Rgs9 Variant Search Result - Rat Genome Database

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710 records found for search term Rgs9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405117351	CV2949583	single nucleotide variant	NM_003835.4(RGS9):c.58-6T>C	not provided [RCV003667064]	likely benign	17	65153416	65153416	Human		name
38476557	CV940428	single nucleotide variant	NM_003835.4(RGS9):c.57+6C>T	not provided [RCV001204739]	uncertain significance	17	65137603	65137603	Human		name
126750790	CV997820	single nucleotide variant	NM_003835.4(RGS9):c.58-1G>T	not provided [RCV001306916]	likely pathogenic\|uncertain significance	17	65153421	65153421	Human		name
126912760	CV1050532	single nucleotide variant	NM_003835.4(RGS9):c.746+6T>C	not provided [RCV001358931]	uncertain significance	17	65190242	65190242	Human		name
127275429	CV1083400	single nucleotide variant	NM_003835.4(RGS9):c.57+10G>A	not provided [RCV001406723]	likely benign	17	65137607	65137607	Human		name
127235271	CV1105204	single nucleotide variant	NM_003835.4(RGS9):c.58-12T>C	not provided [RCV001433065]	likely benign	17	65153410	65153410	Human		name
127271055	CV1105208	single nucleotide variant	NM_003835.4(RGS9):c.205+8C>T	not provided [RCV001430812]	likely benign	17	65158353	65158353	Human		name
127273748	CV1105211	single nucleotide variant	NM_003835.4(RGS9):c.501-8C>T	not provided [RCV001442663]	likely benign	17	65168192	65168192	Human		name
127235830	CV1105212	single nucleotide variant	NM_003835.4(RGS9):c.583-5T>C	not provided [RCV001433196]	likely benign	17	65177727	65177727	Human		name
127274880	CV1105213	single nucleotide variant	NM_003835.4(RGS9):c.976+9T>C	not provided [RCV001432106]	likely benign	17	65197250	65197250	Human		name
127297842	CV1126579	single nucleotide variant	NM_003835.4(RGS9):c.364+8C>T	not provided [RCV001477727]	likely benign	17	65160595	65160595	Human		name
127301856	CV1126580	single nucleotide variant	NM_003835.4(RGS9):c.364+9T>G	not provided [RCV001461493]	likely benign	17	65160596	65160596	Human		name
127332346	CV1126588	single nucleotide variant	NM_003835.4(RGS9):c.977-5T>C	not provided [RCV001472164]	likely benign	17	65201988	65201988	Human		name
127307198	CV1147497	single nucleotide variant	NM_003835.4(RGS9):c.861-6T>C	not provided [RCV001500405]	likely benign	17	65197120	65197120	Human		name
151878527	CV1395381	single nucleotide variant	NM_003835.4(RGS9):c.746+1G>A	not provided [RCV001999236]	likely pathogenic\|uncertain significance	17	65190237	65190237	Human		name
151823786	CV1412318	single nucleotide variant	NM_003835.4(RGS9):c.861-5T>G	not provided [RCV001901142]	uncertain significance	17	65197121	65197121	Human		name
151884513	CV1412403	single nucleotide variant	NM_003835.4(RGS9):c.654+2T>C	not provided [RCV001887167]	likely pathogenic\|uncertain significance	17	65177805	65177805	Human		name
151874006	CV1493443	single nucleotide variant	NM_003835.4(RGS9):c.976+3G>A	not provided [RCV001906840]	uncertain significance	17	65197244	65197244	Human		name
151728849	CV1515206	single nucleotide variant	NM_003835.4(RGS9):c.861-2A>C	not provided [RCV002040988]	likely pathogenic\|uncertain significance	17	65197124	65197124	Human		name
152155887	CV1549881	single nucleotide variant	NM_003835.4(RGS9):c.57+14C>T	not provided [RCV002158835]	likely benign	17	65137611	65137611	Human		name
152134488	CV1634269	single nucleotide variant	NM_003835.4(RGS9):c.977-6A>G	not provided [RCV002218523]	likely benign	17	65201987	65201987	Human		name
156446535	CV1947882	single nucleotide variant	NM_003835.4(RGS9):c.501-3C>A	not provided [RCV003118044]	uncertain significance	17	65168197	65168197	Human		name
156319819	CV1966000	single nucleotide variant	NM_003835.4(RGS9):c.861-7C>T	not provided [RCV002600156]	likely benign	17	65197119	65197119	Human		name
155915346	CV1980783	single nucleotide variant	NM_003835.4(RGS9):c.976+4G>A	not provided [RCV002614280]	uncertain significance	17	65197245	65197245	Human		name
155910646	CV2017645	single nucleotide variant	NM_003835.4(RGS9):c.364+6T>C	not provided [RCV002681690]	uncertain significance	17	65160593	65160593	Human		name
156288402	CV2050287	single nucleotide variant	NM_003835.4(RGS9):c.155-1G>T	not provided [RCV002807244]	likely pathogenic	17	65158294	65158294	Human		name
156235586	CV2072458	single nucleotide variant	NM_003835.4(RGS9):c.860+8T>C	not provided [RCV002830216]	likely benign	17	65193664	65193664	Human		name
155951122	CV2076386	single nucleotide variant	NM_003835.4(RGS9):c.365-2A>G	not provided [RCV002862353]	likely pathogenic	17	65160849	65160849	Human		name
156309261	CV2150160	single nucleotide variant	NM_003835.4(RGS9):c.206-1G>A	not provided [RCV003028482]	likely pathogenic	17	65160232	65160232	Human		name
155970795	CV2158078	single nucleotide variant	NM_003835.4(RGS9):c.860+7A>G	not provided [RCV003033426]	likely benign	17	65193663	65193663	Human		name
156361956	CV2158926	deletion	NM_003835.4(RGS9):c.205+2del	not provided [RCV003031629]	likely pathogenic	17	65158347	65158347	Human		name
156194257	CV2175406	single nucleotide variant	NM_003835.4(RGS9):c.365-7T>C	not provided [RCV003057939]	likely benign	17	65160844	65160844	Human		name
156203558	CV2179141	single nucleotide variant	NM_003835.4(RGS9):c.684+3A>C	not provided [RCV003024536]	uncertain significance	17	65189318	65189318	Human		name
402472058	CV2912137	single nucleotide variant	NM_003835.4(RGS9):c.313-6T>C	not provided [RCV003570705]	likely benign	17	65160530	65160530	Human		name
405221910	CV3154782	single nucleotide variant	NM_003835.4(RGS9):c.746+1G>C	not provided [RCV003847277]	likely pathogenic	17	65190237	65190237	Human		name
597951191	CV3756409	single nucleotide variant	NM_003835.4(RGS9):c.500+1G>T	not provided [RCV005079466]	likely pathogenic	17	65163090	65163090	Human		name
26919308	CV852244	single nucleotide variant	NM_003835.4(RGS9):c.976+2T>C	Retinal dystrophy [RCV004813591]\|not provided [RCV001045233]	likely pathogenic\|uncertain significance	17	65197243	65197243	Human	2	name
26886529	CV852787	single nucleotide variant	NM_003835.4(RGS9):c.977-7C>A	RGS9-related disorder [RCV003938422]\|not provided [RCV001055084]	likely benign\|uncertain significance	17	65201986	65201986	Human	1	name , trait , alternate_id
126733770	CV997821	single nucleotide variant	NM_003835.4(RGS9):c.154+6G>A	not provided [RCV001294802]	uncertain significance	17	65153524	65153524	Human		name
126757781	CV997822	single nucleotide variant	NM_003835.4(RGS9):c.206-3C>A	not provided [RCV001308524]	uncertain significance	17	65160230	65160230	Human		name
126727664	CV997825	single nucleotide variant	NM_003835.4(RGS9):c.423+3A>G	not provided [RCV001303211]	uncertain significance	17	65160912	65160912	Human		name
127230504	CV1083403	single nucleotide variant	NM_003835.4(RGS9):c.312+15T>C	not provided [RCV001412487]	likely benign	17	65160354	65160354	Human		name
127251186	CV1083404	single nucleotide variant	NM_003835.4(RGS9):c.365-13C>T	not provided [RCV001400023]	likely benign	17	65160838	65160838	Human		name
127233087	CV1083405	deletion	NM_003835.4(RGS9):c.976+10del	not provided [RCV001395989]	likely benign	17	65197249	65197249	Human		name
127232721	CV1083406	single nucleotide variant	NM_003835.4(RGS9):c.1064+8T>A	not provided [RCV001413590]	likely benign	17	65202088	65202088	Human		name
127243448	CV1105210	single nucleotide variant	NM_003835.4(RGS9):c.501-20C>T	not provided [RCV001434821]	likely benign	17	65168180	65168180	Human		name
127251637	CV1105214	deletion	NM_003835.4(RGS9):c.1203+9del	not provided [RCV001425647]	likely benign	17	65204308	65204308	Human		name
127318191	CV1126581	single nucleotide variant	NM_003835.4(RGS9):c.364+19A>G	not provided [RCV001466103]	likely benign	17	65160606	65160606	Human		name
127312192	CV1126585	single nucleotide variant	NM_003835.4(RGS9):c.684+17T>C	not provided [RCV001464310]	likely benign	17	65189332	65189332	Human		name
127300695	CV1126587	single nucleotide variant	NM_003835.4(RGS9):c.860+14A>G	not provided [RCV001461155]	likely benign	17	65193670	65193670	Human		name
127308623	CV1126593	single nucleotide variant	NM_003835.4(RGS9):c.1892+7A>T	not provided [RCV001463351]	likely benign	17	65225493	65225493	Human		name
127311521	CV1147501	single nucleotide variant	NM_003835.4(RGS9):c.1204-5A>T	not provided [RCV001501630]	likely benign	17	65207917	65207917	Human		name
127301520	CV1158095	single nucleotide variant	NM_003835.4(RGS9):c.312+10G>A	not provided [RCV001514723]	benign	17	65160349	65160349	Human		name
127305965	CV1158096	single nucleotide variant	NM_003835.4(RGS9):c.500+16C>A	not provided [RCV001516469]	benign	17	65163105	65163105	Human		name
127321848	CV1158097	single nucleotide variant	NM_003835.4(RGS9):c.861-16C>A	not provided [RCV001523250]	benign	17	65197110	65197110	Human		name
127321719	CV1158098	duplication	NM_003835.4(RGS9):c.976+25dup	not provided [RCV001523179]	benign	17	65197257	65197258	Human		name
151821127	CV1443228	single nucleotide variant	NM_003835.4(RGS9):c.861-13A>G	not provided [RCV002049811]	uncertain significance	17	65197113	65197113	Human		name
152039008	CV1538244	single nucleotide variant	NM_003835.4(RGS9):c.364+10T>G	not provided [RCV002206056]	likely benign	17	65160597	65160597	Human		name
152145733	CV1543322	deletion	NM_003835.4(RGS9):c.976+25del	not provided [RCV002178696]	benign	17	65197258	65197258	Human		name
152136331	CV1560618	single nucleotide variant	NM_003835.4(RGS9):c.582+17C>G	not provided [RCV002137590]	likely benign	17	65168298	65168298	Human		name
152068996	CV1566710	single nucleotide variant	NM_003835.4(RGS9):c.313-11T>A	not provided [RCV002111191]	likely benign	17	65160525	65160525	Human		name
152099646	CV1595606	single nucleotide variant	NM_003835.4(RGS9):c.977-20G>A	not provided [RCV002213829]	likely benign	17	65201973	65201973	Human		name
152062743	CV1613061	single nucleotide variant	NM_003835.4(RGS9):c.501-15C>G	not provided [RCV002073874]	likely benign	17	65168185	65168185	Human		name
152026734	CV1626588	single nucleotide variant	NM_003835.4(RGS9):c.205+11A>T	not provided [RCV002185258]	likely benign	17	65158356	65158356	Human		name
152099180	CV1627208	single nucleotide variant	NM_003835.4(RGS9):c.1204-8C>T	not provided [RCV002095283]	likely benign	17	65207914	65207914	Human		name
152027502	CV1628792	single nucleotide variant	NM_003835.4(RGS9):c.423+10T>A	not provided [RCV002104913]	likely benign	17	65160919	65160919	Human		name
152055037	CV1648681	single nucleotide variant	NM_003835.4(RGS9):c.1064+7A>C	not provided [RCV002072827]	likely benign	17	65202087	65202087	Human		name
152170181	CV1650931	single nucleotide variant	NM_003835.4(RGS9):c.582+13C>T	not provided [RCV002143036]	likely benign	17	65168294	65168294	Human		name
