Tmem20 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

311 records found for search term Tmem20

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8590396	CV125088	single nucleotide variant	NM_032842.3(TMEM209):c.*1117T>G	Lung cancer [RCV000105607]	uncertain significance	7	130165334	130165334	Human		name
15135413	CV743778	single nucleotide variant	NM_001130924.3(TMEM201):c.429+7C>T	not provided [RCV000898453]	benign	1	9597060	9597060	Human		name
8649156	CV119128	single nucleotide variant	NM_001080462.1(TMEM202):c.619+13C>A	Lung cancer [RCV000099648]	uncertain significance	15	72407230	72407230	Human		name
407487985	CV3482578	single nucleotide variant	NM_024600.6(TMEM204):c.7G>A (p.Val3Met)	not specified [RCV004679604]	uncertain significance	16	1534282	1534282	Human		name
407526334	CV3482584	single nucleotide variant	NM_198536.3(TMEM205):c.7G>A (p.Glu3Lys)	not specified [RCV004679608]	uncertain significance	19	11345613	11345613	Human		name
597753888	CV3613671	single nucleotide variant	NM_053045.2(TMEM203):c.4C>T (p.Leu2Phe)	not specified [RCV004867475]	uncertain significance	9	137205411	137205411	Human		name
401874885	CV2781341	single nucleotide variant	NM_198536.3(TMEM205):c.26G>C (p.Gly9Ala)	not specified [RCV004352353]	uncertain significance	19	11345594	11345594	Human		name
596947213	CV3548763	single nucleotide variant	NM_024600.6(TMEM204):c.273C>T (p.Thr91=)	not provided [RCV004811087]	likely benign	16	1534548	1534548	Human		name
597753897	CV3613673	single nucleotide variant	NM_053045.2(TMEM203):c.11C>T (p.Ser4Leu)	not specified [RCV004867477]	uncertain significance	9	137205404	137205404	Human		name
151352850	CV1326167	single nucleotide variant	NM_024600.6(TMEM204):c.396G>A (p.Pro132=)	not provided [RCV001815784]	likely benign	16	1542036	1542036	Human		name
156072766	CV2331536	single nucleotide variant	NM_014187.4(TMEM208):c.83G>A (p.Arg28Gln)	not specified [RCV004182138]	uncertain significance	16	67227912	67227912	Human		name
156004353	CV2400976	single nucleotide variant	NM_207316.3(TMEM207):c.35C>T (p.Ala12Val)	not specified [RCV004244261]	likely benign	3	190449775	190449775	Human		name
405753680	CV3336263	single nucleotide variant	NM_198536.3(TMEM205):c.81G>A (p.Met27Ile)	not specified [RCV004467490]	uncertain significance	19	11345539	11345539	Human		name
405753701	CV3336266	single nucleotide variant	NM_207316.3(TMEM207):c.86C>T (p.Ser29Leu)	not specified [RCV004467493]	uncertain significance	3	190447817	190447817	Human		name
407526340	CV3482587	single nucleotide variant	NM_198536.3(TMEM205):c.39G>A (p.Met13Ile)	not specified [RCV004679610]	uncertain significance	19	11345581	11345581	Human		name
407526348	CV3482590	single nucleotide variant	NM_207316.3(TMEM207):c.50G>A (p.Gly17Glu)	not specified [RCV004679612]	uncertain significance	3	190449760	190449760	Human		name
598129897	CV3887321	single nucleotide variant	NM_024600.6(TMEM204):c.513G>C (p.Leu171=)	not provided [RCV005245381]	likely benign	16	1554858	1554858	Human		name
598213743	CV3917598	single nucleotide variant	NM_207316.3(TMEM207):c.79G>A (p.Val27Met)	not specified [RCV005292381]	uncertain significance	3	190447824	190447824	Human		name
598252168	CV3917605	single nucleotide variant	NM_032842.4(TMEM209):c.57G>A (p.Met19Ile)	not specified [RCV005278039]	uncertain significance	7	130204057	130204057	Human		name
15182049	CV715010	single nucleotide variant	NM_014187.4(TMEM208):c.366C>T (p.Val122=)	not provided [RCV000974540]	benign	16	67228863	67228863	Human		name
156174510	CV2194430	single nucleotide variant	NM_024600.6(TMEM204):c.241G>A (p.Glu81Lys)	not specified [RCV004079530]	uncertain significance	16	1534516	1534516	Human		name
156169246	CV2197770	single nucleotide variant	NM_032842.4(TMEM209):c.215C>G (p.Ser72Cys)	not specified [RCV004074967]	uncertain significance	7	130202648	130202648	Human		name
155971453	CV2227849	single nucleotide variant	NM_024600.6(TMEM204):c.166C>T (p.Arg56Trp)	not specified [RCV004094490]	uncertain significance	16	1534441	1534441	Human		name
156048265	CV2245062	single nucleotide variant	NM_024600.6(TMEM204):c.224C>T (p.Ala75Val)	not specified [RCV004104781]	uncertain significance	16	1534499	1534499	Human		name
156059889	CV2263015	single nucleotide variant	NM_014187.4(TMEM208):c.293T>C (p.Met98Thr)	not specified [RCV004131276]	uncertain significance	16	67228625	67228625	Human		name
155924609	CV2277152	single nucleotide variant	NM_198536.3(TMEM205):c.257C>A (p.Ala86Asp)	not specified [RCV004142796]	uncertain significance	19	11345259	11345259	Human		name
156250396	CV2311217	single nucleotide variant	NM_207316.3(TMEM207):c.138C>A (p.His46Gln)	not specified [RCV004166304]	uncertain significance	3	190441458	190441458	Human		name
329369023	CV2450500	single nucleotide variant	NM_024600.6(TMEM204):c.208G>A (p.Ala70Thr)	not specified [RCV004265418]	likely benign	16	1534483	1534483	Human		name
329359528	CV2451063	single nucleotide variant	NM_207316.3(TMEM207):c.237A>T (p.Arg79Ser)	not specified [RCV004269719]	uncertain significance	3	190440311	190440311	Human		name
329388455	CV2471940	single nucleotide variant	NM_024600.6(TMEM204):c.239C>G (p.Ser80Cys)	not specified [RCV004280957]	uncertain significance	16	1534514	1534514	Human		name
401732979	CV2702316	single nucleotide variant	NM_198536.3(TMEM205):c.160T>C (p.Phe54Leu)	not specified [RCV004314642]	uncertain significance	19	11345356	11345356	Human		name
401780241	CV2725949	single nucleotide variant	NM_014187.4(TMEM208):c.112T>G (p.Cys38Gly)	not specified [RCV004324319]	uncertain significance	16	67228364	67228364	Human		name
401881408	CV2759405	single nucleotide variant	NM_198536.3(TMEM205):c.191G>C (p.Cys64Ser)	not specified [RCV004338406]	uncertain significance	19	11345325	11345325	Human		name
401865975	CV2786217	single nucleotide variant	NM_198536.3(TMEM205):c.128G>A (p.Arg43Gln)	not specified [RCV004360012]	uncertain significance	19	11345388	11345388	Human		name
401907286	CV2805664	single nucleotide variant	NM_001130924.3(TMEM201):c.42C>G (p.Ala14=)	not provided [RCV003422529]	likely benign	1	9588972	9588972	Human		name
405753621	CV3336255	single nucleotide variant	NM_024600.6(TMEM204):c.176C>T (p.Pro59Leu)	not specified [RCV004467482]	likely benign	16	1534451	1534451	Human		name
405753650	CV3336259	single nucleotide variant	NM_198536.3(TMEM205):c.203A>G (p.Asn68Ser)	not specified [RCV004467486]	uncertain significance	19	11345313	11345313	Human		name
405753709	CV3336267	single nucleotide variant	NM_014187.4(TMEM208):c.104C>T (p.Ala35Val)	not specified [RCV004467494]	uncertain significance	16	67228356	67228356	Human		name
405753716	CV3336268	single nucleotide variant	NM_014187.4(TMEM208):c.202T>C (p.Tyr68His)	not specified [RCV004467495]	uncertain significance	16	67228534	67228534	Human		name
