Cck Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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101 records found for search term Cck

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405739703	CV3292419	single nucleotide variant	NM_000729.6(CCK):c.14T>C (p.Val5Ala)	not specified [RCV004430508]	uncertain significance	3	42263617	42263617	Human		name
598228150	CV3943603	single nucleotide variant	NM_000729.6(CCK):c.37G>A (p.Val13Ile)	not specified [RCV005319041]	uncertain significance	3	42263594	42263594	Human		name
156068897	CV2222172	single nucleotide variant	NM_000729.6(CCK):c.104G>A (p.Arg35Gln)	not specified [RCV004104924]	likely benign	3	42263527	42263527	Human		name
405739710	CV3292420	single nucleotide variant	NM_000729.6(CCK):c.284G>A (p.Arg95Gln)	not specified [RCV004430509]	uncertain significance	3	42258162	42258162	Human		name
598228157	CV3943604	single nucleotide variant	NM_000729.6(CCK):c.208C>G (p.Arg70Gly)	not specified [RCV005319042]	uncertain significance	3	42263423	42263423	Human		name
598192669	CV3943602	single nucleotide variant	NM_000729.6(CCK):c.325G>A (p.Glu109Lys)	not specified [RCV005312826]	uncertain significance	3	42258121	42258121	Human		name
598192683	CV3943606	single nucleotide variant	NM_000729.6(CCK):c.317G>A (p.Arg106His)	not specified [RCV005312828]	uncertain significance	3	42258129	42258129	Human		name
15166542	CV778149	single nucleotide variant	NM_176875.4(CCKBR):c.404-10C>G	not provided [RCV000948859]	benign	11	6270078	6270078	Human		name
8579672	CV114074	single nucleotide variant	NM_000730.2(CCKAR):c.365-1571T>C	Lung cancer [RCV000094597]	uncertain significance	4	26487469	26487469	Human		name
156294172	CV2233615	single nucleotide variant	NM_176875.4(CCKBR):c.8T>G (p.Leu3Arg)	not specified [RCV004100081]	uncertain significance	11	6259936	6259936	Human		name
156032686	CV2275038	single nucleotide variant	NM_000730.3(CCKAR):c.68A>G (p.Glu23Gly)	not specified [RCV004135075]	uncertain significance	4	26490200	26490200	Human		name
329374004	CV2452763	single nucleotide variant	NM_176875.4(CCKBR):c.76G>A (p.Ala26Thr)	not specified [RCV004275304]	uncertain significance	11	6260004	6260004	Human		name
8566273	CV32568	single nucleotide variant	NM_000730.3(CCKAR):c.61G>C (p.Gly21Arg)	CHOLECYSTOKININ A RECEPTOR POLYMORPHISM [RCV000019081]\|not provided [RCV004715645]	benign	4	26490207	26490207	Human		name
15106306	CV764441	single nucleotide variant	NM_000730.3(CCKAR):c.651C>T (p.Leu217=)	not provided [RCV000937755]	likely benign	4	26483259	26483259	Human		name
156236141	CV2193454	single nucleotide variant	NM_176875.4(CCKBR):c.280C>T (p.Leu94Phe)	not specified [RCV004072944]	uncertain significance	11	6269797	6269797	Human		name
155970853	CV2214028	single nucleotide variant	NM_176875.4(CCKBR):c.218T>C (p.Met73Thr)	not specified [RCV004084075]	uncertain significance	11	6269735	6269735	Human		name
155971659	CV2227911	single nucleotide variant	NM_176875.4(CCKBR):c.190A>G (p.Ile64Val)	not specified [RCV004096170]	uncertain significance	11	6269707	6269707	Human		name
156127905	CV2244760	single nucleotide variant	NM_176875.4(CCKBR):c.142G>A (p.Gly48Arg)	not specified [RCV004102749]	uncertain significance	11	6260070	6260070	Human		name
156085914	CV2340890	single nucleotide variant	NM_176875.4(CCKBR):c.184G>A (p.Ala62Thr)	not specified [RCV004188245]	uncertain significance	11	6269701	6269701	Human		name
401752044	CV2682682	single nucleotide variant	NM_176875.4(CCKBR):c.115T>G (p.Cys39Gly)	not specified [RCV004281664]	uncertain significance	11	6260043	6260043	Human		name
