Adcy10 Variant Search Result - Rat Genome Database

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580 records found for search term Adcy10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8558517	CV20217	single nucleotide variant	ADCY10, 923C-T	Familial idiopathic hypercalciuria [RCV001844008]	risk factor				Human		name
8558518	CV20218	single nucleotide variant	ADCY10, 1438+30T-C	Familial idiopathic hypercalciuria [RCV001844009]	risk factor				Human	1	name
150494141	CV1238808	single nucleotide variant	NM_018417.6(ADCY10):c.*72C>T	not provided [RCV001655352]	benign	1	167809606	167809606	Human		name
150456795	CV1219534	single nucleotide variant	NM_018417.6(ADCY10):c.*210T>G	not provided [RCV001612749]	benign	1	167809468	167809468	Human		name
126917202	CV1039594	single nucleotide variant	NM_018417.6(ADCY10):c.253+4A>G	Familial idiopathic hypercalciuria [RCV002504591]\|not provided [RCV001361027]	uncertain significance	1	167903883	167903883	Human	1	name
150485799	CV1262169	single nucleotide variant	NM_018417.6(ADCY10):c.254-273=	not provided [RCV001686860]	benign	1	167902327	167902327	Human		name
152087682	CV1594740	single nucleotide variant	NM_018417.6(ADCY10):c.643-8T>G	not provided [RCV002113631]	likely benign	1	167896699	167896699	Human		name
156274621	CV1957344	single nucleotide variant	NM_018417.6(ADCY10):c.437-8C>G	not provided [RCV002577280]	likely benign	1	167899636	167899636	Human		name
156336879	CV2057817	single nucleotide variant	NM_018417.6(ADCY10):c.253+1G>A	not provided [RCV002810988]	likely pathogenic	1	167903886	167903886	Human		name
405209813	CV3117377	single nucleotide variant	NM_018417.6(ADCY10):c.292+6G>A	not provided [RCV003823164]	uncertain significance	1	167902010	167902010	Human		name
597888812	CV3739310	single nucleotide variant	NM_018417.6(ADCY10):c.829-4G>C	not provided [RCV005070857]	likely benign	1	167883632	167883632	Human		name
15164007	CV777013	deletion	NM_018417.6(ADCY10):c.254-6del	Familial idiopathic hypercalciuria [RCV002489295]\|not provided [RCV000948232]	benign	1	167902060	167902060	Human	1	name
127245242	CV1054755	single nucleotide variant	NM_018417.6(ADCY10):c.4168+1G>A	not provided [RCV001377382]	likely pathogenic	1	167823007	167823007	Human		name
127323349	CV1130578	single nucleotide variant	NM_018417.6(ADCY10):c.740-10G>C	not provided [RCV001485207]	likely benign	1	167893951	167893951	Human		name
127326030	CV1130579	single nucleotide variant	NM_018417.6(ADCY10):c.292+18G>A	not provided [RCV001506153]	likely benign	1	167901998	167901998	Human		name
150494152	CV1238810	single nucleotide variant	NM_018417.6(ADCY10):c.739+93C>T	not provided [RCV001655354]	benign	1	167896502	167896502	Human		name
150450914	CV1254168	deletion	NM_018417.6(ADCY10):c.149-92del	not provided [RCV001667806]	benign	1	167904083	167904083	Human		name
150479196	CV1273426	single nucleotide variant	NM_018417.6(ADCY10):c.436+95G>A	not provided [RCV001696630]	benign	1	167901567	167901567	Human		name
150545279	CV1307703	duplication	NM_018417.6(ADCY10):c.828+82dup	not provided [RCV001774981]	likely benign	1	167893770	167893771	Human		name
150532891	CV1308175	single nucleotide variant	NM_018417.6(ADCY10):c.292+79G>A	not provided [RCV001753166]	likely benign	1	167901937	167901937	Human		name
150532931	CV1308196	single nucleotide variant	NM_018417.6(ADCY10):c.293-70T>C	not provided [RCV001753187]	likely benign	1	167901875	167901875	Human		name
151233073	CV1316969	single nucleotide variant	NM_018417.6(ADCY10):c.149-60C>A	not provided [RCV001786789]	likely benign	1	167904051	167904051	Human		name
152053398	CV1619399	duplication	NM_018417.6(ADCY10):c.4483-7dup	ADCY10-related disorder [RCV004756348]\|not provided [RCV002167150]	benign\|likely benign	1	167810919	167810920	Human	1	name , trait , alternate_id
152126042	CV1641887	single nucleotide variant	NM_018417.6(ADCY10):c.254-20A>T	not provided [RCV002176192]	likely benign	1	167902074	167902074	Human		name
156197124	CV1912384	single nucleotide variant	NM_018417.6(ADCY10):c.3078-9T>C	not provided [RCV002595572]	likely benign	1	167836549	167836549	Human		name
156168423	CV1960017	single nucleotide variant	NM_018417.6(ADCY10):c.829-15C>T	not provided [RCV002573738]	benign	1	167883643	167883643	Human		name
156327302	CV1980720	single nucleotide variant	NM_018417.6(ADCY10):c.3078-3C>T	not provided [RCV002630725]	uncertain significance	1	167836543	167836543	Human		name
156141440	CV2002767	single nucleotide variant	NM_018417.6(ADCY10):c.739+18A>G	not provided [RCV002663582]	likely benign	1	167896577	167896577	Human		name
401933138	CV2806138	single nucleotide variant	NM_018417.6(ADCY10):c.1021-8C>T	not provided [RCV003409224]	likely benign	1	167880617	167880617	Human		name
402478372	CV2854549	single nucleotide variant	NM_018417.6(ADCY10):c.253+13A>G	not provided [RCV003543739]	likely benign	1	167903874	167903874	Human		name
405197297	CV2869826	single nucleotide variant	NM_018417.6(ADCY10):c.4052+2T>C	not provided [RCV003550982]	likely pathogenic	1	167824474	167824474	Human		name
405226846	CV2888861	single nucleotide variant	NM_018417.6(ADCY10):c.1896+5G>C	not provided [RCV003554812]	uncertain significance	1	167859802	167859802	Human		name
402490782	CV2949041	single nucleotide variant	NM_018417.6(ADCY10):c.149-11A>G	not provided [RCV003660524]	likely benign	1	167904002	167904002	Human		name
405186892	CV2964005	single nucleotide variant	NM_018417.6(ADCY10):c.3007+7T>C	not provided [RCV003676778]	likely benign	1	167845556	167845556	Human		name
402480591	CV3041477	single nucleotide variant	NM_018417.6(ADCY10):c.1617-6A>C	not provided [RCV003712802]	likely benign	1	167861069	167861069	Human		name
405152635	CV3063833	single nucleotide variant	NM_018417.6(ADCY10):c.3007+2T>C	not provided [RCV003726474]	likely pathogenic	1	167845561	167845561	Human		name
405162492	CV3125189	deletion	NM_018417.6(ADCY10):c.4483-7del	not provided [RCV003818461]	benign	1	167810920	167810920	Human		name
405225555	CV3142382	single nucleotide variant	NM_018417.6(ADCY10):c.3750+1G>A	not provided [RCV003847921]	likely pathogenic	1	167829266	167829266	Human		name
405292715	CV3193003	single nucleotide variant	NM_018417.6(ADCY10):c.1810-9T>G	ADCY10-related disorder [RCV003964663]	likely benign	1	167859902	167859902	Human		name , trait , alternate_id
405279321	CV3217411	single nucleotide variant	NM_018417.6(ADCY10):c.293-20C>T	ADCY10-related disorder [RCV003976834]	likely benign	1	167901825	167901825	Human		name , trait , alternate_id
597903177	CV3741565	single nucleotide variant	NM_018417.6(ADCY10):c.148+17T>C	not provided [RCV005072536]	likely benign	1	167904976	167904976	Human		name
597940775	CV3836771	single nucleotide variant	NM_018417.6(ADCY10):c.437-10T>C	not provided [RCV005187791]	likely benign	1	167899638	167899638	Human		name
597924946	CV3840485	single nucleotide variant	NM_018417.6(ADCY10):c.3593+2T>C	not provided [RCV005184956]	likely pathogenic	1	167832985	167832985	Human		name
597925881	CV3840611	single nucleotide variant	NM_018417.6(ADCY10):c.3593+6G>A	not provided [RCV005185082]	uncertain significance	1	167832981	167832981	Human		name
597965415	CV3848350	single nucleotide variant	NM_018417.6(ADCY10):c.2171+1G>A	not provided [RCV005194230]	likely pathogenic	1	167856164	167856164	Human		name
15098245	CV777010	single nucleotide variant	NM_018417.6(ADCY10):c.4482+3G>A	not provided [RCV000958511]	benign	1	167818069	167818069	Human		name
15155591	CV777031	duplication	NM_018417.6(ADCY10):c.254-19dup	Familial idiopathic hypercalciuria [RCV002488027]\|not provided [RCV000946522]	benign\|likely benign	1	167902059	167902060	Human	1	name
15169613	CV778734	single nucleotide variant	NM_018417.6(ADCY10):c.3750+8A>T	not provided [RCV000971846]	benign	1	167829259	167829259	Human		name
38481933	CV940606	single nucleotide variant	NM_018417.6(ADCY10):c.1139+6T>G	Familial idiopathic hypercalciuria [RCV002497743]\|not provided [RCV001218234]	uncertain significance	1	167880485	167880485	Human	1	name
127268432	CV1088155	single nucleotide variant	NM_018417.6(ADCY10):c.1616+13G>A	not provided [RCV001429943]	likely benign	1	167870244	167870244	Human		name
127316723	CV1153346	single nucleotide variant	NM_018417.6(ADCY10):c.2438-13C>T	not provided [RCV001520656]	benign	1	167846276	167846276	Human		name
127313665	CV1153355	single nucleotide variant	NM_018417.6(ADCY10):c.1020+20T>A	Familial idiopathic hypercalciuria [RCV002501820]\|not provided [RCV001519322]	benign\|likely benign	1	167883417	167883417	Human	1	name
150335825	CV1164849	single nucleotide variant	NM_018417.6(ADCY10):c.2716+56A>G	not provided [RCV001530569]	benign	1	167845929	167845929	Human		name
150335657	CV1170621	single nucleotide variant	NM_018417.6(ADCY10):c.436+171A>G	not provided [RCV001540658]	benign	1	167901491	167901491	Human		name
150514258	CV1210940	single nucleotide variant	NM_018417.6(ADCY10):c.3078-87G>A	not provided [RCV001598983]	benign	1	167836627	167836627	Human		name
150440527	CV1220173	single nucleotide variant	NM_018417.6(ADCY10):c.149-127A>G	not provided [RCV001610156]	benign	1	167904118	167904118	Human		name
150438660	CV1221193	single nucleotide variant	NM_018417.6(ADCY10):c.2308+86C>T	not provided [RCV001609887]	benign	1	167854267	167854267	Human		name
150504320	CV1223926	deletion	NM_018417.6(ADCY10):c.828+157del	not provided [RCV001621575]	benign	1	167893696	167893696	Human		name
150506314	CV1226316	single nucleotide variant	NM_018417.6(ADCY10):c.4482+45G>A	not provided [RCV001635684]	benign	1	167818027	167818027	Human		name
150515689	CV1227637	single nucleotide variant	NM_018417.6(ADCY10):c.1897-41G>A	not provided [RCV001638911]	benign	1	167856480	167856480	Human		name
150454938	CV1232367	single nucleotide variant	NM_018417.6(ADCY10):c.3751-37C>T	not provided [RCV001648381]	benign	1	167824892	167824892	Human		name
150442726	CV1233747	single nucleotide variant	NM_018417.6(ADCY10):c.1406+36G>A	not provided [RCV001645435]	benign	1	167878410	167878410	Human		name
150498475	CV1235572	single nucleotide variant	NM_018417.6(ADCY10):c.1216+26C>T	not provided [RCV001656255]	benign	1	167880089	167880089	Human		name
150438595	CV1238044	single nucleotide variant	NM_018417.6(ADCY10):c.2308+79A>G	not provided [RCV001644542]	benign	1	167854274	167854274	Human		name
150494522	CV1238880	single nucleotide variant	NM_018417.6(ADCY10):c.1139+28C>T	not provided [RCV001655424]	benign	1	167880463	167880463	Human		name
150476726	CV1239924	single nucleotide variant	NM_018417.6(ADCY10):c.4671+97T>G	not provided [RCV001652102]	benign	1	167810628	167810628	Human		name
150502961	CV1241690	single nucleotide variant	NM_018417.6(ADCY10):c.1216+35T>C	not provided [RCV001657281]	benign	1	167880080	167880080	Human		name
150430352	CV1242945	single nucleotide variant	NM_018417.6(ADCY10):c.3008-91A>T	not provided [RCV001662878]	benign	1	167837409	167837409	Human		name
150477091	CV1251962	single nucleotide variant	NM_018417.6(ADCY10):c.149-338C>T	not provided [RCV001672161]	benign	1	167904329	167904329	Human		name
150499700	CV1254402	single nucleotide variant	NM_018417.6(ADCY10):c.3007+68A>C	not provided [RCV001676576]	benign	1	167845495	167845495	Human		name
150449380	CV1260814	single nucleotide variant	NM_018417.6(ADCY10):c.253+243C>G	not provided [RCV001680483]	benign	1	167903644	167903644	Human		name
150447449	CV1261820	single nucleotide variant	NM_018417.6(ADCY10):c.1217-82T>C	not provided [RCV001680204]	benign	1	167878717	167878717	Human		name
150448011	CV1261905	single nucleotide variant	NM_018417.6(ADCY10):c.1406+74C>T	not provided [RCV001680290]	benign	1	167878372	167878372	Human		name
150460585	CV1264195	single nucleotide variant	NM_018417.6(ADCY10):c.1616+75T>C	not provided [RCV001682111]	benign	1	167870182	167870182	Human		name
150443951	CV1264663	single nucleotide variant	NM_018417.6(ADCY10):c.3078-35A>G	not provided [RCV001679647]	benign	1	167836575	167836575	Human		name
150439150	CV1264930	single nucleotide variant	NM_018417.6(ADCY10):c.148+229C>G	not provided [RCV001678923]	benign	1	167904764	167904764	Human		name
150443225	CV1266364	single nucleotide variant	NM_018417.6(ADCY10):c.1463-31G>A	not provided [RCV001690800]	benign	1	167870441	167870441	Human		name
150448197	CV1270427	single nucleotide variant	NM_018417.6(ADCY10):c.3310-34A>T	not provided [RCV001691564]	benign	1	167834111	167834111	Human		name
150464464	CV1276397	single nucleotide variant	NM_018417.6(ADCY10):c.3008-86G>C	not provided [RCV001710342]	benign	1	167837404	167837404	Human		name
150490226	CV1279548	single nucleotide variant	NM_018417.6(ADCY10):c.1139+71G>C	not provided [RCV001716431]	benign	1	167880420	167880420	Human		name