407488906	CV3482579	single nucleotide variant	NM_024600.6(TMEM204):c.274G>A (p.Val92Ile)	not specified [RCV004686917]	uncertain significance	16	1534549	1534549	Human		name
407488912	CV3482581	single nucleotide variant	NM_024600.6(TMEM204):c.173G>T (p.Gly58Val)	not specified [RCV004686918]	uncertain significance	16	1534448	1534448	Human		name
407487994	CV3482583	single nucleotide variant	NM_024600.6(TMEM204):c.272C>T (p.Thr91Ile)	not specified [RCV004679607]	uncertain significance	16	1534547	1534547	Human		name
407526344	CV3482589	single nucleotide variant	NM_207316.3(TMEM207):c.265A>G (p.Met89Val)	not specified [RCV004679611]	likely benign	3	190440283	190440283	Human		name
407526354	CV3482592	single nucleotide variant	NM_014187.4(TMEM208):c.160T>C (p.Trp54Arg)	not specified [RCV004679614]	uncertain significance	16	67228412	67228412	Human		name
407526370	CV3482597	single nucleotide variant	NM_032842.4(TMEM209):c.129A>G (p.Ile43Met)	not specified [RCV004679619]	uncertain significance	7	130203985	130203985	Human		name
597753905	CV3613676	single nucleotide variant	NM_024600.6(TMEM204):c.115C>A (p.Arg39Ser)	not specified [RCV004867479]	uncertain significance	16	1534390	1534390	Human		name
597753926	CV3613681	single nucleotide variant	NM_198536.3(TMEM205):c.250T>C (p.Trp84Arg)	not specified [RCV004867484]	uncertain significance	19	11345266	11345266	Human		name
597753935	CV3613684	single nucleotide variant	NM_207316.3(TMEM207):c.114G>C (p.Met38Ile)	not specified [RCV004867486]	uncertain significance	3	190441482	190441482	Human		name
597753952	CV3613688	single nucleotide variant	NM_032842.4(TMEM209):c.281G>T (p.Ser94Ile)	not specified [RCV004867490]	uncertain significance	7	130202582	130202582	Human		name
597753984	CV3613696	single nucleotide variant	NM_032842.4(TMEM209):c.126G>T (p.Met42Ile)	not specified [RCV004867498]	uncertain significance	7	130203988	130203988	Human		name
598213736	CV3917595	single nucleotide variant	NM_053045.2(TMEM203):c.125C>G (p.Pro42Arg)	not specified [RCV005292380]	uncertain significance	9	137205290	137205290	Human		name
598252150	CV3917596	single nucleotide variant	NM_024600.6(TMEM204):c.196G>C (p.Gly66Arg)	not specified [RCV005278036]	uncertain significance	16	1534471	1534471	Human		name
598213748	CV3917599	single nucleotide variant	NM_207316.3(TMEM207):c.200G>A (p.Gly67Glu)	not specified [RCV005292382]	uncertain significance	3	190440348	190440348	Human		name
598252161	CV3917600	single nucleotide variant	NM_207316.3(TMEM207):c.292G>C (p.Asp98His)	not specified [RCV005278038]	uncertain significance	3	190440256	190440256	Human		name
156080106	CV2198440	single nucleotide variant	NM_032842.4(TMEM209):c.658C>T (p.Arg220Cys)	not specified [RCV004081970]	uncertain significance	7	130192739	130192739	Human		name
156038786	CV2215035	single nucleotide variant	NM_032842.4(TMEM209):c.551C>T (p.Ser184Leu)	not specified [RCV004084804]	uncertain significance	7	130201872	130201872	Human		name
156388100	CV2221715	single nucleotide variant	NM_024600.6(TMEM204):c.391G>A (p.Ala131Thr)	not specified [RCV004098477]	uncertain significance	16	1542031	1542031	Human		name
156233522	CV2227772	single nucleotide variant	NM_024600.6(TMEM204):c.620G>A (p.Arg207His)	not specified [RCV004094155]	uncertain significance	16	1554965	1554965	Human		name
156358208	CV2250949	single nucleotide variant	NM_032842.4(TMEM209):c.556G>A (p.Val186Ile)	not specified [RCV004123527]	likely benign	7	130201867	130201867	Human		name
155988499	CV2251221	single nucleotide variant	NM_014187.4(TMEM208):c.433T>G (p.Trp145Gly)	not specified [RCV004115446]	uncertain significance	16	67229024	67229024	Human		name
155994352	CV2253682	single nucleotide variant	NM_032842.4(TMEM209):c.338A>T (p.Gln113Leu)	not specified [RCV004125352]	uncertain significance	7	130202085	130202085	Human		name
155918812	CV2254743	single nucleotide variant	NM_024600.6(TMEM204):c.647G>A (p.Gly216Glu)	not specified [RCV004115216]	uncertain significance	16	1554992	1554992	Human		name
156146864	CV2289291	single nucleotide variant	NM_198536.3(TMEM205):c.382G>T (p.Gly128Trp)	not specified [RCV004152271]	uncertain significance	19	11343003	11343003	Human		name
155931820	CV2293715	single nucleotide variant	NM_032842.4(TMEM209):c.350C>A (p.Pro117Gln)	not specified [RCV004155002]	uncertain significance	7	130202073	130202073	Human		name
156270236	CV2312141	single nucleotide variant	NM_198536.3(TMEM205):c.382G>A (p.Gly128Arg)	not specified [RCV004165048]	uncertain significance	19	11343003	11343003	Human		name
156275357	CV2316449	single nucleotide variant	NM_024600.6(TMEM204):c.473G>A (p.Arg158Lys)	not specified [RCV004169935]	uncertain significance	16	1554818	1554818	Human		name
156284358	CV2349016	single nucleotide variant	NM_014187.4(TMEM208):c.488G>A (p.Arg163His)	not specified [RCV004203442]	uncertain significance	16	67229079	67229079	Human		name
156283588	CV2360589	single nucleotide variant	NM_053045.2(TMEM203):c.317C>A (p.Ala106Glu)	not specified [RCV004211346]	uncertain significance	9	137205098	137205098	Human		name
156087862	CV2366428	single nucleotide variant	NM_198536.3(TMEM205):c.493T>C (p.Ser165Pro)	not specified [RCV004212472]	uncertain significance	19	11342892	11342892	Human		name
156227810	CV2388312	single nucleotide variant	NM_032842.4(TMEM209):c.680A>G (p.Asn227Ser)	not specified [RCV004234764]	uncertain significance	7	130192717	130192717	Human		name
329382874	CV2424582	single nucleotide variant	NM_198536.3(TMEM205):c.514G>A (p.Val172Ile)	not specified [RCV004254081]	uncertain significance	19	11342871	11342871	Human		name
329376292	CV2438078	single nucleotide variant	NM_014187.4(TMEM208):c.500G>A (p.Arg167Gln)	not specified [RCV004256866]	uncertain significance	16	67229091	67229091	Human		name
329370839	CV2461809	single nucleotide variant	NM_024600.6(TMEM204):c.499T>C (p.Trp167Arg)	not specified [RCV004271731]	uncertain significance	16	1554844	1554844	Human		name
329382924	CV2465477	single nucleotide variant	NM_032842.4(TMEM209):c.730A>G (p.Thr244Ala)	not specified [RCV004281241]	uncertain significance	7	130192667	130192667	Human		name
401741995	CV2676870	single nucleotide variant	NM_024600.6(TMEM204):c.325G>A (p.Ala109Thr)	not specified [RCV004291035]	uncertain significance	16	1541965	1541965	Human		name
401730108	CV2700437	single nucleotide variant	NM_014187.4(TMEM208):c.487C>T (p.Arg163Cys)	not specified [RCV004311081]	uncertain significance	16	67229078	67229078	Human		name
401778935	CV2701892	single nucleotide variant	NM_032842.4(TMEM209):c.635G>T (p.Ser212Ile)	not specified [RCV004320511]	uncertain significance	7	130192762	130192762	Human		name
401720449	CV2701893	single nucleotide variant	NM_032842.4(TMEM209):c.765G>C (p.Arg255Ser)	not specified [RCV004320512]	uncertain significance	7	130192632	130192632	Human		name
