Adcy4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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98 records found for search term Adcy4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15191323	CV778281	single nucleotide variant	NM_001198568.2(ADCY4):c.3082-4G>T	not provided [RCV000954741]	benign	14	24318572	24318572	Human		name
407463778	CV3419911	single nucleotide variant	NM_001198568.2(ADCY4):c.32C>A (p.Pro11His)	not specified [RCV004613280]	uncertain significance	14	24334621	24334621	Human		name
407463862	CV3419932	single nucleotide variant	NM_001198568.2(ADCY4):c.59A>G (p.Tyr20Cys)	not specified [RCV004613301]	uncertain significance	14	24334594	24334594	Human		name
598230543	CV3948024	single nucleotide variant	NM_001198568.2(ADCY4):c.35G>T (p.Ser12Ile)	not specified [RCV005319411]	uncertain significance	14	24334618	24334618	Human		name
156203828	CV2300767	single nucleotide variant	NM_001198568.2(ADCY4):c.167C>G (p.Thr56Ser)	not specified [RCV004155698]	uncertain significance	14	24332981	24332981	Human		name
401910362	CV2810320	single nucleotide variant	NM_001198568.2(ADCY4):c.2275C>T (p.Leu759=)	not provided [RCV003424994]	likely benign	14	24322971	24322971	Human		name
401910363	CV2810321	single nucleotide variant	NM_001198568.2(ADCY4):c.1524G>A (p.Pro508=)	not provided [RCV003424995]	likely benign	14	24329061	24329061	Human		name
401910364	CV2810322	single nucleotide variant	NM_001198568.2(ADCY4):c.1404G>A (p.Glu468=)	not provided [RCV003424996]	likely benign	14	24329181	24329181	Human		name
401910365	CV2810323	single nucleotide variant	NM_001198568.2(ADCY4):c.1137C>T (p.Ile379=)	not provided [RCV003424997]	likely benign	14	24329940	24329940	Human		name
597771687	CV3650719	single nucleotide variant	NM_001198568.2(ADCY4):c.143C>G (p.Ala48Gly)	not specified [RCV004897184]	uncertain significance	14	24334510	24334510	Human		name
155958904	CV2197570	single nucleotide variant	NM_001198568.2(ADCY4):c.737G>A (p.Arg246Gln)	not specified [RCV004081290]	uncertain significance	14	24331289	24331289	Human		name
155970429	CV2241400	single nucleotide variant	NM_001198568.2(ADCY4):c.856G>C (p.Ala286Pro)	not specified [RCV004102530]	uncertain significance	14	24331092	24331092	Human		name
155989571	CV2282791	single nucleotide variant	NM_001198568.2(ADCY4):c.947G>A (p.Arg316Gln)	not specified [RCV004141643]	uncertain significance	14	24330279	24330279	Human		name
156239648	CV2285985	single nucleotide variant	NM_001198568.2(ADCY4):c.410G>T (p.Gly137Val)	not specified [RCV004143897]	uncertain significance	14	24332631	24332631	Human		name
156067770	CV2317945	single nucleotide variant	NM_001198568.2(ADCY4):c.599G>C (p.Arg200Pro)	not specified [RCV004177068]	uncertain significance	14	24331858	24331858	Human		name
156081022	CV2337629	single nucleotide variant	NM_001198568.2(ADCY4):c.754G>A (p.Gly252Arg)	not specified [RCV004181192]	uncertain significance	14	24331272	24331272	Human		name
329379912	CV2456555	single nucleotide variant	NM_001198568.2(ADCY4):c.490C>A (p.Pro164Thr)	not specified [RCV004277481]	uncertain significance	14	24332551	24332551	Human		name
329392221	CV2470489	single nucleotide variant	NM_001198568.2(ADCY4):c.547T>C (p.Cys183Arg)	not specified [RCV004273509]	uncertain significance	14	24331910	24331910	Human		name
401736965	CV2699637	single nucleotide variant	NM_001198568.2(ADCY4):c.916G>C (p.Asp306His)	not specified [RCV004299820]	uncertain significance	14	24331032	24331032	Human		name
