909467]	likely benign	14	95196656	95196656	Human		name , trait , alternate_id
405283696	CV3191805	single nucleotide variant	NM_024734.4(CLMN):c.1437G>A (p.Ser479=)	CLMN-related disorder [RCV003921903]	likely benign	14	95203912	95203912	Human		name , trait , alternate_id
405292594	CV3192522	single nucleotide variant	NM_024734.4(CLMN):c.2112C>T (p.Ser704=)	CLMN-related disorder [RCV003929776]	likely benign	14	95203237	95203237	Human		name , trait , alternate_id
405272491	CV3221753	single nucleotide variant	NM_024734.4(CLMN):c.2784T>C (p.Tyr928=)	CLMN-related disorder [RCV003972163]	benign	14	95193905	95193905	Human		name , trait , alternate_id
405782593	CV3305707	single nucleotide variant	NM_024734.4(CLMN):c.152C>G (p.Pro51Arg)	not specified [RCV004437219]	uncertain significance	14	95223848	95223848	Human		name
405782599	CV3305708	single nucleotide variant	NM_024734.4(CLMN):c.155C>G (p.Pro52Arg)	not specified [RCV004437220]	uncertain significance	14	95223845	95223845	Human		name
405782619	CV3305711	single nucleotide variant	NM_024734.4(CLMN):c.183T>G (p.Asp61Glu)	not specified [RCV004437223]	uncertain significance	14	95223817	95223817	Human		name
597791906	CV3656811	single nucleotide variant	NM_024734.4(CLMN):c.269G>C (p.Arg90Pro)	not specified [RCV004902456]	uncertain significance	14	95221746	95221746	Human		name
597791910	CV3656812	single nucleotide variant	NM_024734.4(CLMN):c.181G>A (p.Asp61Asn)	not specified [RCV004902457]	uncertain significance	14	95223819	95223819	Human		name
598244513	CV3944767	single nucleotide variant	NM_024734.4(CLMN):c.236A>C (p.Asn79Thr)	not specified [RCV005322059]	uncertain significance	14	95223764	95223764	Human		name
598244521	CV3944768	single nucleotide variant	NM_024734.4(CLMN):c.208G>T (p.Ala70Ser)	not specified [RCV005322060]	uncertain significance	14	95223792	95223792	Human		name
598244529	CV3944769	single nucleotide variant	NM_024734.4(CLMN):c.268C>G (p.Arg90Gly)	not specified [RCV005322061]	uncertain significance	14	95221747	95221747	Human		name
15173515	CV703047	single nucleotide variant	NM_024734.4(CLMN):c.2352G>A (p.Ser784=)	not provided [RCV000950232]	benign	14	95202997	95202997	Human		name
15162466	CV714287	single nucleotide variant	NM_024734.4(CLMN):c.1776C>T (p.Asp592=)	CLMN-related disorder [RCV003962870]\|not provided [RCV000970275]	benign	14	95203573	95203573	Human		name , trait , alternate_id
15152114	CV714288	single nucleotide variant	NM_024734.4(CLMN):c.1554C>T (p.His518=)	not provided [RCV000968284]	benign	14	95203795	95203795	Human		name
15191972	CV739434	single nucleotide variant	NM_024734.4(CLMN):c.2199G>A (p.Glu733=)	not provided [RCV000910402]	benign	14	95203150	95203150	Human		name
156179184	CV2229507	single nucleotide variant	NM_024734.4(CLMN):c.568A>G (p.Ile190Val)	not specified [RCV004103049]	uncertain significance	14	95213259	95213259	Human		name
155919266	CV2333165	single nucleotide variant	NM_024734.4(CLMN):c.979G>A (p.Val327Ile)	not specified [RCV004194454]	uncertain significance	14	95204370	95204370	Human		name
156329481	CV2342412	single nucleotide variant	NM_024734.4(CLMN):c.668C>G (p.Ala223Gly)	not specified [RCV004194023]	uncertain significance	14	95210820	95210820	Human		name
329372194	CV2455094	single nucleotide variant	NM_024734.4(CLMN):c.776A>G (p.His259Arg)	not specified [RCV004272341]	uncertain significance	14	95210712	95210712	Human		name