152039575	CV1658117	single nucleotide variant	NM_003835.4(RGS9):c.1892+8C>A	not provided [RCV002206138]	likely benign	17	65225494	65225494	Human		name
156067502	CV1971856	single nucleotide variant	NM_003835.4(RGS9):c.312+20C>T	not provided [RCV002621146]	likely benign	17	65160359	65160359	Human		name
156420070	CV1979438	single nucleotide variant	NM_003835.4(RGS9):c.1289+7G>A	not provided [RCV002613321]	likely benign	17	65208014	65208014	Human		name
156244699	CV1991663	single nucleotide variant	NM_003835.4(RGS9):c.1289+2C>A	not provided [RCV002645696]	likely pathogenic\|uncertain significance	17	65208009	65208009	Human		name
156404961	CV1994132	single nucleotide variant	NM_003835.4(RGS9):c.206-11G>C	not provided [RCV002658185]	likely benign	17	65160222	65160222	Human		name
156291830	CV2009765	single nucleotide variant	NM_003835.4(RGS9):c.501-19G>A	not provided [RCV002715685]	likely benign	17	65168181	65168181	Human		name
156094788	CV2010501	single nucleotide variant	NM_003835.4(RGS9):c.746+16G>A	not provided [RCV002695075]	likely benign	17	65190252	65190252	Human		name
156083149	CV2098787	single nucleotide variant	NM_003835.4(RGS9):c.747-15C>T	not provided [RCV002912769]	likely benign	17	65193528	65193528	Human		name
155946200	CV2130244	single nucleotide variant	NM_003835.4(RGS9):c.746+11G>A	not provided [RCV002971593]	likely benign	17	65190247	65190247	Human		name
155986869	CV2153935	single nucleotide variant	NM_003835.4(RGS9):c.500+17C>T	not provided [RCV003016635]	likely benign	17	65163106	65163106	Human		name
155931241	CV2155901	single nucleotide variant	NM_003835.4(RGS9):c.364+20C>G	not provided [RCV003013644]	likely benign\|uncertain significance	17	65160607	65160607	Human		name
156357520	CV2162111	single nucleotide variant	NM_003835.4(RGS9):c.583-19T>C	not provided [RCV003031334]	likely benign	17	65177713	65177713	Human		name
156195437	CV2175496	single nucleotide variant	NM_003835.4(RGS9):c.1408-6C>G	not provided [RCV003057977]	likely benign	17	65224996	65224996	Human		name
156037729	CV2189812	single nucleotide variant	NM_003835.4(RGS9):c.1065-5C>A	not provided [RCV003036444]	likely benign	17	65204158	65204158	Human		name
402467377	CV2910456	single nucleotide variant	NM_003835.4(RGS9):c.501-17G>C	not provided [RCV003569660]	likely benign	17	65168183	65168183	Human		name
405233333	CV2965490	single nucleotide variant	NM_003835.4(RGS9):c.976+10T>G	not provided [RCV003682616]	likely benign	17	65197251	65197251	Human		name
405145330	CV3023858	single nucleotide variant	NM_003835.4(RGS9):c.313-17C>G	not provided [RCV003702876]	likely benign	17	65160519	65160519	Human		name
402480430	CV3041439	single nucleotide variant	NM_003835.4(RGS9):c.424-11T>C	not provided [RCV003712784]	likely benign	17	65163002	65163002	Human		name
405121632	CV3131606	single nucleotide variant	NM_003835.4(RGS9):c.205+12T>C	not provided [RCV003837470]	likely benign	17	65158357	65158357	Human		name
405108470	CV3136674	single nucleotide variant	NM_003835.4(RGS9):c.582+19G>C	not provided [RCV003835828]	likely benign	17	65168300	65168300	Human		name
597971224	CV3750662	single nucleotide variant	NM_003835.4(RGS9):c.583-12T>C	not provided [RCV005084406]	likely benign	17	65177720	65177720	Human		name
597898823	CV3807002	single nucleotide variant	NM_003835.4(RGS9):c.654+11G>C	not provided [RCV005152389]	likely benign	17	65177814	65177814	Human		name
597859057	CV3817104	single nucleotide variant	NM_003835.4(RGS9):c.685-20A>G	not provided [RCV005146485]	likely benign	17	65190155	65190155	Human		name
597970653	CV3832570	single nucleotide variant	NM_003835.4(RGS9):c.685-11G>C	not provided [RCV005166649]	likely benign	17	65190164	65190164	Human		name
597934115	CV3858720	single nucleotide variant	NM_003835.4(RGS9):c.205+18A>G	not provided [RCV005207190]	likely benign	17	65158363	65158363	Human		name
597938115	CV3862714	single nucleotide variant	NM_003835.4(RGS9):c.1892+9C>G	not provided [RCV005207986]	likely benign	17	65225495	65225495	Human		name
38467267	CV940429	single nucleotide variant	NM_003835.4(RGS9):c.1203+5G>A	not provided [RCV001201992]	uncertain significance	17	65204306	65204306	Human		name
38468353	CV940430	single nucleotide variant	NM_003835.4(RGS9):c.1204-1G>A	not provided [RCV001202191]	likely pathogenic\|uncertain significance	17	65207921	65207921	Human		name
127312611	CV1147499	single nucleotide variant	NM_003835.4(RGS9):c.1065-14C>G	not provided [RCV001481719]	likely benign	17	65204149	65204149	Human		name
127320999	CV1158100	single nucleotide variant	NM_003835.4(RGS9):c.1893-20C>T	not provided [RCV001522896]	benign	17	65227255	65227255	Human		name
151746886	CV1428385	single nucleotide variant	NM_003835.4(RGS9):c.1290-18A>G	not provided [RCV001927073]	likely benign\|uncertain significance	17	65210470	65210470	Human		name
152145636	CV1564197	single nucleotide variant	NM_003835.4(RGS9):c.1290-20C>T	not provided [RCV002138765]	likely benign	17	65210468	65210468	Human		name
152173800	CV1567224	single nucleotide variant	NM_003835.4(RGS9):c.1892+20G>A	not provided [RCV002144231]	likely benign	17	65225506	65225506	Human		name
152170442	CV1592434	single nucleotide variant	NM_003835.4(RGS9):c.1203+13G>A	not provided [RCV002161777]	likely benign	17	65204314	65204314	Human		name
152091253	CV1594270	single nucleotide variant	NM_003835.4(RGS9):c.1407+20G>A	not provided [RCV002171853]	likely benign	17	65210625	65210625	Human		name
152160963	CV1598822	duplication	NM_003835.4(RGS9):c.1893-15dup	not provided [RCV002140913]	likely benign	17	65227258	65227259	Human		name
152098729	CV1611768	single nucleotide variant	NM_003835.4(RGS9):c.1203+19T>C	not provided [RCV002172815]	likely benign	17	65204320	65204320	Human		name
152141264	CV1619811	single nucleotide variant	NM_003835.4(RGS9):c.1203+12C>T	not provided [RCV002200605]	likely benign	17	65204313	65204313	Human		name
152136314	CV1624860	single nucleotide variant	NM_003835.4(RGS9):c.1892+10C>T	not provided [RCV002177464]	likely benign	17	65225496	65225496	Human		name
152088251	CV1626125	single nucleotide variant	NM_003835.4(RGS9):c.1893-15C>T	not provided [RCV002131723]	benign	17	65227260	65227260	Human		name
152127090	CV1642015	single nucleotide variant	NM_003835.4(RGS9):c.1065-16C>T	not provided [RCV002176312]	likely benign	17	65204147	65204147	Human		name
152058399	CV1652008	single nucleotide variant	NM_003835.4(RGS9):c.1407+19C>T	not provided [RCV002190238]	likely benign	17	65210624	65210624	Human		name
152073928	CV1660528	single nucleotide variant	NM_003835.4(RGS9):c.1204-11G>C	not provided [RCV002169651]	likely benign	17	65207911	65207911	Human		name
156194603	CV1970900	single nucleotide variant	NM_003835.4(RGS9):c.1289+14T>A	not provided [RCV002625526]	likely benign	17	65208021	65208021	Human		name
156100207	CV1981908	single nucleotide variant	NM_003835.4(RGS9):c.1892+19C>T	not provided [RCV002622183]	likely benign	17	65225505	65225505	Human		name
156013304	CV2071988	single nucleotide variant	NM_003835.4(RGS9):c.1408-19C>T	not provided [RCV002843993]	likely benign	17	65224983	65224983	Human		name
156105340	CV2180924	single nucleotide variant	NM_003835.4(RGS9):c.1065-18A>G	not provided [RCV003054877]	likely benign	17	65204145	65204145	Human		name
155961328	CV2183515	single nucleotide variant	NM_003835.4(RGS9):c.1408-20T>G	not provided [RCV003032952]	uncertain significance	17	65224982	65224982	Human		name
156357053	CV2188973	single nucleotide variant	NM_003835.4(RGS9):c.1064+19G>C	not provided [RCV003048760]	likely benign	17	65202099	65202099	Human		name
156335496	CV2191896	single nucleotide variant	NM_003835.4(RGS9):c.1892+17G>A	not provided [RCV003063941]	likely benign	17	65225503	65225503	Human		name
405076675	CV2948659	single nucleotide variant	NM_003835.4(RGS9):c.1204-14C>G	not provided [RCV003664301]	likely benign	17	65207908	65207908	Human		name
405195589	CV2975860	single nucleotide variant	NM_003835.4(RGS9):c.1289+10A>G	not provided [RCV003677623]	likely benign	17	65208017	65208017	Human		name
405022509	CV3002751	single nucleotide variant	NM_003835.4(RGS9):c.1892+19C>G	not provided [RCV003694951]	likely benign	17	65225505	65225505	Human		name
405201107	CV3041206	single nucleotide variant	NM_003835.4(RGS9):c.1289+13A>G	not provided [RCV003707371]	likely benign	17	65208020	65208020	Human		name
597887402	CV3741960	single nucleotide variant	NM_003835.4(RGS9):c.1892+11G>A	not provided [RCV005070680]	likely benign	17	65225497	65225497	Human		name
597924182	CV3808611	single nucleotide variant	NM_003835.4(RGS9):c.1290-14G>A	not provided [RCV005156125]	likely benign	17	65210474	65210474	Human		name
597882874	CV3857640	deletion	NM_003835.4(RGS9):c.1065-11del	not provided [RCV005199267]	likely benign	17	65204152	65204152	Human		name
126911503	CV1050528	deletion	NM_003835.4(RGS9):c.145_154+18del	not provided [RCV001369243]	likely pathogenic\|uncertain significance	17	65153508	65153535	Human		name
38480019	CV960233	deletion	NM_003835.4(RGS9):c.976+1_976+5del	not provided [RCV001234494]	likely pathogenic\|uncertain significance	17	65197241	65197245	Human		name
127257633	CV1105203	single nucleotide variant	NM_003835.4(RGS9):c.21C>G (p.Gly7=)	not provided [RCV001437932]	likely benign	17	65137561	65137561	Human		name
152172527	CV1660343	single nucleotide variant	NM_003835.4(RGS9):c.15C>T (p.His5=)	not provided [RCV002162488]	likely benign	17	65137555	65137555	Human		name
127237024	CV1105205	single nucleotide variant	NM_003835.4(RGS9):c.78C>T (p.Asp26=)	not provided [RCV001433460]	likely benign	17	65153442	65153442	Human		name
127257557	CV1105206	single nucleotide variant	NM_003835.4(RGS9):c.96A>C (p.Thr32=)	not provided [RCV001437920]	likely benign	17	65153460	65153460	Human		name
156097304	CV2010832	deletion	NM_003835.4(RGS9):c.501-28_501-16del	not provided [RCV002695168]	likely benign	17	65168171	65168183	Human		name
11644095	CV270610	single nucleotide variant	NM_003835.4(RGS9):c.69C>T (p.Leu23=)	not provided [RCV000405035]	conflicting interpretations of pathogenicity\|uncertain significance	17	65153433	65153433	Human		name
402493221	CV2945961	single nucleotide variant	NM_003835.4(RGS9):c.99G>A (p.Gly33=)	not provided [RCV003660755]	likely benign	17	65153463	65153463	Human		name
405234139	CV2975631	single nucleotide variant	NM_003835.4(RGS9):c.39G>A (p.Arg13=)	not provided [RCV003682752]	likely benign	17	65137579	65137579	Human		name
597917193	CV3741131	single nucleotide variant	NM_003835.4(RGS9):c.96A>G (p.Thr32=)	not provided [RCV005074278]	likely benign	17	65153460	65153460	Human		name