150441771	CV1287620	single nucleotide variant	NM_018417.6(ADCY10):c.4052+44G>A	not provided [RCV001725340]	benign	1	167824432	167824432	Human		name
150541684	CV1306502	single nucleotide variant	NM_018417.6(ADCY10):c.1463-93A>G	not provided [RCV001768124]	likely benign	1	167870503	167870503	Human		name
150535761	CV1307064	single nucleotide variant	NM_018417.6(ADCY10):c.1810-21T>G	not provided [RCV001759119]	likely benign	1	167859914	167859914	Human		name
150532888	CV1308174	duplication	NM_018417.6(ADCY10):c.828+157dup	not provided [RCV001753165]	likely benign	1	167893695	167893696	Human		name
150535232	CV1311819	single nucleotide variant	NM_018417.6(ADCY10):c.3077+88T>C	not provided [RCV001779629]	likely benign	1	167837161	167837161	Human		name
151662204	CV1332912	single nucleotide variant	NM_018417.6(ADCY10):c.254-198T>C	not provided [RCV001837159]	likely benign	1	167902252	167902252	Human		name
152089381	CV1580652	single nucleotide variant	NM_018417.6(ADCY10):c.1021-11C>T	Familial idiopathic hypercalciuria [RCV002500127]\|not provided [RCV002093957]	benign\|likely benign	1	167880620	167880620	Human	1	name
152174628	CV1602187	single nucleotide variant	NM_018417.6(ADCY10):c.2308+10G>A	not provided [RCV002144501]	likely benign	1	167854343	167854343	Human		name
152031654	CV1629209	single nucleotide variant	NM_018417.6(ADCY10):c.2308+11C>A	not provided [RCV002106209]	benign	1	167854342	167854342	Human		name
152059947	CV1659383	single nucleotide variant	NM_018417.6(ADCY10):c.2308+11C>T	Familial idiopathic hypercalciuria [RCV002479889]\|not provided [RCV002073553]	benign\|likely benign	1	167854342	167854342	Human	1	name
152054349	CV1665419	single nucleotide variant	NM_018417.6(ADCY10):c.2438-20G>T	not provided [RCV002089525]	benign	1	167846283	167846283	Human		name
156331674	CV1954142	single nucleotide variant	NM_018417.6(ADCY10):c.1216+15C>T	not provided [RCV002580034]	uncertain significance	1	167880100	167880100	Human		name
156224985	CV1956613	single nucleotide variant	NM_018417.6(ADCY10):c.1021-13C>G	not provided [RCV002575668]	benign	1	167880622	167880622	Human		name
156209218	CV1959539	single nucleotide variant	NM_018417.6(ADCY10):c.4053-20C>T	not provided [RCV002575087]	likely benign	1	167823143	167823143	Human		name
156407052	CV1963882	single nucleotide variant	NM_018417.6(ADCY10):c.1809+19A>T	not provided [RCV002586106]	benign	1	167860852	167860852	Human		name
156384723	CV1971848	single nucleotide variant	NM_018417.6(ADCY10):c.2308+12G>A	not provided [RCV002604216]	likely benign	1	167854341	167854341	Human		name
156333644	CV1987425	single nucleotide variant	NM_018417.6(ADCY10):c.4168+10G>A	not provided [RCV002631071]	likely benign\|uncertain significance	1	167822998	167822998	Human		name
155960500	CV2040437	duplication	NM_018417.6(ADCY10):c.1897-12dup	not provided [RCV002776245]	benign	1	167856450	167856451	Human		name
156140051	CV2044436	single nucleotide variant	NM_018417.6(ADCY10):c.2437+17G>A	not provided [RCV002800916]	likely benign	1	167848344	167848344	Human		name
155907453	CV2048294	single nucleotide variant	NM_018417.6(ADCY10):c.4168+17G>A	not provided [RCV002771343]	likely benign	1	167822991	167822991	Human		name
156093144	CV2151927	single nucleotide variant	NM_018417.6(ADCY10):c.3417+15A>T	not provided [RCV003020760]	likely benign	1	167833955	167833955	Human		name
405018632	CV2991955	single nucleotide variant	NM_018417.6(ADCY10):c.1217-12T>A	not provided [RCV003694630]	likely benign	1	167878647	167878647	Human		name
405018645	CV2991956	single nucleotide variant	NM_018417.6(ADCY10):c.1217-20C>A	not provided [RCV003694631]	likely benign	1	167878655	167878655	Human		name
404980118	CV3127859	single nucleotide variant	NM_018417.6(ADCY10):c.2437+20C>T	not provided [RCV003825891]	likely benign	1	167848341	167848341	Human		name
405139152	CV3130857	single nucleotide variant	NM_018417.6(ADCY10):c.3955+17C>G	not provided [RCV003839091]	likely benign	1	167824634	167824634	Human		name
405127413	CV3132888	single nucleotide variant	NM_018417.6(ADCY10):c.3310-18T>A	not provided [RCV003838051]	likely benign	1	167834095	167834095	Human		name
597837630	CV3740230	single nucleotide variant	NM_018417.6(ADCY10):c.3309+16C>T	not provided [RCV005064258]	likely benign	1	167836293	167836293	Human		name
597853717	CV3758637	single nucleotide variant	NM_018417.6(ADCY10):c.3077+16A>G	not provided [RCV005088198]	likely benign	1	167837233	167837233	Human		name
597925499	CV3808802	single nucleotide variant	NM_018417.6(ADCY10):c.2717-10C>T	not provided [RCV005156317]	likely benign	1	167845863	167845863	Human		name
150339631	CV1167171	single nucleotide variant	NM_018417.6(ADCY10):c.1809+103C>G	not provided [RCV001534391]	benign	1	167860768	167860768	Human		name
150333211	CV1168793	deletion	NM_018417.6(ADCY10):c.3417+225del	not provided [RCV001537213]	benign	1	167833745	167833745	Human		name
150337153	CV1170620	single nucleotide variant	NM_018417.6(ADCY10):c.2438-109G>T	not provided [RCV001541450]	benign	1	167846372	167846372	Human		name
150504984	CV1211508	duplication	NM_018417.6(ADCY10):c.1407-245dup	not provided [RCV001595673]	benign	1	167875430	167875431	Human		name
150461116	CV1215766	single nucleotide variant	NM_018417.6(ADCY10):c.1406+100A>G	not provided [RCV001613468]	benign	1	167878346	167878346	Human		name
150472692	CV1217222	single nucleotide variant	NM_018417.6(ADCY10):c.1217-111A>G	not provided [RCV001615517]	benign	1	167878746	167878746	Human		name
150514920	CV1217319	single nucleotide variant	NM_018417.6(ADCY10):c.1617-167A>C	not provided [RCV001608223]	benign	1	167861230	167861230	Human		name
150485461	CV1223001	single nucleotide variant	NM_018417.6(ADCY10):c.3007+196A>G	not provided [RCV001617713]	benign	1	167845367	167845367	Human		name
150499080	CV1224528	single nucleotide variant	NM_018417.6(ADCY10):c.2171+287G>C	not provided [RCV001620359]	benign	1	167855878	167855878	Human		name
150517025	CV1227464	single nucleotide variant	NM_018417.6(ADCY10):c.1809+254A>G	not provided [RCV001639565]	benign	1	167860617	167860617	Human		name
150512245	CV1228458	single nucleotide variant	NM_018417.6(ADCY10):c.4053-301G>T	not provided [RCV001637590]	benign	1	167823424	167823424	Human		name
150430370	CV1230846	single nucleotide variant	NM_018417.6(ADCY10):c.1406+164A>G	not provided [RCV001641395]	benign	1	167878282	167878282	Human		name
150434978	CV1231227	single nucleotide variant	NM_018417.6(ADCY10):c.2172-301A>T	not provided [RCV001643872]	benign	1	167854790	167854790	Human		name
150454882	CV1232355	single nucleotide variant	NM_018417.6(ADCY10):c.3593+157T>C	not provided [RCV001648369]	benign	1	167832830	167832830	Human		name
150446011	CV1233274	single nucleotide variant	NM_018417.6(ADCY10):c.3309+108C>T	not provided [RCV001645947]	benign	1	167836201	167836201	Human		name
150442734	CV1233748	single nucleotide variant	NM_018417.6(ADCY10):c.1020+295T>A	not provided [RCV001645436]	benign	1	167883142	167883142	Human		name
150435130	CV1233783	single nucleotide variant	NM_018417.6(ADCY10):c.4168+167C>A	not provided [RCV001643910]	benign	1	167822841	167822841	Human		name
150460761	CV1234685	single nucleotide variant	NM_018417.6(ADCY10):c.2308+136T>C	not provided [RCV001649267]	benign	1	167854217	167854217	Human		name
150461353	CV1234768	single nucleotide variant	NM_018417.6(ADCY10):c.4053-256G>A	not provided [RCV001649350]	benign	1	167823379	167823379	Human		name
150459716	CV1236134	single nucleotide variant	NM_018417.6(ADCY10):c.1407-129G>T	not provided [RCV001649105]	benign	1	167875315	167875315	Human		name
150496822	CV1236915	single nucleotide variant	NM_018417.6(ADCY10):c.3310-117G>A	not provided [RCV001655979]	benign	1	167834194	167834194	Human		name
150506746	CV1242289	single nucleotide variant	NM_018417.6(ADCY10):c.3008-140A>G	not provided [RCV001658644]	benign	1	167837458	167837458	Human		name
150511915	CV1242833	single nucleotide variant	NM_018417.6(ADCY10):c.4052+209C>T	not provided [RCV001661186]	benign	1	167824267	167824267	Human		name
150458476	CV1248941	single nucleotide variant	NM_018417.6(ADCY10):c.2309-194G>T	not provided [RCV001669117]	benign	1	167848683	167848683	Human		name
150469130	CV1249044	single nucleotide variant	NM_018417.6(ADCY10):c.3008-158C>T	not provided [RCV001670805]	benign	1	167837476	167837476	Human		name
150447336	CV1250813	single nucleotide variant	NM_018417.6(ADCY10):c.4168+196G>A	not provided [RCV001667318]	benign	1	167822812	167822812	Human		name
150505677	CV1255534	single nucleotide variant	NM_018417.6(ADCY10):c.2437+189A>C	not provided [RCV001677981]	benign	1	167848172	167848172	Human		name
150498127	CV1256823	single nucleotide variant	NM_018417.6(ADCY10):c.1462+265G>A	not provided [RCV001676316]	benign	1	167874866	167874866	Human		name
150480632	CV1258762	single nucleotide variant	NM_018417.6(ADCY10):c.3077+193A>G	not provided [RCV001685892]	benign	1	167837056	167837056	Human		name
150481258	CV1258885	single nucleotide variant	NM_018417.6(ADCY10):c.2172-246G>T	not provided [RCV001686015]	benign	1	167854735	167854735	Human		name
150469722	CV1259706	single nucleotide variant	NM_018417.6(ADCY10):c.2171+269T>C	not provided [RCV001684007]	benign	1	167855896	167855896	Human		name
150445266	CV1261170	single nucleotide variant	NM_018417.6(ADCY10):c.4482+278T>C	not provided [RCV001679844]	benign	1	167817794	167817794	Human		name
150460498	CV1264183	single nucleotide variant	NM_018417.6(ADCY10):c.1217-124G>T	not provided [RCV001682099]	benign	1	167878759	167878759	Human		name
150441959	CV1264356	duplication	NM_018417.6(ADCY10):c.3417+207dup	not provided [RCV001679339]	benign	1	167833744	167833745	Human		name
150443801	CV1266443	single nucleotide variant	NM_018417.6(ADCY10):c.2437+240C>T	not provided [RCV001690879]	benign	1	167848121	167848121	Human		name
150493689	CV1267198	single nucleotide variant	NM_018417.6(ADCY10):c.1616+285T>G	not provided [RCV001688226]	benign	1	167869972	167869972	Human		name
150456102	CV1269031	single nucleotide variant	NM_018417.6(ADCY10):c.2172-245A>G	not provided [RCV001692855]	benign	1	167854734	167854734	Human		name
150470442	CV1269845	duplication	NM_018417.6(ADCY10):c.4053-321dup	not provided [RCV001695132]	benign	1	167823424	167823425	Human		name
150473217	CV1271959	single nucleotide variant	NM_018417.6(ADCY10):c.2437+218C>T	not provided [RCV001695672]	benign	1	167848143	167848143	Human		name
150474090	CV1272278	single nucleotide variant	NM_018417.6(ADCY10):c.2438-315A>C	not provided [RCV001695816]	benign	1	167846578	167846578	Human		name
150484782	CV1274022	single nucleotide variant	NM_018417.6(ADCY10):c.1407-135C>T	not provided [RCV001698569]	benign	1	167875321	167875321	Human		name
150460534	CV1275835	single nucleotide variant	NM_018417.6(ADCY10):c.2309-312T>C	not provided [RCV001709773]	benign	1	167848801	167848801	Human		name
150468138	CV1277689	single nucleotide variant	NM_018417.6(ADCY10):c.4052+237A>G	not provided [RCV001710984]	benign	1	167824239	167824239	Human		name
150456643	CV1278527	duplication	NM_018417.6(ADCY10):c.1463-249dup	not provided [RCV001709142]	benign	1	167870638	167870639	Human		name
150489951	CV1279353	single nucleotide variant	NM_018417.6(ADCY10):c.2309-222G>A	not provided [RCV001716386]	benign	1	167848711	167848711	Human		name
150490884	CV1280022	single nucleotide variant	NM_018417.6(ADCY10):c.3750+163C>T	not provided [RCV001716550]	benign	1	167829104	167829104	Human		name
150484346	CV1280428	single nucleotide variant	NM_018417.6(ADCY10):c.3750+114C>T	not provided [RCV001715356]	benign	1	167829153	167829153	Human		name
150487927	CV1283919	single nucleotide variant	NM_018417.6(ADCY10):c.1407-158G>C	not provided [RCV001716026]	benign	1	167875344	167875344	Human		name
150512196	CV1284887	single nucleotide variant	NM_018417.6(ADCY10):c.3417+252G>A	not provided [RCV001721756]	benign	1	167833718	167833718	Human		name
150545282	CV1307704	single nucleotide variant	NM_018417.6(ADCY10):c.3418-155A>G	not provided [RCV001774982]	likely benign	1	167833317	167833317	Human		name
150545285	CV1307705	single nucleotide variant	NM_018417.6(ADCY10):c.3751-224T>C	not provided [RCV001774983]	likely benign	1	167825079	167825079	Human		name
150545288	CV1307707	single nucleotide variant	NM_018417.6(ADCY10):c.3750+216C>T	not provided [RCV001774985]	likely benign	1	167829051	167829051	Human		name
150532665	CV1308044	deletion	NM_018417.6(ADCY10):c.4053-302del	not provided [RCV001753034]	likely benign	1	167823425	167823425	Human		name
150543378	CV1308958	single nucleotide variant	NM_018417.6(ADCY10):c.2172-320T>C	not provided [RCV001769871]	likely benign	1	167854809	167854809	Human		name
151232563	CV1316839	duplication	NM_018417.6(ADCY10):c.2309-166dup	not provided [RCV001786659]	likely benign	1	167848654	167848655	Human		name