401778663	CV2705461	single nucleotide variant	NM_024734.4(CLMN):c.616G>A (p.Val206Met)	not specified [RCV004316552]	uncertain significance	14	95210872	95210872	Human		name
401877682	CV2779907	single nucleotide variant	NM_024734.4(CLMN):c.496G>A (p.Asp166Asn)	not specified [RCV004353519]	uncertain significance	14	95213331	95213331	Human		name
405782694	CV3305723	single nucleotide variant	NM_024734.4(CLMN):c.584C>T (p.Ala195Val)	not specified [RCV004437235]	uncertain significance	14	95213243	95213243	Human		name
405782701	CV3305724	single nucleotide variant	NM_024734.4(CLMN):c.659C>T (p.Ala220Val)	not specified [RCV004437236]	uncertain significance	14	95210829	95210829	Human		name
405782707	CV3305725	single nucleotide variant	NM_024734.4(CLMN):c.743A>G (p.Glu248Gly)	not specified [RCV004437237]	uncertain significance	14	95210745	95210745	Human		name
407463031	CV3429241	single nucleotide variant	NM_024734.4(CLMN):c.509C>T (p.Pro170Leu)	not specified [RCV004613095]	uncertain significance	14	95213318	95213318	Human		name
597791883	CV3656802	single nucleotide variant	NM_024734.4(CLMN):c.620C>T (p.Ala207Val)	not specified [RCV004902448]	uncertain significance	14	95210868	95210868	Human		name
597791912	CV3656813	single nucleotide variant	NM_024734.4(CLMN):c.430A>G (p.Thr144Ala)	not specified [RCV004902458]	uncertain significance	14	95213397	95213397	Human		name
598244457	CV3944759	single nucleotide variant	NM_024734.4(CLMN):c.922G>A (p.Glu308Lys)	not specified [RCV005322052]	uncertain significance	14	95204427	95204427	Human		name
598244491	CV3944764	single nucleotide variant	NM_024734.4(CLMN):c.979G>T (p.Val327Phe)	not specified [RCV005322056]	uncertain significance	14	95204370	95204370	Human		name
15141600	CV714290	single nucleotide variant	NM_024734.4(CLMN):c.826G>A (p.Glu276Lys)	CLMN-related disorder [RCV003960776]\|not provided [RCV000966332]	likely benign	14	95209454	95209454	Human		name , trait , alternate_id
15109341	CV754253	single nucleotide variant	NM_024734.4(CLMN):c.370C>G (p.Pro124Ala)	CLMN-related disorder [RCV003950832]\|not provided [RCV000916316]	likely benign	14	95215688	95215688	Human		name , trait , alternate_id
156400026	CV2198912	single nucleotide variant	NM_024734.4(CLMN):c.1724C>G (p.Ser575Cys)	not specified [RCV004078290]	uncertain significance	14	95203625	95203625	Human		name
156038259	CV2214901	single nucleotide variant	NM_024734.4(CLMN):c.1295C>T (p.Thr432Ile)	not specified [RCV004084693]	uncertain significance	14	95204054	95204054	Human		name
156259260	CV2216205	single nucleotide variant	NM_024734.4(CLMN):c.1538A>C (p.Glu513Ala)	not specified [RCV004097178]	uncertain significance	14	95203811	95203811	Human		name
156257225	CV2219844	single nucleotide variant	NM_024734.4(CLMN):c.1112C>T (p.Ala371Val)	not specified [RCV004095497]	uncertain significance	14	95204237	95204237	Human		name
155974377	CV2221081	single nucleotide variant	NM_024734.4(CLMN):c.1037C>G (p.Pro346Arg)	not specified [RCV004094537]	uncertain significance	14	95204312	95204312	Human		name
155935555	CV2225632	single nucleotide variant	NM_024734.4(CLMN):c.2455C>T (p.His819Tyr)	not specified [RCV004101002]	uncertain significance	14	95202894	95202894	Human		name
156062719	CV2232038	single nucleotide variant	NM_024734.4(CLMN):c.2425C>T (p.Pro809Ser)	not specified [RCV004093088]	uncertain significance	14	95202924	95202924	Human		name
156141362	CV2243804	single nucleotide variant	NM_024734.4(CLMN):c.1281C>A (p.His427Gln)	not specified [RCV004114769]	uncertain significance	14	95204068	95204068	Human		name
