Crim1 Variant Search Result - Rat Genome Database

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135 records found for search term Crim1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405270397	CV3211412	single nucleotide variant	NM_016441.3(CRIM1):c.506-8C>T	CRIM1-related disorder [RCV003949306]	likely benign	2	36441250	36441250	Human		name , trait , alternate_id
408385090	CV3505502	single nucleotide variant	NM_016441.3(CRIM1):c.749-9C>T	CRIM1-related disorder [RCV004732333]	likely benign	2	36442606	36442606	Human		name , trait , alternate_id
15098444	CV777203	single nucleotide variant	NM_016441.3(CRIM1):c.331+5G>A	CRIM1-related disorder [RCV003960692]\|not provided [RCV000958560]	benign	2	36356628	36356628	Human		name , trait , alternate_id
405291671	CV3205930	single nucleotide variant	NM_016441.3(CRIM1):c.2747-8T>C	CRIM1-related disorder [RCV003964039]\|not provided [RCV003992820]	likely benign	2	36546976	36546976	Human		name , trait , alternate_id
15195408	CV777284	single nucleotide variant	NM_016441.3(CRIM1):c.1501+10C>G	CRIM1-related disorder [RCV003915888]\|not provided [RCV000955915]	benign	2	36499357	36499357	Human		name , trait , alternate_id
8577151	CV111522	single nucleotide variant	NM_016441.2(CRIM1):c.505+4947G>T	Lung cancer [RCV000092045]	uncertain significance	2	36401734	36401734	Human		name
8577152	CV111523	single nucleotide variant	NM_016441.2(CRIM1):c.992-3373C>T	Lung cancer [RCV000092046]	uncertain significance	2	36473516	36473516	Human		name
156084454	CV2244545	single nucleotide variant	NM_016441.3(CRIM1):c.7T>G (p.Leu3Val)	not specified [RCV004102279]	uncertain significance	2	36356299	36356299	Human		name
405276770	CV3193492	single nucleotide variant	NM_016441.3(CRIM1):c.26G>T (p.Gly9Val)	CRIM1-related disorder [RCV003974660]	benign	2	36356318	36356318	Human		name , trait , alternate_id
15196132	CV747621	single nucleotide variant	NM_016441.3(CRIM1):c.141G>A (p.Glu47=)	not provided [RCV000911611]	likely benign	2	36356433	36356433	Human		name
329354705	CV2444740	single nucleotide variant	NM_016441.3(CRIM1):c.65G>T (p.Gly22Val)	not specified [RCV004258991]	uncertain significance	2	36356357	36356357	Human		name
401877015	CV2793317	single nucleotide variant	NM_016441.3(CRIM1):c.37T>C (p.Cys13Arg)	not specified [RCV004362133]	uncertain significance	2	36356329	36356329	Human		name
405266748	CV3202080	single nucleotide variant	NM_016441.3(CRIM1):c.76C>A (p.Leu26Met)	CRIM1-related disorder [RCV003911561]	benign	2	36356368	36356368	Human		name , trait , alternate_id
15171520	CV708264	single nucleotide variant	NM_016441.3(CRIM1):c.699A>G (p.Lys233=)	CRIM1-related disorder [RCV003918486]\|not provided [RCV000972216]	benign	2	36441451	36441451	Human		name , trait , alternate_id
15152005	CV719868	single nucleotide variant	NM_016441.3(CRIM1):c.324T>C (p.Val108=)	CRIM1-related disorder [RCV003967964]\|not provided [RCV000879717]	benign	2	36356616	36356616	Human		name , trait , alternate_id
15116080	CV733465	single nucleotide variant	NM_016441.3(CRIM1):c.678C>T (p.Asn226=)	not provided [RCV000895138]	likely benign	2	36441430	36441430	Human		name
15191770	CV733466	single nucleotide variant	NM_016441.3(CRIM1):c.807C>G (p.Pro269=)	not provided [RCV000910344]	benign	2	36442673	36442673	Human		name
156267398	CV2296637	single nucleotide variant	NM_016441.3(CRIM1):c.290A>G (p.Asn97Ser)	not specified [RCV004154692]	uncertain significance	2	36356582	36356582	Human		name