155267709	CV1705109	single nucleotide variant	NM_018417.6(ADCY10):c.1407-140G>A	not provided [RCV002285714]	likely benign	1	167875326	167875326	Human		name
8575046	CV109387	single nucleotide variant	NM_018417.5(ADCY10):c.1463-2119C>G	Lung cancer [RCV000089912]	uncertain significance	1	167872529	167872529	Human		name
404985600	CV2851874	deletion	NM_018417.6(ADCY10):c.4483-12_4484del	not provided [RCV003489529]	uncertain significance	1	167810912	167810925	Human		name
405127423	CV3132889	single nucleotide variant	NM_018417.6(ADCY10):c.27G>A (p.Gln9=)	not provided [RCV003838052]	likely benign	1	167905114	167905114	Human		name
150441853	CV1246802	duplication	NM_018417.6(ADCY10):c.293-79_293-78dup	not provided [RCV001666456]	benign	1	167901882	167901883	Human		name
597948321	CV3800928	single nucleotide variant	NM_018417.6(ADCY10):c.75C>A (p.Val25=)	not provided [RCV005135328]	likely benign	1	167905066	167905066	Human		name
151797809	CV1446820	single nucleotide variant	NM_018417.6(ADCY10):c.20A>C (p.Glu7Ala)	ADCY10-related disorder [RCV003978469]\|not provided [RCV002027808]\|not specified [RCV004612115]	likely benign\|uncertain significance	1	167905121	167905121	Human	1	name , trait , alternate_id
151839414	CV1487588	single nucleotide variant	NM_018417.6(ADCY10):c.147A>C (p.Ser49=)	not provided [RCV001935922]	uncertain significance	1	167904994	167904994	Human		name
156276670	CV2185955	single nucleotide variant	NM_018417.6(ADCY10):c.105T>C (p.Phe35=)	not provided [RCV003044640]	likely benign	1	167905036	167905036	Human		name
405274388	CV3211725	single nucleotide variant	NM_018417.6(ADCY10):c.213G>A (p.Leu71=)	ADCY10-related disorder [RCV003951525]	likely benign	1	167903927	167903927	Human		name , trait , alternate_id
597932549	CV3862069	single nucleotide variant	NM_018417.6(ADCY10):c.211T>C (p.Leu71=)	not provided [RCV005206933]	likely benign	1	167903929	167903929	Human		name
127337265	CV1109677	single nucleotide variant	NM_018417.6(ADCY10):c.324G>A (p.Glu108=)	ADCY10-related disorder [RCV003965958]\|Familial idiopathic hypercalciuria [RCV002506550]\|not provided [RCV001475546]	likely benign	1	167901774	167901774	Human	1	name , trait , alternate_id
150517532	CV1226983	deletion	NM_018417.6(ADCY10):c.828+155_828+157del	not provided [RCV001640079]	benign	1	167893696	167893698	Human		name
150496804	CV1255993	deletion	NM_018417.6(ADCY10):c.828+156_828+157del	not provided [RCV001676088]	benign	1	167893696	167893697	Human		name
150447847	CV1261876	deletion	NM_018417.6(ADCY10):c.828+147_828+157del	not provided [RCV001680261]	benign	1	167893696	167893706	Human		name
152087219	CV1608503	single nucleotide variant	NM_018417.6(ADCY10):c.426A>G (p.Arg142=)	not provided [RCV002212210]	likely benign	1	167901672	167901672	Human		name
156186277	CV2033870	single nucleotide variant	NM_018417.6(ADCY10):c.534C>A (p.Ala178=)	not provided [RCV002765771]	likely benign	1	167899531	167899531	Human		name
156002582	CV2106854	single nucleotide variant	NM_018417.6(ADCY10):c.828G>A (p.Gln276=)	not provided [RCV002947862]	uncertain significance	1	167893853	167893853	Human		name
156006277	CV2126589	single nucleotide variant	NM_018417.6(ADCY10):c.945G>A (p.Gln315=)	not provided [RCV002975416]	benign	1	167883512	167883512	Human		name
156301299	CV2129510	single nucleotide variant	NM_018417.6(ADCY10):c.423C>T (p.Ile141=)	not provided [RCV002962156]	likely benign	1	167901675	167901675	Human		name
402477527	CV2914367	single nucleotide variant	NM_018417.6(ADCY10):c.82C>G (p.His28Asp)	not provided [RCV003571676]	uncertain significance	1	167905059	167905059	Human		name
402478381	CV2914382	single nucleotide variant	NM_018417.6(ADCY10):c.402G>A (p.Glu134=)	not provided [RCV003571686]	likely benign	1	167901696	167901696	Human		name
405138386	CV3029524	single nucleotide variant	NM_018417.6(ADCY10):c.28G>C (p.Asp10His)	not provided [RCV003702297]	uncertain significance	1	167905113	167905113	Human		name
405128538	CV3132887	deletion	NM_018417.6(ADCY10):c.3310-17_3310-13del	not provided [RCV003838050]	likely benign	1	167834090	167834094	Human		name
405106394	CV3136114	single nucleotide variant	NM_018417.6(ADCY10):c.702G>A (p.Thr234=)	not provided [RCV003835460]	likely benign	1	167896632	167896632	Human		name
405107805	CV3136305	single nucleotide variant	NM_018417.6(ADCY10):c.705C>T (p.Thr235=)	not provided [RCV003835651]	likely benign	1	167896629	167896629	Human		name
597960714	CV3756254	microsatellite	NM_018417.6(ADCY10):c.1897-19_1897-14del	not provided [RCV005081571]	likely benign	1	167856453	167856458	Human		name
597872914	CV3769795	single nucleotide variant	NM_018417.6(ADCY10):c.654A>G (p.Leu218=)	not provided [RCV005108053]	likely benign	1	167896680	167896680	Human		name
597972322	CV3790237	single nucleotide variant	NM_018417.6(ADCY10):c.87C>A (p.Phe29Leu)	not provided [RCV005142660]	uncertain significance	1	167905054	167905054	Human		name
127281062	CV1066425	single nucleotide variant	NM_018417.6(ADCY10):c.1620T>C (p.Ile540=)	not provided [RCV001410195]	likely benign	1	167861060	167861060	Human		name
127268439	CV1088154	single nucleotide variant	NM_018417.6(ADCY10):c.1902G>A (p.Val634=)	Familial idiopathic hypercalciuria [RCV002501550]\|not provided [RCV001440784]	likely benign	1	167856434	167856434	Human	1	name
127304206	CV1109676	single nucleotide variant	NM_018417.6(ADCY10):c.2259A>G (p.Gln753=)	not provided [RCV001454918]	likely benign	1	167854402	167854402	Human		name
127301293	CV1153345	single nucleotide variant	NM_018417.6(ADCY10):c.2778T>C (p.Ile926=)	not provided [RCV001514594]	benign	1	167845792	167845792	Human		name
127308493	CV1153347	single nucleotide variant	NM_018417.6(ADCY10):c.2397T>C (p.Gly799=)	not provided [RCV001517528]	benign	1	167848401	167848401	Human		name
127291303	CV1153350	single nucleotide variant	NM_018417.6(ADCY10):c.1968T>C (p.Phe656=)	not provided [RCV001510286]	benign	1	167856368	167856368	Human		name
127308799	CV1153351	single nucleotide variant	NM_018417.6(ADCY10):c.1668C>T (p.Thr556=)	ADCY10-related disorder [RCV003956183]\|Familial idiopathic hypercalciuria [RCV002495814]\|not provided [RCV001517642]	benign\|likely benign	1	167861012	167861012	Human	1	name , trait , alternate_id
127291308	CV1153352	single nucleotide variant	NM_018417.6(ADCY10):c.1533C>T (p.Val511=)	not provided [RCV001510287]	benign	1	167870340	167870340	Human		name
127311613	CV1153353	single nucleotide variant	NM_018417.6(ADCY10):c.1260C>T (p.Tyr420=)	Familial idiopathic hypercalciuria [RCV002501808]\|not provided [RCV001518673]	benign\|likely benign	1	167878592	167878592	Human	1	name
127308504	CV1153354	single nucleotide variant	NM_018417.6(ADCY10):c.1155T>C (p.Gly385=)	not provided [RCV001517530]	benign	1	167880176	167880176	Human		name
151870776	CV1351573	single nucleotide variant	NM_018417.6(ADCY10):c.1185C>A (p.Ile395=)	not provided [RCV002018909]	uncertain significance	1	167880146	167880146	Human		name
151771405	CV1366375	single nucleotide variant	NM_018417.6(ADCY10):c.229T>C (p.Tyr77His)	Familial idiopathic hypercalciuria [RCV002507598]\|not provided [RCV001929552]	uncertain significance	1	167903911	167903911	Human	1	name
151863199	CV1374347	single nucleotide variant	NM_018417.6(ADCY10):c.239G>A (p.Ser80Asn)	not provided [RCV001884200]	uncertain significance	1	167903901	167903901	Human		name
151886992	CV1441356	duplication	NM_018417.6(ADCY10):c.952dup (p.Tyr318fs)	not provided [RCV001962878]	pathogenic	1	167883504	167883505	Human		name
152111055	CV1537094	single nucleotide variant	NM_018417.6(ADCY10):c.2406G>A (p.Leu802=)	ADCY10-related disorder [RCV003968817]\|Familial idiopathic hypercalciuria [RCV002486840]\|not provided [RCV002215494]	likely benign	1	167848392	167848392	Human	1	name , trait , alternate_id
152142030	CV1629039	single nucleotide variant	NM_018417.6(ADCY10):c.1926C>A (p.Ile642=)	not provided [RCV002100907]	likely benign	1	167856410	167856410	Human		name
152059666	CV1650276	single nucleotide variant	NM_018417.6(ADCY10):c.1860A>G (p.Lys620=)	not provided [RCV002128192]	likely benign	1	167859843	167859843	Human		name
156223308	CV1879441	single nucleotide variant	NM_018417.6(ADCY10):c.1626C>G (p.Ala542=)	not provided [RCV003059029]	likely benign	1	167861054	167861054	Human		name
156161126	CV1933213	single nucleotide variant	NM_018417.6(ADCY10):c.1311A>T (p.Leu437=)	not provided [RCV002624373]	likely benign	1	167878541	167878541	Human		name
156382271	CV1960952	single nucleotide variant	NM_018417.6(ADCY10):c.1275G>A (p.Val425=)	not provided [RCV002583259]	likely benign	1	167878577	167878577	Human		name
156415182	CV1983235	single nucleotide variant	NM_018417.6(ADCY10):c.1164T>C (p.Ser388=)	not provided [RCV002609551]	likely benign	1	167880167	167880167	Human		name
156130867	CV2125133	single nucleotide variant	NM_018417.6(ADCY10):c.2955C>T (p.Asn985=)	not provided [RCV002953873]	likely benign	1	167845615	167845615	Human		name
156034123	CV2132791	single nucleotide variant	NM_018417.6(ADCY10):c.2814C>T (p.Tyr938=)	not provided [RCV002999265]	likely benign	1	167845756	167845756	Human		name
155924270	CV2212688	single nucleotide variant	NM_018417.6(ADCY10):c.230A>G (p.Tyr77Cys)	not specified [RCV004085194]	uncertain significance	1	167903910	167903910	Human		name
401855343	CV2752876	single nucleotide variant	NM_018417.6(ADCY10):c.257T>C (p.Val86Ala)	Familial idiopathic hypercalciuria [RCV003337930]	uncertain significance	1	167902051	167902051	Human	1	name
405199647	CV2877046	single nucleotide variant	NM_018417.6(ADCY10):c.1119C>T (p.Cys373=)	not provided [RCV003551258]	likely benign	1	167880511	167880511	Human		name
405147674	CV2881730	single nucleotide variant	NM_018417.6(ADCY10):c.2766G>A (p.Glu922=)	not provided [RCV003561488]	likely benign	1	167845804	167845804	Human		name
405209404	CV2910142	duplication	NM_018417.6(ADCY10):c.697dup (p.Cys233fs)	not provided [RCV003566945]	pathogenic	1	167896636	167896637	Human		name
402495804	CV2942709	single nucleotide variant	NM_018417.6(ADCY10):c.2136C>T (p.Asp712=)	not provided [RCV003661093]	likely benign	1	167856200	167856200	Human		name
405226927	CV2963399	single nucleotide variant	NM_018417.6(ADCY10):c.2916C>T (p.Phe972=)	not provided [RCV003681583]	likely benign	1	167845654	167845654	Human		name
405133781	CV3051822	single nucleotide variant	NM_018417.6(ADCY10):c.1206C>T (p.His402=)	not provided [RCV003725061]	benign	1	167880125	167880125	Human		name
405254426	CV3055356	single nucleotide variant	NM_018417.6(ADCY10):c.1071C>T (p.Asp357=)	not provided [RCV003723006]	likely benign	1	167880559	167880559	Human		name
405144218	CV3056252	single nucleotide variant	NM_018417.6(ADCY10):c.1362A>T (p.Ala454=)	ADCY10-related disorder [RCV003929315]\|not provided [RCV003725911]	benign\|likely benign	1	167878490	167878490	Human	1	name , trait , alternate_id
405012594	CV3128205	insertion	NM_018417.6(ADCY10):c.3593+10_3593+11insA	not provided [RCV003829085]	likely benign	1	167832976	167832977	Human		name
405187925	CV3149213	single nucleotide variant	NM_018417.6(ADCY10):c.2931C>T (p.His977=)	not provided [RCV003843139]	likely benign	1	167845639	167845639	Human		name
405163620	CV3160366	single nucleotide variant	NM_018417.6(ADCY10):c.1023C>T (p.Gly341=)	not provided [RCV003857245]	likely benign	1	167880607	167880607	Human		name
405165696	CV3160523	single nucleotide variant	NM_018417.6(ADCY10):c.2724T>G (p.Gly908=)	not provided [RCV003857403]	likely benign	1	167845846	167845846	Human		name
405667972	CV3240004	single nucleotide variant	NM_018417.6(ADCY10):c.163A>T (p.Thr55Ser)	not specified [RCV004368056]	uncertain significance	1	167903977	167903977	Human		name
597930935	CV3745902	single nucleotide variant	NM_018417.6(ADCY10):c.2763C>A (p.Ile921=)	not provided [RCV005075887]	likely benign	1	167845807	167845807	Human		name
597878826	CV3763289	single nucleotide variant	NM_018417.6(ADCY10):c.184A>G (p.Met62Val)	not provided [RCV005108884]	uncertain significance	1	167903956	167903956	Human		name
597903757	CV3793156	single nucleotide variant	NM_018417.6(ADCY10):c.2583G>A (p.Leu861=)	not provided [RCV005153124]	likely benign	1	167846118	167846118	Human		name
597930207	CV3826933	single nucleotide variant	NM_018417.6(ADCY10):c.2250C>A (p.Leu750=)	not provided [RCV005156946]	likely benign	1	167854411	167854411	Human		name
598214792	CV3951647	single nucleotide variant	NM_018417.6(ADCY10):c.193G>A (p.Asp65Asn)	not specified [RCV005316634]	uncertain significance	1	167903947	167903947	Human		name
15160856	CV706833	single nucleotide variant	NM_018417.6(ADCY10):c.2565G>A (p.Lys855=)	ADCY10-related disorder [RCV003972891]\|not provided [RCV000969982]	benign\|likely benign	1	167846136	167846136	Human	1	name , trait , alternate_id