15193778	CV704300	single nucleotide variant	NM_003835.4(RGS9):c.66G>A (p.Ala22=)	not provided [RCV000955468]\|not specified [RCV001699477]	benign\|likely benign	17	65153430	65153430	Human		name
126917522	CV1050526	single nucleotide variant	NM_003835.4(RGS9):c.19G>C (p.Gly7Arg)	not provided [RCV001372119]	uncertain significance	17	65137559	65137559	Human		name
127272692	CV1083401	single nucleotide variant	NM_003835.4(RGS9):c.171A>G (p.Gln57=)	not provided [RCV001405779]	likely benign	17	65158311	65158311	Human		name
127251120	CV1083402	single nucleotide variant	NM_003835.4(RGS9):c.297C>T (p.Ser99=)	not provided [RCV001400011]	likely benign	17	65160324	65160324	Human		name
127259620	CV1105207	single nucleotide variant	NM_003835.4(RGS9):c.132C>G (p.Thr44=)	not provided [RCV001427636]	likely benign	17	65153496	65153496	Human		name
127241349	CV1105209	single nucleotide variant	NM_003835.4(RGS9):c.255C>A (p.Pro85=)	not provided [RCV001434388]	likely benign	17	65160282	65160282	Human		name
127321098	CV1158093	single nucleotide variant	NM_003835.4(RGS9):c.135C>T (p.Ser45=)	RGS9-related disorder [RCV003921178]\|not provided [RCV001522946]	benign\|likely benign	17	65153499	65153499	Human	1	name , trait , alternate_id
152055224	CV1522547	single nucleotide variant	NM_003835.4(RGS9):c.126G>A (p.Leu42=)	not provided [RCV002146142]	likely benign	17	65153490	65153490	Human		name
152145896	CV1543342	single nucleotide variant	NM_003835.4(RGS9):c.102C>T (p.Val34=)	not provided [RCV002178716]	likely benign	17	65153466	65153466	Human		name
152111907	CV1640471	single nucleotide variant	NM_003835.4(RGS9):c.180C>A (p.Val60=)	not provided [RCV002174443]	likely benign	17	65158320	65158320	Human		name
156199554	CV1968116	single nucleotide variant	NM_003835.4(RGS9):c.16C>A (p.Gln6Lys)	Inborn genetic diseases [RCV002625679]\|not provided [RCV002598490]	uncertain significance	17	65137556	65137556	Human	1	name
155944062	CV2130089	single nucleotide variant	NM_003835.4(RGS9):c.11G>T (p.Arg4Leu)	not provided [RCV002971476]	uncertain significance	17	65137551	65137551	Human		name
402524230	CV2940462	single nucleotide variant	NM_003835.4(RGS9):c.177C>T (p.Ile59=)	not provided [RCV003663532]	likely benign	17	65158317	65158317	Human		name
405227011	CV3039549	single nucleotide variant	NM_003835.4(RGS9):c.132C>T (p.Thr44=)	not provided [RCV003710879]	likely benign	17	65153496	65153496	Human		name
596941896	CV3408355	single nucleotide variant	NM_003835.4(RGS9):c.16C>T (p.Gln6Ter)	Retinal dystrophy [RCV004816026]	likely pathogenic	17	65137556	65137556	Human	2	name
15201522	CV704301	single nucleotide variant	NM_003835.4(RGS9):c.255C>G (p.Pro85=)	not provided [RCV000957646]	benign	17	65160282	65160282	Human		name
26917024	CV845939	single nucleotide variant	NM_003835.4(RGS9):c.23A>G (p.Gln8Arg)	not provided [RCV001041264]	uncertain significance	17	65137563	65137563	Human		name
26903347	CV845941	single nucleotide variant	NM_003835.4(RGS9):c.204G>T (p.Leu68=)	not provided [RCV001069777]	likely benign\|uncertain significance	17	65158344	65158344	Human		name
38464746	CV958261	single nucleotide variant	NM_003835.4(RGS9):c.222C>T (p.Gly74=)	not provided [RCV001247443]	likely benign\|uncertain significance	17	65160249	65160249	Human		name
126921756	CV1050527	single nucleotide variant	NM_003835.4(RGS9):c.65C>T (p.Ala22Val)	not provided [RCV001363868]	uncertain significance	17	65153429	65153429	Human		name
127299573	CV1126582	single nucleotide variant	NM_003835.4(RGS9):c.538C>T (p.Leu180=)	not provided [RCV001453622]	likely benign	17	65168237	65168237	Human		name
127289920	CV1126583	single nucleotide variant	NM_003835.4(RGS9):c.666C>T (p.Val222=)	not provided [RCV001458258]	likely benign	17	65189297	65189297	Human		name
127332977	CV1126586	single nucleotide variant	NM_003835.4(RGS9):c.807C>T (p.Pro269=)	not provided [RCV001472606]	likely benign	17	65193603	65193603	Human		name
127329185	CV1147496	single nucleotide variant	NM_003835.4(RGS9):c.657A>G (p.Lys219=)	not provided [RCV001487276]	likely benign	17	65189288	65189288	Human		name
127327558	CV1147498	single nucleotide variant	NM_003835.4(RGS9):c.939A>T (p.Arg313=)	not provided [RCV001486396]	likely benign	17	65197204	65197204	Human		name
127295756	CV1158094	single nucleotide variant	NM_003835.4(RGS9):c.303C>T (p.Tyr101=)	RGS9-related disorder [RCV003966074]\|not provided [RCV001512305]	benign\|likely benign	17	65160330	65160330	Human	1	name , trait , alternate_id
151732832	CV1386470	single nucleotide variant	NM_003835.4(RGS9):c.615G>A (p.Leu205=)	not provided [RCV001911055]	likely benign\|uncertain significance	17	65177764	65177764	Human		name
151824358	CV1404097	single nucleotide variant	NM_003835.4(RGS9):c.70G>A (p.Val24Met)	not provided [RCV001976047]	uncertain significance	17	65153434	65153434	Human		name
151731261	CV1420747	single nucleotide variant	NM_003835.4(RGS9):c.86A>T (p.Asn29Ile)	not provided [RCV002021319]	uncertain significance	17	65153450	65153450	Human		name
151854911	CV1473689	single nucleotide variant	NM_003835.4(RGS9):c.35C>G (p.Pro12Arg)	not provided [RCV001904566]	uncertain significance	17	65137575	65137575	Human		name
151854769	CV1481823	deletion	NM_003835.4(RGS9):c.239del (p.Tyr80fs)	not provided [RCV002033635]	pathogenic\|uncertain significance	17	65160266	65160266	Human		name
152110779	CV1551141	single nucleotide variant	NM_003835.4(RGS9):c.771C>T (p.Phe257=)	not provided [RCV002196744]	likely benign	17	65193567	65193567	Human		name
152071025	CV1551999	single nucleotide variant	NM_003835.4(RGS9):c.408G>A (p.Leu136=)	not provided [RCV002148077]	likely benign	17	65160894	65160894	Human		name
152151690	CV1559725	single nucleotide variant	NM_003835.4(RGS9):c.513G>A (p.Glu171=)	not provided [RCV002220916]	likely benign	17	65168212	65168212	Human		name
152088808	CV1562991	single nucleotide variant	NM_003835.4(RGS9):c.537C>T (p.Ala179=)	not provided [RCV002113785]	likely benign	17	65168236	65168236	Human		name
152026341	CV1594390	single nucleotide variant	NM_003835.4(RGS9):c.318G>A (p.Pro106=)	not provided [RCV002104522]	likely benign	17	65160541	65160541	Human		name
152094989	CV1603798	single nucleotide variant	NM_003835.4(RGS9):c.855C>A (p.Ala285=)	not provided [RCV002213237]	likely benign	17	65193651	65193651	Human		name
152027584	CV1628919	single nucleotide variant	NM_003835.4(RGS9):c.432C>T (p.Tyr144=)	RGS9-related disorder [RCV003903334]\|not provided [RCV002104943]	likely benign	17	65163021	65163021	Human	1	name , trait , alternate_id
152127235	CV1642039	single nucleotide variant	NM_003835.4(RGS9):c.357C>T (p.Thr119=)	not provided [RCV002176329]	likely benign	17	65160580	65160580	Human		name
152170378	CV1651054	single nucleotide variant	NM_003835.4(RGS9):c.669T>C (p.Val223=)	not provided [RCV002143099]	likely benign	17	65189300	65189300	Human		name
152068092	CV1660202	single nucleotide variant	NM_003835.4(RGS9):c.378C>T (p.Ala126=)	not provided [RCV002147702]	likely benign	17	65160864	65160864	Human		name
156444433	CV1938294	single nucleotide variant	NM_003835.4(RGS9):c.510G>A (p.Lys170=)	not provided [RCV003115357]	likely benign	17	65168209	65168209	Human		name
156379333	CV1968334	single nucleotide variant	NM_003835.4(RGS9):c.780C>T (p.Asn260=)	not provided [RCV002603852]	likely benign	17	65193576	65193576	Human		name
156226456	CV1991550	single nucleotide variant	NM_003835.4(RGS9):c.37A>G (p.Arg13Gly)	not provided [RCV002626635]	uncertain significance	17	65137577	65137577	Human		name
156212203	CV1997175	single nucleotide variant	NM_003835.4(RGS9):c.87C>G (p.Asn29Lys)	not provided [RCV002666886]	uncertain significance	17	65153451	65153451	Human		name
155943700	CV2002907	single nucleotide variant	NM_003835.4(RGS9):c.828T>C (p.Asp276=)	not provided [RCV002685623]	likely benign	17	65193624	65193624	Human		name
156182690	CV2033632	single nucleotide variant	NM_003835.4(RGS9):c.549G>A (p.Gln183=)	not provided [RCV002765662]	likely benign	17	65168248	65168248	Human		name
156142067	CV2040882	single nucleotide variant	NM_003835.4(RGS9):c.369C>T (p.Ile123=)	not provided [RCV002786559]	likely benign	17	65160855	65160855	Human		name
156031517	CV2059165	single nucleotide variant	NM_003835.4(RGS9):c.525A>G (p.Ala175=)	not provided [RCV002796072]	likely benign	17	65168224	65168224	Human		name
155933184	CV2064163	single nucleotide variant	NM_003835.4(RGS9):c.738C>G (p.Ser246=)	not provided [RCV002861258]	likely benign	17	65190228	65190228	Human		name
155986743	CV2091220	deletion	NM_003835.4(RGS9):c.1892+12_1892+25del	not provided [RCV002907962]	likely benign	17	65225495	65225508	Human		name
156128046	CV2158585	single nucleotide variant	NM_003835.4(RGS9):c.726G>A (p.Lys242=)	not provided [RCV003022065]	likely benign	17	65190216	65190216	Human		name
11640800	CV270609	single nucleotide variant	NM_003835.4(RGS9):c.495G>A (p.Gln165=)	not provided [RCV000884018]\|not specified [RCV000344048]	benign\|likely benign	17	65163084	65163084	Human		name
405210949	CV2867915	single nucleotide variant	NM_003835.4(RGS9):c.474C>T (p.Val158=)	not provided [RCV003552590]	likely benign	17	65163063	65163063	Human		name
402508710	CV3042290	single nucleotide variant	NM_003835.4(RGS9):c.330C>T (p.Pro110=)	not provided [RCV003715468]	likely benign	17	65160553	65160553	Human		name
405236074	CV3079623	single nucleotide variant	NM_003835.4(RGS9):c.825C>T (p.Thr275=)	not provided [RCV003735924]	likely benign	17	65193621	65193621	Human		name
405217920	CV3135644	single nucleotide variant	NM_003835.4(RGS9):c.333C>G (p.Thr111=)	not provided [RCV003824269]	likely benign	17	65160556	65160556	Human		name
405143703	CV3141302	single nucleotide variant	NM_003835.4(RGS9):c.892C>A (p.Arg298=)	not provided [RCV003839418]	likely benign	17	65197157	65197157	Human		name
405216591	CV3160861	single nucleotide variant	NM_003835.4(RGS9):c.912C>T (p.Ser304=)	not provided [RCV003862923]	likely benign	17	65197177	65197177	Human		name
597971856	CV3798933	single nucleotide variant	NM_003835.4(RGS9):c.840C>T (p.Phe280=)	not provided [RCV005142345]	likely benign	17	65193636	65193636	Human		name
597973567	CV3820583	single nucleotide variant	NM_003835.4(RGS9):c.636T>C (p.Asn212=)	not provided [RCV005168100]	likely benign	17	65177785	65177785	Human		name
15201737	CV704302	single nucleotide variant	NM_003835.4(RGS9):c.642C>G (p.Val214=)	not provided [RCV000957710]	likely benign	17	65177791	65177791	Human		name
15123073	CV740961	single nucleotide variant	NM_003835.4(RGS9):c.570G>C (p.Val190=)	not provided [RCV000896348]	benign	17	65168269	65168269	Human		name
15155052	CV756044	single nucleotide variant	NM_003835.4(RGS9):c.609C>T (p.Tyr203=)	not provided [RCV000924384]	benign\|likely benign	17	65177758	65177758	Human		name