401776040	CV2724308	single nucleotide variant	NM_207316.3(TMEM207):c.380C>A (p.Ala127Asp)	not specified [RCV004328181]	uncertain significance	3	190429656	190429656	Human		name
401893269	CV2755393	single nucleotide variant	NM_032842.4(TMEM209):c.578C>T (p.Ala193Val)	not specified [RCV004337555]	uncertain significance	7	130192819	130192819	Human		name
405753576	CV3336248	single nucleotide variant	NM_001080462.3(TMEM202):c.17A>C (p.His6Pro)	not specified [RCV004467475]	uncertain significance	15	72398343	72398343	Human		name
405753630	CV3336256	single nucleotide variant	NM_024600.6(TMEM204):c.379C>G (p.Leu127Val)	not specified [RCV004467483]	uncertain significance	16	1542019	1542019	Human		name
405753657	CV3336260	single nucleotide variant	NM_198536.3(TMEM205):c.371G>A (p.Arg124Gln)	not specified [RCV004467487]	uncertain significance	19	11343014	11343014	Human		name
405753664	CV3336261	single nucleotide variant	NM_198536.3(TMEM205):c.460C>T (p.Arg154Cys)	not specified [RCV004467488]	uncertain significance	19	11342925	11342925	Human		name
405753672	CV3336262	single nucleotide variant	NM_198536.3(TMEM205):c.514G>T (p.Val172Phe)	not specified [RCV004467489]	uncertain significance	19	11342871	11342871	Human		name
405753695	CV3336265	single nucleotide variant	NM_207316.3(TMEM207):c.334G>A (p.Gly112Arg)	not specified [RCV004467492]	uncertain significance	3	190429702	190429702	Human		name
405753730	CV3336270	single nucleotide variant	NM_014187.4(TMEM208):c.514C>T (p.Arg172Trp)	not specified [RCV004467497]	uncertain significance	16	67229105	67229105	Human		name
405753748	CV3336273	single nucleotide variant	NM_032842.4(TMEM209):c.421A>C (p.Ser141Arg)	not specified [RCV004467500]	uncertain significance	7	130202002	130202002	Human		name
405753754	CV3336274	single nucleotide variant	NM_032842.4(TMEM209):c.605C>T (p.Pro202Leu)	not specified [RCV004467501]	uncertain significance	7	130192792	130192792	Human		name
405753760	CV3336275	single nucleotide variant	NM_032842.4(TMEM209):c.658C>A (p.Arg220Ser)	not specified [RCV004467502]	uncertain significance	7	130192739	130192739	Human		name
405753772	CV3336277	single nucleotide variant	NM_032842.4(TMEM209):c.943G>T (p.Ala315Ser)	not specified [RCV004467504]	uncertain significance	7	130185200	130185200	Human		name
407487990	CV3482580	single nucleotide variant	NM_024600.6(TMEM204):c.585G>T (p.Glu195Asp)	not specified [RCV004679605]	uncertain significance	16	1554930	1554930	Human		name
407458730	CV3482585	single nucleotide variant	NM_198536.3(TMEM205):c.421C>T (p.Arg141Cys)	not specified [RCV004686919]	uncertain significance	19	11342964	11342964	Human		name
407526337	CV3482586	single nucleotide variant	NM_198536.3(TMEM205):c.310C>T (p.Arg104Cys)	not specified [RCV004679609]	uncertain significance	19	11343075	11343075	Human		name
407458733	CV3482588	single nucleotide variant	NM_198536.3(TMEM205):c.521G>A (p.Ser174Asn)	not specified [RCV004686920]	uncertain significance	19	11342864	11342864	Human		name
407526351	CV3482591	single nucleotide variant	NM_207316.3(TMEM207):c.311A>G (p.Glu104Gly)	not specified [RCV004679613]	uncertain significance	3	190429725	190429725	Human		name
407526361	CV3482594	single nucleotide variant	NM_032842.4(TMEM209):c.790A>G (p.Thr264Ala)	not specified [RCV004679616]	uncertain significance	7	130185353	130185353	Human		name
597753901	CV3613674	single nucleotide variant	NM_053045.2(TMEM203):c.308A>G (p.Gln103Arg)	not specified [RCV004867478]	uncertain significance	9	137205107	137205107	Human		name
597795235	CV3613675	single nucleotide variant	NM_024600.6(TMEM204):c.632C>G (p.Ala211Gly)	not specified [RCV004878147]	uncertain significance	16	1554977	1554977	Human		name
597753909	CV3613677	single nucleotide variant	NM_024600.6(TMEM204):c.644G>A (p.Arg215His)	not specified [RCV004867480]	uncertain significance	16	1554989	1554989	Human		name
597753913	CV3613678	single nucleotide variant	NM_198536.3(TMEM205):c.412G>A (p.Asp138Asn)	not specified [RCV004867481]	uncertain significance	19	11342973	11342973	Human		name
597753918	CV3613679	single nucleotide variant	NM_198536.3(TMEM205):c.524A>G (p.Asn175Ser)	not specified [RCV004867482]	uncertain significance	19	11342861	11342861	Human		name
597753922	CV3613680	single nucleotide variant	NM_198536.3(TMEM205):c.443C>G (p.Pro148Arg)	not specified [RCV004867483]	uncertain significance	19	11342942	11342942	Human		name
597795238	CV3613682	single nucleotide variant	NM_198536.3(TMEM205):c.515T>A (p.Val172Asp)	not specified [RCV004878148]	uncertain significance	19	11342870	11342870	Human		name
597753938	CV3613685	single nucleotide variant	NM_014187.4(TMEM208):c.482G>A (p.Arg161Gln)	not specified [RCV004867487]	uncertain significance	16	67229073	67229073	Human		name
597753944	CV3613686	single nucleotide variant	NM_014187.4(TMEM208):c.512A>T (p.Lys171Met)	not specified [RCV004867488]	uncertain significance	16	67229103	67229103	Human		name
597753948	CV3613687	single nucleotide variant	NM_014187.4(TMEM208):c.371C>T (p.Ser124Phe)	not specified [RCV004867489]	uncertain significance	16	67228868	67228868	Human		name
597753956	CV3613689	single nucleotide variant	NM_032842.4(TMEM209):c.556G>T (p.Val186Phe)	not specified [RCV004867491]	uncertain significance	7	130201867	130201867	Human		name
597753965	CV3613691	single nucleotide variant	NM_032842.4(TMEM209):c.437G>A (p.Arg146His)	not specified [RCV004867493]	uncertain significance	7	130201986	130201986	Human		name
597753976	CV3613694	single nucleotide variant	NM_032842.4(TMEM209):c.652C>T (p.Arg218Cys)	not specified [RCV004867496]	uncertain significance	7	130192745	130192745	Human		name
597753981	CV3613695	single nucleotide variant	NM_032842.4(TMEM209):c.451A>G (p.Ser151Gly)	not specified [RCV004867497]	uncertain significance	7	130201972	130201972	Human		name
598252145	CV3917593	single nucleotide variant	NM_053045.2(TMEM203):c.349A>C (p.Ile117Leu)	not specified [RCV005278035]	uncertain significance	9	137205066	137205066	Human		name
598252156	CV3917597	single nucleotide variant	NM_024600.6(TMEM204):c.367G>A (p.Gly123Ser)	not specified [RCV005278037]	uncertain significance	16	1542007	1542007	Human		name
598213753	CV3917601	single nucleotide variant	NM_207316.3(TMEM207):c.314C>A (p.Ala105Glu)	not specified [RCV005292383]	uncertain significance	3	190429722	190429722	Human		name
598213770	CV3917604	single nucleotide variant	NM_032842.4(TMEM209):c.560G>T (p.Ser187Ile)	not specified [RCV005292386]	uncertain significance	7	130201863	130201863	Human		name
15194507	CV696919	single nucleotide variant	NM_001130924.3(TMEM201):c.255G>A (p.Pro85=)	not provided [RCV000955666]	benign	1	9596879	9596879	Human		name
8631823	CV87029	single nucleotide variant	NM_052913.2(TMEM200A):c.1041G>A (p.Arg347=)	Malignant melanoma [RCV000067120]	not provided	6	130441463	130441463	Human		name