401746600	CV2694889	single nucleotide variant	NM_176875.4(CCKBR):c.226A>G (p.Ile76Val)	not specified [RCV004300957]	uncertain significance	11	6269743	6269743	Human		name
405739716	CV3292421	single nucleotide variant	NM_000730.3(CCKAR):c.109A>G (p.Lys37Glu)	not specified [RCV004430510]	uncertain significance	4	26490159	26490159	Human		name
405739729	CV3292423	single nucleotide variant	NM_000730.3(CCKAR):c.163A>G (p.Ser55Gly)	not specified [RCV004430512]	uncertain significance	4	26489434	26489434	Human		name
405739735	CV3292424	single nucleotide variant	NM_000730.3(CCKAR):c.284T>C (p.Met95Thr)	not specified [RCV004430513]	uncertain significance	4	26489313	26489313	Human		name
405739781	CV3292431	single nucleotide variant	NM_176875.4(CCKBR):c.229G>T (p.Val77Leu)	not specified [RCV004430520]	uncertain significance	11	6269746	6269746	Human		name
407491448	CV3428539	single nucleotide variant	NM_000730.3(CCKAR):c.265A>G (p.Met89Val)	not specified [RCV004604749]	uncertain significance	4	26489332	26489332	Human		name
407491457	CV3428541	single nucleotide variant	NM_176875.4(CCKBR):c.192C>G (p.Ile64Met)	not specified [RCV004604751]	uncertain significance	11	6269709	6269709	Human		name
598192736	CV3939672	single nucleotide variant	NM_176875.4(CCKBR):c.121C>T (p.Pro41Ser)	not specified [RCV005312837]	uncertain significance	11	6260049	6260049	Human		name
15125910	CV738073	single nucleotide variant	NM_176875.4(CCKBR):c.109C>T (p.Leu37Phe)	not provided [RCV000896844]	benign	11	6260037	6260037	Human		name
156239325	CV2193713	single nucleotide variant	NM_000730.3(CCKAR):c.425C>T (p.Ala142Val)	not specified [RCV004074306]	uncertain significance	4	26485838	26485838	Human		name
156271176	CV2237123	single nucleotide variant	NM_176875.4(CCKBR):c.662T>C (p.Leu221Pro)	not specified [RCV004114876]	uncertain significance	11	6270654	6270654	Human		name
156176869	CV2258133	single nucleotide variant	NM_000730.3(CCKAR):c.632C>G (p.Thr211Arg)	not specified [RCV004121521]	uncertain significance	4	26483278	26483278	Human		name
156274819	CV2279848	single nucleotide variant	NM_176875.4(CCKBR):c.832C>A (p.Arg278Ser)	not specified [RCV004144447]	uncertain significance	11	6271031	6271031	Human		name
156132534	CV2280075	single nucleotide variant	NM_000730.3(CCKAR):c.570C>A (p.Asn190Lys)	not specified [RCV004146431]	uncertain significance	4	26485693	26485693	Human		name
156267129	CV2304988	single nucleotide variant	NM_176875.4(CCKBR):c.439G>A (p.Ala147Thr)	not specified [RCV004168883]	uncertain significance	11	6270123	6270123	Human		name
156255043	CV2311580	single nucleotide variant	NM_000730.3(CCKAR):c.694A>G (p.Ile232Val)	not specified [RCV004168394]	uncertain significance	4	26483216	26483216	Human		name
156048864	CV2336476	single nucleotide variant	NM_000730.3(CCKAR):c.524C>T (p.Pro175Leu)	not specified [RCV004194688]	uncertain significance	4	26485739	26485739	Human		name
156291068	CV2342806	single nucleotide variant	NM_000730.3(CCKAR):c.799G>A (p.Asp267Asn)	not specified [RCV004189847]	uncertain significance	4	26482126	26482126	Human		name
156127715	CV2351249	single nucleotide variant	NM_000730.3(CCKAR):c.893G>T (p.Ser298Ile)	not specified [RCV004214095]	uncertain significance	4	26482032	26482032	Human		name
156174127	CV2377149	single nucleotide variant	NM_000730.3(CCKAR):c.575C>T (p.Thr192Ile)	not specified [RCV004231826]	uncertain significance	4	26485688	26485688	Human		name