15200063	CV771731	single nucleotide variant	NM_003835.4(RGS9):c.916T>C (p.Leu306=)	not provided [RCV000935279]	likely benign	17	65197181	65197181	Human		name
26895672	CV845940	single nucleotide variant	NM_003835.4(RGS9):c.79A>G (p.Met27Val)	not provided [RCV001064189]	uncertain significance	17	65153443	65153443	Human		name
26917979	CV845942	single nucleotide variant	NM_003835.4(RGS9):c.363C>T (p.Tyr121=)	not provided [RCV001042586]	uncertain significance	17	65160586	65160586	Human		name
8636299	CV91522	single nucleotide variant	NM_003835.3(RGS9):c.402G>A (p.Gly134=)	Malignant melanoma [RCV000071620]	not provided	17	65160888	65160888	Human		name
38484150	CV950174	single nucleotide variant	NM_003835.4(RGS9):c.82C>T (p.Gln28Ter)	not provided [RCV001236216]	pathogenic	17	65153446	65153446	Human		name
38499385	CV958260	single nucleotide variant	NM_003835.4(RGS9):c.46T>C (p.Phe16Leu)	not provided [RCV001244586]	uncertain significance	17	65137586	65137586	Human		name
126745449	CV1013005	single nucleotide variant	NM_003835.4(RGS9):c.140C>T (p.Pro47Leu)	not provided [RCV001325893]	uncertain significance	17	65153504	65153504	Human		name
126741812	CV1013006	single nucleotide variant	NM_003835.4(RGS9):c.157A>G (p.Ser53Gly)	Inborn genetic diseases [RCV004671343]\|not provided [RCV001325393]	uncertain significance	17	65158297	65158297	Human	1	name
126745575	CV1013007	single nucleotide variant	NM_003835.4(RGS9):c.272A>G (p.Asn91Ser)	not provided [RCV001315090]	uncertain significance	17	65160299	65160299	Human		name
126755047	CV1013008	single nucleotide variant	NM_003835.4(RGS9):c.286C>G (p.Pro96Ala)	not provided [RCV001327648]	uncertain significance	17	65160313	65160313	Human		name
126752926	CV1013015	single nucleotide variant	NM_003835.4(RGS9):c.1290C>T (p.Ser430=)	not provided [RCV001316397]	likely benign\|uncertain significance	17	65210488	65210488	Human		name
126768564	CV1033537	single nucleotide variant	NM_003835.4(RGS9):c.177C>G (p.Ile59Met)	not provided [RCV001343429]	uncertain significance	17	65158317	65158317	Human		name
126758888	CV1033544	single nucleotide variant	NM_003835.4(RGS9):c.1080G>A (p.Pro360=)	not provided [RCV001339976]	likely benign\|uncertain significance	17	65204178	65204178	Human		name
126919318	CV1050529	single nucleotide variant	NM_003835.4(RGS9):c.157A>C (p.Ser53Arg)	not provided [RCV001362222]	uncertain significance	17	65158297	65158297	Human		name
127251290	CV1083407	single nucleotide variant	NM_003835.4(RGS9):c.1101C>T (p.Asn367=)	not provided [RCV001400040]	likely benign	17	65204199	65204199	Human		name
127268041	CV1083408	single nucleotide variant	NM_003835.4(RGS9):c.1437T>C (p.His479=)	not provided [RCV001404301]	likely benign	17	65225031	65225031	Human		name
127233149	CV1083409	single nucleotide variant	NM_003835.4(RGS9):c.1506C>A (p.Ser502=)	not provided [RCV001396009]	likely benign	17	65225100	65225100	Human		name
127230538	CV1083410	single nucleotide variant	NM_003835.4(RGS9):c.1830G>A (p.Arg610=)	not provided [RCV001394729]	likely benign	17	65225424	65225424	Human		name
127257651	CV1083411	single nucleotide variant	NM_003835.4(RGS9):c.1872G>A (p.Leu624=)	not provided [RCV001419357]	likely benign	17	65225466	65225466	Human		name
127247130	CV1083412	single nucleotide variant	NM_003835.4(RGS9):c.1974G>A (p.Ser658=)	not provided [RCV001399087]	likely benign	17	65227356	65227356	Human		name
127232161	CV1105215	single nucleotide variant	NM_003835.4(RGS9):c.1377A>C (p.Arg459=)	not provided [RCV001421177]	likely benign	17	65210575	65210575	Human		name
127268121	CV1105217	single nucleotide variant	NM_003835.4(RGS9):c.1824C>T (p.His608=)	not provided [RCV001440692]	likely benign	17	65225418	65225418	Human		name
127265078	CV1105218	single nucleotide variant	NM_003835.4(RGS9):c.1929C>T (p.Ser643=)	not provided [RCV001439794]	likely benign	17	65227311	65227311	Human		name
127298599	CV1126589	single nucleotide variant	NM_003835.4(RGS9):c.1005C>T (p.Cys335=)	not provided [RCV001477947]	likely benign	17	65202021	65202021	Human		name
127292194	CV1126590	single nucleotide variant	NM_003835.4(RGS9):c.1470G>A (p.Pro490=)	not provided [RCV001458915]	likely benign	17	65225064	65225064	Human		name
127291461	CV1126591	single nucleotide variant	NM_003835.4(RGS9):c.1545G>A (p.Arg515=)	not provided [RCV001451495]	likely benign	17	65225139	65225139	Human		name
127327327	CV1126592	single nucleotide variant	NM_003835.4(RGS9):c.1867C>A (p.Arg623=)	not provided [RCV001469043]	likely benign	17	65225461	65225461	Human		name
127300435	CV1126594	single nucleotide variant	NM_003835.4(RGS9):c.1939T>C (p.Leu647=)	not provided [RCV001478416]	likely benign	17	65227321	65227321	Human		name
127329206	CV1147500	single nucleotide variant	NM_003835.4(RGS9):c.1170C>T (p.Ala390=)	not provided [RCV001487287]	likely benign	17	65204268	65204268	Human		name
127286430	CV1147502	single nucleotide variant	NM_003835.4(RGS9):c.1392T>C (p.Thr464=)	not provided [RCV001494184]	likely benign	17	65210590	65210590	Human		name
127321683	CV1147503	single nucleotide variant	NM_003835.4(RGS9):c.1410G>T (p.Pro470=)	not provided [RCV001504824]	likely benign	17	65225004	65225004	Human		name
127293933	CV1147504	single nucleotide variant	NM_003835.4(RGS9):c.1524C>T (p.Ala508=)	not provided [RCV001496881]	likely benign	17	65225118	65225118	Human		name
127290877	CV1147505	single nucleotide variant	NM_003835.4(RGS9):c.1602G>A (p.Ser534=)	not provided [RCV001496086]	likely benign	17	65225196	65225196	Human		name
127321623	CV1147506	single nucleotide variant	NM_003835.4(RGS9):c.1602G>C (p.Ser534=)	not provided [RCV001504808]	likely benign	17	65225196	65225196	Human		name
127330033	CV1147507	single nucleotide variant	NM_003835.4(RGS9):c.1848C>T (p.Asp616=)	not provided [RCV001487827]	likely benign	17	65225442	65225442	Human		name
151882059	CV1364049	single nucleotide variant	NM_003835.4(RGS9):c.1521C>T (p.Phe507=)	not provided [RCV001999751]	likely benign	17	65225115	65225115	Human		name
151851307	CV1365894	single nucleotide variant	NM_003835.4(RGS9):c.143A>C (p.His48Pro)	not provided [RCV001922824]	uncertain significance	17	65153507	65153507	Human		name
151822963	CV1378233	deletion	NM_003835.4(RGS9):c.407del (p.Leu136fs)	not provided [RCV002049984]	pathogenic\|uncertain significance	17	65160890	65160890	Human		name
151737397	CV1410758	single nucleotide variant	NM_003835.4(RGS9):c.1854C>T (p.Gly618=)	not provided [RCV002005459]	uncertain significance	17	65225448	65225448	Human		name
151744049	CV1431835	single nucleotide variant	NM_003835.4(RGS9):c.233T>C (p.Val78Ala)	not provided [RCV001926762]	uncertain significance	17	65160260	65160260	Human		name
151829772	CV1489392	single nucleotide variant	NM_003835.4(RGS9):c.1410G>A (p.Pro470=)	not provided [RCV001934940]	likely benign\|uncertain significance	17	65225004	65225004	Human		name
151733970	CV1509964	single nucleotide variant	NM_003835.4(RGS9):c.136G>A (p.Val46Ile)	Bradyopsia [RCV002482651]\|not provided [RCV001892539]	uncertain significance	17	65153500	65153500	Human	2	name
152132330	CV1522045	single nucleotide variant	NM_003835.4(RGS9):c.1569C>T (p.Pro523=)	not provided [RCV002199486]	likely benign	17	65225163	65225163	Human		name
152064568	CV1535826	single nucleotide variant	NM_003835.4(RGS9):c.1230T>G (p.Ser410=)	not provided [RCV002168456]	likely benign	17	65207948	65207948	Human		name
152129518	CV1538974	single nucleotide variant	NM_003835.4(RGS9):c.1779A>T (p.Ser593=)	not provided [RCV002217873]	likely benign	17	65225373	65225373	Human		name
152133428	CV1547168	single nucleotide variant	NM_003835.4(RGS9):c.1683C>G (p.Leu561=)	not provided [RCV002155836]	likely benign	17	65225277	65225277	Human		name
152135053	CV1549913	single nucleotide variant	NM_003835.4(RGS9):c.1743C>T (p.Ser581=)	not provided [RCV002199834]	likely benign	17	65225337	65225337	Human		name
152164414	CV1557599	single nucleotide variant	NM_003835.4(RGS9):c.1026T>C (p.Asp342=)	not provided [RCV002141515]	likely benign	17	65202042	65202042	Human		name
152113622	CV1559051	single nucleotide variant	NM_003835.4(RGS9):c.1317C>T (p.His439=)	not provided [RCV002174642]	likely benign	17	65210515	65210515	Human		name
152136059	CV1560539	single nucleotide variant	NM_003835.4(RGS9):c.1086G>A (p.Ala362=)	not provided [RCV002137557]	likely benign	17	65204184	65204184	Human		name
152076872	CV1565580	single nucleotide variant	NM_003835.4(RGS9):c.1332A>C (p.Pro444=)	not provided [RCV002148802]	likely benign	17	65210530	65210530	Human		name
152102720	CV1579095	single nucleotide variant	NM_003835.4(RGS9):c.1590G>A (p.Leu530=)	not provided [RCV002079200]	likely benign	17	65225184	65225184	Human		name
152153808	CV1579377	single nucleotide variant	NM_003835.4(RGS9):c.1281C>A (p.Thr427=)	not provided [RCV002158584]	likely benign	17	65207999	65207999	Human		name
152089968	CV1580748	single nucleotide variant	NM_003835.4(RGS9):c.1701C>T (p.Arg567=)	not provided [RCV002094034]	likely benign	17	65225295	65225295	Human		name
152081894	CV1589489	single nucleotide variant	NM_003835.4(RGS9):c.1452C>T (p.Thr484=)	not provided [RCV002112867]	likely benign	17	65225046	65225046	Human		name
152135420	CV1594978	single nucleotide variant	NM_003835.4(RGS9):c.1851G>A (p.Val617=)	not provided [RCV002199877]	likely benign	17	65225445	65225445	Human		name
152172448	CV1599128	single nucleotide variant	NM_003835.4(RGS9):c.1632G>A (p.Gly544=)	not provided [RCV002143781]	likely benign	17	65225226	65225226	Human		name
152062153	CV1629559	single nucleotide variant	NM_003835.4(RGS9):c.1125C>T (p.Ile375=)	not provided [RCV002208821]	likely benign	17	65204223	65204223	Human		name
152085958	CV1645288	single nucleotide variant	NM_003835.4(RGS9):c.1527A>G (p.Ser509=)	not provided [RCV002131429]	likely benign	17	65225121	65225121	Human		name
152083893	CV1645568	single nucleotide variant	NM_003835.4(RGS9):c.1546C>A (p.Arg516=)	not provided [RCV002170904]	likely benign	17	65225140	65225140	Human		name
152159731	CV1649903	single nucleotide variant	NM_003835.4(RGS9):c.1854C>A (p.Gly618=)	not provided [RCV002159423]	likely benign	17	65225448	65225448	Human		name
152119726	CV1654774	single nucleotide variant	NM_003835.4(RGS9):c.1683C>T (p.Leu561=)	RGS9-related disorder [RCV003893190]\|not provided [RCV002216616]	likely benign	17	65225277	65225277	Human	1	name , trait , alternate_id
156210515	CV1909719	single nucleotide variant	NM_003835.4(RGS9):c.274C>G (p.Leu92Val)	Inborn genetic diseases [RCV002596045]\|not provided [RCV002596044]	uncertain significance	17	65160301	65160301	Human	1	name
156265464	CV1973849	single nucleotide variant	NM_003835.4(RGS9):c.1776C>T (p.Ala592=)	not provided [RCV002597920]	likely benign	17	65225370	65225370	Human		name