15159788	CV706835	single nucleotide variant	NM_018417.6(ADCY10):c.2097A>G (p.Ala699=)	ADCY10-related disorder [RCV004756139]\|not provided [RCV000969774]	benign\|likely benign	1	167856239	167856239	Human	1	name , trait , alternate_id
15190371	CV761313	single nucleotide variant	NM_018417.6(ADCY10):c.2070G>A (p.Arg690=)	not provided [RCV000932499]	likely benign	1	167856266	167856266	Human		name
26915208	CV822979	single nucleotide variant	NM_018417.6(ADCY10):c.224T>C (p.Leu75Pro)	not provided [RCV001038624]	uncertain significance	1	167903916	167903916	Human		name
126911007	CV1036969	single nucleotide variant	NM_018417.6(ADCY10):c.307G>T (p.Ala103Ser)	Familial idiopathic hypercalciuria [RCV002493816]\|not provided [RCV001354905]	uncertain significance	1	167901791	167901791	Human	1	name
127260704	CV1058470	single nucleotide variant	NM_018417.6(ADCY10):c.581G>A (p.Trp194Ter)	not provided [RCV001387407]	pathogenic	1	167899484	167899484	Human		name
127302423	CV1109674	single nucleotide variant	NM_018417.6(ADCY10):c.4815C>T (p.Thr1605=)	Familial idiopathic hypercalciuria [RCV002495648]\|not provided [RCV001454441]	likely benign	1	167809696	167809696	Human	1	name
127298573	CV1109675	single nucleotide variant	NM_018417.6(ADCY10):c.4059G>T (p.Pro1353=)	ADCY10-related disorder [RCV003955989]\|not provided [RCV001453352]	likely benign	1	167823117	167823117	Human	1	name , trait , alternate_id
127313115	CV1153344	single nucleotide variant	NM_018417.6(ADCY10):c.3565C>A (p.Arg1189=)	not provided [RCV001519162]	benign	1	167833015	167833015	Human		name
127308509	CV1153356	single nucleotide variant	NM_018417.6(ADCY10):c.701C>T (p.Thr234Met)	Familial idiopathic hypercalciuria [RCV002221629]\|not provided [RCV001517531]	risk factor\|benign	1	167896633	167896633	Human	1	name
150503047	CV1223370	duplication	NM_018417.6(ADCY10):c.4053-321_4053-320dup	not provided [RCV001621305]	benign	1	167823424	167823425	Human		name
150507784	CV1229175	duplication	NM_018417.6(ADCY10):c.1463-249_1463-248dup	not provided [RCV001636046]	benign	1	167870638	167870639	Human		name
150437260	CV1249840	duplication	NM_018417.6(ADCY10):c.1463-249_1463-247dup	not provided [RCV001665754]	benign	1	167870638	167870639	Human		name
150476312	CV1279231	deletion	NM_018417.6(ADCY10):c.2172-167_2172-166del	not provided [RCV001713965]	benign	1	167854655	167854656	Human		name
150545291	CV1307708	deletion	NM_018417.6(ADCY10):c.3417+222_3417+225del	not provided [RCV001774986]	likely benign	1	167833745	167833748	Human		name
150531393	CV1310838	deletion	NM_018417.6(ADCY10):c.3417+224_3417+225del	not provided [RCV001776572]	likely benign	1	167833745	167833746	Human		name
151736880	CV1391582	single nucleotide variant	NM_018417.6(ADCY10):c.349A>G (p.Thr117Ala)	Familial idiopathic hypercalciuria [RCV002478093]\|not provided [RCV002041813]	uncertain significance	1	167901749	167901749	Human	1	name
151871852	CV1451476	single nucleotide variant	NM_018417.6(ADCY10):c.651C>A (p.Phe217Leu)	not provided [RCV001960538]	likely benign	1	167896683	167896683	Human		name
151821725	CV1452363	single nucleotide variant	NM_018417.6(ADCY10):c.758G>A (p.Cys253Tyr)	Familial idiopathic hypercalciuria [RCV002478080]\|not provided [RCV002049866]	uncertain significance	1	167893923	167893923	Human	1	name
151845381	CV1501598	single nucleotide variant	NM_018417.6(ADCY10):c.878C>G (p.Thr293Arg)	not provided [RCV002015834]	uncertain significance	1	167883579	167883579	Human		name
152034610	CV1634963	single nucleotide variant	NM_018417.6(ADCY10):c.3429T>C (p.Asn1143=)	ADCY10-related disorder [RCV003978475]\|Familial idiopathic hypercalciuria [RCV002507844]\|not provided [RCV002087000]	likely benign	1	167833151	167833151	Human	1	name , trait , alternate_id
152137790	CV1657734	single nucleotide variant	NM_018417.6(ADCY10):c.3840G>A (p.Glu1280=)	not provided [RCV002177651]	likely benign	1	167824766	167824766	Human		name
155695806	CV1777048	single nucleotide variant	NM_018417.6(ADCY10):c.849G>C (p.Gln283His)	not provided [RCV002295213]	uncertain significance	1	167883608	167883608	Human		name
156248564	CV1886780	single nucleotide variant	NM_018417.6(ADCY10):c.4030A>C (p.Arg1344=)	not provided [RCV003086018]	likely benign	1	167824498	167824498	Human		name
156404223	CV1898164	single nucleotide variant	NM_018417.6(ADCY10):c.4212C>T (p.His1404=)	ADCY10-related disorder [RCV003898822]\|not provided [RCV002585358]	likely benign	1	167822098	167822098	Human	1	name , trait , alternate_id
156324571	CV1972593	single nucleotide variant	NM_018417.6(ADCY10):c.3354C>T (p.Leu1118=)	not provided [RCV002600446]	likely benign	1	167834033	167834033	Human		name
156324355	CV1975501	single nucleotide variant	NM_018417.6(ADCY10):c.3921C>T (p.Leu1307=)	not provided [RCV002630560]	likely benign	1	167824685	167824685	Human		name
156185561	CV1997759	single nucleotide variant	NM_018417.6(ADCY10):c.4147T>C (p.Leu1383=)	not provided [RCV002643158]	likely benign	1	167823029	167823029	Human		name
156168680	CV2041430	single nucleotide variant	NM_018417.6(ADCY10):c.3855C>T (p.Leu1285=)	not provided [RCV002741794]	likely benign	1	167824751	167824751	Human		name
155938078	CV2045215	single nucleotide variant	NM_018417.6(ADCY10):c.4248T>C (p.Ser1416=)	not provided [RCV002775013]	likely benign	1	167822062	167822062	Human		name
156033585	CV2122922	single nucleotide variant	NM_018417.6(ADCY10):c.4047C>T (p.Asn1349=)	not provided [RCV002949335]	likely benign	1	167824481	167824481	Human		name
156360259	CV2126397	single nucleotide variant	NM_018417.6(ADCY10):c.3558T>C (p.Tyr1186=)	not provided [RCV002966935]	likely benign	1	167833022	167833022	Human		name
155945805	CV2130220	single nucleotide variant	NM_018417.6(ADCY10):c.325C>T (p.Arg109Ter)	not provided [RCV002971573]	pathogenic	1	167901773	167901773	Human		name
156148903	CV2175216	single nucleotide variant	NM_018417.6(ADCY10):c.497T>A (p.Leu166Gln)	not provided [RCV003040303]	uncertain significance	1	167899568	167899568	Human		name
156331807	CV2188069	single nucleotide variant	NM_018417.6(ADCY10):c.3225T>C (p.Phe1075=)	not provided [RCV003063739]	likely benign	1	167836393	167836393	Human		name
155980750	CV2223062	single nucleotide variant	NM_018417.6(ADCY10):c.959A>C (p.His320Pro)	not specified [RCV004103641]	uncertain significance	1	167883498	167883498	Human		name
156068709	CV2280717	single nucleotide variant	NM_018417.6(ADCY10):c.801G>T (p.Lys267Asn)	not specified [RCV004143174]	uncertain significance	1	167893880	167893880	Human		name
155906991	CV2302127	single nucleotide variant	NM_018417.6(ADCY10):c.448G>A (p.Gly150Ser)	not specified [RCV004159144]	uncertain significance	1	167899617	167899617	Human		name
156338926	CV2370820	single nucleotide variant	NM_018417.6(ADCY10):c.586C>T (p.Leu196Phe)	not specified [RCV004209213]	uncertain significance	1	167899479	167899479	Human		name
401750791	CV2712147	single nucleotide variant	NM_018417.6(ADCY10):c.315G>C (p.Trp105Cys)	not specified [RCV004311871]	uncertain significance	1	167901783	167901783	Human		name
401743183	CV2715418	single nucleotide variant	NM_018417.6(ADCY10):c.709A>T (p.Met237Leu)	not provided [RCV003549047]\|not specified [RCV004324737]	uncertain significance	1	167896625	167896625	Human		name
401764144	CV2717240	single nucleotide variant	NM_018417.6(ADCY10):c.512C>G (p.Ala171Gly)	not specified [RCV004324073]	uncertain significance	1	167899553	167899553	Human		name
401915236	CV2795186	single nucleotide variant	NM_018417.6(ADCY10):c.386T>C (p.Leu129Ser)	Familial idiopathic hypercalciuria [RCV003388970]	uncertain significance	1	167901712	167901712	Human	1	name
404985594	CV2851873	single nucleotide variant	NM_018417.6(ADCY10):c.710T>C (p.Met237Thr)	not provided [RCV003489528]	uncertain significance	1	167896624	167896624	Human		name
405210175	CV2870700	single nucleotide variant	NM_018417.6(ADCY10):c.4383C>T (p.Asp1461=)	not provided [RCV003552327]	likely benign	1	167818171	167818171	Human		name
402476031	CV2916752	single nucleotide variant	NM_018417.6(ADCY10):c.889G>A (p.Val297Met)	not provided [RCV003571357]	uncertain significance	1	167883568	167883568	Human		name
405068942	CV2923808	single nucleotide variant	NM_018417.6(ADCY10):c.331C>G (p.Gln111Glu)	not provided [RCV003580875]	uncertain significance	1	167901767	167901767	Human		name
402469966	CV2931274	single nucleotide variant	NM_018417.6(ADCY10):c.3501C>T (p.Tyr1167=)	not provided [RCV003570251]	likely benign	1	167833079	167833079	Human		name
405252584	CV3047374	single nucleotide variant	NM_018417.6(ADCY10):c.3171T>C (p.Ser1057=)	not provided [RCV003722270]	likely benign	1	167836447	167836447	Human		name
405176789	CV3049477	single nucleotide variant	NM_018417.6(ADCY10):c.369C>G (p.Ser123Arg)	not provided [RCV003728411]	uncertain significance	1	167901729	167901729	Human		name
405103974	CV3120053	single nucleotide variant	NM_018417.6(ADCY10):c.3147C>T (p.Asp1049=)	not provided [RCV003812123]	likely benign	1	167836471	167836471	Human		name
405220445	CV3154412	single nucleotide variant	NM_018417.6(ADCY10):c.3618C>T (p.Tyr1206=)	not provided [RCV003847104]	likely benign	1	167829399	167829399	Human		name
404985281	CV3183754	single nucleotide variant	NM_018417.6(ADCY10):c.595C>T (p.Arg199Trp)	not provided [RCV003881031]\|not specified [RCV005063205]	uncertain significance	1	167899470	167899470	Human		name
405668894	CV3240194	single nucleotide variant	NM_018417.6(ADCY10):c.761C>T (p.Thr254Met)	not specified [RCV004368246]	likely benign	1	167893920	167893920	Human		name
405668905	CV3240196	single nucleotide variant	NM_018417.6(ADCY10):c.767A>G (p.Lys256Arg)	not specified [RCV004368248]	uncertain significance	1	167893914	167893914	Human		name
405668932	CV3240201	single nucleotide variant	NM_018417.6(ADCY10):c.878C>T (p.Thr293Met)	not specified [RCV004368253]	uncertain significance	1	167883579	167883579	Human		name
407457296	CV3419685	single nucleotide variant	NM_018417.6(ADCY10):c.526C>T (p.Arg176Cys)	not specified [RCV004611079]	uncertain significance	1	167899539	167899539	Human		name
407457322	CV3419695	single nucleotide variant	NM_018417.6(ADCY10):c.520G>A (p.Asp174Asn)	not specified [RCV004611089]	uncertain significance	1	167899545	167899545	Human		name
408384677	CV3503281	deletion	NM_018417.6(ADCY10):c.1572del (p.Ile525fs)	ADCY10-related disorder [RCV004732011]	likely pathogenic	1	167870301	167870301	Human		name , trait , alternate_id
597798862	CV3653853	single nucleotide variant	NM_018417.6(ADCY10):c.869G>A (p.Arg290His)	not specified [RCV004904911]	uncertain significance	1	167883588	167883588	Human		name
597954309	CV3754000	single nucleotide variant	NM_018417.6(ADCY10):c.667A>C (p.Asn223His)	not provided [RCV005080043]	uncertain significance	1	167896667	167896667	Human		name
597849658	CV3761705	single nucleotide variant	NM_018417.6(ADCY10):c.3510C>T (p.Ile1170=)	not provided [RCV005087801]	likely benign	1	167833070	167833070	Human		name
597939784	CV3775397	single nucleotide variant	NM_018417.6(ADCY10):c.3570G>A (p.Gln1190=)	not provided [RCV005118223]	likely benign	1	167833010	167833010	Human		name
597949762	CV3797710	single nucleotide variant	NM_018417.6(ADCY10):c.4677A>C (p.Ser1559=)	not provided [RCV005135702]	likely benign	1	167809834	167809834	Human		name
597948139	CV3800884	duplication	NM_018417.6(ADCY10):c.1738dup (p.Leu580fs)	not provided [RCV005135284]	pathogenic	1	167860941	167860942	Human		name
597889831	CV3804890	single nucleotide variant	NM_018417.6(ADCY10):c.3303C>T (p.Asn1101=)	not provided [RCV005151152]	likely benign	1	167836315	167836315	Human		name
597944194	CV3812502	single nucleotide variant	NM_018417.6(ADCY10):c.4497G>A (p.Leu1499=)	not provided [RCV005159712]	likely benign	1	167810899	167810899	Human		name
597951743	CV3815395	single nucleotide variant	NM_018417.6(ADCY10):c.983T>C (p.Phe328Ser)	not provided [RCV005161345]	uncertain significance	1	167883474	167883474	Human		name
597946546	CV3841679	single nucleotide variant	NM_018417.6(ADCY10):c.4179T>C (p.Tyr1393=)	not provided [RCV005189113]	likely benign	1	167822131	167822131	Human		name
597903075	CV3845911	single nucleotide variant	NM_018417.6(ADCY10):c.661C>A (p.Pro221Thr)	not provided [RCV005181533]	uncertain significance	1	167896673	167896673	Human		name
598214726	CV3951637	single nucleotide variant	NM_018417.6(ADCY10):c.547C>G (p.Gln183Glu)	not specified [RCV005316625]	uncertain significance	1	167899518	167899518	Human		name
598215168	CV3951716	single nucleotide variant	NM_018417.6(ADCY10):c.727G>C (p.Gly243Arg)	not specified [RCV005316699]	uncertain significance	1	167896607	167896607	Human		name
15155585	CV696240	single nucleotide variant	NM_018417.6(ADCY10):c.3696C>T (p.His1232=)	ADCY10-related disorder [RCV003970662]\|Familial idiopathic hypercalciuria [RCV002502903]\|not provided [RCV000946520]	benign\|likely benign	1	167829321	167829321	Human	1	name , trait , alternate_id