329381922	CV2424266	single nucleotide variant	NM_000730.3(CCKAR):c.796A>G (p.Ser266Gly)	not specified [RCV004252177]	uncertain significance	4	26482129	26482129	Human		name
329393645	CV2472052	single nucleotide variant	NM_176875.4(CCKBR):c.870C>A (p.Ser290Arg)	not specified [RCV004283194]	uncertain significance	11	6271069	6271069	Human		name
401740605	CV2679763	single nucleotide variant	NM_176875.4(CCKBR):c.958C>T (p.Pro320Ser)	not specified [RCV004282228]	uncertain significance	11	6271157	6271157	Human		name
401769029	CV2686478	single nucleotide variant	NM_176875.4(CCKBR):c.317C>T (p.Ala106Val)	not specified [RCV004290632]	uncertain significance	11	6269834	6269834	Human		name
401895677	CV2775087	single nucleotide variant	NM_000730.3(CCKAR):c.979A>G (p.Met327Val)	not specified [RCV004346454]	uncertain significance	4	26481946	26481946	Human		name
401894896	CV2782046	single nucleotide variant	NM_000730.3(CCKAR):c.379G>A (p.Val127Ile)	not specified [RCV004359051]	uncertain significance	4	26485884	26485884	Human		name
401864075	CV2784970	single nucleotide variant	NM_176875.4(CCKBR):c.877T>C (p.Cys293Arg)	not specified [RCV004354700]	uncertain significance	11	6271076	6271076	Human		name
405739741	CV3292425	single nucleotide variant	NM_000730.3(CCKAR):c.353C>T (p.Thr118Ile)	not specified [RCV004430514]	uncertain significance	4	26489244	26489244	Human		name
405739748	CV3292426	single nucleotide variant	NM_000730.3(CCKAR):c.449G>C (p.Arg150Pro)	not specified [RCV004430515]	uncertain significance	4	26485814	26485814	Human		name
405739755	CV3292427	single nucleotide variant	NM_000730.3(CCKAR):c.796A>T (p.Ser266Cys)	not specified [RCV004430516]	uncertain significance	4	26482129	26482129	Human		name
405739762	CV3292428	single nucleotide variant	NM_000730.3(CCKAR):c.994G>A (p.Ala332Thr)	not specified [RCV004430517]	uncertain significance	4	26481931	26481931	Human		name
405739769	CV3292429	single nucleotide variant	NM_000730.3(CCKAR):c.999C>A (p.Asn333Lys)	not specified [RCV004430518]	uncertain significance	4	26481926	26481926	Human		name
405739788	CV3292432	single nucleotide variant	NM_176875.4(CCKBR):c.301C>T (p.Leu101Phe)	not specified [RCV004430521]	uncertain significance	11	6269818	6269818	Human		name
405739794	CV3292433	single nucleotide variant	NM_176875.4(CCKBR):c.406G>T (p.Val136Leu)	not specified [RCV004430522]	uncertain significance	11	6270090	6270090	Human		name
405739802	CV3292434	single nucleotide variant	NM_176875.4(CCKBR):c.449T>C (p.Leu150Pro)	not specified [RCV004430523]	uncertain significance	11	6270133	6270133	Human		name
405739809	CV3292435	single nucleotide variant	NM_176875.4(CCKBR):c.535T>G (p.Trp179Gly)	not specified [RCV004430524]	uncertain significance	11	6270219	6270219	Human		name
405739815	CV3292436	single nucleotide variant	NM_176875.4(CCKBR):c.602G>A (p.Arg201His)	not specified [RCV004430525]	uncertain significance	11	6270286	6270286	Human		name
405739822	CV3292437	single nucleotide variant	NM_176875.4(CCKBR):c.809C>T (p.Pro270Leu)	not specified [RCV004430526]	uncertain significance	11	6270801	6270801	Human		name
405739829	CV3292438	single nucleotide variant	NM_176875.4(CCKBR):c.830G>C (p.Gly277Ala)	not specified [RCV004430527]	uncertain significance	11	6271029	6271029	Human		name
405739834	CV3292439	single nucleotide variant	NM_176875.4(CCKBR):c.887A>C (p.Gln296Pro)	not specified [RCV004430528]	uncertain significance	11	6271086	6271086	Human		name
405739841	CV3292440	single nucleotide variant	NM_176875.4(CCKBR):c.902G>T (p.Arg301Leu)	not specified [RCV004430529]	uncertain significance	11	6271101	6271101	Human		name