401749658	CV2719357	single nucleotide variant	NM_001198568.2(ADCY4):c.886C>T (p.Leu296Phe)	not specified [RCV004324987]	uncertain significance	14	24331062	24331062	Human		name
401879987	CV2783056	single nucleotide variant	NM_001198568.2(ADCY4):c.896A>G (p.Asn299Ser)	not specified [RCV004363424]	uncertain significance	14	24331052	24331052	Human		name
405680793	CV3237147	single nucleotide variant	NM_001198568.2(ADCY4):c.472C>G (p.Leu158Val)	not specified [RCV004371107]	uncertain significance	14	24332569	24332569	Human		name
405681207	CV3237150	single nucleotide variant	NM_001198568.2(ADCY4):c.589C>T (p.Arg197Cys)	not specified [RCV004371110]	uncertain significance	14	24331868	24331868	Human		name
405680848	CV3237159	single nucleotide variant	NM_001198568.2(ADCY4):c.721G>T (p.Ala241Ser)	not specified [RCV004371119]	uncertain significance	14	24331305	24331305	Human		name
405680875	CV3237165	single nucleotide variant	NM_001198568.2(ADCY4):c.732G>A (p.Met244Ile)	not specified [RCV004371125]	uncertain significance	14	24331294	24331294	Human		name
405680905	CV3237171	single nucleotide variant	NM_001198568.2(ADCY4):c.736C>T (p.Arg246Trp)	not specified [RCV004371131]	uncertain significance	14	24331290	24331290	Human		name
407463748	CV3419903	single nucleotide variant	NM_001198568.2(ADCY4):c.469G>A (p.Gly157Arg)	not specified [RCV004613272]	uncertain significance	14	24332572	24332572	Human		name
597771659	CV3650693	single nucleotide variant	NM_001198568.2(ADCY4):c.376G>C (p.Val126Leu)	not specified [RCV004897178]	uncertain significance	14	24332665	24332665	Human		name
598229978	CV3951871	single nucleotide variant	NM_001198568.2(ADCY4):c.491C>T (p.Pro164Leu)	not specified [RCV005319320]	uncertain significance	14	24332550	24332550	Human		name
156253922	CV2209602	single nucleotide variant	NM_001198568.2(ADCY4):c.1730G>A (p.Arg577Gln)	not specified [RCV004093699]	uncertain significance	14	24325470	24325470	Human		name
156226960	CV2216085	single nucleotide variant	NM_001198568.2(ADCY4):c.2576G>A (p.Arg859Gln)	not specified [RCV004097104]	uncertain significance	14	24322076	24322076	Human		name
156271081	CV2237104	single nucleotide variant	NM_001198568.2(ADCY4):c.1304A>G (p.Tyr435Cys)	not specified [RCV004114861]	uncertain significance	14	24329447	24329447	Human		name
156154557	CV2242317	single nucleotide variant	NM_001198568.2(ADCY4):c.2614G>A (p.Val872Ile)	not specified [RCV004111332]	uncertain significance	14	24319861	24319861	Human		name
156317554	CV2251061	single nucleotide variant	NM_001198568.2(ADCY4):c.2297C>T (p.Ser766Leu)	not specified [RCV004123612]	uncertain significance	14	24322949	24322949	Human		name
155998858	CV2296131	single nucleotide variant	NM_001198568.2(ADCY4):c.2684G>A (p.Gly895Asp)	not specified [RCV004154061]	uncertain significance	14	24319791	24319791	Human		name
156007578	CV2299741	single nucleotide variant	NM_001198568.2(ADCY4):c.1829C>T (p.Pro610Leu)	not specified [RCV004148902]	uncertain significance	14	24324386	24324386	Human		name
156346518	CV2300599	single nucleotide variant	NM_001198568.2(ADCY4):c.2876T>C (p.Met959Thr)	not specified [RCV004155558]	uncertain significance	14	24319178	24319178	Human		name
156065223	CV2316332	single nucleotide variant	NM_001198568.2(ADCY4):c.2108C>T (p.Ser703Phe)	not specified [RCV004174345]	likely benign	14	24323393	24323393	Human		name
156081934	CV2333424	single nucleotide variant	NM_001198568.2(ADCY4):c.1583G>A (p.Arg528Gln)	not specified [RCV004190130]	uncertain significance	14	24326151	24326151	Human		name