401929460	CV2815682	single nucleotide variant	NM_016441.3(CRIM1):c.1791T>C (p.Ala597=)	CRIM1-related disorder [RCV003980907]\|not provided [RCV003407201]	benign\|likely benign	2	36513566	36513566	Human		name , trait , alternate_id
401911074	CV2815684	single nucleotide variant	NM_016441.3(CRIM1):c.2541C>A (p.Thr847=)	CRIM1-related disorder [RCV003929109]\|not provided [RCV003425577]	benign\|likely benign	2	36537464	36537464	Human		name , trait , alternate_id
405258557	CV3203855	single nucleotide variant	NM_016441.3(CRIM1):c.1308C>G (p.Thr436=)	CRIM1-related disorder [RCV003942022]	likely benign	2	36479630	36479630	Human		name , trait , alternate_id
405290161	CV3206139	single nucleotide variant	NM_016441.3(CRIM1):c.2958A>C (p.Leu986=)	CRIM1-related disorder [RCV003962158]	likely benign	2	36548548	36548548	Human		name , trait , alternate_id
408367274	CV3509708	single nucleotide variant	NM_016441.3(CRIM1):c.1680C>T (p.Asp560=)	CRIM1-related disorder [RCV004758349]	likely benign	2	36512294	36512294	Human		name , trait , alternate_id
598249484	CV3941774	single nucleotide variant	NM_016441.3(CRIM1):c.215A>G (p.Glu72Gly)	not specified [RCV005322752]	uncertain significance	2	36356507	36356507	Human		name
598249491	CV3941775	single nucleotide variant	NM_016441.3(CRIM1):c.271G>C (p.Val91Leu)	not specified [RCV005322753]	uncertain significance	2	36356563	36356563	Human		name
15191723	CV697562	single nucleotide variant	NM_016441.3(CRIM1):c.1323C>G (p.Thr441=)	CRIM1-related disorder [RCV003935842]\|not provided [RCV000954859]	benign	2	36479645	36479645	Human		name , trait , alternate_id
15177594	CV708265	single nucleotide variant	NM_016441.3(CRIM1):c.1077C>T (p.Cys359=)	CRIM1-related disorder [RCV003906064]\|not provided [RCV000973466]	benign	2	36476974	36476974	Human		name , trait , alternate_id
15110075	CV708266	single nucleotide variant	NM_016441.3(CRIM1):c.1305G>A (p.Ala435=)	CRIM1-related disorder [RCV003935932]\|not provided [RCV000960829]	benign	2	36479627	36479627	Human		name , trait , alternate_id
15116038	CV708267	single nucleotide variant	NM_016441.3(CRIM1):c.2730C>T (p.Ile910=)	CRIM1-related disorder [RCV003916062]\|not provided [RCV000961965]	benign	2	36544482	36544482	Human		name , trait , alternate_id
15175910	CV719869	single nucleotide variant	NM_016441.3(CRIM1):c.1206C>G (p.Gly402=)	not provided [RCV000884472]	benign	2	36479528	36479528	Human		name
15126538	CV733467	single nucleotide variant	NM_016441.3(CRIM1):c.1869C>T (p.His623=)	CRIM1-related disorder [RCV003922886]\|not provided [RCV000896948]	benign	2	36513644	36513644	Human		name , trait , alternate_id
152980421	CV1678608	single nucleotide variant	NM_016441.3(CRIM1):c.881T>C (p.Leu294Pro)	not specified [RCV002247116]	uncertain significance	2	36464545	36464545	Human		name
155907289	CV2276326	single nucleotide variant	NM_016441.3(CRIM1):c.899T>C (p.Phe300Ser)	not specified [RCV004144071]	uncertain significance	2	36464563	36464563	Human		name
155903888	CV2282311	single nucleotide variant	NM_016441.3(CRIM1):c.713C>T (p.Pro238Leu)	not specified [RCV004133138]	uncertain significance	2	36441465	36441465	Human		name
156115385	CV2349295	single nucleotide variant	NM_016441.3(CRIM1):c.437G>A (p.Arg146Gln)	not specified [RCV004199242]	uncertain significance	2	36396719	36396719	Human		name
156391518	CV2382346	single nucleotide variant	NM_016441.3(CRIM1):c.874G>A (p.Glu292Lys)	not specified [RCV004230688]	uncertain significance	2	36464538	36464538	Human		name