156416238	CV1976476	single nucleotide variant	NM_003835.4(RGS9):c.1680C>T (p.Ser560=)	not provided [RCV002589597]	likely benign	17	65225274	65225274	Human		name
156336590	CV1988352	single nucleotide variant	NM_003835.4(RGS9):c.1923G>A (p.Thr641=)	not provided [RCV002631215]	uncertain significance	17	65227305	65227305	Human		name
156390543	CV1990083	single nucleotide variant	NM_003835.4(RGS9):c.125T>A (p.Leu42Gln)	not provided [RCV002604631]	uncertain significance	17	65153489	65153489	Human		name
156106289	CV2008397	single nucleotide variant	NM_003835.4(RGS9):c.1194C>T (p.Leu398=)	not provided [RCV002695492]	likely benign	17	65204292	65204292	Human		name
156059441	CV2034445	single nucleotide variant	NM_003835.4(RGS9):c.184C>T (p.Arg62Trp)	not provided [RCV002736785]	uncertain significance	17	65158324	65158324	Human		name
156248474	CV2049577	single nucleotide variant	NM_003835.4(RGS9):c.1914T>C (p.Asp638=)	not provided [RCV002791609]	likely benign	17	65227296	65227296	Human		name
156029316	CV2059018	single nucleotide variant	NM_003835.4(RGS9):c.1971G>A (p.Glu657=)	not provided [RCV002795982]	likely benign	17	65227353	65227353	Human		name
156034309	CV2059312	single nucleotide variant	NM_003835.4(RGS9):c.1359A>G (p.Glu453=)	not provided [RCV002796185]	likely benign	17	65210557	65210557	Human		name
156103537	CV2061101	single nucleotide variant	NM_003835.4(RGS9):c.1506C>T (p.Ser502=)	not provided [RCV002824645]	likely benign	17	65225100	65225100	Human		name
156178471	CV2061251	single nucleotide variant	NM_003835.4(RGS9):c.290A>T (p.Asp97Val)	not provided [RCV002802181]	uncertain significance	17	65160317	65160317	Human		name
156020816	CV2110995	single nucleotide variant	NM_003835.4(RGS9):c.1467C>G (p.Pro489=)	not provided [RCV002909603]	likely benign	17	65225061	65225061	Human		name
156037672	CV2120085	single nucleotide variant	NM_003835.4(RGS9):c.1689C>T (p.Thr563=)	not provided [RCV002949492]	likely benign	17	65225283	65225283	Human		name
156316700	CV2140343	single nucleotide variant	NM_003835.4(RGS9):c.1233G>A (p.Pro411=)	not provided [RCV003011430]	likely benign	17	65207951	65207951	Human		name
155978598	CV2157091	single nucleotide variant	NM_003835.4(RGS9):c.237G>C (p.Arg79Ser)	not provided [RCV003016265]	uncertain significance	17	65160264	65160264	Human		name
155988033	CV2159887	single nucleotide variant	NM_003835.4(RGS9):c.1767C>T (p.Gly589=)	not provided [RCV003034194]	likely benign	17	65225361	65225361	Human		name
156228845	CV2164880	single nucleotide variant	NM_003835.4(RGS9):c.1935C>G (p.Thr645=)	not provided [RCV003043006]	likely benign	17	65227317	65227317	Human		name
156176215	CV2166355	single nucleotide variant	NM_003835.4(RGS9):c.1491C>T (p.Ser497=)	not provided [RCV003023679]	likely benign	17	65225085	65225085	Human		name
156136980	CV2177610	single nucleotide variant	NM_003835.4(RGS9):c.185G>T (p.Arg62Leu)	not provided [RCV003039903]	uncertain significance	17	65158325	65158325	Human		name
401763426	CV2703836	single nucleotide variant	NM_003835.4(RGS9):c.289G>C (p.Asp97His)	Inborn genetic diseases [RCV003281523]	uncertain significance	17	65160316	65160316	Human	1	name
405065208	CV2937184	deletion	NM_003835.4(RGS9):c.681del (p.Glu228fs)	not provided [RCV003663642]	pathogenic	17	65189307	65189307	Human		name
405114780	CV2953035	single nucleotide variant	NM_003835.4(RGS9):c.1416G>A (p.Gln472=)	not provided [RCV003666788]	likely benign	17	65225010	65225010	Human		name
405193871	CV2975163	single nucleotide variant	NM_003835.4(RGS9):c.1746C>T (p.Phe582=)	not provided [RCV003677458]	likely benign	17	65225340	65225340	Human		name
405187737	CV2977581	single nucleotide variant	NM_003835.4(RGS9):c.1605C>G (p.Gly535=)	not provided [RCV003706122]	likely benign	17	65225199	65225199	Human		name
405241914	CV3014622	single nucleotide variant	NM_003835.4(RGS9):c.1989A>G (p.Thr663=)	not provided [RCV003719378]	likely benign	17	65227371	65227371	Human		name
405220824	CV3059821	single nucleotide variant	NM_003835.4(RGS9):c.1671C>T (p.Ser557=)	not provided [RCV003733183]	likely benign	17	65225265	65225265	Human		name
404996943	CV3123829	single nucleotide variant	NM_003835.4(RGS9):c.1533C>T (p.Ser511=)	not provided [RCV003827736]	likely benign	17	65225127	65225127	Human		name
405218811	CV3154172	single nucleotide variant	NM_003835.4(RGS9):c.1758G>A (p.Leu586=)	not provided [RCV003846864]	likely benign	17	65225352	65225352	Human		name
597718177	CV3586426	single nucleotide variant	NM_003835.4(RGS9):c.236G>A (p.Arg79Lys)	Inborn genetic diseases [RCV004960095]	likely benign	17	65160263	65160263	Human	1	name
597933287	CV3742770	single nucleotide variant	NM_003835.4(RGS9):c.1152C>T (p.His384=)	not provided [RCV005076209]	likely benign	17	65204250	65204250	Human		name
597872645	CV3747199	single nucleotide variant	NM_003835.4(RGS9):c.1650G>A (p.Gly550=)	not provided [RCV005068883]	likely benign	17	65225244	65225244	Human		name
597969234	CV3791284	single nucleotide variant	NM_003835.4(RGS9):c.1920C>T (p.Pro640=)	not provided [RCV005141316]	likely benign	17	65227302	65227302	Human		name
597938485	CV3808255	single nucleotide variant	NM_003835.4(RGS9):c.1623G>A (p.Glu541=)	not provided [RCV005158443]	likely benign	17	65225217	65225217	Human		name
598189465	CV3902622	single nucleotide variant	NM_003835.4(RGS9):c.270G>T (p.Lys90Asn)	Inborn genetic diseases [RCV005266716]	uncertain significance	17	65160297	65160297	Human	1	name
13516220	CV491378	single nucleotide variant	NM_003835.4(RGS9):c.1662C>T (p.Thr554=)	not provided [RCV000595249]	conflicting interpretations of pathogenicity\|uncertain significance	17	65225256	65225256	Human		name
15164001	CV727358	single nucleotide variant	NM_003835.4(RGS9):c.1851G>C (p.Val617=)	not provided [RCV000882099]\|not specified [RCV001701465]	benign	17	65225445	65225445	Human		name
15134636	CV740960	single nucleotide variant	NM_003835.4(RGS9):c.178G>A (p.Val60Ile)	not provided [RCV000898325]\|not specified [RCV001701475]	benign	17	65158318	65158318	Human		name
15168766	CV740962	single nucleotide variant	NM_003835.4(RGS9):c.1863G>A (p.Leu621=)	not provided [RCV000904925]	likely benign	17	65225457	65225457	Human		name
8628057	CV83201	single nucleotide variant	NM_003835.3(RGS9):c.1845G>A (p.Gly615=)	Malignant melanoma [RCV000063281]	not provided	17	65225439	65225439	Human		name
26886805	CV845948	deletion	NM_003835.4(RGS9):c.727del (p.Ser243fs)	not provided [RCV001055443]	pathogenic\|uncertain significance	17	65190217	65190217	Human		name
38477267	CV950175	single nucleotide variant	NM_003835.4(RGS9):c.103C>T (p.Arg35Ter)	not provided [RCV001233416]	pathogenic\|uncertain significance	17	65153467	65153467	Human		name
38496157	CV950176	single nucleotide variant	NM_003835.4(RGS9):c.104G>A (p.Arg35Gln)	not provided [RCV001226199]	uncertain significance	17	65153468	65153468	Human		name
38482663	CV950177	single nucleotide variant	NM_003835.4(RGS9):c.296G>A (p.Ser99Asn)	Inborn genetic diseases [RCV002563831]\|Retinal dystrophy [RCV004813953]\|not provided [RCV001235614]	uncertain significance	17	65160323	65160323	Human	3	name
38477101	CV950184	single nucleotide variant	NM_003835.4(RGS9):c.1629C>T (p.Ser543=)	not provided [RCV001233346]	likely benign\|uncertain significance	17	65225223	65225223	Human		name
38458711	CV950187	single nucleotide variant	NM_003835.4(RGS9):c.1950G>A (p.Ser650=)	not provided [RCV001228937]	likely benign\|uncertain significance	17	65227332	65227332	Human		name
38463207	CV958262	single nucleotide variant	NM_003835.4(RGS9):c.262G>T (p.Asp88Tyr)	Inborn genetic diseases [RCV002568675]\|not provided [RCV001247221]	uncertain significance	17	65160289	65160289	Human	1	name
126731402	CV997823	single nucleotide variant	NM_003835.4(RGS9):c.232G>A (p.Val78Ile)	Inborn genetic diseases [RCV002541821]\|not provided [RCV001294374]	uncertain significance	17	65160259	65160259	Human	1	name
126770525	CV1013009	single nucleotide variant	NM_003835.4(RGS9):c.516G>C (p.Arg172Ser)	not provided [RCV001322623]	uncertain significance	17	65168215	65168215	Human		name
126747365	CV1013010	single nucleotide variant	NM_003835.4(RGS9):c.589A>G (p.Met197Val)	not provided [RCV001315338]	uncertain significance	17	65177738	65177738	Human		name
126771764	CV1013011	single nucleotide variant	NM_003835.4(RGS9):c.629A>G (p.Asn210Ser)	not provided [RCV001323346]	uncertain significance	17	65177778	65177778	Human		name
126773548	CV1013012	single nucleotide variant	NM_003835.4(RGS9):c.658C>G (p.Gln220Glu)	Inborn genetic diseases [RCV002546111]\|not provided [RCV001324396]	uncertain significance	17	65189289	65189289	Human	1	name
126764776	CV1013013	single nucleotide variant	NM_003835.4(RGS9):c.781G>A (p.Asp261Asn)	Inborn genetic diseases [RCV004034986]\|not provided [RCV001319784]	uncertain significance	17	65193577	65193577	Human	1	name
126742861	CV1021681	single nucleotide variant	NM_003835.4(RGS9):c.382C>T (p.Arg128Ter)	Bradyopsia [RCV003229575]\|not provided [RCV002972151]	pathogenic\|drug response	17	65160868	65160868	Human	2	name
126747774	CV1033538	single nucleotide variant	NM_003835.4(RGS9):c.317C>T (p.Pro106Leu)	not provided [RCV001337532]	uncertain significance	17	65160540	65160540	Human		name
126746286	CV1033539	single nucleotide variant	NM_003835.4(RGS9):c.383G>A (p.Arg128Gln)	not provided [RCV001337306]	uncertain significance	17	65160869	65160869	Human		name
126769216	CV1033540	single nucleotide variant	NM_003835.4(RGS9):c.667G>T (p.Val223Phe)	Inborn genetic diseases [RCV002546995]\|not provided [RCV001343803]	uncertain significance	17	65189298	65189298	Human	1	name
126726602	CV1033541	single nucleotide variant	NM_003835.4(RGS9):c.709A>G (p.Met237Val)	Inborn genetic diseases [RCV004656546]\|not provided [RCV001348502]	uncertain significance	17	65190199	65190199	Human	1	name
126736137	CV1033542	single nucleotide variant	NM_003835.4(RGS9):c.748A>G (p.Ile250Val)	not provided [RCV001350185]	uncertain significance	17	65193544	65193544	Human		name
126773630	CV1033543	single nucleotide variant	NM_003835.4(RGS9):c.785C>T (p.Ala262Val)	not provided [RCV001346291]	uncertain significance	17	65193581	65193581	Human		name
126919141	CV1050530	single nucleotide variant	NM_003835.4(RGS9):c.453G>A (p.Met151Ile)	not provided [RCV001362123]	uncertain significance	17	65163042	65163042	Human		name
126916269	CV1050531	single nucleotide variant	NM_003835.4(RGS9):c.499A>G (p.Arg167Gly)	not provided [RCV001360478]	uncertain significance	17	65163088	65163088	Human		name
126918553	CV1050533	single nucleotide variant	NM_003835.4(RGS9):c.880A>T (p.Met294Leu)	not provided [RCV001361792]	uncertain significance	17	65197145	65197145	Human		name