156072915	CV2365419	single nucleotide variant	NM_001198568.2(ADCY4):c.1028G>A (p.Arg343His)	not specified [RCV004209498]	uncertain significance	14	24330198	24330198	Human		name
155929265	CV2369697	single nucleotide variant	NM_001198568.2(ADCY4):c.1507A>C (p.Thr503Pro)	not specified [RCV004215097]	uncertain significance	14	24329078	24329078	Human		name
156161154	CV2398245	single nucleotide variant	NM_001198568.2(ADCY4):c.2119T>C (p.Trp707Arg)	not specified [RCV004235158]	uncertain significance	14	24323382	24323382	Human		name
329366925	CV2441980	single nucleotide variant	NM_001198568.2(ADCY4):c.1403A>G (p.Glu468Gly)	not specified [RCV004262152]	uncertain significance	14	24329182	24329182	Human		name
329378184	CV2446886	single nucleotide variant	NM_001198568.2(ADCY4):c.2099C>G (p.Ser700Cys)	not specified [RCV004257736]	uncertain significance	14	24323402	24323402	Human		name
401719685	CV2675658	single nucleotide variant	NM_001198568.2(ADCY4):c.1567C>T (p.Arg523Trp)	not specified [RCV004287911]	uncertain significance	14	24326300	24326300	Human		name
401770389	CV2678652	single nucleotide variant	NM_001198568.2(ADCY4):c.2045T>C (p.Leu682Pro)	not specified [RCV004294693]	uncertain significance	14	24324063	24324063	Human		name
401752770	CV2682931	single nucleotide variant	NM_001198568.2(ADCY4):c.2967T>A (p.His989Gln)	not specified [RCV004283725]	uncertain significance	14	24318768	24318768	Human		name
401730306	CV2711192	single nucleotide variant	NM_001198568.2(ADCY4):c.1510T>C (p.Ser504Pro)	not specified [RCV004312988]	uncertain significance	14	24329075	24329075	Human		name
401776893	CV2721515	single nucleotide variant	NM_001198568.2(ADCY4):c.1096C>T (p.Arg366Cys)	not specified [RCV004316031]	uncertain significance	14	24329981	24329981	Human		name
401884388	CV2761247	single nucleotide variant	NM_001198568.2(ADCY4):c.2638C>T (p.Pro880Ser)	not specified [RCV004341124]	uncertain significance	14	24319837	24319837	Human		name
401856787	CV2761787	single nucleotide variant	NM_001198568.2(ADCY4):c.1609G>A (p.Gly537Arg)	not specified [RCV004339438]	uncertain significance	14	24326125	24326125	Human		name
401876767	CV2783009	single nucleotide variant	NM_001198568.2(ADCY4):c.2710G>A (p.Glu904Lys)	not specified [RCV004361797]	uncertain significance	14	24319765	24319765	Human		name
401896622	CV2791793	single nucleotide variant	NM_001198568.2(ADCY4):c.2863C>A (p.His955Asn)	not specified [RCV004353111]	uncertain significance	14	24319191	24319191	Human		name
401882183	CV2793396	single nucleotide variant	NM_001198568.2(ADCY4):c.1713G>C (p.Glu571Asp)	not specified [RCV004362495]	uncertain significance	14	24325830	24325830	Human		name
405680321	CV3237031	single nucleotide variant	NM_001198568.2(ADCY4):c.1049G>A (p.Arg350Gln)	not specified [RCV004370991]	uncertain significance	14	24330177	24330177	Human		name
405680388	CV3237044	single nucleotide variant	NM_001198568.2(ADCY4):c.1292A>T (p.His431Leu)	not specified [RCV004371004]	uncertain significance	14	24329459	24329459	Human		name
405680531	CV3237073	single nucleotide variant	NM_001198568.2(ADCY4):c.1976G>A (p.Arg659Gln)	not specified [RCV004371033]	uncertain significance	14	24324132	24324132	Human		name
405680556	CV3237078	single nucleotide variant	NM_001198568.2(ADCY4):c.2000G>A (p.Gly667Asp)	not specified [RCV004371038]	uncertain significance	14	24324108	24324108	Human		name
405681170	CV3237087	single nucleotide variant	NM_001198568.2(ADCY4):c.2084C>T (p.Ala695Val)	not specified [RCV004371047]	uncertain significance	14	24323417	24323417	Human		name