15173839	CV706830	single nucleotide variant	NM_018417.6(ADCY10):c.4389A>T (p.Ile1463=)	not provided [RCV000972657]	benign	1	167818165	167818165	Human		name
15180485	CV706831	single nucleotide variant	NM_018417.6(ADCY10):c.4377C>T (p.Tyr1459=)	Familial idiopathic hypercalciuria [RCV002505483]\|not provided [RCV000974164]	benign\|likely benign	1	167818177	167818177	Human	1	name
15180488	CV706832	single nucleotide variant	NM_018417.6(ADCY10):c.3720T>C (p.Asn1240=)	Familial idiopathic hypercalciuria [RCV002479141]\|not provided [RCV000974165]	benign\|likely benign	1	167829297	167829297	Human	1	name
15112154	CV718352	single nucleotide variant	NM_018417.6(ADCY10):c.4752T>C (p.Ile1584=)	Familial idiopathic hypercalciuria [RCV002495411]\|not provided [RCV000894411]	benign\|likely benign	1	167809759	167809759	Human	1	name
15168264	CV718353	single nucleotide variant	NM_018417.6(ADCY10):c.4075C>T (p.Leu1359=)	Familial idiopathic hypercalciuria [RCV002501401]\|not provided [RCV000883026]	benign	1	167823101	167823101	Human	1	name
15200494	CV718354	single nucleotide variant	NM_018417.6(ADCY10):c.3765C>T (p.Tyr1255=)	Familial idiopathic hypercalciuria [RCV002501465]\|not provided [RCV000890929]	benign\|likely benign	1	167824841	167824841	Human	1	name
15175509	CV731841	single nucleotide variant	NM_018417.6(ADCY10):c.3999C>T (p.Asn1333=)	not provided [RCV000906232]	benign	1	167824529	167824529	Human		name
38468257	CV930149	deletion	NM_018417.6(ADCY10):c.2402del (p.Arg801fs)	not provided [RCV001202172]	pathogenic	1	167848396	167848396	Human		name
38470865	CV930151	single nucleotide variant	NM_018417.6(ADCY10):c.461T>A (p.Met154Lys)	not provided [RCV001202730]	uncertain significance	1	167899604	167899604	Human		name
38476742	CV941567	single nucleotide variant	NM_018417.6(ADCY10):c.489C>G (p.Ser163Arg)	not provided [RCV001233213]	uncertain significance	1	167899576	167899576	Human		name
41408158	CV966128	single nucleotide variant	NM_018417.6(ADCY10):c.366T>A (p.Cys122Ter)	Male infertility [RCV001283748]	uncertain significance	1	167901732	167901732	Human	2	name
126746377	CV1022748	single nucleotide variant	NM_018417.6(ADCY10):c.2102A>G (p.Gln701Arg)	not provided [RCV001337318]	uncertain significance	1	167856234	167856234	Human		name
126920327	CV1039592	single nucleotide variant	NM_018417.6(ADCY10):c.2903G>C (p.Arg968Pro)	not provided [RCV001373741]	uncertain significance	1	167845667	167845667	Human		name
126919161	CV1039593	single nucleotide variant	NM_018417.6(ADCY10):c.1595T>C (p.Leu532Pro)	not provided [RCV001373075]\|not specified [RCV004037554]	uncertain significance	1	167870278	167870278	Human		name
127272870	CV1058467	deletion	NM_018417.6(ADCY10):c.4477del (p.Leu1493fs)	not provided [RCV001390597]	pathogenic	1	167818077	167818077	Human		name
127253774	CV1058469	single nucleotide variant	NM_018417.6(ADCY10):c.1825G>T (p.Glu609Ter)	not provided [RCV001386001]	pathogenic	1	167859878	167859878	Human		name
127306292	CV1153348	single nucleotide variant	NM_018417.6(ADCY10):c.2125A>G (p.Ile709Val)	not provided [RCV001516576]	benign\|likely benign	1	167856211	167856211	Human		name
127308498	CV1153349	single nucleotide variant	NM_018417.6(ADCY10):c.2089A>G (p.Ile697Val)	not provided [RCV001517529]	benign	1	167856247	167856247	Human		name
150330571	CV1168600	single nucleotide variant	NM_018417.6(ADCY10):c.2215G>T (p.Glu739Ter)	Familial idiopathic hypercalciuria [RCV001535865]	likely pathogenic	1	167854446	167854446	Human	1	name
151836619	CV1367285	single nucleotide variant	NM_018417.6(ADCY10):c.2474C>G (p.Ser825Cys)	not provided [RCV001994260]	uncertain significance	1	167846227	167846227	Human		name
151813541	CV1373224	single nucleotide variant	NM_018417.6(ADCY10):c.1897A>C (p.Ile633Leu)	not provided [RCV001900187]	uncertain significance	1	167856439	167856439	Human		name
151796883	CV1392689	single nucleotide variant	NM_018417.6(ADCY10):c.1025G>T (p.Cys342Phe)	Familial idiopathic hypercalciuria [RCV002503545]\|not provided [RCV001898699]	uncertain significance	1	167880605	167880605	Human	1	name
151857481	CV1410618	single nucleotide variant	NM_018417.6(ADCY10):c.2278A>C (p.Lys760Gln)	Familial idiopathic hypercalciuria [RCV002492086]\|not provided [RCV001996715]\|not specified [RCV004043803]	uncertain significance	1	167854383	167854383	Human	1	name
151794653	CV1420598	single nucleotide variant	NM_018417.6(ADCY10):c.1415G>A (p.Gly472Asp)	not provided [RCV002027541]	uncertain significance	1	167875178	167875178	Human		name
151819914	CV1422412	single nucleotide variant	NM_018417.6(ADCY10):c.1401G>C (p.Glu467Asp)	See cases [RCV003493886]\|not provided [RCV001900781]	uncertain significance	1	167878451	167878451	Human		name
151849604	CV1427599	single nucleotide variant	NM_018417.6(ADCY10):c.1354G>A (p.Gly452Ser)	not provided [RCV001922590]	uncertain significance	1	167878498	167878498	Human		name
151718462	CV1458697	single nucleotide variant	NM_018417.6(ADCY10):c.2026G>A (p.Val676Ile)	not provided [RCV002003292]	uncertain significance	1	167856310	167856310	Human		name
152175076	CV1601842	single nucleotide variant	NM_018417.6(ADCY10):c.2996A>G (p.His999Arg)	not provided [RCV002163365]	likely benign	1	167845574	167845574	Human		name
155728002	CV1773821	single nucleotide variant	NM_018417.6(ADCY10):c.1202G>A (p.Arg401Lys)	not provided [RCV002301577]	uncertain significance	1	167880129	167880129	Human		name
155686648	CV1777661	single nucleotide variant	NM_018417.6(ADCY10):c.1451A>G (p.Tyr484Cys)	not provided [RCV002299040]\|not specified [RCV004047648]	uncertain significance	1	167875142	167875142	Human		name
156400925	CV1889033	single nucleotide variant	NM_018417.6(ADCY10):c.2859T>A (p.Cys953Ter)	not provided [RCV003069125]	pathogenic	1	167845711	167845711	Human		name
156025993	CV1896264	single nucleotide variant	NM_018417.6(ADCY10):c.2251G>A (p.Val751Ile)	ADCY10-related disorder [RCV003973673]\|not provided [RCV003100427]	likely benign\|uncertain significance	1	167854410	167854410	Human	1	name , trait , alternate_id
156087820	CV1953339	single nucleotide variant	NM_018417.6(ADCY10):c.1795A>G (p.Ile599Val)	not provided [RCV002570121]	uncertain significance	1	167860885	167860885	Human		name
156393475	CV1965160	single nucleotide variant	NM_018417.6(ADCY10):c.2897A>G (p.His966Arg)	not provided [RCV002584108]	uncertain significance	1	167845673	167845673	Human		name
156413172	CV1968973	single nucleotide variant	NM_018417.6(ADCY10):c.2956G>A (p.Ala986Thr)	not provided [RCV002608762]	uncertain significance	1	167845614	167845614	Human		name
156133994	CV1998752	single nucleotide variant	NM_018417.6(ADCY10):c.2353C>A (p.His785Asn)	not provided [RCV002663326]\|not specified [RCV004066789]	uncertain significance	1	167848445	167848445	Human		name
156287952	CV2001846	single nucleotide variant	NM_018417.6(ADCY10):c.2779C>T (p.Arg927Ter)	not provided [RCV002647081]	pathogenic	1	167845791	167845791	Human		name
156394172	CV2015625	single nucleotide variant	NM_018417.6(ADCY10):c.1970T>G (p.Met657Arg)	not provided [RCV002725365]	uncertain significance	1	167856366	167856366	Human		name
156372048	CV2028151	single nucleotide variant	NM_018417.6(ADCY10):c.2548C>A (p.Pro850Thr)	not provided [RCV002721597]	uncertain significance	1	167846153	167846153	Human		name
156238539	CV2031839	single nucleotide variant	NM_018417.6(ADCY10):c.1934A>G (p.Glu645Gly)	not provided [RCV002745581]	uncertain significance	1	167856402	167856402	Human		name
155931534	CV2096089	single nucleotide variant	NM_018417.6(ADCY10):c.1415G>T (p.Gly472Val)	not provided [RCV002903855]	uncertain significance	1	167875178	167875178	Human		name
156002882	CV2103441	single nucleotide variant	NM_018417.6(ADCY10):c.2864G>A (p.Arg955His)	not provided [RCV002908719]\|not specified [RCV004614254]	uncertain significance	1	167845706	167845706	Human		name
156241544	CV2105325	single nucleotide variant	NM_018417.6(ADCY10):c.1664A>G (p.Tyr555Cys)	not provided [RCV002933215]	uncertain significance	1	167861016	167861016	Human		name
156127514	CV2112409	single nucleotide variant	NM_018417.6(ADCY10):c.1153G>A (p.Gly385Ser)	not provided [RCV002928065]	uncertain significance	1	167880178	167880178	Human		name
156372476	CV2127641	single nucleotide variant	NM_018417.6(ADCY10):c.1373C>G (p.Pro458Arg)	not provided [RCV002942446]	uncertain significance	1	167878479	167878479	Human		name
156213537	CV2127865	single nucleotide variant	NM_018417.6(ADCY10):c.2903G>A (p.Arg968Gln)	ADCY10-related disorder [RCV003973571]\|not provided [RCV002957846]	likely benign	1	167845667	167845667	Human	1	name , trait , alternate_id
156215958	CV2167361	single nucleotide variant	NM_018417.6(ADCY10):c.1937C>G (p.Ala646Gly)	not provided [RCV003042521]	uncertain significance	1	167856399	167856399	Human		name
156335677	CV2168373	single nucleotide variant	NM_018417.6(ADCY10):c.1307A>G (p.Asn436Ser)	not provided [RCV003030011]	uncertain significance	1	167878545	167878545	Human		name
156299765	CV2169982	single nucleotide variant	NM_018417.6(ADCY10):c.1090G>A (p.Glu364Lys)	not provided [RCV003045494]	uncertain significance	1	167880540	167880540	Human		name
156271797	CV2187453	single nucleotide variant	NM_018417.6(ADCY10):c.1355G>T (p.Gly452Val)	not provided [RCV003044478]	uncertain significance	1	167878497	167878497	Human		name
156063712	CV2199963	single nucleotide variant	NM_018417.6(ADCY10):c.1283A>G (p.Asp428Gly)	not specified [RCV004074134]	uncertain significance	1	167878569	167878569	Human		name
156386888	CV2221345	single nucleotide variant	NM_018417.6(ADCY10):c.2215G>C (p.Glu739Gln)	not specified [RCV004095026]	uncertain significance	1	167854446	167854446	Human		name
156140448	CV2247072	single nucleotide variant	NM_018417.6(ADCY10):c.1052C>G (p.Pro351Arg)	not specified [RCV004114618]	uncertain significance	1	167880578	167880578	Human		name
155983967	CV2247710	single nucleotide variant	NM_018417.6(ADCY10):c.1604G>T (p.Gly535Val)	not specified [RCV004119398]	uncertain significance	1	167870269	167870269	Human		name
156308378	CV2249503	single nucleotide variant	NM_018417.6(ADCY10):c.2167G>A (p.Asp723Asn)	not specified [RCV004120542]	uncertain significance	1	167856169	167856169	Human		name
156179311	CV2298368	single nucleotide variant	NM_018417.6(ADCY10):c.2189G>A (p.Ser730Asn)	not specified [RCV004160260]	uncertain significance	1	167854472	167854472	Human		name
156200645	CV2313091	single nucleotide variant	NM_018417.6(ADCY10):c.2516C>A (p.Thr839Asn)	not specified [RCV004161364]	uncertain significance	1	167846185	167846185	Human		name
156051832	CV2336690	single nucleotide variant	NM_018417.6(ADCY10):c.2723G>A (p.Gly908Asp)	not provided [RCV005099920]\|not specified [RCV004196930]	uncertain significance	1	167845847	167845847	Human		name
155969143	CV2337923	single nucleotide variant	NM_018417.6(ADCY10):c.1372C>T (p.Pro458Ser)	not specified [RCV004183929]	uncertain significance	1	167878480	167878480	Human		name
156221801	CV2343889	single nucleotide variant	NM_018417.6(ADCY10):c.2404C>A (p.Leu802Met)	not provided [RCV003491293]\|not specified [RCV004193467]	uncertain significance	1	167848394	167848394	Human		name
156195413	CV2347491	single nucleotide variant	NM_018417.6(ADCY10):c.1199T>C (p.Val400Ala)	not specified [RCV004200440]	uncertain significance	1	167880132	167880132	Human		name
156195818	CV2347597	single nucleotide variant	NM_018417.6(ADCY10):c.1207G>A (p.Glu403Lys)	not specified [RCV004200535]	uncertain significance	1	167880124	167880124	Human		name
155993320	CV2381778	single nucleotide variant	NM_018417.6(ADCY10):c.1780T>C (p.Cys594Arg)	not provided [RCV005099116]\|not specified [RCV004232227]	uncertain significance	1	167860900	167860900	Human		name
329362905	CV2464828	single nucleotide variant	NM_018417.6(ADCY10):c.2623A>G (p.Asn875Asp)	not specified [RCV004284776]	uncertain significance	1	167846078	167846078	Human		name
401753088	CV2674775	single nucleotide variant	NM_018417.6(ADCY10):c.1580T>C (p.Met527Thr)	not provided [RCV003561270]\|not specified [RCV004294055]	likely benign\|uncertain significance	1	167870293	167870293	Human		name
401732773	CV2685330	single nucleotide variant	NM_018417.6(ADCY10):c.1878T>A (p.Phe626Leu)	not provided [RCV003779894]\|not specified [RCV004292328]	uncertain significance	1	167859825	167859825	Human		name
401731035	CV2686849	single nucleotide variant	NM_018417.6(ADCY10):c.1421C>T (p.Ala474Val)	not specified [RCV004302028]	uncertain significance	1	167875172	167875172	Human		name
401728506	CV2693604	single nucleotide variant	NM_018417.6(ADCY10):c.2255T>C (p.Phe752Ser)	not provided [RCV003720825]\|not specified [RCV004297948]	uncertain significance	1	167854406	167854406	Human		name