156398238	CV2204477	single nucleotide variant	NM_001080462.3(TMEM202):c.88G>A (p.Val30Ile)	not specified [RCV004079279]	uncertain significance	15	72398659	72398659	Human		name
156063530	CV2240161	single nucleotide variant	NM_001080462.3(TMEM202):c.52A>C (p.Lys18Gln)	not specified [RCV004110920]	uncertain significance	15	72398378	72398378	Human		name
156344259	CV2364252	single nucleotide variant	NM_032842.4(TMEM209):c.1091G>A (p.Arg364Gln)	not specified [RCV004223484]	uncertain significance	7	130181652	130181652	Human		name
156161404	CV2398269	single nucleotide variant	NM_032842.4(TMEM209):c.1280G>A (p.Arg427Gln)	not specified [RCV004235179]	uncertain significance	7	130175576	130175576	Human		name
155930639	CV2399696	single nucleotide variant	NM_001080462.3(TMEM202):c.50C>A (p.Pro17His)	not specified [RCV004245515]	uncertain significance	15	72398376	72398376	Human		name
401730293	CV2711181	single nucleotide variant	NM_032842.4(TMEM209):c.1619C>T (p.Ser540Leu)	not specified [RCV004312980]	uncertain significance	7	130170412	130170412	Human		name
401935575	CV2812569	single nucleotide variant	NM_001003682.4(TMEM200B):c.111C>G (p.Pro37=)	not provided [RCV003413008]	likely benign	1	29121718	29121718	Human		name
405753590	CV3336250	single nucleotide variant	NM_001080462.3(TMEM202):c.50C>T (p.Pro17Leu)	not specified [RCV004467477]	uncertain significance	15	72398376	72398376	Human		name
405753737	CV3336271	single nucleotide variant	NM_032842.4(TMEM209):c.1026G>T (p.Trp342Cys)	not specified [RCV004467498]	uncertain significance	7	130181717	130181717	Human		name
407526364	CV3482595	single nucleotide variant	NM_032842.4(TMEM209):c.1196A>C (p.Gln399Pro)	not specified [RCV004679617]	uncertain significance	7	130178452	130178452	Human		name
407526367	CV3482596	single nucleotide variant	NM_032842.4(TMEM209):c.1447C>A (p.Pro483Thr)	not specified [RCV004679618]	uncertain significance	7	130173837	130173837	Human		name
407526302	CV3486510	single nucleotide variant	NM_001130924.3(TMEM201):c.65T>C (p.Val22Ala)	not specified [RCV004679595]	uncertain significance	1	9588995	9588995	Human		name
597753881	CV3613669	single nucleotide variant	NM_001080462.3(TMEM202):c.32T>C (p.Phe11Ser)	not specified [RCV004867473]	uncertain significance	15	72398358	72398358	Human		name
597753960	CV3613690	single nucleotide variant	NM_032842.4(TMEM209):c.1058A>C (p.Gln353Pro)	not specified [RCV004867492]	uncertain significance	7	130181685	130181685	Human		name
597753969	CV3613692	single nucleotide variant	NM_032842.4(TMEM209):c.1192G>A (p.Val398Ile)	not specified [RCV004867494]	uncertain significance	7	130178456	130178456	Human		name
15194512	CV696920	single nucleotide variant	NM_001130924.3(TMEM201):c.633G>A (p.Pro211=)	not provided [RCV000955667]	benign	1	9601131	9601131	Human		name
15194515	CV696921	single nucleotide variant	NM_001130924.3(TMEM201):c.795C>A (p.Thr265=)	not provided [RCV000955668]	benign	1	9601293	9601293	Human		name
15161646	CV732667	single nucleotide variant	NM_001130924.3(TMEM201):c.600C>T (p.His200=)	not provided [RCV000903389]	benign	1	9598619	9598619	Human		name
8627696	CV82840	single nucleotide variant	NM_001080462.1(TMEM202):c.62G>A (p.Gly21Glu)	Malignant melanoma [RCV000062920]	not provided	15	72398388	72398388	Human		name
8631820	CV87026	single nucleotide variant	NM_052913.2(TMEM200A):c.649C>T (p.Arg217Trp)	Malignant melanoma [RCV000067117]	not provided	6	130441071	130441071	Human		name
8631821	CV87027	single nucleotide variant	NM_052913.2(TMEM200A):c.661C>T (p.Arg221Ter)	Malignant melanoma [RCV000067118]	not provided	6	130441083	130441083	Human		name
8631822	CV87028	single nucleotide variant	NM_052913.2(TMEM200A):c.733C>T (p.Pro245Ser)	Malignant melanoma [RCV000067119]	not provided	6	130441155	130441155	Human		name
156398666	CV2194713	single nucleotide variant	NM_001080462.3(TMEM202):c.220A>G (p.Met74Val)	not specified [RCV004075268]	uncertain significance	15	72398791	72398791	Human		name
156267002	CV2243861	single nucleotide variant	NM_001003682.4(TMEM200B):c.92G>C (p.Arg31Pro)	not specified [RCV004114805]	uncertain significance	1	29121737	29121737	Human		name
156078336	CV2281727	single nucleotide variant	NM_001080462.3(TMEM202):c.210G>A (p.Met70Ile)	not specified [RCV004147873]	uncertain significance	15	72398781	72398781	Human		name
156047361	CV2319158	single nucleotide variant	NM_001080462.3(TMEM202):c.173C>T (p.Thr58Met)	not specified [RCV004178224]	likely benign	15	72398744	72398744	Human		name
401735141	CV2706682	single nucleotide variant	NM_001258277.2(TMEM200A):c.55T>C (p.Ser19Pro)	not specified [RCV004319255]	uncertain significance	6	130440477	130440477	Human		name
401752383	CV2706991	single nucleotide variant	NM_001003682.4(TMEM200B):c.76C>G (p.Arg26Gly)	not specified [RCV004321589]	uncertain significance	1	29121753	29121753	Human		name
401860781	CV2758626	single nucleotide variant	NM_001080462.3(TMEM202):c.170G>A (p.Arg57Gln)	not specified [RCV004337701]	uncertain significance	15	72398741	72398741	Human		name
401864367	CV2760812	single nucleotide variant	NM_001130924.3(TMEM201):c.241G>A (p.Asp81Asn)	not specified [RCV004336452]	uncertain significance	1	9596865	9596865	Human		name
401906659	CV2818172	single nucleotide variant	NM_001395400.1(TMEM200C):c.963C>G (p.Ala321=)	not provided [RCV003421583]	likely benign	18	5891101	5891101	Human		name
401907976	CV2818174	single nucleotide variant	NM_001395400.1(TMEM200C):c.435C>T (p.Ser145=)	not provided [RCV003423012]	likely benign	18	5891629	5891629	Human		name
405867136	CV2842657	single nucleotide variant	NM_001395400.1(TMEM200C):c.441G>A (p.Thr147=)	EBV-positive nodal T- and NK-cell lymphoma [RCV004558014]	likely benign	18	5891623	5891623	Human		name
405753278	CV3336229	single nucleotide variant	NM_001003682.4(TMEM200B):c.47C>G (p.Pro16Arg)	not specified [RCV004467456]	uncertain significance	1	29121782	29121782	Human		name
405753286	CV3336230	single nucleotide variant	NM_001003682.4(TMEM200B):c.80T>G (p.Leu27Arg)	not specified [RCV004467457]	uncertain significance	1	29121749	29121749	Human		name
405753295	CV3336231	single nucleotide variant	NM_001003682.4(TMEM200B):c.82G>C (p.Gly28Arg)	not specified [RCV004467458]	uncertain significance	1	29121747	29121747	Human		name
405753340	CV3336237	single nucleotide variant	NM_001130924.3(TMEM201):c.155A>G (p.Asn52Ser)	not specified [RCV004467464]	uncertain significance	1	9595931	9595931	Human		name
405753347	CV3336238	single nucleotide variant	NM_001130924.3(TMEM201):c.163A>G (p.Thr55Ala)	not specified [RCV004467465]	uncertain significance	1	9595939	9595939	Human		name
405753522	CV3336241	single nucleotide variant	NM_001130924.3(TMEM201):c.185G>A (p.Arg62His)	not specified [RCV004467468]	uncertain significance	1	9595961	9595961	Human		name
407526327	CV3482577	single nucleotide variant	NM_001080462.3(TMEM202):c.224C>G (p.Ser75Cys)	not specified [RCV004679603]	uncertain significance	15	72398795	72398795	Human		name