405680805	CV3237104	single nucleotide variant	NM_001198568.2(ADCY4):c.2423G>A (p.Arg808His)	not specified [RCV004371064]	uncertain significance	14	24322628	24322628	Human		name
405680634	CV3237117	single nucleotide variant	NM_001198568.2(ADCY4):c.2660C>T (p.Ser887Phe)	not specified [RCV004371077]	uncertain significance	14	24319815	24319815	Human		name
405680698	CV3237129	single nucleotide variant	NM_001198568.2(ADCY4):c.2825G>A (p.Gly942Glu)	not specified [RCV004371089]	uncertain significance	14	24319345	24319345	Human		name
405680708	CV3237131	single nucleotide variant	NM_001198568.2(ADCY4):c.2860A>G (p.Ser954Gly)	not specified [RCV004371091]	uncertain significance	14	24319194	24319194	Human		name
407457676	CV3419850	single nucleotide variant	NM_001198568.2(ADCY4):c.2210A>G (p.His737Arg)	not specified [RCV004611244]	uncertain significance	14	24323036	24323036	Human		name
407457715	CV3419867	single nucleotide variant	NM_001198568.2(ADCY4):c.1216G>C (p.Gly406Arg)	not specified [RCV004611261]	uncertain significance	14	24329861	24329861	Human		name
407457735	CV3419877	single nucleotide variant	NM_001198568.2(ADCY4):c.2498C>T (p.Thr833Met)	not specified [RCV004611271]	uncertain significance	14	24322154	24322154	Human		name
407463682	CV3419887	single nucleotide variant	NM_001198568.2(ADCY4):c.2551G>A (p.Ala851Thr)	not specified [RCV004613256]	uncertain significance	14	24322101	24322101	Human		name
407463719	CV3419896	single nucleotide variant	NM_001198568.2(ADCY4):c.2834C>T (p.Ala945Val)	not specified [RCV004613265]	uncertain significance	14	24319336	24319336	Human		name
407463819	CV3419922	single nucleotide variant	NM_001198568.2(ADCY4):c.2134T>C (p.Ser712Pro)	not specified [RCV004613291]	uncertain significance	14	24323367	24323367	Human		name
597799297	CV3650642	single nucleotide variant	NM_001198568.2(ADCY4):c.1294C>T (p.Arg432Trp)	not specified [RCV004905136]	uncertain significance	14	24329457	24329457	Human		name
597799334	CV3650660	single nucleotide variant	NM_001198568.2(ADCY4):c.1582C>T (p.Arg528Trp)	not specified [RCV004905154]	uncertain significance	14	24326152	24326152	Human		name
597771555	CV3650670	single nucleotide variant	NM_001198568.2(ADCY4):c.1310G>A (p.Arg437Gln)	not specified [RCV004897156]	uncertain significance	14	24329441	24329441	Human		name
597771607	CV3650681	single nucleotide variant	NM_001198568.2(ADCY4):c.1342G>A (p.Asp448Asn)	not specified [RCV004897167]	uncertain significance	14	24329409	24329409	Human		name
597771662	CV3650699	single nucleotide variant	NM_001198568.2(ADCY4):c.2861G>A (p.Ser954Asn)	not specified [RCV004897179]	uncertain significance	14	24319193	24319193	Human		name
597771667	CV3650705	single nucleotide variant	NM_001198568.2(ADCY4):c.1913G>A (p.Cys638Tyr)	not specified [RCV004897180]	uncertain significance	14	24324195	24324195	Human		name
597771672	CV3650709	single nucleotide variant	NM_001198568.2(ADCY4):c.1810C>A (p.Leu604Ile)	not specified [RCV004897181]	uncertain significance	14	24325390	24325390	Human		name
597771729	CV3650728	single nucleotide variant	NM_001198568.2(ADCY4):c.1684C>T (p.Pro562Ser)	not specified [RCV004897193]	uncertain significance	14	24325859	24325859	Human		name
597771779	CV3650739	single nucleotide variant	NM_001198568.2(ADCY4):c.1723G>A (p.Glu575Lys)	not specified [RCV004897204]	uncertain significance	14	24325820	24325820	Human		name
597771828	CV3650750	single nucleotide variant	NM_001198568.2(ADCY4):c.2014C>T (p.Leu672Phe)	not specified [RCV004897215]	uncertain significance	14	24324094	24324094	Human		name