401726614	CV2695740	single nucleotide variant	NM_018417.6(ADCY10):c.1336C>T (p.Pro446Ser)	not specified [RCV004299540]	uncertain significance	1	167878516	167878516	Human		name
401855597	CV2753015	single nucleotide variant	NM_018417.6(ADCY10):c.2414T>A (p.Leu805Gln)	Familial idiopathic hypercalciuria [RCV003338070]	uncertain significance	1	167848384	167848384	Human	1	name
401889674	CV2758372	single nucleotide variant	NM_018417.6(ADCY10):c.1385A>G (p.Tyr462Cys)	not provided [RCV003720856]\|not specified [RCV004341720]	likely benign\|uncertain significance	1	167878467	167878467	Human		name
401863836	CV2770857	single nucleotide variant	NM_018417.6(ADCY10):c.2466G>A (p.Met822Ile)	not specified [RCV004343535]	uncertain significance	1	167846235	167846235	Human		name
401891514	CV2780495	single nucleotide variant	NM_018417.6(ADCY10):c.2848C>A (p.His950Asn)	not specified [RCV004358188]	uncertain significance	1	167845722	167845722	Human		name
401897112	CV2789832	single nucleotide variant	NM_018417.6(ADCY10):c.2425A>G (p.Thr809Ala)	not specified [RCV004362225]	likely benign	1	167848373	167848373	Human		name
401921808	CV2800029	single nucleotide variant	NM_018417.6(ADCY10):c.1933G>A (p.Glu645Lys)	ADCY10-related disorder [RCV003403099]	uncertain significance	1	167856403	167856403	Human		name , trait , alternate_id
404985586	CV2851872	single nucleotide variant	NM_018417.6(ADCY10):c.1787T>C (p.Leu596Pro)	not provided [RCV003489527]	uncertain significance	1	167860893	167860893	Human		name
404985607	CV2851875	single nucleotide variant	NM_018417.6(ADCY10):c.2971G>T (p.Ala991Ser)	not provided [RCV003489530]	uncertain significance	1	167845599	167845599	Human		name
404982947	CV2851876	single nucleotide variant	NM_018417.6(ADCY10):c.2585C>G (p.Ala862Gly)	not provided [RCV003489531]\|not specified [RCV005323454]	uncertain significance	1	167846116	167846116	Human		name
405218066	CV2873645	single nucleotide variant	NM_018417.6(ADCY10):c.2525C>G (p.Thr842Ser)	not provided [RCV003553480]	uncertain significance	1	167846176	167846176	Human		name
402522474	CV2900136	single nucleotide variant	NM_018417.6(ADCY10):c.1823G>A (p.Arg608Gln)	not provided [RCV003575966]\|not specified [RCV005323492]	uncertain significance	1	167859880	167859880	Human		name
405165126	CV2905847	single nucleotide variant	NM_018417.6(ADCY10):c.2241T>A (p.His747Gln)	not provided [RCV003562677]	uncertain significance	1	167854420	167854420	Human		name
405083996	CV2946433	single nucleotide variant	NM_018417.6(ADCY10):c.1196C>T (p.Thr399Ile)	not provided [RCV003664821]	uncertain significance	1	167880135	167880135	Human		name
405127419	CV2954738	single nucleotide variant	NM_018417.6(ADCY10):c.1378T>C (p.Tyr460His)	not provided [RCV003668058]	uncertain significance	1	167878474	167878474	Human		name
405139114	CV2970322	single nucleotide variant	NM_018417.6(ADCY10):c.2938G>A (p.Val980Met)	not provided [RCV003669044]	uncertain significance	1	167845632	167845632	Human		name
405013986	CV2994317	single nucleotide variant	NM_018417.6(ADCY10):c.1625C>T (p.Ala542Val)	not provided [RCV003694227]	uncertain significance	1	167861055	167861055	Human		name
404998319	CV3008812	single nucleotide variant	NM_018417.6(ADCY10):c.2741G>A (p.Arg914His)	not provided [RCV003692908]\|not specified [RCV004897811]	uncertain significance	1	167845829	167845829	Human		name
402484205	CV3036789	single nucleotide variant	NM_018417.6(ADCY10):c.2348C>G (p.Thr783Ser)	not provided [RCV003713141]	uncertain significance	1	167848450	167848450	Human		name
405254050	CV3045199	single nucleotide variant	NM_018417.6(ADCY10):c.1490T>A (p.Met497Lys)	not provided [RCV003722801]	uncertain significance	1	167870383	167870383	Human		name
405162115	CV3062667	single nucleotide variant	NM_018417.6(ADCY10):c.2141A>G (p.Asn714Ser)	not provided [RCV003727172]	uncertain significance	1	167856195	167856195	Human		name
405234193	CV3073638	single nucleotide variant	NM_018417.6(ADCY10):c.2620C>T (p.Arg874Trp)	not provided [RCV003735551]	uncertain significance	1	167846081	167846081	Human		name
405151050	CV3123372	single nucleotide variant	NM_018417.6(ADCY10):c.1839G>A (p.Met613Ile)	not provided [RCV003817605]	uncertain significance	1	167859864	167859864	Human		name
402518462	CV3135995	single nucleotide variant	NM_018417.6(ADCY10):c.1793A>G (p.Asp598Gly)	not provided [RCV003824621]	uncertain significance	1	167860887	167860887	Human		name
405176757	CV3152372	single nucleotide variant	NM_018417.6(ADCY10):c.2893G>T (p.Asp965Tyr)	not provided [RCV003858327]	uncertain significance	1	167845677	167845677	Human		name
405045448	CV3154495	single nucleotide variant	NM_018417.6(ADCY10):c.2863C>A (p.Arg955Ser)	not provided [RCV003849171]	uncertain significance	1	167845707	167845707	Human		name
405083106	CV3167169	single nucleotide variant	NM_018417.6(ADCY10):c.2948G>A (p.Arg983Gln)	not provided [RCV003851748]\|not specified [RCV004369502]	uncertain significance	1	167845622	167845622	Human		name
404985899	CV3183824	single nucleotide variant	NM_018417.6(ADCY10):c.1996A>G (p.Ile666Val)	not provided [RCV003881101]	uncertain significance	1	167856340	167856340	Human		name
405667898	CV3239989	single nucleotide variant	NM_018417.6(ADCY10):c.1489A>T (p.Met497Leu)	not specified [RCV004368041]	uncertain significance	1	167870384	167870384	Human		name
405668042	CV3240019	single nucleotide variant	NM_018417.6(ADCY10):c.2061A>G (p.Ile687Met)	not specified [RCV004368071]	likely benign	1	167856275	167856275	Human		name
405668063	CV3240023	single nucleotide variant	NM_018417.6(ADCY10):c.2121C>A (p.Asn707Lys)	not specified [RCV004368075]	uncertain significance	1	167856215	167856215	Human		name
405668132	CV3240036	single nucleotide variant	NM_018417.6(ADCY10):c.2201C>T (p.Pro734Leu)	not specified [RCV004368088]	uncertain significance	1	167854460	167854460	Human		name
405668298	CV3240069	single nucleotide variant	NM_018417.6(ADCY10):c.2933T>C (p.Phe978Ser)	not specified [RCV004368121]	uncertain significance	1	167845637	167845637	Human		name
405668349	CV3240079	single nucleotide variant	NM_018417.6(ADCY10):c.2992T>C (p.Ser998Pro)	not specified [RCV004368131]	uncertain significance	1	167845578	167845578	Human		name
407457336	CV3419701	single nucleotide variant	NM_018417.6(ADCY10):c.1937C>T (p.Ala646Val)	not specified [RCV004611095]	uncertain significance	1	167856399	167856399	Human		name
407457388	CV3419720	single nucleotide variant	NM_018417.6(ADCY10):c.2098G>A (p.Val700Ile)	not specified [RCV004611114]	uncertain significance	1	167856238	167856238	Human		name
407457408	CV3419727	single nucleotide variant	NM_018417.6(ADCY10):c.2855A>T (p.Lys952Ile)	not specified [RCV004611121]	uncertain significance	1	167845715	167845715	Human		name
12838696	CV364598	single nucleotide variant	NM_018417.6(ADCY10):c.2872G>T (p.Glu958Ter)	Familial idiopathic hypercalciuria [RCV002480315]\|not provided [RCV000427423]	uncertain significance	1	167845698	167845698	Human	1	name
597798860	CV3653848	single nucleotide variant	NM_018417.6(ADCY10):c.1633T>G (p.Leu545Val)	not specified [RCV004904910]	uncertain significance	1	167861047	167861047	Human		name
597798864	CV3653861	single nucleotide variant	NM_018417.6(ADCY10):c.1393C>T (p.Arg465Cys)	not specified [RCV004904912]	uncertain significance	1	167878459	167878459	Human		name
597798926	CV3653899	single nucleotide variant	NM_018417.6(ADCY10):c.1264C>T (p.Pro422Ser)	not specified [RCV004904945]	uncertain significance	1	167878588	167878588	Human		name
597798967	CV3653928	single nucleotide variant	NM_018417.6(ADCY10):c.2009T>C (p.Met670Thr)	not specified [RCV004904966]	uncertain significance	1	167856327	167856327	Human		name
597798974	CV3653939	single nucleotide variant	NM_018417.6(ADCY10):c.2791C>G (p.Pro931Ala)	not specified [RCV004904970]	uncertain significance	1	167845779	167845779	Human		name
597798976	CV3653949	single nucleotide variant	NM_018417.6(ADCY10):c.2612A>G (p.Tyr871Cys)	not specified [RCV004904971]	uncertain significance	1	167846089	167846089	Human		name
597919755	CV3737997	single nucleotide variant	NM_018417.6(ADCY10):c.1559A>G (p.Tyr520Cys)	not provided [RCV005074596]	uncertain significance	1	167870314	167870314	Human		name
597863868	CV3742135	duplication	NM_018417.6(ADCY10):c.3094dup (p.Glu1032fs)	not provided [RCV005067751]	pathogenic	1	167836523	167836524	Human		name
597864012	CV3742153	single nucleotide variant	NM_018417.6(ADCY10):c.1358T>C (p.Val453Ala)	not provided [RCV005067769]	uncertain significance	1	167878494	167878494	Human		name
597881146	CV3744903	single nucleotide variant	NM_018417.6(ADCY10):c.1850A>G (p.Lys617Arg)	not provided [RCV005069928]	uncertain significance	1	167859853	167859853	Human		name
597933966	CV3750373	single nucleotide variant	NM_018417.6(ADCY10):c.2402G>C (p.Arg801Thr)	not provided [RCV005076298]	uncertain significance	1	167848396	167848396	Human		name
597939186	CV3756786	single nucleotide variant	NM_018417.6(ADCY10):c.1397C>T (p.Thr466Ile)	not provided [RCV005077167]	uncertain significance	1	167878455	167878455	Human		name
597877533	CV3766800	single nucleotide variant	NM_018417.6(ADCY10):c.2662C>T (p.Pro888Ser)	not provided [RCV005108740]	uncertain significance	1	167846039	167846039	Human		name
597899492	CV3782898	single nucleotide variant	NM_018417.6(ADCY10):c.2507T>C (p.Ile836Thr)	not provided [RCV005126918]	uncertain significance	1	167846194	167846194	Human		name
597941859	CV3785893	single nucleotide variant	NM_018417.6(ADCY10):c.2516C>T (p.Thr839Ile)	not provided [RCV005133786]	uncertain significance	1	167846185	167846185	Human		name
597892247	CV3809764	single nucleotide variant	NM_018417.6(ADCY10):c.1915A>C (p.Ile639Leu)	not provided [RCV005151485]	uncertain significance	1	167856421	167856421	Human		name
597861115	CV3822469	single nucleotide variant	NM_018417.6(ADCY10):c.1932T>A (p.Asp644Glu)	not provided [RCV005174999]	uncertain significance	1	167856404	167856404	Human		name
597881562	CV3822913	single nucleotide variant	NM_018417.6(ADCY10):c.2464A>T (p.Met822Leu)	not provided [RCV005178239]	uncertain significance	1	167846237	167846237	Human		name
597866568	CV3834478	single nucleotide variant	NM_018417.6(ADCY10):c.1376T>C (p.Leu459Ser)	not provided [RCV005175845]	uncertain significance	1	167878476	167878476	Human		name
597831932	CV3863998	single nucleotide variant	NM_018417.6(ADCY10):c.2576A>G (p.Lys859Arg)	Familial idiopathic hypercalciuria [RCV005208414]	uncertain significance	1	167846125	167846125	Human	1	name
598214403	CV3951574	single nucleotide variant	NM_018417.6(ADCY10):c.1349T>C (p.Met450Thr)	not specified [RCV005316562]	uncertain significance	1	167878503	167878503	Human		name
598214856	CV3951657	single nucleotide variant	NM_018417.6(ADCY10):c.2711G>A (p.Gly904Glu)	not specified [RCV005316644]	uncertain significance	1	167845990	167845990	Human		name
598264391	CV3951667	single nucleotide variant	NM_018417.6(ADCY10):c.1333C>G (p.Leu445Val)	not specified [RCV005326120]	uncertain significance	1	167878519	167878519	Human		name
598214991	CV3951684	single nucleotide variant	NM_018417.6(ADCY10):c.1914G>T (p.Arg638Ser)	not specified [RCV005316668]	uncertain significance	1	167856422	167856422	Human		name
598215051	CV3951695	single nucleotide variant	NM_018417.6(ADCY10):c.1228A>G (p.Lys410Glu)	not specified [RCV005316678]	uncertain significance	1	167878624	167878624	Human		name
15193051	CV696241	single nucleotide variant	NM_018417.6(ADCY10):c.1691T>C (p.Val564Ala)	not provided [RCV000955258]	benign	1	167860989	167860989	Human		name
15183417	CV706834	single nucleotide variant	NM_018417.6(ADCY10):c.2236C>T (p.His746Tyr)	ADCY10-related disorder [RCV003906088]\|not provided [RCV000974869]	benign\|likely benign	1	167854425	167854425	Human	1	name , trait , alternate_id
15167209	CV706836	single nucleotide variant	NM_018417.6(ADCY10):c.1418T>C (p.Met473Thr)	ADCY10-related disorder [RCV003928510]\|not provided [RCV000971351]	likely benign	1	167875175	167875175	Human	1	name , trait , alternate_id
15183422	CV706837	single nucleotide variant	NM_018417.6(ADCY10):c.1394G>A (p.Arg465His)	ADCY10-related disorder [RCV003928593]\|not provided [RCV000974870]	benign	1	167878458	167878458	Human	1	name , trait , alternate_id
15105939	CV718355	single nucleotide variant	NM_018417.6(ADCY10):c.2895C>A (p.Asp965Glu)	ADCY10-related disorder [RCV003920792]\|not provided [RCV000893176]	likely benign	1	167845675	167845675	Human	1	name , trait , alternate_id
15151221	CV718356	single nucleotide variant	NM_018417.6(ADCY10):c.1742G>A (p.Arg581Gln)	Familial idiopathic hypercalciuria [RCV002507548]\|not provided [RCV000879549]\|not specified [RCV001817059]	likely benign	1	167860938	167860938	Human	1	name