329383320	CV2445814	single nucleotide variant	NM_016441.3(CRIM1):c.772G>A (p.Val258Met)	not specified [RCV004259868]	uncertain significance	2	36442638	36442638	Human		name
329393893	CV2449941	single nucleotide variant	NM_016441.3(CRIM1):c.861G>T (p.Leu287Phe)	not specified [RCV004269011]	uncertain significance	2	36442727	36442727	Human		name
329369153	CV2450547	single nucleotide variant	NM_016441.3(CRIM1):c.805C>G (p.Pro269Ala)	not specified [RCV004265454]	uncertain significance	2	36442671	36442671	Human		name
329397438	CV2456168	single nucleotide variant	NM_016441.3(CRIM1):c.929G>A (p.Arg310His)	not specified [RCV004273360]	uncertain significance	2	36464593	36464593	Human		name
401742573	CV2715264	single nucleotide variant	NM_016441.3(CRIM1):c.532C>T (p.Arg178Cys)	not specified [RCV004324607]	uncertain significance	2	36441284	36441284	Human		name
401894852	CV2781909	single nucleotide variant	NM_016441.3(CRIM1):c.614C>G (p.Pro205Arg)	not specified [RCV004357152]	uncertain significance	2	36441366	36441366	Human		name
401865918	CV2786198	single nucleotide variant	NM_016441.3(CRIM1):c.743A>C (p.Lys248Thr)	not specified [RCV004359995]	uncertain significance	2	36441495	36441495	Human		name
405664366	CV3242782	single nucleotide variant	NM_016441.3(CRIM1):c.328G>C (p.Glu110Gln)	not specified [RCV004367323]	uncertain significance	2	36356620	36356620	Human		name
405664369	CV3242783	single nucleotide variant	NM_016441.3(CRIM1):c.406A>G (p.Ile136Val)	not specified [RCV004367324]	uncertain significance	2	36396688	36396688	Human		name
405664383	CV3242786	single nucleotide variant	NM_016441.3(CRIM1):c.904G>A (p.Val302Met)	not specified [RCV004367327]	uncertain significance	2	36464568	36464568	Human		name
407463897	CV3429630	single nucleotide variant	NM_016441.3(CRIM1):c.304A>C (p.Thr102Pro)	not specified [RCV004613317]	uncertain significance	2	36356596	36356596	Human		name
407463902	CV3429631	single nucleotide variant	NM_016441.3(CRIM1):c.598C>G (p.Pro200Ala)	not specified [RCV004613318]	uncertain significance	2	36441350	36441350	Human		name
407463906	CV3429632	single nucleotide variant	NM_016441.3(CRIM1):c.766A>G (p.Arg256Gly)	not specified [RCV004613319]	uncertain significance	2	36442632	36442632	Human		name
597671544	CV3661326	single nucleotide variant	NM_016441.3(CRIM1):c.928C>T (p.Arg310Cys)	not specified [RCV004913115]	uncertain significance	2	36464592	36464592	Human		name
597671536	CV3661327	single nucleotide variant	NM_016441.3(CRIM1):c.410A>G (p.Asn137Ser)	not specified [RCV004913116]	uncertain significance	2	36396692	36396692	Human		name
597671510	CV3661330	single nucleotide variant	NM_016441.3(CRIM1):c.468T>A (p.Ser156Arg)	not specified [RCV004913119]	likely benign	2	36396750	36396750	Human		name
597671466	CV3661335	single nucleotide variant	NM_016441.3(CRIM1):c.639C>A (p.Asn213Lys)	not specified [RCV004913124]	uncertain significance	2	36441391	36441391	Human		name
598249446	CV3941768	single nucleotide variant	NM_016441.3(CRIM1):c.655C>T (p.Arg219Cys)	not specified [RCV005322746]	uncertain significance	2	36441407	36441407	Human		name
598249459	CV3941770	single nucleotide variant	NM_016441.3(CRIM1):c.521G>T (p.Cys174Phe)	not specified [RCV005322748]	uncertain significance	2	36441273	36441273	Human		name
598249473	CV3941772	single nucleotide variant	NM_016441.3(CRIM1):c.908G>A (p.Cys303Tyr)	not specified [RCV005322750]	uncertain significance	2	36464572	36464572	Human		name