597771874	CV3650760	single nucleotide variant	NM_001198568.2(ADCY4):c.1489G>A (p.Gly497Arg)	not specified [RCV004897225]	uncertain significance	14	24329096	24329096	Human		name
598230419	CV3948005	single nucleotide variant	NM_001198568.2(ADCY4):c.2603C>T (p.Ser868Phe)	not specified [RCV005319392]	uncertain significance	14	24319872	24319872	Human		name
598230590	CV3948033	single nucleotide variant	NM_001198568.2(ADCY4):c.2884T>A (p.Phe962Ile)	not specified [RCV005319420]	uncertain significance	14	24319170	24319170	Human		name
598230634	CV3948042	single nucleotide variant	NM_001198568.2(ADCY4):c.1194C>G (p.His398Gln)	not specified [RCV005319429]	uncertain significance	14	24329883	24329883	Human		name
598230685	CV3948052	single nucleotide variant	NM_001198568.2(ADCY4):c.1262C>T (p.Ala421Val)	not specified [RCV005319439]	uncertain significance	14	24329489	24329489	Human		name
598215808	CV3951846	single nucleotide variant	NM_001198568.2(ADCY4):c.2474G>A (p.Arg825Lys)	not specified [RCV005316823]	uncertain significance	14	24322178	24322178	Human		name
598229908	CV3951856	single nucleotide variant	NM_001198568.2(ADCY4):c.2312T>A (p.Val771Asp)	not specified [RCV005319307]	uncertain significance	14	24322934	24322934	Human		name
598229955	CV3951865	single nucleotide variant	NM_001198568.2(ADCY4):c.1760A>G (p.Tyr587Cys)	not specified [RCV005319315]	uncertain significance	14	24325440	24325440	Human		name
598230029	CV3951882	single nucleotide variant	NM_001198568.2(ADCY4):c.1162G>A (p.Val388Ile)	not specified [RCV005319331]	uncertain significance	14	24329915	24329915	Human		name
598230179	CV3951908	single nucleotide variant	NM_001198568.2(ADCY4):c.1391T>C (p.Leu464Pro)	not specified [RCV005319353]	uncertain significance	14	24329194	24329194	Human		name
598230242	CV3951919	single nucleotide variant	NM_001198568.2(ADCY4):c.1991T>C (p.Ile664Thr)	not specified [RCV005319363]	uncertain significance	14	24324117	24324117	Human		name
598230352	CV3951938	single nucleotide variant	NM_001198568.2(ADCY4):c.1537G>C (p.Ala513Pro)	not specified [RCV005319382]	uncertain significance	14	24326330	24326330	Human		name
155986434	CV2247976	single nucleotide variant	NM_001198568.2(ADCY4):c.3211C>T (p.Pro1071Ser)	not specified [RCV004121404]	uncertain significance	14	24318439	24318439	Human		name
156064074	CV2287055	single nucleotide variant	NM_001198568.2(ADCY4):c.3135C>A (p.Ser1045Arg)	not specified [RCV004144935]	uncertain significance	14	24318515	24318515	Human		name
155959127	CV2313875	single nucleotide variant	NM_001198568.2(ADCY4):c.3094A>G (p.Thr1032Ala)	not specified [RCV004164192]	uncertain significance	14	24318556	24318556	Human		name
407457700	CV3419860	single nucleotide variant	NM_001198568.2(ADCY4):c.3124A>C (p.Thr1042Pro)	not specified [RCV004611254]	uncertain significance	14	24318526	24318526	Human		name
597799317	CV3650652	single nucleotide variant	NM_001198568.2(ADCY4):c.3212C>T (p.Pro1071Leu)	not specified [RCV004905146]	uncertain significance	14	24318438	24318438	Human		name
598230493	CV3948016	single nucleotide variant	NM_001198568.2(ADCY4):c.3054G>C (p.Glu1018Asp)	not specified [RCV005319403]	uncertain significance	14	24318681	24318681	Human		name
598230295	CV3951929	single nucleotide variant	NM_001198568.2(ADCY4):c.3092A>C (p.Glu1031Ala)	not specified [RCV005319373]	uncertain significance	14	24318558	24318558	Human		name

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