127304304	CV1126578	single nucleotide variant	NM_003835.4(RGS9):c.317C>A (p.Pro106Gln)	not provided [RCV001462180]	likely benign	17	65160540	65160540	Human		name
127295262	CV1126584	single nucleotide variant	NM_003835.4(RGS9):c.682G>A (p.Glu228Lys)	Inborn genetic diseases [RCV005271286]\|not provided [RCV001452452]	likely benign\|uncertain significance	17	65189313	65189313	Human	1	name
127324082	CV1147495	single nucleotide variant	NM_003835.4(RGS9):c.445C>A (p.Gln149Lys)	not provided [RCV001505595]	likely benign	17	65163034	65163034	Human		name
151887659	CV1341571	single nucleotide variant	NM_003835.4(RGS9):c.722T>C (p.Val241Ala)	not provided [RCV001887806]	uncertain significance	17	65190212	65190212	Human		name
151810759	CV1345186	deletion	NM_003835.4(RGS9):c.1681del (p.Leu561fs)	not provided [RCV001878246]	pathogenic\|uncertain significance	17	65225273	65225273	Human		name
151721587	CV1347714	single nucleotide variant	NM_003835.4(RGS9):c.833C>G (p.Thr278Ser)	not provided [RCV001966060]	uncertain significance	17	65193629	65193629	Human		name
151863061	CV1353582	single nucleotide variant	NM_003835.4(RGS9):c.562T>G (p.Trp188Gly)	not provided [RCV001924252]	uncertain significance	17	65168261	65168261	Human		name
151724706	CV1357067	single nucleotide variant	NM_003835.4(RGS9):c.524C>T (p.Ala175Val)	not provided [RCV001966437]	uncertain significance	17	65168223	65168223	Human		name
151812638	CV1367565	single nucleotide variant	NM_003835.4(RGS9):c.689T>C (p.Met230Thr)	not provided [RCV001878424]	uncertain significance	17	65190179	65190179	Human		name
151855970	CV1373015	single nucleotide variant	NM_003835.4(RGS9):c.298C>T (p.Leu100Phe)	not provided [RCV001996542]	uncertain significance	17	65160325	65160325	Human		name
151750788	CV1377704	single nucleotide variant	NM_003835.4(RGS9):c.619C>T (p.Arg207Ter)	not provided [RCV001948118]	pathogenic\|uncertain significance	17	65177768	65177768	Human		name
151737542	CV1389853	single nucleotide variant	NM_003835.4(RGS9):c.659A>G (p.Gln220Arg)	not provided [RCV001892935]	uncertain significance	17	65189290	65189290	Human		name
151866218	CV1399424	single nucleotide variant	NM_003835.4(RGS9):c.305G>T (p.Arg102Ile)	not provided [RCV001884566]	uncertain significance	17	65160332	65160332	Human		name
151867465	CV1422660	single nucleotide variant	NM_003835.4(RGS9):c.455A>G (p.Asn152Ser)	not provided [RCV001884713]	uncertain significance	17	65163044	65163044	Human		name
151848135	CV1433464	single nucleotide variant	NM_003835.4(RGS9):c.310C>T (p.Gln104Ter)	not provided [RCV001978567]	pathogenic\|uncertain significance	17	65160337	65160337	Human		name
151776694	CV1439573	single nucleotide variant	NM_003835.4(RGS9):c.383G>C (p.Arg128Pro)	not provided [RCV002009357]	uncertain significance	17	65160869	65160869	Human		name
151741076	CV1455403	single nucleotide variant	NM_003835.4(RGS9):c.629A>T (p.Asn210Ile)	Inborn genetic diseases [RCV004043248]\|not provided [RCV002005824]	uncertain significance	17	65177778	65177778	Human	1	name
151759763	CV1459312	single nucleotide variant	NM_003835.4(RGS9):c.965A>T (p.Lys322Ile)	not provided [RCV002044137]	uncertain significance	17	65197230	65197230	Human		name
151815138	CV1507559	single nucleotide variant	NM_003835.4(RGS9):c.899C>A (p.Ala300Asp)	Inborn genetic diseases [RCV004044460]\|not provided [RCV001954209]	uncertain significance	17	65197164	65197164	Human	1	name
151876316	CV1508079	single nucleotide variant	NM_003835.4(RGS9):c.364G>A (p.Ala122Thr)	not provided [RCV001961086]	uncertain significance	17	65160587	65160587	Human		name
151868949	CV1514649	single nucleotide variant	NM_003835.4(RGS9):c.327G>A (p.Trp109Ter)	not provided [RCV001998079]	pathogenic\|uncertain significance	17	65160550	65160550	Human		name
9693283	CV177291	single nucleotide variant	NM_003835.4(RGS9):c.773C>T (p.Ser258Leu)	not provided [RCV000968923]\|not specified [RCV000153838]	benign\|uncertain significance	17	65193569	65193569	Human		name
155721877	CV1773512	single nucleotide variant	NM_003835.4(RGS9):c.794C>T (p.Ser265Leu)	not provided [RCV002301327]	uncertain significance	17	65193590	65193590	Human		name
10045129	CV188891	single nucleotide variant	NM_003835.4(RGS9):c.704C>T (p.Ala235Val)	Inborn genetic diseases [RCV004955296]\|not provided [RCV000171265]	likely pathogenic\|uncertain significance	17	65190194	65190194	Human	1	name
156412416	CV1972097	single nucleotide variant	NM_003835.4(RGS9):c.614T>C (p.Leu205Pro)	not provided [RCV002608535]	uncertain significance	17	65177763	65177763	Human		name
156124238	CV2036184	single nucleotide variant	NM_003835.4(RGS9):c.392A>G (p.Lys131Arg)	Inborn genetic diseases [RCV003250593]\|not provided [RCV002800352]	uncertain significance	17	65160878	65160878	Human	1	name
156243430	CV2086088	single nucleotide variant	NM_003835.4(RGS9):c.342G>A (p.Trp114Ter)	not provided [RCV002876680]	pathogenic	17	65160565	65160565	Human		name
8596926	CV20901	single nucleotide variant	NM_003835.4(RGS9):c.895T>C (p.Trp299Arg)	Bradyopsia [RCV000006220]\|Leber congenital amaurosis [RCV000787876]\|not provided [RCV001052039]	pathogenic\|drug response	17	65197160	65197160	Human	3	name
156254333	CV2098181	single nucleotide variant	NM_003835.4(RGS9):c.371A>C (p.Tyr124Ser)	not provided [RCV002895367]	uncertain significance	17	65160857	65160857	Human		name
156099611	CV2107205	single nucleotide variant	NM_003835.4(RGS9):c.492G>T (p.Glu164Asp)	not provided [RCV002926999]	uncertain significance	17	65163081	65163081	Human		name
156075758	CV2160322	single nucleotide variant	NM_003835.4(RGS9):c.545G>T (p.Cys182Phe)	not provided [RCV003020182]	uncertain significance	17	65168244	65168244	Human		name
156006951	CV2163040	single nucleotide variant	NM_003835.4(RGS9):c.781G>T (p.Asp261Tyr)	not provided [RCV003017541]	uncertain significance	17	65193577	65193577	Human		name
156293512	CV2166349	single nucleotide variant	NM_003835.4(RGS9):c.651C>A (p.Asn217Lys)	not provided [RCV003045239]	uncertain significance	17	65177800	65177800	Human		name
156248840	CV2174463	single nucleotide variant	NM_003835.4(RGS9):c.713G>C (p.Arg238Thr)	not provided [RCV003043714]	uncertain significance	17	65190203	65190203	Human		name
156372821	CV2185159	single nucleotide variant	NM_003835.4(RGS9):c.592G>A (p.Asp198Asn)	not provided [RCV003049849]	uncertain significance	17	65177741	65177741	Human		name
156302051	CV2189680	single nucleotide variant	NM_003835.4(RGS9):c.595A>G (p.Asn199Asp)	not provided [RCV003062009]	uncertain significance	17	65177744	65177744	Human		name
156037346	CV2250184	single nucleotide variant	NM_003835.4(RGS9):c.521A>G (p.Lys174Arg)	Inborn genetic diseases [RCV002821492]	uncertain significance	17	65168220	65168220	Human	1	name
155907907	CV2302320	single nucleotide variant	NM_003835.4(RGS9):c.610G>A (p.Gly204Ser)	Inborn genetic diseases [RCV002902096]	uncertain significance	17	65177759	65177759	Human	1	name
329376939	CV2456732	single nucleotide variant	NM_003835.4(RGS9):c.631C>T (p.Pro211Ser)	Inborn genetic diseases [RCV003186214]	uncertain significance	17	65177780	65177780	Human	1	name
329393816	CV2472143	single nucleotide variant	NM_003835.4(RGS9):c.694T>A (p.Tyr232Asn)	Inborn genetic diseases [RCV003218479]	uncertain significance	17	65190184	65190184	Human	1	name
401733236	CV2685466	single nucleotide variant	NM_003835.4(RGS9):c.332C>T (p.Thr111Ile)	Inborn genetic diseases [RCV003249131]	uncertain significance	17	65160555	65160555	Human	1	name
401894925	CV2782142	single nucleotide variant	NM_003835.4(RGS9):c.426A>T (p.Glu142Asp)	Inborn genetic diseases [RCV003372012]	uncertain significance	17	65163015	65163015	Human	1	name
405716179	CV3309291	single nucleotide variant	NM_003835.4(RGS9):c.541G>A (p.Asp181Asn)	Inborn genetic diseases [RCV004449230]	uncertain significance	17	65168240	65168240	Human	1	name
405716183	CV3309292	single nucleotide variant	NM_003835.4(RGS9):c.998A>G (p.Glu333Gly)	Inborn genetic diseases [RCV004449231]	uncertain significance	17	65202014	65202014	Human	1	name
407474380	CV3472857	single nucleotide variant	NM_003835.4(RGS9):c.458A>C (p.Tyr153Ser)	Inborn genetic diseases [RCV004662985]	uncertain significance	17	65163047	65163047	Human	1	name
407474385	CV3472859	single nucleotide variant	NM_003835.4(RGS9):c.437T>C (p.Phe146Ser)	Inborn genetic diseases [RCV004662987]	uncertain significance	17	65163026	65163026	Human	1	name
597718164	CV3586424	single nucleotide variant	NM_003835.4(RGS9):c.430T>C (p.Tyr144His)	Inborn genetic diseases [RCV004960093]	uncertain significance	17	65163019	65163019	Human	1	name
598189453	CV3902620	single nucleotide variant	NM_003835.4(RGS9):c.608A>G (p.Tyr203Cys)	Inborn genetic diseases [RCV005266714]	uncertain significance	17	65177757	65177757	Human	1	name
598189468	CV3902623	single nucleotide variant	NM_003835.4(RGS9):c.461A>G (p.Lys154Arg)	Inborn genetic diseases [RCV005266717]	uncertain significance	17	65163050	65163050	Human	1	name
13446168	CV438052	single nucleotide variant	NM_003835.4(RGS9):c.313A>G (p.Thr105Ala)	Inborn genetic diseases [RCV002527406]\|RGS9-related disorder [RCV003915423]\|not provided [RCV000513358]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	17	65160536	65160536	Human	2	name , trait , alternate_id
13836520	CV587795	single nucleotide variant	NM_003835.4(RGS9):c.334C>G (p.Gln112Glu)	not provided [RCV000732658]	uncertain significance	17	65160557	65160557	Human		name
14695721	CV622917	single nucleotide variant	NM_003835.4(RGS9):c.458A>G (p.Tyr153Cys)	Bradyopsia [RCV000785959]\|Inborn genetic diseases [RCV003353021]\|not provided [RCV001371195]	uncertain significance	17	65163047	65163047	Human	3	name
15150829	CV727356	single nucleotide variant	NM_003835.4(RGS9):c.314C>G (p.Thr105Arg)	Inborn genetic diseases [RCV002536815]\|RGS9-related disorder [RCV003920486]\|not provided [RCV000879466]	likely benign\|uncertain significance	17	65160537	65160537	Human	2	name , trait , alternate_id
8628056	CV83200	single nucleotide variant	NM_003835.4(RGS9):c.632C>T (p.Pro211Leu)	Inborn genetic diseases [RCV002548872]\|not provided [RCV002041051]	uncertain significance\|not provided	17	65177781	65177781	Human	1	name
26921294	CV845943	single nucleotide variant	NM_003835.4(RGS9):c.538C>G (p.Leu180Val)	not provided [RCV001049632]	uncertain significance	17	65168237	65168237	Human		name
26884687	CV845944	single nucleotide variant	NM_003835.4(RGS9):c.574C>T (p.Arg192Ter)	not provided [RCV001052371]	pathogenic\|uncertain significance	17	65168273	65168273	Human		name
26886692	CV845945	single nucleotide variant	NM_003835.4(RGS9):c.631C>G (p.Pro211Ala)	not provided [RCV001055294]	uncertain significance	17	65177780	65177780	Human		name