156380094	CV2211779	single nucleotide variant	NM_016441.3(CRIM1):c.1243C>G (p.Arg415Gly)	not specified [RCV004086618]	uncertain significance	2	36479565	36479565	Human		name
155970557	CV2217844	single nucleotide variant	NM_016441.3(CRIM1):c.1101C>G (p.Phe367Leu)	not provided [RCV004695372]\|not specified [RCV004084016]	uncertain significance	2	36476998	36476998	Human		name
155939733	CV2221797	single nucleotide variant	NM_016441.3(CRIM1):c.2150C>T (p.Pro717Leu)	not specified [RCV004102829]	uncertain significance	2	36517486	36517486	Human		name
155944955	CV2237900	single nucleotide variant	NM_016441.3(CRIM1):c.1055A>G (p.Asp352Gly)	not specified [RCV004109127]	uncertain significance	2	36476952	36476952	Human		name
155983829	CV2273119	single nucleotide variant	NM_016441.3(CRIM1):c.1399C>T (p.Pro467Ser)	not specified [RCV004137759]	uncertain significance	2	36499245	36499245	Human		name
156270630	CV2315579	single nucleotide variant	NM_016441.3(CRIM1):c.2426T>G (p.Ile809Arg)	not specified [RCV004169620]	uncertain significance	2	36522311	36522311	Human		name
155977657	CV2321216	single nucleotide variant	NM_016441.3(CRIM1):c.2756A>G (p.His919Arg)	not specified [RCV004175336]	uncertain significance	2	36546993	36546993	Human		name
155976603	CV2324770	single nucleotide variant	NM_016441.3(CRIM1):c.1279G>A (p.Val427Ile)	not specified [RCV004173004]	likely benign	2	36479601	36479601	Human		name
156170563	CV2337450	single nucleotide variant	NM_016441.3(CRIM1):c.2867C>T (p.Ala956Val)	not specified [RCV004187888]	uncertain significance	2	36547104	36547104	Human		name
156200522	CV2350856	single nucleotide variant	NM_016441.3(CRIM1):c.2889G>C (p.Lys963Asn)	not specified [RCV004211694]	uncertain significance	2	36547126	36547126	Human		name
156127387	CV2351197	single nucleotide variant	NM_016441.3(CRIM1):c.1598G>A (p.Arg533His)	not specified [RCV004214045]	uncertain significance	2	36510079	36510079	Human		name
155990991	CV2384097	single nucleotide variant	NM_016441.3(CRIM1):c.2482G>A (p.Asp828Asn)	not specified [RCV004227503]	uncertain significance	2	36537405	36537405	Human		name
155991033	CV2384114	single nucleotide variant	NM_016441.3(CRIM1):c.1522C>T (p.Arg508Cys)	not specified [RCV004227519]	uncertain significance	2	36510003	36510003	Human		name
329363096	CV2445822	single nucleotide variant	NM_016441.3(CRIM1):c.1820C>T (p.Thr607Ile)	not specified [RCV004270448]	uncertain significance	2	36513595	36513595	Human		name
329389008	CV2469695	single nucleotide variant	NM_016441.3(CRIM1):c.2173C>T (p.Arg725Cys)	not specified [RCV004283108]	uncertain significance	2	36517509	36517509	Human		name
401766219	CV2679612	single nucleotide variant	NM_016441.3(CRIM1):c.2116G>A (p.Gly706Arg)	not specified [RCV004282091]	uncertain significance	2	36517452	36517452	Human		name
401736306	CV2688755	single nucleotide variant	NM_016441.3(CRIM1):c.2836C>T (p.Pro946Ser)	not specified [RCV004303782]	uncertain significance	2	36547073	36547073	Human		name
401742115	CV2697701	single nucleotide variant	NM_016441.3(CRIM1):c.2566C>A (p.Pro856Thr)	not specified [RCV004300440]	uncertain significance	2	36537489	36537489	Human		name
401783248	CV2716204	single nucleotide variant	NM_016441.3(CRIM1):c.1237G>C (p.Gly413Arg)	not specified [RCV004323431]	uncertain significance	2	36479559	36479559	Human		name
401773380	CV2716547	single nucleotide variant	NM_016441.3(CRIM1):c.1648C>T (p.Leu550Phe)	not specified [RCV004327623]	likely benign	2	36510129	36510129	Human		name