15192158	CV731842	single nucleotide variant	NM_018417.6(ADCY10):c.2182G>A (p.Glu728Lys)	not provided [RCV000910456]	likely benign	1	167854479	167854479	Human		name
26891522	CV822977	single nucleotide variant	NM_018417.6(ADCY10):c.2740C>T (p.Arg914Cys)	not provided [RCV001060584]	uncertain significance	1	167845830	167845830	Human		name
26921365	CV822978	single nucleotide variant	NM_018417.6(ADCY10):c.2101C>T (p.Gln701Ter)	not provided [RCV001049797]	pathogenic	1	167856235	167856235	Human		name
38484314	CV921737	single nucleotide variant	NM_018417.6(ADCY10):c.2005A>G (p.Ile669Val)	Familial idiopathic hypercalciuria [RCV002480722]\|not provided [RCV001219351]\|not specified [RCV004032357]	uncertain significance	1	167856331	167856331	Human	1	name
38488493	CV921738	single nucleotide variant	NM_018417.6(ADCY10):c.1263C>A (p.Tyr421Ter)	not provided [RCV001221254]	pathogenic\|likely pathogenic	1	167878589	167878589	Human		name
38475795	CV930150	single nucleotide variant	NM_018417.6(ADCY10):c.2111A>G (p.Asp704Gly)	Familial idiopathic hypercalciuria [RCV002484106]\|not provided [RCV001204402]\|not specified [RCV004033616]	uncertain significance	1	167856225	167856225	Human	1	name
38483708	CV941566	single nucleotide variant	NM_018417.6(ADCY10):c.2042C>T (p.Ala681Val)	ADCY10-related disorder [RCV003938570]\|not provided [RCV001236033]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	167856294	167856294	Human	1	name , trait , alternate_id
126732141	CV987033	single nucleotide variant	NM_018417.6(ADCY10):c.2056G>A (p.Val686Ile)	Familial idiopathic hypercalciuria [RCV002486177]\|not provided [RCV001304033]	uncertain significance	1	167856280	167856280	Human	1	name
126746775	CV1002285	single nucleotide variant	NM_018417.6(ADCY10):c.4763G>C (p.Arg1588Thr)	Familial idiopathic hypercalciuria [RCV002476464]\|not provided [RCV001315245]	uncertain significance	1	167809748	167809748	Human	1	name
126759844	CV1002286	single nucleotide variant	NM_018417.6(ADCY10):c.4504C>G (p.Gln1502Glu)	Familial idiopathic hypercalciuria [RCV002476485]\|not provided [RCV001318172]\|not specified [RCV004034927]	uncertain significance	1	167810892	167810892	Human	1	name
126730995	CV1002287	single nucleotide variant	NM_018417.6(ADCY10):c.3667T>C (p.Tyr1223His)	Familial idiopathic hypercalciuria [RCV002499601]\|not provided [RCV001312961]\|not specified [RCV004609748]	uncertain significance	1	167829350	167829350	Human	1	name
126750605	CV1002288	single nucleotide variant	NM_018417.6(ADCY10):c.3619C>T (p.Arg1207Trp)	not provided [RCV001326755]\|not specified [RCV004035218]	uncertain significance	1	167829398	167829398	Human		name
126738811	CV1002289	single nucleotide variant	NM_018417.6(ADCY10):c.3422G>C (p.Cys1141Ser)	Familial idiopathic hypercalciuria [RCV002499605]\|not provided [RCV001314159]	uncertain significance	1	167833158	167833158	Human	1	name
126727608	CV1022747	single nucleotide variant	NM_018417.6(ADCY10):c.4171T>G (p.Phe1391Val)	Familial idiopathic hypercalciuria [RCV002486431]\|not provided [RCV001348736]	uncertain significance	1	167822139	167822139	Human	1	name
126924273	CV1039590	single nucleotide variant	NM_018417.6(ADCY10):c.4816G>A (p.Val1606Met)	Familial idiopathic hypercalciuria [RCV002504604]\|not provided [RCV001366842]\|not specified [RCV004036985]	uncertain significance	1	167809695	167809695	Human	1	name
127268333	CV1058468	single nucleotide variant	NM_018417.6(ADCY10):c.4438G>T (p.Glu1480Ter)	not provided [RCV001389209]	pathogenic	1	167818116	167818116	Human		name
127244386	CV1066424	single nucleotide variant	NM_018417.6(ADCY10):c.4651T>C (p.Cys1551Arg)	not provided [RCV001393702]	likely benign	1	167810745	167810745	Human		name
127292785	CV1153341	single nucleotide variant	NM_018417.6(ADCY10):c.4721C>T (p.Thr1574Met)	not provided [RCV001510980]	benign	1	167809790	167809790	Human		name
127291299	CV1153342	single nucleotide variant	NM_018417.6(ADCY10):c.4562G>A (p.Cys1521Tyr)	not provided [RCV001510285]	benign	1	167810834	167810834	Human		name
127293581	CV1153343	single nucleotide variant	NM_018417.6(ADCY10):c.4058C>T (p.Pro1353Leu)	not provided [RCV001511392]	benign\|likely benign	1	167823118	167823118	Human		name
151777433	CV1342713	single nucleotide variant	NM_018417.6(ADCY10):c.4082G>A (p.Arg1361Gln)	not provided [RCV001988816]	uncertain significance	1	167823094	167823094	Human		name
151890995	CV1344449	single nucleotide variant	NM_018417.6(ADCY10):c.3307A>C (p.Met1103Leu)	Familial idiopathic hypercalciuria [RCV002484470]\|not provided [RCV001943206]\|not specified [RCV005320961]	uncertain significance	1	167836311	167836311	Human	1	name
151811629	CV1359488	single nucleotide variant	NM_018417.6(ADCY10):c.3746T>C (p.Phe1249Ser)	Familial idiopathic hypercalciuria [RCV002486602]\|not provided [RCV001991885]\|not specified [RCV004045498]	uncertain significance	1	167829271	167829271	Human	1	name
151853222	CV1376239	single nucleotide variant	NM_018417.6(ADCY10):c.4573G>A (p.Gly1525Arg)	not provided [RCV001996224]	uncertain significance	1	167810823	167810823	Human		name
151794149	CV1394900	single nucleotide variant	NM_018417.6(ADCY10):c.4378T>C (p.Tyr1460His)	not provided [RCV001973326]	uncertain significance	1	167818176	167818176	Human		name
151764272	CV1478382	single nucleotide variant	NM_018417.6(ADCY10):c.3082G>A (p.Glu1028Lys)	not provided [RCV002008219]	uncertain significance	1	167836536	167836536	Human		name
151872107	CV1487821	single nucleotide variant	NM_018417.6(ADCY10):c.4317T>A (p.Phe1439Leu)	not provided [RCV001981434]\|not specified [RCV004043654]	uncertain significance	1	167818237	167818237	Human		name
152136215	CV1624823	single nucleotide variant	NM_018417.6(ADCY10):c.4334G>C (p.Arg1445Thr)	not provided [RCV002177453]	likely benign	1	167818220	167818220	Human		name
152090552	CV1661892	single nucleotide variant	NM_018417.6(ADCY10):c.3488G>T (p.Arg1163Leu)	not provided [RCV002131990]	benign	1	167833092	167833092	Human		name
156040797	CV1891024	single nucleotide variant	NM_018417.6(ADCY10):c.4754T>C (p.Val1585Ala)	not provided [RCV003078509]\|not specified [RCV004071948]	uncertain significance	1	167809757	167809757	Human		name
156041606	CV1891083	single nucleotide variant	NM_018417.6(ADCY10):c.3823G>T (p.Glu1275Ter)	not provided [RCV003078539]	pathogenic	1	167824783	167824783	Human		name
156371940	CV1916528	single nucleotide variant	NM_018417.6(ADCY10):c.4175T>C (p.Val1392Ala)	not provided [RCV002603251]\|not specified [RCV004614367]	uncertain significance	1	167822135	167822135	Human		name
156138552	CV1963039	single nucleotide variant	NM_018417.6(ADCY10):c.3947T>C (p.Ile1316Thr)	not provided [RCV002572484]	uncertain significance	1	167824659	167824659	Human		name
156379705	CV1968414	single nucleotide variant	NM_018417.6(ADCY10):c.4430A>G (p.Gln1477Arg)	not provided [RCV002603877]	uncertain significance	1	167818124	167818124	Human		name
156344530	CV1970437	single nucleotide variant	NM_018417.6(ADCY10):c.3799T>G (p.Tyr1267Asp)	not provided [RCV002601458]	uncertain significance	1	167824807	167824807	Human		name
156097467	CV2012941	single nucleotide variant	NM_018417.6(ADCY10):c.4399A>G (p.Met1467Val)	not provided [RCV002706540]	uncertain significance	1	167818155	167818155	Human		name
156210323	CV2018839	single nucleotide variant	NM_018417.6(ADCY10):c.4078G>A (p.Gly1360Arg)	not provided [RCV002700602]	uncertain significance	1	167823098	167823098	Human		name
156002550	CV2106853	single nucleotide variant	NM_018417.6(ADCY10):c.3961C>T (p.Arg1321Ter)	not provided [RCV002947861]	pathogenic	1	167824567	167824567	Human		name
156253342	CV2117096	single nucleotide variant	NM_018417.6(ADCY10):c.3565C>T (p.Arg1189Trp)	not provided [RCV002933629]	uncertain significance	1	167833015	167833015	Human		name
156148467	CV2128431	single nucleotide variant	NM_018417.6(ADCY10):c.3235G>A (p.Gly1079Arg)	ADCY10-related disorder [RCV003906377]\|not provided [RCV002928815]	likely benign	1	167836383	167836383	Human	1	name , trait , alternate_id
156303193	CV2129608	single nucleotide variant	NM_018417.6(ADCY10):c.4220A>G (p.Glu1407Gly)	ADCY10-related disorder [RCV003961304]\|not provided [RCV002962238]	benign\|likely benign	1	167822090	167822090	Human	1	name , trait , alternate_id
156086977	CV2134600	single nucleotide variant	NM_018417.6(ADCY10):c.4822A>G (p.Asn1608Asp)	not provided [RCV002979462]	uncertain significance	1	167809689	167809689	Human		name
156158855	CV2140628	single nucleotide variant	NM_018417.6(ADCY10):c.4615C>T (p.Arg1539Trp)	not provided [RCV003004986]	uncertain significance	1	167810781	167810781	Human		name
155956118	CV2144028	single nucleotide variant	NM_018417.6(ADCY10):c.3875T>C (p.Ile1292Thr)	not provided [RCV002994904]	likely benign	1	167824731	167824731	Human		name
156158799	CV2147210	single nucleotide variant	NM_018417.6(ADCY10):c.3856C>T (p.Pro1286Ser)	not provided [RCV003023115]	uncertain significance	1	167824750	167824750	Human		name
156318230	CV2161627	single nucleotide variant	NM_018417.6(ADCY10):c.3812G>T (p.Trp1271Leu)	not provided [RCV003046434]	uncertain significance	1	167824794	167824794	Human		name
156186350	CV2164154	single nucleotide variant	NM_018417.6(ADCY10):c.3829A>G (p.Met1277Val)	not provided [RCV003023990]	uncertain significance	1	167824777	167824777	Human		name
156114051	CV2172450	single nucleotide variant	NM_018417.6(ADCY10):c.3860T>G (p.Leu1287Arg)	not provided [RCV003039057]	uncertain significance	1	167824746	167824746	Human		name
156400143	CV2198992	single nucleotide variant	NM_018417.6(ADCY10):c.4814C>T (p.Thr1605Ile)	not specified [RCV004080402]	likely benign	1	167809697	167809697	Human		name
156190585	CV2226922	single nucleotide variant	NM_018417.6(ADCY10):c.3433G>A (p.Gly1145Ser)	not specified [RCV004103893]	uncertain significance	1	167833147	167833147	Human		name
156021747	CV2264490	single nucleotide variant	NM_018417.6(ADCY10):c.3694C>T (p.His1232Tyr)	not specified [RCV004138383]	uncertain significance	1	167829323	167829323	Human		name
156089281	CV2290781	single nucleotide variant	NM_018417.6(ADCY10):c.3065C>T (p.Pro1022Leu)	not specified [RCV004149288]	uncertain significance	1	167837261	167837261	Human		name
156277272	CV2300134	single nucleotide variant	NM_018417.6(ADCY10):c.4444T>A (p.Ser1482Thr)	not specified [RCV004151324]	uncertain significance	1	167818110	167818110	Human		name
156049492	CV2319310	single nucleotide variant	NM_018417.6(ADCY10):c.4681T>G (p.Tyr1561Asp)	not specified [RCV004180136]	uncertain significance	1	167809830	167809830	Human		name
156356697	CV2320837	single nucleotide variant	NM_018417.6(ADCY10):c.3931C>A (p.His1311Asn)	not specified [RCV004172665]	uncertain significance	1	167824675	167824675	Human		name
156175995	CV2331135	single nucleotide variant	NM_018417.6(ADCY10):c.3085G>A (p.Glu1029Lys)	not provided [RCV003561128]\|not specified [RCV004181746]	likely benign\|uncertain significance	1	167836533	167836533	Human		name
156190028	CV2339487	single nucleotide variant	NM_018417.6(ADCY10):c.4530C>G (p.Cys1510Trp)	ADCY10-related disorder [RCV003410204]\|not specified [RCV004194155]	likely benign\|uncertain significance	1	167810866	167810866	Human	1	name , trait , alternate_id
156092216	CV2384906	single nucleotide variant	NM_018417.6(ADCY10):c.3488G>A (p.Arg1163Gln)	not specified [RCV004225780]	uncertain significance	1	167833092	167833092	Human		name
329385885	CV2428131	single nucleotide variant	NM_018417.6(ADCY10):c.4384G>A (p.Gly1462Arg)	not specified [RCV004251173]	uncertain significance	1	167818170	167818170	Human		name
329356177	CV2430618	single nucleotide variant	NM_018417.6(ADCY10):c.4055A>G (p.Tyr1352Cys)	not provided [RCV005101196]\|not specified [RCV004253812]	uncertain significance	1	167823121	167823121	Human		name
329360207	CV2446641	single nucleotide variant	NM_018417.6(ADCY10):c.3349A>T (p.Thr1117Ser)	not provided [RCV003779621]\|not specified [RCV004251529]	uncertain significance	1	167834038	167834038	Human		name
401752250	CV2682755	single nucleotide variant	NM_018417.6(ADCY10):c.4034G>A (p.Cys1345Tyr)	not specified [RCV004281729]	uncertain significance	1	167824494	167824494	Human		name
401750146	CV2695956	single nucleotide variant	NM_018417.6(ADCY10):c.3233T>C (p.Leu1078Ser)	not specified [RCV004308225]	uncertain significance	1	167836385	167836385	Human		name
401732464	CV2708840	single nucleotide variant	NM_018417.6(ADCY10):c.3603G>C (p.Arg1201Ser)	not specified [RCV004307787]	uncertain significance	1	167829414	167829414	Human		name
401763537	CV2720359	single nucleotide variant	NM_018417.6(ADCY10):c.3998A>G (p.Asn1333Ser)	not specified [RCV004325672]	uncertain significance	1	167824530	167824530	Human		name