156083610	CV2244489	single nucleotide variant	NM_024734.4(CLMN):c.2920C>A (p.Gln974Lys)	not specified [RCV004100446]	uncertain significance	14	95191653	95191653	Human		name
155919426	CV2254864	single nucleotide variant	NM_024734.4(CLMN):c.1103C>G (p.Ser368Cys)	not specified [RCV004115323]	uncertain significance	14	95204246	95204246	Human		name
156101329	CV2260329	single nucleotide variant	NM_024734.4(CLMN):c.1477A>T (p.Ile493Phe)	not specified [RCV004129416]	uncertain significance	14	95203872	95203872	Human		name
155943336	CV2298522	single nucleotide variant	NM_024734.4(CLMN):c.1358C>G (p.Ala453Gly)	not specified [RCV004162180]	uncertain significance	14	95203991	95203991	Human		name
155903581	CV2301668	single nucleotide variant	NM_024734.4(CLMN):c.1254C>G (p.Asn418Lys)	not specified [RCV004162569]	uncertain significance	14	95204095	95204095	Human		name
156193707	CV2302012	single nucleotide variant	NM_024734.4(CLMN):c.1601T>C (p.Met534Thr)	not specified [RCV004158782]	uncertain significance	14	95203748	95203748	Human		name
156040683	CV2310825	single nucleotide variant	NM_024734.4(CLMN):c.2882A>G (p.His961Arg)	not specified [RCV004163873]	uncertain significance	14	95191691	95191691	Human		name
156261488	CV2314733	single nucleotide variant	NM_024734.4(CLMN):c.1129A>G (p.Thr377Ala)	not specified [RCV004170876]	uncertain significance	14	95204220	95204220	Human		name
156363462	CV2329895	single nucleotide variant	NM_024734.4(CLMN):c.2992G>A (p.Asp998Asn)	not specified [RCV004183351]	uncertain significance	14	95191581	95191581	Human		name
156121176	CV2354236	single nucleotide variant	NM_024734.4(CLMN):c.1010C>A (p.Thr337Asn)	not specified [RCV004206661]	uncertain significance	14	95204339	95204339	Human		name
156074115	CV2365505	single nucleotide variant	NM_024734.4(CLMN):c.2849A>G (p.Asn950Ser)	not specified [RCV004211622]	uncertain significance	14	95191724	95191724	Human		name
156387127	CV2372645	single nucleotide variant	NM_024734.4(CLMN):c.1606G>A (p.Asp536Asn)	not specified [RCV004221847]	uncertain significance	14	95203743	95203743	Human		name
155937837	CV2373848	single nucleotide variant	NM_024734.4(CLMN):c.1776C>G (p.Asp592Glu)	not specified [RCV004224783]	uncertain significance	14	95203573	95203573	Human		name
156191189	CV2385166	single nucleotide variant	NM_024734.4(CLMN):c.1349C>T (p.Pro450Leu)	not specified [RCV004228420]	uncertain significance	14	95204000	95204000	Human		name
155908418	CV2387317	single nucleotide variant	NM_024734.4(CLMN):c.2003C>T (p.Pro668Leu)	not specified [RCV004238405]	uncertain significance	14	95203346	95203346	Human		name
156258847	CV2395425	single nucleotide variant	NM_024734.4(CLMN):c.1502A>G (p.Asn501Ser)	not specified [RCV004241298]	likely benign	14	95203847	95203847	Human		name
329391915	CV2445136	single nucleotide variant	NM_024734.4(CLMN):c.1538A>G (p.Glu513Gly)	not specified [RCV004263779]	uncertain significance	14	95203811	95203811	Human		name
329354827	CV2449095	single nucleotide variant	NM_024734.4(CLMN):c.2762C>T (p.Ser921Leu)	not specified [RCV004264159]	likely benign	14	95194543	95194543	Human		name
329372535	CV2451533	single nucleotide variant	NM_024734.4(CLMN):c.1337T>G (p.Phe446Cys)	not specified [RCV004274476]	uncertain significance	14	95204012	95204012	Human		name
329401391	CV2460856	single nucleotide variant	NM_024734.4(CLMN):c.2021G>A (p.Gly674Glu)	not specified [RCV004271162]	uncertain significance	14	95203328	95203328	Human		name