401866415	CV2775541	single nucleotide variant	NM_016441.3(CRIM1):c.2497G>A (p.Asp833Asn)	not specified [RCV004350712]	uncertain significance	2	36537420	36537420	Human		name
401887361	CV2775717	single nucleotide variant	NM_016441.3(CRIM1):c.2200T>A (p.Cys734Ser)	not specified [RCV004350845]	uncertain significance	2	36517536	36517536	Human		name
401890859	CV2778392	single nucleotide variant	NM_016441.3(CRIM1):c.2084T>C (p.Ile695Thr)	not specified [RCV004344076]	uncertain significance	2	36517420	36517420	Human		name
401871813	CV2783607	single nucleotide variant	NM_016441.3(CRIM1):c.2729T>C (p.Ile910Thr)	not specified [RCV004365926]	uncertain significance	2	36544481	36544481	Human		name
401881911	CV2784001	single nucleotide variant	NM_016441.3(CRIM1):c.2861T>C (p.Ile954Thr)	not specified [RCV004362410]	uncertain significance	2	36547098	36547098	Human		name
405285083	CV3202385	single nucleotide variant	NM_016441.3(CRIM1):c.1235A>C (p.His412Pro)	CRIM1-related disorder [RCV003909655]	likely benign	2	36479557	36479557	Human		name , trait , alternate_id
405291012	CV3203635	single nucleotide variant	NM_016441.3(CRIM1):c.1587C>G (p.Ile529Met)	CRIM1-related disorder [RCV003927320]	likely benign	2	36510068	36510068	Human		name , trait , alternate_id
405272389	CV3210049	single nucleotide variant	NM_016441.3(CRIM1):c.1504G>A (p.Glu502Lys)	CRIM1-related disorder [RCV003914300]	benign	2	36509985	36509985	Human	1	name , trait , alternate_id
405278648	CV3216773	single nucleotide variant	NM_016441.3(CRIM1):c.2341G>A (p.Val781Ile)	CRIM1-related disorder [RCV003954645]	likely benign	2	36522226	36522226	Human		name , trait , alternate_id
405696634	CV3226753	single nucleotide variant	NM_016441.3(CRIM1):c.1336G>T (p.Val446Leu)	not provided [RCV003993146]	uncertain significance	2	36479658	36479658	Human		name
405664300	CV3242767	single nucleotide variant	NM_016441.3(CRIM1):c.1043T>C (p.Met348Thr)	not specified [RCV004367308]	uncertain significance	2	36476940	36476940	Human		name
405664305	CV3242768	single nucleotide variant	NM_016441.3(CRIM1):c.1064G>A (p.Arg355Gln)	not specified [RCV004367309]	uncertain significance	2	36476961	36476961	Human		name
405664309	CV3242769	single nucleotide variant	NM_016441.3(CRIM1):c.1244G>A (p.Arg415Gln)	not specified [RCV004367310]	uncertain significance	2	36479566	36479566	Human		name
405664315	CV3242771	single nucleotide variant	NM_016441.3(CRIM1):c.1472A>G (p.Asn491Ser)	not specified [RCV004367312]	uncertain significance	2	36499318	36499318	Human		name
405664321	CV3242772	single nucleotide variant	NM_016441.3(CRIM1):c.1480C>T (p.Arg494Trp)	not specified [RCV004367313]	uncertain significance	2	36499326	36499326	Human		name
405664325	CV3242773	single nucleotide variant	NM_016441.3(CRIM1):c.1530A>C (p.Gln510His)	not specified [RCV004367314]	uncertain significance	2	36510011	36510011	Human		name
405664330	CV3242774	single nucleotide variant	NM_016441.3(CRIM1):c.1810C>A (p.Leu604Met)	not specified [RCV004367315]	uncertain significance	2	36513585	36513585	Human		name
405664333	CV3242775	single nucleotide variant	NM_016441.3(CRIM1):c.1831G>A (p.Val611Met)	not specified [RCV004367316]	likely benign	2	36513606	36513606	Human		name
405664340	CV3242776	single nucleotide variant	NM_016441.3(CRIM1):c.2041G>A (p.Ala681Thr)	not specified [RCV004367317]	uncertain significance	2	36517377	36517377	Human		name
405664347	CV3242778	single nucleotide variant	NM_016441.3(CRIM1):c.2567C>T (p.Pro856Leu)	not specified [RCV004367319]	uncertain significance	2	36537490	36537490	Human		name