597753799	CV3613649	single nucleotide variant	NM_001003682.4(TMEM200B):c.41G>A (p.Arg14Lys)	not specified [RCV004867453]	uncertain significance	1	29121788	29121788	Human		name
597753857	CV3613663	single nucleotide variant	NM_001130924.3(TMEM201):c.176A>G (p.Tyr59Cys)	not specified [RCV004867467]	uncertain significance	1	9595952	9595952	Human		name
15194503	CV696918	single nucleotide variant	NM_001130924.3(TMEM201):c.131C>T (p.Thr44Met)	not provided [RCV000955665]	benign	1	9595907	9595907	Human		name
156096808	CV2210557	single nucleotide variant	NM_001080462.3(TMEM202):c.640T>A (p.Tyr214Asn)	not specified [RCV004083365]	uncertain significance	15	72407711	72407711	Human		name
155975195	CV2211254	single nucleotide variant	NM_001130924.3(TMEM201):c.494G>A (p.Arg165Gln)	not specified [RCV004090190]	uncertain significance	1	9598513	9598513	Human		name
156329409	CV2213833	single nucleotide variant	NM_001130924.3(TMEM201):c.716A>G (p.His239Arg)	not specified [RCV004089889]	uncertain significance	1	9601214	9601214	Human		name
156381688	CV2215151	single nucleotide variant	NM_001080462.3(TMEM202):c.325C>T (p.Pro109Ser)	not specified [RCV004086871]	uncertain significance	15	72398896	72398896	Human		name
155922938	CV2215362	single nucleotide variant	NM_001130924.3(TMEM201):c.962G>A (p.Arg321Gln)	not specified [RCV004089174]	uncertain significance	1	9602074	9602074	Human		name
156191815	CV2223135	single nucleotide variant	NM_001003682.4(TMEM200B):c.275C>G (p.Pro92Arg)	not specified [RCV004103982]	uncertain significance	1	29121554	29121554	Human		name
156241796	CV2231385	single nucleotide variant	NM_001258277.2(TMEM200A):c.192T>A (p.Phe64Leu)	not specified [RCV004096472]	uncertain significance	6	130440614	130440614	Human		name
156296311	CV2236498	single nucleotide variant	NM_001080462.3(TMEM202):c.612G>A (p.Met204Ile)	not specified [RCV004110500]	uncertain significance	15	72407210	72407210	Human		name
156289962	CV2309768	single nucleotide variant	NM_001130924.3(TMEM201):c.794C>T (p.Thr265Ile)	not specified [RCV004160891]	uncertain significance	1	9601292	9601292	Human		name
156304827	CV2338565	single nucleotide variant	NM_001003682.4(TMEM200B):c.281T>G (p.Met94Arg)	not specified [RCV004182160]	uncertain significance	1	29121548	29121548	Human		name
155983692	CV2344334	single nucleotide variant	NM_001003682.4(TMEM200B):c.145C>T (p.Arg49Cys)	not specified [RCV004195091]	uncertain significance	1	29121684	29121684	Human		name
156167698	CV2345333	single nucleotide variant	NM_001080462.3(TMEM202):c.422T>A (p.Ile141Asn)	not specified [RCV004198113]	uncertain significance	15	72406686	72406686	Human		name
156140771	CV2358350	single nucleotide variant	NM_001080462.3(TMEM202):c.544A>T (p.Arg182Trp)	not specified [RCV004214161]	uncertain significance	15	72407142	72407142	Human		name
155986112	CV2363604	single nucleotide variant	NM_001130924.3(TMEM201):c.421C>T (p.Arg141Cys)	not specified [RCV004216559]	uncertain significance	1	9597045	9597045	Human		name
155936707	CV2379885	single nucleotide variant	NM_001130924.3(TMEM201):c.694G>A (p.Ala232Thr)	not specified [RCV004219990]	likely benign	1	9601192	9601192	Human		name
156053544	CV2388540	single nucleotide variant	NM_001130924.3(TMEM201):c.316G>A (p.Asp106Asn)	not specified [RCV004237391]	uncertain significance	1	9596940	9596940	Human		name
401723401	CV2674939	single nucleotide variant	NM_001003682.4(TMEM200B):c.124G>T (p.Val42Leu)	not specified [RCV004296251]	uncertain significance	1	29121705	29121705	Human		name
401781426	CV2681995	single nucleotide variant	NM_001130924.3(TMEM201):c.664T>C (p.Phe222Leu)	not specified [RCV004296972]	uncertain significance	1	9601162	9601162	Human		name
401759956	CV2698687	single nucleotide variant	NM_001130924.3(TMEM201):c.870G>C (p.Trp290Cys)	not specified [RCV004301153]	uncertain significance	1	9601368	9601368	Human		name
401776547	CV2711180	single nucleotide variant	NM_001130924.3(TMEM201):c.435G>T (p.Arg145Ser)	not specified [RCV004312979]	uncertain significance	1	9598454	9598454	Human		name
405753228	CV3336221	single nucleotide variant	NM_001258277.2(TMEM200A):c.172T>C (p.Tyr58His)	not specified [RCV004467448]	uncertain significance	6	130440594	130440594	Human		name
405753248	CV3336224	single nucleotide variant	NM_001003682.4(TMEM200B):c.146G>A (p.Arg49His)	not specified [RCV004467451]	uncertain significance	1	29121683	29121683	Human		name
405753254	CV3336225	single nucleotide variant	NM_001003682.4(TMEM200B):c.266C>T (p.Ala89Val)	not specified [RCV004467452]	uncertain significance	1	29121563	29121563	Human		name
405753551	CV3336245	single nucleotide variant	NM_001130924.3(TMEM201):c.409G>A (p.Ala137Thr)	not specified [RCV004467472]	uncertain significance	1	9597033	9597033	Human		name
405753559	CV3336246	single nucleotide variant	NM_001130924.3(TMEM201):c.493C>T (p.Arg165Trp)	not specified [RCV004467473]	uncertain significance	1	9598512	9598512	Human		name
405753567	CV3336247	single nucleotide variant	NM_001130924.3(TMEM201):c.728G>T (p.Gly243Val)	not specified [RCV004467474]	uncertain significance	1	9601226	9601226	Human		name
405753583	CV3336249	single nucleotide variant	NM_001080462.3(TMEM202):c.476G>A (p.Ser159Asn)	not specified [RCV004467476]	uncertain significance	15	72406740	72406740	Human		name
405753597	CV3336251	single nucleotide variant	NM_001080462.3(TMEM202):c.577T>C (p.Tyr193His)	not specified [RCV004467478]	uncertain significance	15	72407175	72407175	Human		name
405753602	CV3336252	single nucleotide variant	NM_001080462.3(TMEM202):c.719C>T (p.Pro240Leu)	not specified [RCV004467479]	uncertain significance	15	72407790	72407790	Human		name
405753609	CV3336253	single nucleotide variant	NM_001080462.3(TMEM202):c.791A>G (p.Lys264Arg)	not specified [RCV004467480]	uncertain significance	15	72407862	72407862	Human		name
407526305	CV3486511	single nucleotide variant	NM_001130924.3(TMEM201):c.695C>T (p.Ala232Val)	not specified [RCV004679596]	uncertain significance	1	9601193	9601193	Human		name
407526311	CV3486513	single nucleotide variant	NM_001080462.3(TMEM202):c.508C>T (p.Leu170Phe)	not specified [RCV004679598]	uncertain significance	15	72407106	72407106	Human		name
407526318	CV3486515	single nucleotide variant	NM_001080462.3(TMEM202):c.574A>G (p.Thr192Ala)	not specified [RCV004679600]	likely benign	15	72407172	72407172	Human		name
407458724	CV3486516	single nucleotide variant	NM_001080462.3(TMEM202):c.653G>T (p.Arg218Ile)	not specified [RCV004686915]	uncertain significance	15	72407724	72407724	Human		name
407526321	CV3486517	single nucleotide variant	NM_001080462.3(TMEM202):c.676G>A (p.Val226Ile)	not specified [RCV004679601]	uncertain significance	15	72407747	72407747	Human		name
407526324	CV3486518	single nucleotide variant	NM_001080462.3(TMEM202):c.523G>A (p.Ala175Thr)	not specified [RCV004679602]	uncertain significance	15	72407121	72407121	Human		name