407491444	CV3428538	single nucleotide variant	NM_000730.3(CCKAR):c.950T>C (p.Val317Ala)	not specified [RCV004604748]	uncertain significance	4	26481975	26481975	Human		name
597765612	CV3641496	single nucleotide variant	NM_000730.3(CCKAR):c.890G>A (p.Arg297Gln)	not specified [RCV004895910]	uncertain significance	4	26482035	26482035	Human		name
597765620	CV3641499	single nucleotide variant	NM_000730.3(CCKAR):c.577G>A (p.Ala193Thr)	not specified [RCV004895912]	uncertain significance	4	26485686	26485686	Human		name
597765624	CV3641500	single nucleotide variant	NM_000730.3(CCKAR):c.461C>T (p.Thr154Ile)	not specified [RCV004895913]	uncertain significance	4	26485802	26485802	Human		name
597761985	CV3641502	single nucleotide variant	NM_000730.3(CCKAR):c.937C>T (p.Arg313Cys)	not specified [RCV004895060]	uncertain significance	4	26481988	26481988	Human		name
597765630	CV3641504	single nucleotide variant	NM_000730.3(CCKAR):c.962T>C (p.Leu321Pro)	not specified [RCV004895915]	uncertain significance	4	26481963	26481963	Human		name
597765634	CV3641505	single nucleotide variant	NM_000730.3(CCKAR):c.565A>G (p.Asn189Asp)	not specified [RCV004895916]	uncertain significance	4	26485698	26485698	Human		name
597765646	CV3641508	single nucleotide variant	NM_176875.4(CCKBR):c.812G>T (p.Gly271Val)	not specified [RCV004895919]	uncertain significance	11	6271011	6271011	Human		name
597761990	CV3641509	single nucleotide variant	NM_176875.4(CCKBR):c.419T>C (p.Val140Ala)	not specified [RCV004895061]	uncertain significance	11	6270103	6270103	Human		name
597765651	CV3641510	single nucleotide variant	NM_176875.4(CCKBR):c.884T>C (p.Val295Ala)	not specified [RCV004895920]	uncertain significance	11	6271083	6271083	Human		name
597761995	CV3641511	single nucleotide variant	NM_176875.4(CCKBR):c.763A>T (p.Ser255Cys)	not specified [RCV004895062]	uncertain significance	11	6270755	6270755	Human		name
598228175	CV3939670	single nucleotide variant	NM_176875.4(CCKBR):c.551T>C (p.Leu184Pro)	not specified [RCV005319045]	uncertain significance	11	6270235	6270235	Human		name
598192729	CV3939671	single nucleotide variant	NM_176875.4(CCKBR):c.884T>G (p.Val295Gly)	not specified [RCV005312836]	uncertain significance	11	6271083	6271083	Human		name
598228162	CV3943608	single nucleotide variant	NM_000730.3(CCKAR):c.347C>A (p.Thr116Asn)	not specified [RCV005319043]	uncertain significance	4	26489250	26489250	Human		name
598192696	CV3943609	single nucleotide variant	NM_000730.3(CCKAR):c.497G>T (p.Trp166Leu)	not specified [RCV005312830]	uncertain significance	4	26485766	26485766	Human		name
598192701	CV3943610	single nucleotide variant	NM_000730.3(CCKAR):c.608A>G (p.Asp203Gly)	not specified [RCV005312831]	uncertain significance	4	26485655	26485655	Human		name
598192708	CV3943611	single nucleotide variant	NM_176875.4(CCKBR):c.397C>T (p.Leu133Phe)	not specified [RCV005312832]	likely benign	11	6269914	6269914	Human		name
598228168	CV3943612	single nucleotide variant	NM_176875.4(CCKBR):c.701T>C (p.Met234Thr)	not specified [RCV005319044]	uncertain significance	11	6270693	6270693	Human		name
156100061	CV2260225	single nucleotide variant	NM_000730.3(CCKAR):c.1099C>A (p.Pro367Thr)	not specified [RCV004129338]	uncertain significance	4	26481826	26481826	Human		name
156175130	CV2278185	single nucleotide variant	NM_176875.4(CCKBR):c.1243G>A (p.Ala415Thr)	not specified [RCV004141379]	uncertain significance	11	6271442	6271442	Human		name