401869530	CV2772433	single nucleotide variant	NM_018417.6(ADCY10):c.4287G>C (p.Trp1429Cys)	not provided [RCV005104137]\|not specified [RCV004355221]	uncertain significance	1	167818267	167818267	Human		name
401882332	CV2781664	single nucleotide variant	NM_018417.6(ADCY10):c.3898G>A (p.Glu1300Lys)	not specified [RCV004354863]	uncertain significance	1	167824708	167824708	Human		name
401935088	CV2799840	single nucleotide variant	NM_018417.6(ADCY10):c.3833C>A (p.Ala1278Asp)	ADCY10-related disorder [RCV003412506]\|not provided [RCV005099993]	uncertain significance	1	167824773	167824773	Human	1	name , trait , alternate_id
405069979	CV2876414	single nucleotide variant	NM_018417.6(ADCY10):c.3626C>T (p.Thr1209Ile)	not provided [RCV003548470]\|not specified [RCV005323474]	uncertain significance	1	167829391	167829391	Human		name
405198997	CV2876878	single nucleotide variant	NM_018417.6(ADCY10):c.3079C>T (p.Pro1027Ser)	not provided [RCV003551194]	uncertain significance	1	167836539	167836539	Human		name
405121537	CV2888154	single nucleotide variant	NM_018417.6(ADCY10):c.4081C>T (p.Arg1361Trp)	not provided [RCV003559145]	uncertain significance	1	167823095	167823095	Human		name
405149782	CV2892047	single nucleotide variant	NM_018417.6(ADCY10):c.3864A>C (p.Lys1288Asn)	not provided [RCV003561644]	conflicting interpretations of pathogenicity\|uncertain significance	1	167824742	167824742	Human		name
405226534	CV2892570	single nucleotide variant	NM_018417.6(ADCY10):c.4647G>T (p.Glu1549Asp)	not provided [RCV003554761]	uncertain significance	1	167810749	167810749	Human		name
405130808	CV2895181	single nucleotide variant	NM_018417.6(ADCY10):c.4441C>G (p.Gln1481Glu)	not provided [RCV003559987]	uncertain significance	1	167818113	167818113	Human		name
402470333	CV2931327	single nucleotide variant	NM_018417.6(ADCY10):c.4531C>A (p.Pro1511Thr)	not provided [RCV003570277]	uncertain significance	1	167810865	167810865	Human		name
405100676	CV2948146	single nucleotide variant	NM_018417.6(ADCY10):c.3326A>G (p.Asn1109Ser)	not provided [RCV003666125]	uncertain significance	1	167834061	167834061	Human		name
404981259	CV3006224	single nucleotide variant	NM_018417.6(ADCY10):c.4817T>G (p.Val1606Gly)	not provided [RCV003691196]	uncertain significance	1	167809694	167809694	Human		name
402505352	CV3038975	single nucleotide variant	NM_018417.6(ADCY10):c.4669A>T (p.Lys1557Ter)	not provided [RCV003715143]	uncertain significance	1	167810727	167810727	Human		name
405135369	CV3052092	single nucleotide variant	NM_018417.6(ADCY10):c.4227C>A (p.Asn1409Lys)	not provided [RCV003725191]	uncertain significance	1	167822083	167822083	Human		name
405213990	CV3128326	single nucleotide variant	NM_018417.6(ADCY10):c.3148G>A (p.Glu1050Lys)	not provided [RCV003823750]	uncertain significance	1	167836470	167836470	Human		name
405200698	CV3143474	single nucleotide variant	NM_018417.6(ADCY10):c.3140C>T (p.Thr1047Ile)	not provided [RCV003844460]	uncertain significance	1	167836478	167836478	Human		name
405180003	CV3147421	single nucleotide variant	NM_018417.6(ADCY10):c.4715T>C (p.Leu1572Pro)	not provided [RCV003842323]\|not specified [RCV004897821]	uncertain significance	1	167809796	167809796	Human		name
405132365	CV3163799	single nucleotide variant	NM_018417.6(ADCY10):c.4628C>T (p.Thr1543Ile)	not provided [RCV003854787]	uncertain significance	1	167810768	167810768	Human		name
405252447	CV3177977	single nucleotide variant	NM_018417.6(ADCY10):c.3650G>A (p.Arg1217His)	not provided [RCV003870757]	uncertain significance	1	167829367	167829367	Human		name
405668381	CV3240086	single nucleotide variant	NM_018417.6(ADCY10):c.3207G>C (p.Leu1069Phe)	not specified [RCV004368138]	uncertain significance	1	167836411	167836411	Human		name
405668386	CV3240087	single nucleotide variant	NM_018417.6(ADCY10):c.3297T>G (p.Cys1099Trp)	not specified [RCV004368139]	uncertain significance	1	167836321	167836321	Human		name
405668565	CV3240124	single nucleotide variant	NM_018417.6(ADCY10):c.4049G>A (p.Ser1350Asn)	not specified [RCV004368176]	likely benign	1	167824479	167824479	Human		name
405668598	CV3240131	single nucleotide variant	NM_018417.6(ADCY10):c.4244A>T (p.His1415Leu)	not specified [RCV004368183]	uncertain significance	1	167822066	167822066	Human		name
405668623	CV3240136	single nucleotide variant	NM_018417.6(ADCY10):c.4292C>T (p.Ala1431Val)	not specified [RCV004368188]	uncertain significance	1	167818262	167818262	Human		name
405668763	CV3240165	single nucleotide variant	NM_018417.6(ADCY10):c.4713G>C (p.Trp1571Cys)	not specified [RCV004368217]	uncertain significance	1	167809798	167809798	Human		name
405668778	CV3240168	single nucleotide variant	NM_018417.6(ADCY10):c.4769A>T (p.Asn1590Ile)	not specified [RCV004368220]	uncertain significance	1	167809742	167809742	Human		name
405854015	CV3395483	single nucleotide variant	NM_018417.6(ADCY10):c.4136A>G (p.Tyr1379Cys)	Familial idiopathic hypercalciuria [RCV004555739]\|not provided [RCV005059529]	uncertain significance	1	167823040	167823040	Human	1	name
596932704	CV3539331	single nucleotide variant	NM_018417.6(ADCY10):c.3962G>A (p.Arg1321Gln)	not provided [RCV004793955]	uncertain significance	1	167824566	167824566	Human		name
597798834	CV3653821	single nucleotide variant	NM_018417.6(ADCY10):c.3443T>G (p.Val1148Gly)	not specified [RCV004904896]	uncertain significance	1	167833137	167833137	Human		name
597798842	CV3653831	single nucleotide variant	NM_018417.6(ADCY10):c.3868G>A (p.Glu1290Lys)	not specified [RCV004904900]	uncertain significance	1	167824738	167824738	Human		name
597798859	CV3653840	single nucleotide variant	NM_018417.6(ADCY10):c.3343C>G (p.Leu1115Val)	not specified [RCV004904909]	uncertain significance	1	167834044	167834044	Human		name
597798885	CV3653872	single nucleotide variant	NM_018417.6(ADCY10):c.4195T>C (p.Cys1399Arg)	not specified [RCV004904923]	uncertain significance	1	167822115	167822115	Human		name
597798907	CV3653889	single nucleotide variant	NM_018417.6(ADCY10):c.3440T>A (p.Ile1147Lys)	not specified [RCV004904935]	uncertain significance	1	167833140	167833140	Human		name
597798944	CV3653908	single nucleotide variant	NM_018417.6(ADCY10):c.3243T>A (p.Asn1081Lys)	not specified [RCV004904954]	uncertain significance	1	167836375	167836375	Human		name
597798950	CV3653916	single nucleotide variant	NM_018417.6(ADCY10):c.4550T>C (p.Met1517Thr)	not specified [RCV004904957]	uncertain significance	1	167810846	167810846	Human		name
597798972	CV3653931	single nucleotide variant	NM_018417.6(ADCY10):c.4276G>A (p.Val1426Ile)	not specified [RCV004904969]	likely benign	1	167822034	167822034	Human		name
597798980	CV3653959	single nucleotide variant	NM_018417.6(ADCY10):c.4798C>G (p.Leu1600Val)	not specified [RCV004904973]	uncertain significance	1	167809713	167809713	Human		name
597725422	CV3730148	single nucleotide variant	NM_018417.6(ADCY10):c.3760G>T (p.Ala1254Ser)	Familial idiopathic hypercalciuria [RCV005050244]	uncertain significance	1	167824846	167824846	Human	1	name
597853469	CV3743412	single nucleotide variant	NM_018417.6(ADCY10):c.3649C>T (p.Arg1217Cys)	not provided [RCV005060762]	uncertain significance	1	167829368	167829368	Human		name
597850104	CV3746842	single nucleotide variant	NM_018417.6(ADCY10):c.4259T>C (p.Leu1420Pro)	not provided [RCV005060469]	uncertain significance	1	167822051	167822051	Human		name
597957023	CV3754761	single nucleotide variant	NM_018417.6(ADCY10):c.4361C>T (p.Thr1454Ile)	not provided [RCV005080611]	uncertain significance	1	167818193	167818193	Human		name
597951787	CV3798421	single nucleotide variant	NM_018417.6(ADCY10):c.4751T>C (p.Ile1584Thr)	not provided [RCV005136202]	uncertain significance	1	167809760	167809760	Human		name
597906572	CV3804070	single nucleotide variant	NM_018417.6(ADCY10):c.4292C>G (p.Ala1431Gly)	not provided [RCV005153616]	uncertain significance	1	167818262	167818262	Human		name
597961249	CV3812095	single nucleotide variant	NM_018417.6(ADCY10):c.3311C>T (p.Ala1104Val)	not provided [RCV005163748]	uncertain significance	1	167834076	167834076	Human		name
597945213	CV3812888	single nucleotide variant	NM_018417.6(ADCY10):c.4270T>A (p.Ser1424Thr)	not provided [RCV005159901]	uncertain significance	1	167822040	167822040	Human		name
597953250	CV3843940	single nucleotide variant	NM_018417.6(ADCY10):c.3503A>G (p.Asn1168Ser)	not provided [RCV005190802]	uncertain significance	1	167833077	167833077	Human		name
598214774	CV3890727	single nucleotide variant	NM_018417.6(ADCY10):c.3544A>T (p.Arg1182Ter)	Familial idiopathic hypercalciuria [RCV005251591]	likely pathogenic	1	167833036	167833036	Human	1	name
12896952	CV389325	single nucleotide variant	NM_018417.6(ADCY10):c.3542A>G (p.Asn1181Ser)	not provided [RCV000946521]\|not specified [RCV000456041]	benign	1	167833038	167833038	Human		name
598214489	CV3951594	single nucleotide variant	NM_018417.6(ADCY10):c.4186T>C (p.Phe1396Leu)	not specified [RCV005316582]	uncertain significance	1	167822124	167822124	Human		name
598214566	CV3951610	single nucleotide variant	NM_018417.6(ADCY10):c.3502A>C (p.Asn1168His)	not specified [RCV005316598]	uncertain significance	1	167833078	167833078	Human		name
598214949	CV3951675	single nucleotide variant	NM_018417.6(ADCY10):c.4383C>A (p.Asp1461Glu)	not specified [RCV005316661]	likely benign	1	167818171	167818171	Human		name
598215109	CV3951705	single nucleotide variant	NM_018417.6(ADCY10):c.3232T>G (p.Leu1078Val)	not specified [RCV005316688]	uncertain significance	1	167836386	167836386	Human		name
15164005	CV696239	single nucleotide variant	NM_018417.6(ADCY10):c.4313A>G (p.Asn1438Ser)	not provided [RCV000948231]	benign\|likely benign	1	167818241	167818241	Human		name
15127894	CV745813	single nucleotide variant	NM_018417.6(ADCY10):c.4072G>T (p.Val1358Leu)	not provided [RCV000919566]	likely benign	1	167823104	167823104	Human		name
26884915	CV822976	single nucleotide variant	NM_018417.6(ADCY10):c.4625A>G (p.Glu1542Gly)	not provided [RCV001052817]	uncertain significance	1	167810771	167810771	Human		name
38485607	CV921736	single nucleotide variant	NM_018417.6(ADCY10):c.4000C>T (p.Arg1334Ter)	not provided [RCV001219949]	pathogenic	1	167824528	167824528	Human		name
38471348	CV930148	single nucleotide variant	NM_018417.6(ADCY10):c.4424A>G (p.Gln1475Arg)	Familial idiopathic hypercalciuria [RCV002497731]\|not provided [RCV001213755]\|not specified [RCV004033903]	uncertain significance	1	167818130	167818130	Human	1	name
38499095	CV941563	single nucleotide variant	NM_018417.6(ADCY10):c.4558G>A (p.Val1520Ile)	ADCY10-related disorder [RCV003963136]\|not provided [RCV001228168]	likely benign\|uncertain significance	1	167810838	167810838	Human	1	name , trait , alternate_id
38478590	CV941564	single nucleotide variant	NM_018417.6(ADCY10):c.4232T>A (p.Ile1411Asn)	not provided [RCV001233956]	uncertain significance	1	167822078	167822078	Human		name
38478152	CV941565	single nucleotide variant	NM_018417.6(ADCY10):c.3592G>A (p.Gly1198Arg)	not provided [RCV001233802]\|not specified [RCV004033214]	uncertain significance	1	167832988	167832988	Human		name
126731024	CV987032	single nucleotide variant	NM_018417.6(ADCY10):c.4547T>C (p.Leu1516Pro)	Familial idiopathic hypercalciuria [RCV002486108]\|not provided [RCV001294311]\|not specified [RCV004035603]	uncertain significance	1	167810849	167810849	Human	1	name
405212125	CV3063162	microsatellite	NM_018417.6(ADCY10):c.2372AAG[1] (p.Glu792del)	not provided [RCV003732158]	uncertain significance	1	167848421	167848423	Human		name
126920954	CV1039591	microsatellite	NM_018417.6(ADCY10):c.3782ACC[2] (p.His1263del)	not provided [RCV001363187]	uncertain significance	1	167824816	167824818	Human		name
13802360	CV535228	microsatellite	NM_018417.6(ADCY10):c.1205_1206del (p.His402fs)	Abnormal sperm morphology [RCV000714269]	pathogenic	1	167880125	167880126	Human		name
8629070	CV84214	single nucleotide variant	NM_001167749.2(ADCY10):c.4284G>A (p.Trp1428Ter)	Malignant melanoma [RCV000064295]	not provided	1	167809768	167809768	Human		name
156373711	CV1921143	inversion	NM_018417.6(ADCY10):c.2397_2398inv (p.Val800Ile)	not provided [RCV002603406]	uncertain significance	1	167848400	167848401	Human		name
405853851	CV3395261	deletion	NM_018417.6(ADCY10):c.2430del (p.Ser810_Leu811insTer)	Familial idiopathic hypercalciuria [RCV004555403]	likely pathogenic	1	167848368	167848368	Human	1	name
596932714	CV3539341	deletion	NM_018417.6(ADCY10):c.2235_2237del (p.Glu745_His746delinsAsp)	not provided [RCV004793965]	uncertain significance	1	167854424	167854426	Human		name
402513303	CV2860168	duplication	NM_018417.6(ADCY10):c.3193_3302dup (p.Asn1101delinsLysArgLeuSerSerCysLeuTrpProThrIlePheTrpLeuTrpGluLysMetThrLysProTyrIleThrSerTer)	not provided [RCV003575283]	pathogenic	1	167836315	167836316	Human		name

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