405664353	CV3242779	single nucleotide variant	NM_016441.3(CRIM1):c.2651T>C (p.Ile884Thr)	not specified [RCV004367320]	uncertain significance	2	36544403	36544403	Human		name
407463883	CV3419944	single nucleotide variant	NM_016441.3(CRIM1):c.2075C>T (p.Thr692Met)	not specified [RCV004613313]	uncertain significance	2	36517411	36517411	Human		name
407463886	CV3419945	single nucleotide variant	NM_016441.3(CRIM1):c.1582G>A (p.Glu528Lys)	not specified [RCV004613314]	uncertain significance	2	36510063	36510063	Human		name
407463890	CV3429628	single nucleotide variant	NM_016441.3(CRIM1):c.1073G>A (p.Arg358Gln)	not specified [RCV004613315]	uncertain significance	2	36476970	36476970	Human		name
407463894	CV3429629	single nucleotide variant	NM_016441.3(CRIM1):c.2002G>A (p.Val668Met)	not specified [RCV004613316]	uncertain significance	2	36517338	36517338	Human		name
597671571	CV3661323	single nucleotide variant	NM_016441.3(CRIM1):c.2752G>T (p.Gly918Cys)	not specified [RCV004913112]	uncertain significance	2	36546989	36546989	Human		name
597671561	CV3661324	single nucleotide variant	NM_016441.3(CRIM1):c.2362T>A (p.Ser788Thr)	not specified [RCV004913113]	uncertain significance	2	36522247	36522247	Human		name
597671552	CV3661325	single nucleotide variant	NM_016441.3(CRIM1):c.2419T>C (p.Tyr807His)	not specified [RCV004913114]	uncertain significance	2	36522304	36522304	Human		name
597671529	CV3661328	single nucleotide variant	NM_016441.3(CRIM1):c.1300G>A (p.Val434Ile)	not specified [RCV004913117]	uncertain significance	2	36479622	36479622	Human		name
597671518	CV3661329	single nucleotide variant	NM_016441.3(CRIM1):c.1670A>G (p.His557Arg)	not specified [RCV004913118]	uncertain significance	2	36512284	36512284	Human		name
597671491	CV3661332	single nucleotide variant	NM_016441.3(CRIM1):c.1250G>A (p.Arg417Gln)	not specified [RCV004913121]	uncertain significance	2	36479572	36479572	Human		name
597671482	CV3661333	single nucleotide variant	NM_016441.3(CRIM1):c.2614A>G (p.Met872Val)	not specified [RCV004913122]	uncertain significance	2	36537537	36537537	Human		name
597671475	CV3661334	single nucleotide variant	NM_016441.3(CRIM1):c.2218C>T (p.Arg740Trp)	not specified [RCV004913123]	uncertain significance	2	36522103	36522103	Human		name
597671457	CV3661336	single nucleotide variant	NM_016441.3(CRIM1):c.2210A>G (p.Gln737Arg)	not specified [RCV004913125]	uncertain significance	2	36522095	36522095	Human		name
597671449	CV3661337	single nucleotide variant	NM_016441.3(CRIM1):c.1729C>G (p.Pro577Ala)	not specified [RCV004913126]	uncertain significance	2	36512343	36512343	Human		name
598249368	CV3941756	single nucleotide variant	NM_016441.3(CRIM1):c.2658T>G (p.Ile886Met)	not specified [RCV005322734]	uncertain significance	2	36544410	36544410	Human		name
598249373	CV3941757	single nucleotide variant	NM_016441.3(CRIM1):c.2819T>C (p.Ile940Thr)	not specified [RCV005322735]	uncertain significance	2	36547056	36547056	Human		name
598249380	CV3941758	single nucleotide variant	NM_016441.3(CRIM1):c.2675G>A (p.Arg892Gln)	not specified [RCV005322736]	uncertain significance	2	36544427	36544427	Human		name
598249388	CV3941759	single nucleotide variant	NM_016441.3(CRIM1):c.2177C>T (p.Thr726Ile)	not specified [RCV005322737]	uncertain significance	2	36517513	36517513	Human		name
598249393	CV3941760	single nucleotide variant	NM_016441.3(CRIM1):c.1447A>G (p.Ile483Val)	not specified [RCV005322738]	likely benign	2	36499293	36499293	Human		name