401726817	CV2674557	single nucleotide variant	NM_024734.4(CLMN):c.2386C>A (p.Gln796Lys)	not specified [RCV004291435]	uncertain significance	14	95202963	95202963	Human		name
401730403	CV2680301	single nucleotide variant	NM_024734.4(CLMN):c.2499G>A (p.Met833Ile)	not specified [RCV004288554]	uncertain significance	14	95202850	95202850	Human		name
401758599	CV2694183	single nucleotide variant	NM_024734.4(CLMN):c.2654T>C (p.Val885Ala)	not specified [RCV004302606]	uncertain significance	14	95196552	95196552	Human		name
401735310	CV2706746	single nucleotide variant	NM_024734.4(CLMN):c.1717T>G (p.Phe573Val)	not specified [RCV004319308]	uncertain significance	14	95203632	95203632	Human		name
401771656	CV2711820	single nucleotide variant	NM_024734.4(CLMN):c.2231T>C (p.Val744Ala)	not specified [RCV004309459]	likely benign	14	95203118	95203118	Human		name
401781616	CV2722189	single nucleotide variant	NM_024734.4(CLMN):c.2941A>T (p.Ile981Phe)	not specified [RCV004328756]	uncertain significance	14	95191632	95191632	Human		name
401874636	CV2759296	single nucleotide variant	NM_024734.4(CLMN):c.1262C>T (p.Pro421Leu)	not specified [RCV004335885]	uncertain significance	14	95204087	95204087	Human		name
401860421	CV2768584	single nucleotide variant	NM_024734.4(CLMN):c.2236G>A (p.Asp746Asn)	not specified [RCV004344446]	uncertain significance	14	95203113	95203113	Human		name
401899073	CV2786004	single nucleotide variant	NM_024734.4(CLMN):c.2423C>T (p.Thr808Ile)	not specified [RCV004359841]	uncertain significance	14	95202926	95202926	Human		name
401898252	CV2791013	single nucleotide variant	NM_024734.4(CLMN):c.2074A>G (p.Ser692Gly)	not specified [RCV004354629]	uncertain significance	14	95203275	95203275	Human		name
405285079	CV3202434	single nucleotide variant	NM_024734.4(CLMN):c.1550G>A (p.Arg517His)	CLMN-related disorder [RCV003909700]	benign	14	95203799	95203799	Human		name , trait , alternate_id
405256166	CV3208676	single nucleotide variant	NM_024734.4(CLMN):c.2783A>G (p.Tyr928Cys)	CLMN-related disorder [RCV003939737]	likely benign	14	95193906	95193906	Human		name , trait , alternate_id
405782579	CV3305705	single nucleotide variant	NM_024734.4(CLMN):c.1017C>G (p.Asn339Lys)	not specified [RCV004437217]	uncertain significance	14	95204332	95204332	Human		name
405782606	CV3305709	single nucleotide variant	NM_024734.4(CLMN):c.1660G>A (p.Asp554Asn)	not specified [RCV004437221]	uncertain significance	14	95203689	95203689	Human		name
405782613	CV3305710	single nucleotide variant	NM_024734.4(CLMN):c.1789G>T (p.Ala597Ser)	not specified [RCV004437222]	uncertain significance	14	95203560	95203560	Human		name
405782626	CV3305712	single nucleotide variant	NM_024734.4(CLMN):c.2000G>A (p.Arg667His)	not specified [RCV004437224]	uncertain significance	14	95203349	95203349	Human		name
405782633	CV3305713	single nucleotide variant	NM_024734.4(CLMN):c.2059T>C (p.Ser687Pro)	not specified [RCV004437225]	likely benign	14	95203290	95203290	Human		name
405782639	CV3305714	single nucleotide variant	NM_024734.4(CLMN):c.2102G>C (p.Gly701Ala)	not specified [RCV004437226]	uncertain significance	14	95203247	95203247	Human		name
405782645	CV3305715	single nucleotide variant	NM_024734.4(CLMN):c.2120G>T (p.Gly707Val)	not specified [RCV004437227]	uncertain significance	14	95203229	95203229	Human		name