26886362	CV845946	single nucleotide variant	NM_003835.4(RGS9):c.687C>G (p.Ile229Met)	Inborn genetic diseases [RCV002553352]\|not provided [RCV001054826]	uncertain significance	17	65190177	65190177	Human	1	name
26885364	CV845947	single nucleotide variant	NM_003835.4(RGS9):c.718A>T (p.Thr240Ser)	not provided [RCV001053425]	uncertain significance	17	65190208	65190208	Human		name
26886949	CV845949	single nucleotide variant	NM_003835.4(RGS9):c.823A>G (p.Thr275Ala)	not provided [RCV001055606]	uncertain significance	17	65193619	65193619	Human		name
38490284	CV928455	single nucleotide variant	NM_003835.4(RGS9):c.620G>T (p.Arg207Leu)	not provided [RCV001222079]	uncertain significance	17	65177769	65177769	Human		name
38489053	CV928456	single nucleotide variant	NM_003835.4(RGS9):c.937C>T (p.Arg313Ter)	not provided [RCV001221505]	pathogenic\|uncertain significance	17	65197202	65197202	Human		name
38460259	CV938138	single nucleotide variant	NM_003835.4(RGS9):c.502G>T (p.Ala168Ser)	not provided [RCV001211796]	uncertain significance	17	65168201	65168201	Human		name
38488076	CV950178	single nucleotide variant	NM_003835.4(RGS9):c.533A>G (p.Tyr178Cys)	Inborn genetic diseases [RCV003294126]\|not provided [RCV001237869]	uncertain significance	17	65168232	65168232	Human	1	name
38494922	CV950180	single nucleotide variant	NM_003835.4(RGS9):c.659A>C (p.Gln220Pro)	not provided [RCV001225393]	uncertain significance	17	65189290	65189290	Human		name
38481037	CV950181	single nucleotide variant	NM_003835.4(RGS9):c.667G>A (p.Val223Ile)	Inborn genetic diseases [RCV003373072]\|not provided [RCV001234947]	likely benign\|uncertain significance	17	65189298	65189298	Human	1	name
38496241	CV950182	single nucleotide variant	NM_003835.4(RGS9):c.923G>A (p.Arg308Gln)	not provided [RCV001226255]	uncertain significance	17	65197188	65197188	Human		name
126767356	CV997824	single nucleotide variant	NM_003835.4(RGS9):c.358G>A (p.Asp120Asn)	not provided [RCV001302251]	uncertain significance	17	65160581	65160581	Human		name
126758501	CV997826	single nucleotide variant	NM_003835.4(RGS9):c.502G>A (p.Ala168Thr)	not provided [RCV001308739]	uncertain significance	17	65168201	65168201	Human		name
8641295	CV100279	single nucleotide variant	NM_003835.4(RGS9):c.1502G>A (p.Arg501His)	not provided [RCV001519931]\|not specified [RCV000080351]	benign	17	65225096	65225096	Human		name
126733210	CV1013014	single nucleotide variant	NM_003835.4(RGS9):c.1172C>A (p.Ala391Glu)	not provided [RCV001313351]	uncertain significance	17	65204270	65204270	Human		name
126765421	CV1013016	single nucleotide variant	NM_003835.4(RGS9):c.1507C>T (p.Pro503Ser)	not provided [RCV001320037]	uncertain significance	17	65225101	65225101	Human		name
126772061	CV1013017	single nucleotide variant	NM_003835.4(RGS9):c.1534C>A (p.Arg512Ser)	not provided [RCV001323521]	uncertain significance	17	65225128	65225128	Human		name
126732593	CV1013018	single nucleotide variant	NM_003835.4(RGS9):c.1534C>T (p.Arg512Cys)	not provided [RCV001313248]	uncertain significance	17	65225128	65225128	Human		name
126768766	CV1013019	single nucleotide variant	NM_003835.4(RGS9):c.1546C>T (p.Arg516Ter)	not provided [RCV001321557]	pathogenic\|uncertain significance	17	65225140	65225140	Human		name
126767478	CV1013020	single nucleotide variant	NM_003835.4(RGS9):c.1646G>A (p.Arg549His)	not provided [RCV001320867]	uncertain significance	17	65225240	65225240	Human		name
126765425	CV1013021	single nucleotide variant	NM_003835.4(RGS9):c.1718C>T (p.Pro573Leu)	Inborn genetic diseases [RCV004960762]\|not provided [RCV001320038]	uncertain significance	17	65225312	65225312	Human	1	name
126751112	CV1013022	single nucleotide variant	NM_003835.4(RGS9):c.1848C>G (p.Asp616Glu)	not provided [RCV001316046]	uncertain significance	17	65225442	65225442	Human		name
126741880	CV1013023	single nucleotide variant	NM_003835.4(RGS9):c.1964C>T (p.Thr655Ile)	not provided [RCV001314583]	uncertain significance	17	65227346	65227346	Human		name
126770621	CV1033545	single nucleotide variant	NM_003835.4(RGS9):c.1543C>T (p.Arg515Trp)	not provided [RCV001344577]	uncertain significance	17	65225137	65225137	Human		name
126773172	CV1033547	single nucleotide variant	NM_003835.4(RGS9):c.1925G>A (p.Gly642Glu)	Inborn genetic diseases [RCV003346502]\|Retinal dystrophy [RCV004815420]\|not provided [RCV001346034]	uncertain significance	17	65227307	65227307	Human	3	name
126756000	CV1033548	single nucleotide variant	NM_003835.4(RGS9):c.1949C>G (p.Ser650Trp)	not provided [RCV001339170]	uncertain significance	17	65227331	65227331	Human		name
126924438	CV1050534	single nucleotide variant	NM_003835.4(RGS9):c.1159G>A (p.Val387Met)	not provided [RCV001367033]	uncertain significance	17	65204257	65204257	Human		name
126915109	CV1050535	single nucleotide variant	NM_003835.4(RGS9):c.1171G>A (p.Ala391Thr)	not provided [RCV001370722]	uncertain significance	17	65204269	65204269	Human		name
126914825	CV1050536	single nucleotide variant	NM_003835.4(RGS9):c.1453G>A (p.Gly485Arg)	Inborn genetic diseases [RCV002550109]\|not provided [RCV001370606]	uncertain significance	17	65225047	65225047	Human	1	name
126920983	CV1050538	single nucleotide variant	NM_003835.4(RGS9):c.1672G>A (p.Glu558Lys)	not provided [RCV001374132]	uncertain significance	17	65225266	65225266	Human		name
126917545	CV1050539	single nucleotide variant	NM_003835.4(RGS9):c.1696C>A (p.Pro566Thr)	not provided [RCV001361233]	uncertain significance	17	65225290	65225290	Human		name
126924613	CV1050540	single nucleotide variant	NM_003835.4(RGS9):c.1715C>G (p.Ala572Gly)	not provided [RCV001367231]	uncertain significance	17	65225309	65225309	Human		name
126917326	CV1050541	single nucleotide variant	NM_003835.4(RGS9):c.1780C>T (p.Pro594Ser)	not provided [RCV001372010]	uncertain significance	17	65225374	65225374	Human		name
127237864	CV1105216	single nucleotide variant	NM_003835.4(RGS9):c.1706G>A (p.Arg569Gln)	not provided [RCV001433641]	likely benign	17	65225300	65225300	Human		name
127298067	CV1158099	single nucleotide variant	NM_003835.4(RGS9):c.1868G>C (p.Arg623Pro)	RGS9-related disorder [RCV003948509]\|not provided [RCV001513127]	benign\|likely benign	17	65225462	65225462	Human	1	name , trait , alternate_id
150490140	CV1274694	single nucleotide variant	NM_003835.4(RGS9):c.1867C>T (p.Arg623Ter)	Bradyopsia [RCV002488473]\|not provided [RCV001700654]	uncertain significance	17	65225461	65225461	Human	2	name
151893311	CV1338083	single nucleotide variant	NM_003835.4(RGS9):c.1535G>A (p.Arg512His)	not provided [RCV001944908]	uncertain significance	17	65225129	65225129	Human		name
151885867	CV1341036	single nucleotide variant	NM_003835.4(RGS9):c.1001C>A (p.Ala334Asp)	Inborn genetic diseases [RCV004955915]\|not provided [RCV001962639]	uncertain significance	17	65202017	65202017	Human	1	name
151760634	CV1343254	single nucleotide variant	NM_003835.4(RGS9):c.1547G>A (p.Arg516Gln)	not provided [RCV002024324]	uncertain significance	17	65225141	65225141	Human		name
151872480	CV1351624	single nucleotide variant	NM_003835.4(RGS9):c.1922C>T (p.Thr641Met)	Inborn genetic diseases [RCV004956047]\|not provided [RCV001998530]	uncertain significance	17	65227304	65227304	Human	1	name
151862607	CV1353503	single nucleotide variant	NM_003835.4(RGS9):c.1709C>G (p.Pro570Arg)	not provided [RCV001924194]	uncertain significance	17	65225303	65225303	Human		name
151796386	CV1356028	single nucleotide variant	NM_003835.4(RGS9):c.1351C>G (p.Gln451Glu)	not provided [RCV002027683]	uncertain significance	17	65210549	65210549	Human		name
151749630	CV1380946	single nucleotide variant	NM_003835.4(RGS9):c.1322G>A (p.Arg441His)	Inborn genetic diseases [RCV002548763]\|not provided [RCV002023240]	uncertain significance	17	65210520	65210520	Human	1	name
151837935	CV1382686	single nucleotide variant	NM_003835.4(RGS9):c.1136G>A (p.Gly379Glu)	not provided [RCV002031487]	uncertain significance	17	65204234	65204234	Human		name
151715034	CV1388923	single nucleotide variant	NM_003835.4(RGS9):c.1502G>T (p.Arg501Leu)	not provided [RCV002002764]	uncertain significance	17	65225096	65225096	Human		name
151833515	CV1396356	single nucleotide variant	NM_003835.4(RGS9):c.1310G>A (p.Arg437Gln)	not provided [RCV001902044]	uncertain significance	17	65210508	65210508	Human		name
151772626	CV1400988	single nucleotide variant	NM_003835.4(RGS9):c.1849G>A (p.Val617Met)	not provided [RCV002045394]	uncertain significance	17	65225443	65225443	Human		name
151826783	CV1414871	single nucleotide variant	NM_003835.4(RGS9):c.1672G>C (p.Glu558Gln)	not provided [RCV001920098]	uncertain significance	17	65225266	65225266	Human		name
151823041	CV1415212	single nucleotide variant	NM_003835.4(RGS9):c.1862T>C (p.Leu621Pro)	not provided [RCV001954954]	uncertain significance	17	65225456	65225456	Human		name
151859147	CV1422869	single nucleotide variant	NM_003835.4(RGS9):c.1765G>A (p.Gly589Ser)	Inborn genetic diseases [RCV004044109]\|Retinal dystrophy [RCV004816767]\|not provided [RCV001923779]	uncertain significance	17	65225359	65225359	Human	3	name
151773490	CV1424029	single nucleotide variant	NM_003835.4(RGS9):c.1418A>T (p.His473Leu)	not provided [RCV002025588]	uncertain significance	17	65225012	65225012	Human		name
151864043	CV1431494	single nucleotide variant	NM_003835.4(RGS9):c.1313G>A (p.Arg438His)	not provided [RCV001924381]	uncertain significance	17	65210511	65210511	Human		name
151742773	CV1431668	single nucleotide variant	NM_003835.4(RGS9):c.1769G>C (p.Cys590Ser)	Inborn genetic diseases [RCV002561355]\|not provided [RCV001926630]	uncertain significance	17	65225363	65225363	Human	1	name
151744287	CV1432826	single nucleotide variant	NM_003835.4(RGS9):c.1308G>A (p.Met436Ile)	not provided [RCV001968467]	uncertain significance	17	65210506	65210506	Human		name
151739119	CV1437541	single nucleotide variant	NM_003835.4(RGS9):c.1727C>T (p.Ala576Val)	not provided [RCV001870842]	uncertain significance	17	65225321	65225321	Human		name
151767853	CV1444403	single nucleotide variant	NM_003835.4(RGS9):c.1832T>C (p.Val611Ala)	not provided [RCV001949867]	uncertain significance	17	65225426	65225426	Human		name
151716251	CV1448563	single nucleotide variant	NM_003835.4(RGS9):c.1232C>T (p.Pro411Leu)	not provided [RCV001965271]	uncertain significance	17	65207950	65207950	Human		name
151756695	CV1449391	single nucleotide variant	NM_003835.4(RGS9):c.1799C>T (p.Ser600Leu)	not provided [RCV001986818]	uncertain significance	17	65225393	65225393	Human		name
151822710	CV1456455	single nucleotide variant	NM_003835.4(RGS9):c.1684G>A (p.Asp562Asn)	not provided [RCV002030044]	uncertain significance	17	65225278	65225278	Human		name
151818212	CV1463940	single nucleotide variant	NM_003835.4(RGS9):c.1121A>C (p.Asp374Ala)	Inborn genetic diseases [RCV004671539]\|not provided [RCV001933884]	uncertain significance	17	65204219	65204219	Human	1	name