407458727	CV3486519	single nucleotide variant	NM_001080462.3(TMEM202):c.368T>G (p.Leu123Arg)	not specified [RCV004686916]	uncertain significance	15	72406632	72406632	Human		name
597753787	CV3613646	single nucleotide variant	NM_001258277.2(TMEM200A):c.253C>T (p.Pro85Ser)	not specified [RCV004867450]	uncertain significance	6	130440675	130440675	Human		name
597753820	CV3613654	single nucleotide variant	NM_001003682.4(TMEM200B):c.269G>A (p.Ser90Asn)	not specified [RCV004867458]	uncertain significance	1	29121560	29121560	Human		name
597753823	CV3613655	single nucleotide variant	NM_001003682.4(TMEM200B):c.257C>T (p.Ala86Val)	not specified [RCV004867459]	uncertain significance	1	29121572	29121572	Human		name
597753853	CV3613662	single nucleotide variant	NM_001130924.3(TMEM201):c.442G>A (p.Glu148Lys)	not specified [RCV004867466]	uncertain significance	1	9598461	9598461	Human		name
597753861	CV3613664	single nucleotide variant	NM_001130924.3(TMEM201):c.394A>G (p.Ile132Val)	not specified [RCV004867468]	uncertain significance	1	9597018	9597018	Human		name
597753872	CV3613667	single nucleotide variant	NM_001130924.3(TMEM201):c.521A>G (p.Tyr174Cys)	not specified [RCV004867471]	uncertain significance	1	9598540	9598540	Human		name
597753877	CV3613668	single nucleotide variant	NM_001080462.3(TMEM202):c.385A>G (p.Ile129Val)	not specified [RCV004867472]	uncertain significance	15	72406649	72406649	Human		name
597753884	CV3613670	single nucleotide variant	NM_001080462.3(TMEM202):c.530T>C (p.Val177Ala)	not specified [RCV004867474]	uncertain significance	15	72407128	72407128	Human		name
598213681	CV3917576	single nucleotide variant	NM_001258277.2(TMEM200A):c.128G>A (p.Arg43Gln)	not specified [RCV005292366]	uncertain significance	6	130440550	130440550	Human		name
598213693	CV3917580	single nucleotide variant	NM_001003682.4(TMEM200B):c.229C>T (p.His77Tyr)	not specified [RCV005292369]	uncertain significance	1	29121600	29121600	Human		name
598252132	CV3917582	single nucleotide variant	NM_001003682.4(TMEM200B):c.158G>C (p.Gly53Ala)	not specified [RCV005278033]	uncertain significance	1	29121671	29121671	Human		name
598252139	CV3917588	single nucleotide variant	NM_001130924.3(TMEM201):c.904G>A (p.Ala302Thr)	not specified [RCV005278034]	uncertain significance	1	9601402	9601402	Human		name
598213717	CV3917589	single nucleotide variant	NM_001130924.3(TMEM201):c.314G>A (p.Arg105His)	not specified [RCV005292375]	uncertain significance	1	9596938	9596938	Human		name
598213721	CV3917590	single nucleotide variant	NM_001130924.3(TMEM201):c.538C>T (p.Arg180Cys)	not specified [RCV005292376]	uncertain significance	1	9598557	9598557	Human		name
156153672	CV2209462	single nucleotide variant	NM_001130924.3(TMEM201):c.1912G>A (p.Gly638Ser)	not specified [RCV004093607]	uncertain significance	1	9612994	9612994	Human		name
155989408	CV2244247	single nucleotide variant	NM_001130924.3(TMEM201):c.1952C>G (p.Ala651Gly)	not specified [RCV004100245]	uncertain significance	1	9613034	9613034	Human		name
156078180	CV2248267	single nucleotide variant	NM_001130924.3(TMEM201):c.1141C>T (p.Arg381Trp)	not specified [RCV004119436]	uncertain significance	1	9602253	9602253	Human		name
156359108	CV2260993	single nucleotide variant	NM_001003682.4(TMEM200B):c.313G>A (p.Gly105Ser)	not specified [RCV004125870]	uncertain significance	1	29121516	29121516	Human		name
155978278	CV2266500	single nucleotide variant	NM_001130924.3(TMEM201):c.1825G>C (p.Asp609His)	not specified [RCV004131067]	uncertain significance	1	9611812	9611812	Human		name
156118624	CV2279087	single nucleotide variant	NM_001258277.2(TMEM200A):c.925A>G (p.Thr309Ala)	not specified [RCV004145761]	uncertain significance	6	130441347	130441347	Human		name
156034599	CV2282908	single nucleotide variant	NM_001130924.3(TMEM201):c.1928G>A (p.Arg643Gln)	not specified [RCV004143550]	uncertain significance	1	9613010	9613010	Human		name
156274329	CV2293796	single nucleotide variant	NM_001003682.4(TMEM200B):c.916C>T (p.Arg306Trp)	not specified [RCV004155069]	uncertain significance	1	29120913	29120913	Human		name
156348705	CV2309042	single nucleotide variant	NM_001130924.3(TMEM201):c.1750G>A (p.Val584Met)	not specified [RCV004171412]	likely benign	1	9610790	9610790	Human		name
156270540	CV2315556	single nucleotide variant	NM_001130924.3(TMEM201):c.1729C>T (p.Arg577Trp)	not specified [RCV004169601]	uncertain significance	1	9610769	9610769	Human		name
156349965	CV2316114	single nucleotide variant	NM_001258277.2(TMEM200A):c.571G>A (p.Glu191Lys)	not specified [RCV004174166]	uncertain significance	6	130440993	130440993	Human		name
156395425	CV2329183	single nucleotide variant	NM_001130924.3(TMEM201):c.1595G>A (p.Arg532Gln)	not specified [RCV004173937]	uncertain significance	1	9610635	9610635	Human		name
155973671	CV2332428	single nucleotide variant	NM_001003682.4(TMEM200B):c.338G>T (p.Arg113Leu)	not specified [RCV004196159]	uncertain significance	1	29121491	29121491	Human		name
156174414	CV2334533	single nucleotide variant	NM_001130924.3(TMEM201):c.1880C>T (p.Ser627Leu)	not specified [RCV004188493]	uncertain significance	1	9611867	9611867	Human		name
155914742	CV2338987	single nucleotide variant	NM_001003682.4(TMEM200B):c.640C>T (p.Arg214Cys)	not specified [RCV004187044]	uncertain significance	1	29121189	29121189	Human		name
155923073	CV2340731	single nucleotide variant	NM_001003682.4(TMEM200B):c.533C>A (p.Pro178His)	not specified [RCV004190400]	uncertain significance	1	29121296	29121296	Human		name
156188217	CV2342152	single nucleotide variant	NM_001258277.2(TMEM200A):c.691C>T (p.Leu231Phe)	not specified [RCV004191742]	uncertain significance	6	130441113	130441113	Human		name
156134223	CV2346977	single nucleotide variant	NM_001258277.2(TMEM200A):c.955T>A (p.Ser319Thr)	not specified [RCV004202422]	uncertain significance	6	130441377	130441377	Human		name
156283907	CV2348978	single nucleotide variant	NM_001258277.2(TMEM200A):c.811G>A (p.Gly271Ser)	not specified [RCV004203409]	uncertain significance	6	130441233	130441233	Human		name
156344089	CV2349385	single nucleotide variant	NM_001130924.3(TMEM201):c.1715C>T (p.Pro572Leu)	not specified [RCV004199316]	uncertain significance	1	9610755	9610755	Human		name
156078198	CV2351096	single nucleotide variant	NM_001003682.4(TMEM200B):c.660G>C (p.Leu220Phe)	not specified [RCV004213958]	uncertain significance	1	29121169	29121169	Human		name
156106979	CV2355290	single nucleotide variant	NM_001130924.3(TMEM201):c.1528G>T (p.Val510Leu)	not specified [RCV004203141]	uncertain significance	1	9610568	9610568	Human		name
156129846	CV2357880	single nucleotide variant	NM_001130924.3(TMEM201):c.1534G>A (p.Gly512Ser)	not specified [RCV004209670]	uncertain significance	1	9610574	9610574	Human		name