405782651	CV3305716	single nucleotide variant	NM_024734.4(CLMN):c.2137T>C (p.Ser713Pro)	not specified [RCV004437228]	uncertain significance	14	95203212	95203212	Human		name
405782657	CV3305717	single nucleotide variant	NM_024734.4(CLMN):c.2161G>A (p.Val721Ile)	not specified [RCV004437229]	uncertain significance	14	95203188	95203188	Human		name
405782668	CV3305719	single nucleotide variant	NM_024734.4(CLMN):c.2258A>G (p.Glu753Gly)	not specified [RCV004437231]	uncertain significance	14	95203091	95203091	Human		name
405782673	CV3305720	single nucleotide variant	NM_024734.4(CLMN):c.2540T>G (p.Ile847Arg)	not specified [RCV004437232]	uncertain significance	14	95196666	95196666	Human		name
405782680	CV3305721	single nucleotide variant	NM_024734.4(CLMN):c.2552T>C (p.Leu851Pro)	not specified [RCV004437233]	uncertain significance	14	95196654	95196654	Human		name
405782687	CV3305722	single nucleotide variant	NM_024734.4(CLMN):c.2689G>A (p.Asp897Asn)	not specified [RCV004437234]	uncertain significance	14	95196517	95196517	Human		name
407463027	CV3429240	single nucleotide variant	NM_024734.4(CLMN):c.1549C>T (p.Arg517Cys)	not specified [RCV004613094]	uncertain significance	14	95203800	95203800	Human		name
407463037	CV3429242	single nucleotide variant	NM_024734.4(CLMN):c.1999C>T (p.Arg667Cys)	not specified [RCV004613096]	uncertain significance	14	95203350	95203350	Human		name
407463045	CV3429244	single nucleotide variant	NM_024734.4(CLMN):c.2943T>G (p.Ile981Met)	not specified [RCV004613098]	uncertain significance	14	95191630	95191630	Human		name
407463049	CV3429245	single nucleotide variant	NM_024734.4(CLMN):c.1432T>C (p.Ser478Pro)	not specified [RCV004613099]	uncertain significance	14	95203917	95203917	Human		name
407463052	CV3429246	single nucleotide variant	NM_024734.4(CLMN):c.1823G>C (p.Arg608Thr)	not specified [RCV004613100]	uncertain significance	14	95203526	95203526	Human		name
407463061	CV3429248	single nucleotide variant	NM_024734.4(CLMN):c.1379A>G (p.Asp460Gly)	not specified [RCV004613102]	uncertain significance	14	95203970	95203970	Human		name
407463064	CV3429249	single nucleotide variant	NM_024734.4(CLMN):c.1195A>C (p.Ser399Arg)	not specified [RCV004613103]	uncertain significance	14	95204154	95204154	Human		name
407463069	CV3429250	single nucleotide variant	NM_024734.4(CLMN):c.1697T>C (p.Phe566Ser)	not specified [RCV004613104]	uncertain significance	14	95203652	95203652	Human		name
597791879	CV3656801	single nucleotide variant	NM_024734.4(CLMN):c.1856C>T (p.Ser619Leu)	not specified [RCV004902447]	uncertain significance	14	95203493	95203493	Human		name
597791886	CV3656803	single nucleotide variant	NM_024734.4(CLMN):c.1001G>A (p.Arg334His)	not specified [RCV004902449]	uncertain significance	14	95204348	95204348	Human		name
597791888	CV3656804	single nucleotide variant	NM_024734.4(CLMN):c.1037C>A (p.Pro346Gln)	not specified [RCV004902450]	uncertain significance	14	95204312	95204312	Human		name
597791891	CV3656805	single nucleotide variant	NM_024734.4(CLMN):c.2828G>A (p.Arg943Gln)	not specified [RCV004902451]	uncertain significance	14	95193861	95193861	Human		name
597791894	CV3656806	single nucleotide variant	NM_024734.4(CLMN):c.1591A>C (p.Asn531His)	not specified [RCV004902452]	uncertain significance	14	95203758	95203758	Human		name
597791897	CV3656807	single nucleotide variant	NM_024734.4(CLMN):c.1637C>T (p.Thr546Ile)	not specified [RCV004902453]	uncertain significance	14	95203712	95203712	Human		name