156193974	CV2398142	single nucleotide variant	NM_000730.3(CCKAR):c.1021G>A (p.Ala341Thr)	not specified [RCV004241719]	uncertain significance	4	26481904	26481904	Human		name
329352297	CV2452320	single nucleotide variant	NM_000730.3(CCKAR):c.1085C>A (p.Ser362Tyr)	not specified [RCV004272654]	uncertain significance	4	26481840	26481840	Human		name
401762162	CV2722667	single nucleotide variant	NM_000730.3(CCKAR):c.1202G>A (p.Gly401Glu)	not specified [RCV004325115]	uncertain significance	4	26481723	26481723	Human		name
401860549	CV2758521	single nucleotide variant	NM_000730.3(CCKAR):c.1034G>A (p.Arg345His)	not specified [RCV004335568]	uncertain significance	4	26481891	26481891	Human		name
401870674	CV2792470	single nucleotide variant	NM_176875.4(CCKBR):c.1225T>C (p.Cys409Arg)	not specified [RCV004363212]	uncertain significance	11	6271424	6271424	Human		name
8566274	CV32569	single nucleotide variant	NM_000730.3(CCKAR):c.1093G>A (p.Val365Ile)	CHOLECYSTOKININ A RECEPTOR POLYMORPHISM [RCV000019082]\|not provided [RCV004715646]	benign	4	26481832	26481832	Human	4	name
8566274	CV32569	single nucleotide variant	NM_000730.3(CCKAR):c.1093G>A (p.Val365Ile)	CHOLECYSTOKININ A RECEPTOR POLYMORPHISM [RCV000019082]\|not provided [RCV004715646]	benign	4	26481832	26481833	Human	4	name
405739723	CV3292422	single nucleotide variant	NM_000730.3(CCKAR):c.1262T>A (p.Met421Lys)	not specified [RCV004430511]	uncertain significance	4	26481663	26481663	Human		name
405739776	CV3292430	single nucleotide variant	NM_176875.4(CCKBR):c.1319C>T (p.Thr440Ile)	not specified [RCV004430519]	uncertain significance	11	6271518	6271518	Human		name
407491453	CV3428540	single nucleotide variant	NM_176875.4(CCKBR):c.1324A>G (p.Ser442Gly)	not specified [RCV004604750]	uncertain significance	11	6271523	6271523	Human		name
597765608	CV3641495	single nucleotide variant	NM_000730.3(CCKAR):c.1249T>C (p.Ser417Pro)	not specified [RCV004895909]	uncertain significance	4	26481676	26481676	Human		name
597765616	CV3641498	single nucleotide variant	NM_000730.3(CCKAR):c.1204G>C (p.Glu402Gln)	not specified [RCV004895911]	uncertain significance	4	26481721	26481721	Human		name
597761979	CV3641501	single nucleotide variant	NM_000730.3(CCKAR):c.1163G>T (p.Cys388Phe)	not specified [RCV004895059]	uncertain significance	4	26481762	26481762	Human		name
597765627	CV3641503	single nucleotide variant	NM_000730.3(CCKAR):c.1117A>C (p.Met373Leu)	not specified [RCV004895914]	uncertain significance	4	26481808	26481808	Human		name
597765638	CV3641506	single nucleotide variant	NM_176875.4(CCKBR):c.1184G>C (p.Arg395Pro)	not specified [RCV004895917]	uncertain significance	11	6271383	6271383	Human		name
597765655	CV3641512	single nucleotide variant	NM_176875.4(CCKBR):c.1273C>T (p.Pro425Ser)	not specified [RCV004895921]	uncertain significance	11	6271472	6271472	Human		name
597765658	CV3641513	single nucleotide variant	NM_176875.4(CCKBR):c.1280C>G (p.Thr427Ser)	not specified [RCV004895922]	uncertain significance	11	6271479	6271479	Human		name
598192689	CV3943607	single nucleotide variant	NM_000730.3(CCKAR):c.1006C>T (p.Arg336Trp)	not specified [RCV005312829]	uncertain significance	4	26481919	26481919	Human		name
598192713	CV3943613	single nucleotide variant	NM_176875.4(CCKBR):c.1223G>A (p.Cys408Tyr)	not specified [RCV005312833]	uncertain significance	11	6271422	6271422	Human		name
598192723	CV3943615	single nucleotide variant	NM_176875.4(CCKBR):c.1274C>T (p.Pro425Leu)	not specified [RCV005312835]	uncertain significance	11	6271473	6271473	Human		name

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