156259332	CV2366266	single nucleotide variant	NM_001003682.4(TMEM200B):c.631G>A (p.Ala211Thr)	not specified [RCV004210282]	uncertain significance	1	29121198	29121198	Human		name
156178922	CV2374633	single nucleotide variant	NM_001258277.2(TMEM200A):c.626C>G (p.Thr209Arg)	not specified [RCV004225253]	uncertain significance	6	130441048	130441048	Human		name
156049017	CV2378160	single nucleotide variant	NM_001258277.2(TMEM200A):c.721C>T (p.His241Tyr)	not specified [RCV004233077]	uncertain significance	6	130441143	130441143	Human		name
155992180	CV2379286	single nucleotide variant	NM_001130924.3(TMEM201):c.1571G>A (p.Arg524His)	not specified [RCV004223755]	uncertain significance	1	9610611	9610611	Human		name
155939512	CV2385686	single nucleotide variant	NM_001130924.3(TMEM201):c.1778A>C (p.Lys593Thr)	not specified [RCV004233313]	uncertain significance	1	9611765	9611765	Human		name
156100374	CV2386716	single nucleotide variant	NM_001258277.2(TMEM200A):c.715T>A (p.Ser239Thr)	not specified [RCV004233409]	uncertain significance	6	130441137	130441137	Human		name
156221033	CV2392360	single nucleotide variant	NM_001130924.3(TMEM201):c.1954G>A (p.Ala652Thr)	not specified [RCV004243953]	uncertain significance	1	9613036	9613036	Human		name
156228329	CV2392946	single nucleotide variant	NM_001130924.3(TMEM201):c.1315C>T (p.Arg439Trp)	not specified [RCV004247290]	uncertain significance	1	9607711	9607711	Human		name
155998659	CV2396278	single nucleotide variant	NM_001130924.3(TMEM201):c.1748A>G (p.Asp583Gly)	not specified [RCV004240225]	uncertain significance	1	9610788	9610788	Human		name
156247508	CV2396913	single nucleotide variant	NM_001130924.3(TMEM201):c.1726C>G (p.Pro576Ala)	not specified [RCV004234030]	uncertain significance	1	9610766	9610766	Human		name
155932383	CV2400013	single nucleotide variant	NM_001130924.3(TMEM201):c.1351C>T (p.Arg451Trp)	not specified [RCV004246937]	uncertain significance	1	9607747	9607747	Human		name
329354096	CV2436947	single nucleotide variant	NM_001130924.3(TMEM201):c.1988A>G (p.Gln663Arg)	not specified [RCV004260325]	uncertain significance	1	9613070	9613070	Human		name
329379629	CV2443490	single nucleotide variant	NM_001130924.3(TMEM201):c.1157G>A (p.Arg386Gln)	not specified [RCV004262325]	uncertain significance	1	9602269	9602269	Human		name
329401838	CV2457484	single nucleotide variant	NM_001258277.2(TMEM200A):c.980T>C (p.Leu327Pro)	not specified [RCV004267301]	uncertain significance	6	130441402	130441402	Human		name
401722151	CV2680842	single nucleotide variant	NM_001258277.2(TMEM200A):c.914T>C (p.Ile305Thr)	not specified [RCV004293489]	uncertain significance	6	130441336	130441336	Human		name
401732038	CV2690265	single nucleotide variant	NM_001003682.4(TMEM200B):c.476C>T (p.Pro159Leu)	not specified [RCV004302268]	uncertain significance	1	29121353	29121353	Human		name
401759033	CV2694397	single nucleotide variant	NM_001258277.2(TMEM200A):c.730C>T (p.Pro244Ser)	not specified [RCV004304580]	uncertain significance	6	130441152	130441152	Human		name
401719309	CV2701043	single nucleotide variant	NM_001130924.3(TMEM201):c.1709T>C (p.Met570Thr)	not specified [RCV004309648]	uncertain significance	1	9610749	9610749	Human		name
401874830	CV2756081	single nucleotide variant	NM_001130924.3(TMEM201):c.1714C>T (p.Pro572Ser)	not specified [RCV004338197]	uncertain significance	1	9610754	9610754	Human		name
401860538	CV2758517	single nucleotide variant	NM_001258277.2(TMEM200A):c.815C>G (p.Ser272Cys)	not specified [RCV004335565]	uncertain significance	6	130441237	130441237	Human		name
401860021	CV2768447	single nucleotide variant	NM_001003682.4(TMEM200B):c.674C>G (p.Pro225Arg)	not specified [RCV004344336]	uncertain significance	1	29121155	29121155	Human		name
401866932	CV2769831	single nucleotide variant	NM_001003682.4(TMEM200B):c.905A>T (p.Asp302Val)	not specified [RCV004353693]	uncertain significance	1	29120924	29120924	Human		name
401876074	CV2777646	single nucleotide variant	NM_001130924.3(TMEM201):c.1168C>G (p.Pro390Ala)	not specified [RCV004343486]	uncertain significance	1	9607564	9607564	Human		name
401882364	CV2793465	single nucleotide variant	NM_001258277.2(TMEM200A):c.528G>C (p.Lys176Asn)	not specified [RCV004362552]	uncertain significance	6	130440950	130440950	Human		name
405753234	CV3336222	single nucleotide variant	NM_001258277.2(TMEM200A):c.662G>T (p.Arg221Leu)	not specified [RCV004467449]	uncertain significance	6	130441084	130441084	Human		name
405753260	CV3336226	single nucleotide variant	NM_001003682.4(TMEM200B):c.298G>C (p.Glu100Gln)	not specified [RCV004467453]	uncertain significance	1	29121531	29121531	Human		name
405753266	CV3336227	single nucleotide variant	NM_001003682.4(TMEM200B):c.333C>G (p.His111Gln)	not specified [RCV004467454]	uncertain significance	1	29121496	29121496	Human		name
405753302	CV3336232	single nucleotide variant	NM_001003682.4(TMEM200B):c.878G>A (p.Gly293Asp)	not specified [RCV004467459]	uncertain significance	1	29120951	29120951	Human		name
405753311	CV3336233	single nucleotide variant	NM_001130924.3(TMEM201):c.1223C>T (p.Pro408Leu)	not specified [RCV004467460]	uncertain significance	1	9607619	9607619	Human		name
405753317	CV3336234	single nucleotide variant	NM_001130924.3(TMEM201):c.1302C>A (p.Phe434Leu)	not specified [RCV004467461]	uncertain significance	1	9607698	9607698	Human		name
405753326	CV3336235	single nucleotide variant	NM_001130924.3(TMEM201):c.1327T>A (p.Ser443Thr)	not specified [RCV004467462]	uncertain significance	1	9607723	9607723	Human		name
405753333	CV3336236	single nucleotide variant	NM_001130924.3(TMEM201):c.1403A>G (p.Tyr468Cys)	not specified [RCV004467463]	uncertain significance	1	9609849	9609849	Human		name
405753353	CV3336239	single nucleotide variant	NM_001130924.3(TMEM201):c.1681T>G (p.Ser561Ala)	not specified [RCV004467466]	uncertain significance	1	9610721	9610721	Human		name
405753528	CV3336242	single nucleotide variant	NM_001130924.3(TMEM201):c.1864A>G (p.Thr622Ala)	not specified [RCV004467469]	uncertain significance	1	9611851	9611851	Human		name
405753537	CV3336243	single nucleotide variant	NM_001130924.3(TMEM201):c.1907G>A (p.Arg636His)	not specified [RCV004467470]	uncertain significance	1	9612989	9612989	Human		name
407526299	CV3486509	single nucleotide variant	NM_001258277.2(TMEM200A):c.629T>C (p.Ile210Thr)	not specified [RCV004679594]	uncertain significance	6	130441051	130441051	Human		name
407526308	CV3486512	single nucleotide variant	NM_001130924.3(TMEM201):c.1886A>G (p.Glu629Gly)	not specified [RCV004679597]	uncertain significance	1	9611873	9611873	Human		name
597753782	CV3613645	single nucleotide variant	NM_001258277.2(TMEM200A):c.436A>G (p.Ile146Val)	not specified [RCV004867449]	uncertain significance	6	130440858	130440858	Human		name