597791903	CV3656810	single nucleotide variant	NM_024734.4(CLMN):c.2096C>T (p.Thr699Ile)	not specified [RCV004902455]	uncertain significance	14	95203253	95203253	Human		name
597791916	CV3656814	single nucleotide variant	NM_024734.4(CLMN):c.1698T>G (p.Phe566Leu)	not specified [RCV004902459]	uncertain significance	14	95203651	95203651	Human		name
597791918	CV3656815	single nucleotide variant	NM_024734.4(CLMN):c.2040G>C (p.Gln680His)	not specified [RCV004902460]	uncertain significance	14	95203309	95203309	Human		name
597792116	CV3656816	single nucleotide variant	NM_024734.4(CLMN):c.2210C>G (p.Ala737Gly)	not specified [RCV004902461]	uncertain significance	14	95203139	95203139	Human		name
597792113	CV3656817	single nucleotide variant	NM_024734.4(CLMN):c.1436C>T (p.Ser479Leu)	not specified [RCV004902462]	likely benign	14	95203913	95203913	Human		name
597792110	CV3656818	single nucleotide variant	NM_024734.4(CLMN):c.1487T>G (p.Val496Gly)	not specified [RCV004902463]	uncertain significance	14	95203862	95203862	Human		name
597792107	CV3656819	single nucleotide variant	NM_024734.4(CLMN):c.1946C>T (p.Thr649Ile)	not specified [RCV004902464]	uncertain significance	14	95203403	95203403	Human		name
597792099	CV3656821	single nucleotide variant	NM_024734.4(CLMN):c.2911C>T (p.Leu971Phe)	not specified [RCV004902466]	likely benign	14	95191662	95191662	Human		name
597792096	CV3656822	single nucleotide variant	NM_024734.4(CLMN):c.2452C>A (p.Pro818Thr)	not specified [RCV004902467]	uncertain significance	14	95202897	95202897	Human		name
597792093	CV3656823	single nucleotide variant	NM_024734.4(CLMN):c.1334G>T (p.Cys445Phe)	not specified [RCV004902468]	uncertain significance	14	95204015	95204015	Human		name
598244450	CV3944758	single nucleotide variant	NM_024734.4(CLMN):c.1001G>C (p.Arg334Pro)	not specified [RCV005322051]	uncertain significance	14	95204348	95204348	Human		name
598244466	CV3944761	single nucleotide variant	NM_024734.4(CLMN):c.1159G>A (p.Val387Ile)	not specified [RCV005322053]	uncertain significance	14	95204190	95204190	Human		name
598244475	CV3944762	single nucleotide variant	NM_024734.4(CLMN):c.1468G>C (p.Ala490Pro)	not specified [RCV005322054]	likely benign	14	95203881	95203881	Human		name
598244482	CV3944763	single nucleotide variant	NM_024734.4(CLMN):c.1580C>T (p.Pro527Leu)	not specified [RCV005322055]	uncertain significance	14	95203769	95203769	Human		name
598244506	CV3944766	single nucleotide variant	NM_024734.4(CLMN):c.2252A>G (p.Lys751Arg)	not specified [RCV005322058]	uncertain significance	14	95203097	95203097	Human		name
15200125	CV703046	single nucleotide variant	NM_024734.4(CLMN):c.2698A>T (p.Ile900Phe)	CLMN-related disorder [RCV003935873]\|not provided [RCV000957240]	benign	14	95196508	95196508	Human		name , trait , alternate_id
15152108	CV714286	single nucleotide variant	NM_024734.4(CLMN):c.2888C>T (p.Pro963Leu)	not provided [RCV000968283]	benign	14	95191685	95191685	Human		name
15135383	CV714289	single nucleotide variant	NM_024734.4(CLMN):c.1465G>T (p.Val489Phe)	not provided [RCV000965279]	benign	14	95203884	95203884	Human		name
15198079	CV725880	single nucleotide variant	NM_024734.4(CLMN):c.2312A>C (p.Glu771Ala)	not provided [RCV000890250]	likely benign	14	95203037	95203037	Human		name
15185956	CV725881	single nucleotide variant	NM_024734.4(CLMN):c.1069G>A (p.Glu357Lys)	not provided [RCV000886840]	benign	14	95204280	95204280	Human		name

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