598249401	CV3941761	single nucleotide variant	NM_016441.3(CRIM1):c.2921G>A (p.Arg974Gln)	not specified [RCV005322739]	uncertain significance	2	36547158	36547158	Human		name
598249411	CV3941763	single nucleotide variant	NM_016441.3(CRIM1):c.1243C>T (p.Arg415Trp)	not specified [RCV005322741]	uncertain significance	2	36479565	36479565	Human		name
598249418	CV3941764	single nucleotide variant	NM_016441.3(CRIM1):c.1574A>C (p.Gln525Pro)	not specified [RCV005322742]	uncertain significance	2	36510055	36510055	Human		name
598249425	CV3941765	single nucleotide variant	NM_016441.3(CRIM1):c.2821G>A (p.Ala941Thr)	not specified [RCV005322743]	uncertain significance	2	36547058	36547058	Human		name
598249439	CV3941767	single nucleotide variant	NM_016441.3(CRIM1):c.2920C>G (p.Arg974Gly)	not specified [RCV005322745]	uncertain significance	2	36547157	36547157	Human		name
598249452	CV3941769	single nucleotide variant	NM_016441.3(CRIM1):c.1469A>G (p.His490Arg)	not specified [RCV005322747]	uncertain significance	2	36499315	36499315	Human		name
598249466	CV3941771	single nucleotide variant	NM_016441.3(CRIM1):c.1381A>G (p.Ile461Val)	not specified [RCV005322749]	uncertain significance	2	36499227	36499227	Human		name
598249497	CV3941776	single nucleotide variant	NM_016441.3(CRIM1):c.1139A>T (p.Tyr380Phe)	not specified [RCV005322754]	uncertain significance	2	36477036	36477036	Human		name
598249503	CV3941777	single nucleotide variant	NM_016441.3(CRIM1):c.1249C>T (p.Arg417Trp)	not specified [RCV005322755]	uncertain significance	2	36479571	36479571	Human		name
598249509	CV3941778	single nucleotide variant	NM_016441.3(CRIM1):c.2443A>G (p.Lys815Glu)	not specified [RCV005322756]	uncertain significance	2	36537366	36537366	Human		name
15164406	CV719870	single nucleotide variant	NM_016441.3(CRIM1):c.2566C>T (p.Pro856Ser)	CRIM1-related disorder [RCV003955845]\|not provided [RCV000882187]	likely benign	2	36537489	36537489	Human		name , trait , alternate_id
15175914	CV719871	single nucleotide variant	NM_016441.3(CRIM1):c.2986A>G (p.Arg996Gly)	not provided [RCV000884473]	benign	2	36548576	36548576	Human		name
15103337	CV747624	single nucleotide variant	NM_016441.3(CRIM1):c.2929A>G (p.Thr977Ala)	CRIM1-related disorder [RCV003933036]\|not provided [RCV000915141]	likely benign	2	36547166	36547166	Human		name , trait , alternate_id
8625360	CV80483	single nucleotide variant	NM_016441.2(CRIM1):c.1187C>T (p.Pro396Leu)	Malignant melanoma [RCV000060560]	not provided	2	36479509	36479509	Human		name
156284517	CV2231244	single nucleotide variant	NM_016441.3(CRIM1):c.3061A>G (p.Met1021Val)	not specified [RCV004094442]	uncertain significance	2	36548651	36548651	Human		name
405664358	CV3242780	single nucleotide variant	NM_016441.3(CRIM1):c.3047G>T (p.Ser1016Ile)	not specified [RCV004367321]	uncertain significance	2	36548637	36548637	Human		name
405664363	CV3242781	single nucleotide variant	NM_016441.3(CRIM1):c.3089A>T (p.Asp1030Val)	not specified [RCV004367322]	uncertain significance	2	36548679	36548679	Human		name
598249433	CV3941766	single nucleotide variant	NM_016441.3(CRIM1):c.3074A>C (p.Asn1025Thr)	not specified [RCV005322744]	uncertain significance	2	36548664	36548664	Human		name
401937510	CV2815683	deletion	NM_016441.3(CRIM1):c.1997_1998del (p.Phe666fs)	not provided [RCV003415545]	uncertain significance	2	36517332	36517333	Human		name

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