597753791	CV3613647	single nucleotide variant	NM_001258277.2(TMEM200A):c.437T>A (p.Ile146Asn)	not specified [RCV004867451]	uncertain significance	6	130440859	130440859	Human		name
597753795	CV3613648	single nucleotide variant	NM_001258277.2(TMEM200A):c.590A>T (p.Asn197Ile)	not specified [RCV004867452]	uncertain significance	6	130441012	130441012	Human		name
597753807	CV3613651	single nucleotide variant	NM_001003682.4(TMEM200B):c.488C>G (p.Pro163Arg)	not specified [RCV004867455]	uncertain significance	1	29121341	29121341	Human		name
597753811	CV3613652	single nucleotide variant	NM_001003682.4(TMEM200B):c.400A>C (p.Thr134Pro)	not specified [RCV004867456]	uncertain significance	1	29121429	29121429	Human		name
597753816	CV3613653	single nucleotide variant	NM_001003682.4(TMEM200B):c.562A>T (p.Ile188Phe)	not specified [RCV004867457]	uncertain significance	1	29121267	29121267	Human		name
597753827	CV3613656	single nucleotide variant	NM_001003682.4(TMEM200B):c.571C>G (p.Pro191Ala)	not specified [RCV004867460]	uncertain significance	1	29121258	29121258	Human		name
597753831	CV3613657	single nucleotide variant	NM_001130924.3(TMEM201):c.1601A>G (p.Asn534Ser)	not specified [RCV004867461]	uncertain significance	1	9610641	9610641	Human		name
597753835	CV3613658	single nucleotide variant	NM_001130924.3(TMEM201):c.1808G>A (p.Arg603His)	not specified [RCV004867462]	likely benign	1	9611795	9611795	Human		name
597753840	CV3613659	single nucleotide variant	NM_001130924.3(TMEM201):c.1388G>A (p.Arg463Gln)	not specified [RCV004867463]	uncertain significance	1	9607784	9607784	Human		name
597753843	CV3613660	single nucleotide variant	NM_001130924.3(TMEM201):c.1980T>G (p.Phe660Leu)	not specified [RCV004867464]	uncertain significance	1	9613062	9613062	Human		name
597753865	CV3613665	single nucleotide variant	NM_001130924.3(TMEM201):c.1316G>A (p.Arg439Gln)	not specified [RCV004867469]	uncertain significance	1	9607712	9607712	Human		name
597753868	CV3613666	single nucleotide variant	NM_001130924.3(TMEM201):c.1810T>C (p.Ser604Pro)	not specified [RCV004867470]	uncertain significance	1	9611797	9611797	Human		name
598213673	CV3917574	single nucleotide variant	NM_001258277.2(TMEM200A):c.740T>C (p.Leu247Pro)	not specified [RCV005292364]	uncertain significance	6	130441162	130441162	Human		name
598213677	CV3917575	single nucleotide variant	NM_001258277.2(TMEM200A):c.643G>A (p.Gly215Ser)	not specified [RCV005292365]	uncertain significance	6	130441065	130441065	Human		name
598213685	CV3917577	single nucleotide variant	NM_001258277.2(TMEM200A):c.388C>G (p.Pro130Ala)	not specified [RCV005292367]	uncertain significance	6	130440810	130440810	Human		name
598213689	CV3917578	single nucleotide variant	NM_001003682.4(TMEM200B):c.755G>C (p.Gly252Ala)	not specified [RCV005292368]	uncertain significance	1	29121074	29121074	Human		name
598178669	CV3917579	single nucleotide variant	NM_001003682.4(TMEM200B):c.908T>C (p.Leu303Ser)	not specified [RCV005286009]	uncertain significance	1	29120921	29120921	Human		name
598252127	CV3917581	single nucleotide variant	NM_001003682.4(TMEM200B):c.512C>T (p.Pro171Leu)	not specified [RCV005278032]	uncertain significance	1	29121317	29121317	Human		name
598213697	CV3917583	single nucleotide variant	NM_001003682.4(TMEM200B):c.764T>C (p.Ile255Thr)	not specified [RCV005292370]	uncertain significance	1	29121065	29121065	Human		name
598213704	CV3917585	single nucleotide variant	NM_001130924.3(TMEM201):c.1304G>A (p.Arg435Gln)	not specified [RCV005292372]	likely benign	1	9607700	9607700	Human		name
598213709	CV3917586	single nucleotide variant	NM_001130924.3(TMEM201):c.1723G>A (p.Val575Ile)	not specified [RCV005292373]	uncertain significance	1	9610763	9610763	Human		name
598213713	CV3917587	single nucleotide variant	NM_001130924.3(TMEM201):c.1991G>A (p.Ser664Asn)	not specified [RCV005292374]	uncertain significance	1	9613073	9613073	Human		name
598213727	CV3917591	single nucleotide variant	NM_001130924.3(TMEM201):c.1484C>T (p.Ser495Leu)	not specified [RCV005292377]	uncertain significance	1	9610524	9610524	Human		name
598213730	CV3917592	single nucleotide variant	NM_001130924.3(TMEM201):c.1927C>T (p.Arg643Trp)	not specified [RCV005292378]	uncertain significance	1	9613009	9613009	Human		name
15194519	CV696922	single nucleotide variant	NM_001130924.3(TMEM201):c.1906C>T (p.Arg636Cys)	not provided [RCV000955669]	benign	1	9612988	9612988	Human		name
15150223	CV707602	single nucleotide variant	NM_001130924.3(TMEM201):c.1640C>A (p.Pro547His)	not provided [RCV000967902]	benign	1	9610680	9610680	Human		name
156151558	CV2197951	single nucleotide variant	NM_001258277.2(TMEM200A):c.1151C>A (p.Ser384Tyr)	not specified [RCV004077165]	uncertain significance	6	130441573	130441573	Human		name
156382103	CV2227189	single nucleotide variant	NM_001258277.2(TMEM200A):c.1074G>T (p.Gln358His)	not specified [RCV004091798]	uncertain significance	6	130441496	130441496	Human		name
155901641	CV2242068	single nucleotide variant	NM_001258277.2(TMEM200A):c.1127G>C (p.Gly376Ala)	not specified [RCV004109002]	uncertain significance	6	130441549	130441549	Human		name
156387764	CV2383353	single nucleotide variant	NM_001258277.2(TMEM200A):c.1021G>A (p.Val341Ile)	not specified [RCV004222386]	uncertain significance	6	130441443	130441443	Human		name
156268491	CV2398439	single nucleotide variant	NM_001258277.2(TMEM200A):c.1349T>A (p.Ile450Asn)	not specified [RCV004237767]	uncertain significance	6	130441771	130441771	Human		name
401907975	CV2818170	single nucleotide variant	NM_001395400.1(TMEM200C):c.1199G>T (p.Ser400Ile)	not provided [RCV003423011]	likely benign	18	5890865	5890865	Human		name
401906658	CV2818171	single nucleotide variant	NM_001395400.1(TMEM200C):c.1198A>C (p.Ser400Arg)	not provided [RCV003421582]	likely benign	18	5890866	5890866	Human		name
405753223	CV3336220	single nucleotide variant	NM_001258277.2(TMEM200A):c.1205G>A (p.Arg402Gln)	not specified [RCV004467447]	uncertain significance	6	130441627	130441627	Human		name
407526292	CV3486507	single nucleotide variant	NM_001258277.2(TMEM200A):c.1367A>G (p.Asn456Ser)	not specified [RCV004679592]	uncertain significance	6	130441789	130441789	Human		name
407526295	CV3486508	single nucleotide variant	NM_001258277.2(TMEM200A):c.1450A>T (p.Arg484Trp)	not specified [RCV004679593]	uncertain significance	6	130441872	130441872	Human		name
597753778	CV3613644	single nucleotide variant	NM_001258277.2(TMEM200A):c.1441A>C (p.Asn481His)	not specified [RCV004867448]	uncertain significance	6	130441863	130441863	Human		name
152978554	CV1671719	microsatellite	NM_001130924.3(TMEM201):c.1178_1179del (p.Ser393fs)	not provided [RCV002227824]	uncertain significance	1	9607572	9607573	Human		name
401935940	CV2818173	deletion	NM_001395400.1(TMEM200C):c.676_690del (p.Ala226_Ala230del)	not provided [RCV003413404]	likely benign	18	5891374	5891388	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message