151749267	CV1465284	single nucleotide variant	NM_003835.4(RGS9):c.1981C>T (p.Arg661Trp)	Inborn genetic diseases [RCV002545563]\|not provided [RCV002043109]	uncertain significance	17	65227363	65227363	Human	1	name
151860503	CV1482970	single nucleotide variant	NM_003835.4(RGS9):c.2019C>A (p.Ser673Arg)	not provided [RCV001883856]	uncertain significance	17	65227401	65227401	Human		name
151844591	CV1496371	single nucleotide variant	NM_003835.4(RGS9):c.1417C>T (p.His473Tyr)	not provided [RCV001921948]	uncertain significance	17	65225011	65225011	Human		name
151719283	CV1497987	single nucleotide variant	NM_003835.4(RGS9):c.1949C>T (p.Ser650Leu)	not provided [RCV001965714]	uncertain significance	17	65227331	65227331	Human		name
151772642	CV1504703	single nucleotide variant	NM_003835.4(RGS9):c.1582G>A (p.Val528Met)	Inborn genetic diseases [RCV002592570]\|not provided [RCV002008993]	uncertain significance	17	65225176	65225176	Human	1	name
151723742	CV1507748	single nucleotide variant	NM_003835.4(RGS9):c.1774G>C (p.Ala592Pro)	not provided [RCV001983422]	uncertain significance	17	65225368	65225368	Human		name
151734681	CV1508726	single nucleotide variant	NM_003835.4(RGS9):c.1700G>A (p.Arg567His)	not provided [RCV002021663]	uncertain significance	17	65225294	65225294	Human		name
151829123	CV1510289	single nucleotide variant	NM_003835.4(RGS9):c.1730G>A (p.Arg577His)	not provided [RCV001920319]	uncertain significance	17	65225324	65225324	Human		name
151757664	CV1514281	single nucleotide variant	NM_003835.4(RGS9):c.1090C>T (p.Arg364Cys)	not provided [RCV001948785]	uncertain significance	17	65204188	65204188	Human		name
9693284	CV177159	single nucleotide variant	NM_003835.4(RGS9):c.1645C>T (p.Arg549Cys)	not provided [RCV000153839]	conflicting interpretations of pathogenicity\|uncertain significance	17	65225239	65225239	Human		name
156413104	CV1904730	single nucleotide variant	NM_003835.4(RGS9):c.1888G>A (p.Ala630Thr)	Inborn genetic diseases [RCV004073404]\|not provided [RCV002588053]	uncertain significance	17	65225482	65225482	Human	1	name
10050493	CV192006	single nucleotide variant	NM_003835.4(RGS9):c.1658T>C (p.Val553Ala)	Inborn genetic diseases [RCV004020078]\|not provided [RCV000175308]	conflicting interpretations of pathogenicity\|uncertain significance	17	65225252	65225252	Human	1	name
156443934	CV1941211	single nucleotide variant	NM_003835.4(RGS9):c.1372G>A (p.Ala458Thr)	not provided [RCV003114846]	uncertain significance	17	65210570	65210570	Human		name
156444942	CV1948993	single nucleotide variant	NM_003835.4(RGS9):c.1312C>T (p.Arg438Cys)	Inborn genetic diseases [RCV004245922]\|not provided [RCV003115876]	uncertain significance	17	65210510	65210510	Human	1	name
156236053	CV1952785	single nucleotide variant	NM_003835.4(RGS9):c.1663G>A (p.Glu555Lys)	not provided [RCV002576056]	uncertain significance	17	65225257	65225257	Human		name
155990326	CV1990461	single nucleotide variant	NM_003835.4(RGS9):c.1729C>T (p.Arg577Cys)	not provided [RCV002617992]	uncertain significance	17	65225323	65225323	Human		name
156189213	CV1997970	single nucleotide variant	NM_003835.4(RGS9):c.1811C>T (p.Pro604Leu)	not provided [RCV002643261]	uncertain significance	17	65225405	65225405	Human		name
156014524	CV2009060	single nucleotide variant	NM_003835.4(RGS9):c.1381G>A (p.Ala461Thr)	not provided [RCV002690695]	uncertain significance	17	65210579	65210579	Human		name
156206888	CV2021510	single nucleotide variant	NM_003835.4(RGS9):c.1837C>A (p.Pro613Thr)	not provided [RCV002711609]	uncertain significance	17	65225431	65225431	Human		name
156022595	CV2025502	single nucleotide variant	NM_003835.4(RGS9):c.1469C>T (p.Pro490Leu)	not provided [RCV002735446]	uncertain significance	17	65225063	65225063	Human		name
156144824	CV2033112	single nucleotide variant	NM_003835.4(RGS9):c.1714G>T (p.Ala572Ser)	not provided [RCV002741027]	uncertain significance	17	65225308	65225308	Human		name
156095287	CV2050835	single nucleotide variant	NM_003835.4(RGS9):c.1533C>A (p.Ser511Arg)	Inborn genetic diseases [RCV002824345]\|not provided [RCV002824344]	uncertain significance	17	65225127	65225127	Human	1	name
156322723	CV2067719	single nucleotide variant	NM_003835.4(RGS9):c.1371G>C (p.Lys457Asn)	not provided [RCV002834814]	uncertain significance	17	65210569	65210569	Human		name
155983945	CV2070265	single nucleotide variant	NM_003835.4(RGS9):c.1942A>T (p.Met648Leu)	not provided [RCV002842655]	uncertain significance	17	65227324	65227324	Human		name
156324130	CV2101286	single nucleotide variant	NM_003835.4(RGS9):c.1930G>A (p.Gly644Arg)	not provided [RCV002899505]	uncertain significance	17	65227312	65227312	Human		name
155986079	CV2108875	single nucleotide variant	NM_003835.4(RGS9):c.1565G>T (p.Cys522Phe)	Inborn genetic diseases [RCV004958845]\|not provided [RCV002947103]	uncertain significance	17	65225159	65225159	Human	1	name
156366465	CV2116584	single nucleotide variant	NM_003835.4(RGS9):c.1397A>G (p.Asp466Gly)	not provided [RCV002941987]	uncertain significance	17	65210595	65210595	Human		name
156374266	CV2123939	single nucleotide variant	NM_003835.4(RGS9):c.1376G>A (p.Arg459Gln)	not provided [RCV002942578]	uncertain significance	17	65210574	65210574	Human		name
156217176	CV2136216	single nucleotide variant	NM_003835.4(RGS9):c.1679C>T (p.Ser560Phe)	not provided [RCV003007231]	uncertain significance	17	65225273	65225273	Human		name
156228279	CV2146120	single nucleotide variant	NM_003835.4(RGS9):c.1462A>G (p.Met488Val)	not provided [RCV003025545]	uncertain significance	17	65225056	65225056	Human		name
155976360	CV2146571	single nucleotide variant	NM_003835.4(RGS9):c.1499G>A (p.Cys500Tyr)	not provided [RCV003016172]	uncertain significance	17	65225093	65225093	Human		name
155939620	CV2147530	single nucleotide variant	NM_003835.4(RGS9):c.1969G>C (p.Glu657Gln)	not provided [RCV003014178]	uncertain significance	17	65227351	65227351	Human		name
156035084	CV2150119	single nucleotide variant	NM_003835.4(RGS9):c.1933A>G (p.Thr645Ala)	not provided [RCV003018842]	uncertain significance	17	65227315	65227315	Human		name
156018046	CV2151462	single nucleotide variant	NM_003835.4(RGS9):c.1168G>A (p.Ala390Thr)	not provided [RCV003018090]	uncertain significance	17	65204266	65204266	Human		name
155950095	CV2164895	single nucleotide variant	NM_003835.4(RGS9):c.1684G>C (p.Asp562His)	not provided [RCV003032389]	uncertain significance	17	65225278	65225278	Human		name
155966622	CV2216720	single nucleotide variant	NM_003835.4(RGS9):c.1700G>C (p.Arg567Pro)	Inborn genetic diseases [RCV002687124]	uncertain significance	17	65225294	65225294	Human	1	name
155975866	CV2231488	single nucleotide variant	NM_003835.4(RGS9):c.1876T>C (p.Ser626Pro)	Inborn genetic diseases [RCV002732023]	likely benign	17	65225470	65225470	Human	1	name
156047239	CV2244817	single nucleotide variant	NM_003835.4(RGS9):c.1643C>T (p.Pro548Leu)	Inborn genetic diseases [RCV002781805]	uncertain significance	17	65225237	65225237	Human	1	name
156060053	CV2305373	single nucleotide variant	NM_003835.4(RGS9):c.1301C>A (p.Pro434His)	Inborn genetic diseases [RCV002911726]	uncertain significance	17	65210499	65210499	Human	1	name
401725529	CV2721814	single nucleotide variant	NM_003835.4(RGS9):c.1676C>T (p.Ala559Val)	Inborn genetic diseases [RCV003269012]	uncertain significance	17	65225270	65225270	Human	1	name
405086073	CV3122065	single nucleotide variant	NM_003835.4(RGS9):c.1375C>T (p.Arg459Ter)	not provided [RCV003810820]	pathogenic	17	65210573	65210573	Human		name
405716173	CV3309290	single nucleotide variant	NM_003835.4(RGS9):c.1763G>A (p.Arg588Gln)	Inborn genetic diseases [RCV004449229]	uncertain significance	17	65225357	65225357	Human	1	name
596942231	CV3408472	single nucleotide variant	NM_003835.4(RGS9):c.1325C>T (p.Ser442Phe)	Retinal dystrophy [RCV004816143]	uncertain significance	17	65210523	65210523	Human	2	name
596944545	CV3408936	single nucleotide variant	NM_003835.4(RGS9):c.1726G>T (p.Ala576Ser)	Optic atrophy [RCV004817589]	uncertain significance	17	65225320	65225320	Human	2	name
407474383	CV3472858	single nucleotide variant	NM_003835.4(RGS9):c.1873A>G (p.Lys625Glu)	Inborn genetic diseases [RCV004662986]	uncertain significance	17	65225467	65225467	Human	1	name
597718157	CV3586423	single nucleotide variant	NM_003835.4(RGS9):c.1124T>G (p.Ile375Ser)	Inborn genetic diseases [RCV004960092]	uncertain significance	17	65204222	65204222	Human	1	name
597718169	CV3586425	single nucleotide variant	NM_003835.4(RGS9):c.1483C>T (p.Pro495Ser)	Inborn genetic diseases [RCV004960094]	uncertain significance	17	65225077	65225077	Human	1	name
597718181	CV3586428	single nucleotide variant	NM_003835.4(RGS9):c.1259C>T (p.Ala420Val)	Inborn genetic diseases [RCV004960096]	uncertain significance	17	65207977	65207977	Human	1	name
597891184	CV3749350	single nucleotide variant	NM_003835.4(RGS9):c.1187A>G (p.Tyr396Cys)	not provided [RCV005071134]	uncertain significance	17	65204285	65204285	Human		name
598189459	CV3902621	single nucleotide variant	NM_003835.4(RGS9):c.1082G>A (p.Gly361Glu)	Inborn genetic diseases [RCV005266715]	uncertain significance	17	65204180	65204180	Human	1	name
13522030	CV489333	single nucleotide variant	NM_003835.4(RGS9):c.1868G>A (p.Arg623Gln)	Inborn genetic diseases [RCV002531006]\|not provided [RCV000591214]	uncertain significance	17	65225462	65225462	Human	1	name
15103293	CV704303	single nucleotide variant	NM_003835.4(RGS9):c.1424C>T (p.Ala475Val)	not provided [RCV000959451]	benign	17	65225018	65225018	Human		name
15163995	CV727357	single nucleotide variant	NM_003835.4(RGS9):c.1630G>A (p.Gly544Arg)	RGS9-related disorder [RCV003910404]\|not provided [RCV000882098]	benign	17	65225224	65225224	Human	1	name , trait , alternate_id
21075661	CV797592	single nucleotide variant	NM_003835.4(RGS9):c.1521C>G (p.Phe507Leu)	RGS9-related disorder [RCV003906136]\|not provided [RCV000996600]	benign\|conflicting interpretations of pathogenicity\|uncertain significance	17	65225115	65225115	Human	1	name , trait , alternate_id
26904944	CV845950	single nucleotide variant	NM_003835.4(RGS9):c.1087A>G (p.Arg363Gly)	not provided [RCV001071362]	uncertain significance	17	65204185	65204185	Human		name
26887207	CV845951	single nucleotide variant	NM_003835.4(RGS9):c.1120G>A (p.Asp374Asn)	not provided [RCV001055978]	uncertain significance	17	65204218	65204218	Human		name
26900331	CV845952	single nucleotide variant	NM_003835.4(RGS9):c.1256A>G (p.Lys419Arg)	Inborn genetic diseases [RCV004960427]\|not provided [RCV001067709]	uncertain significance	17	65207974	65207974	Human	1	name
26912911	CV845953	single nucleotide variant	NM_003835.4(RGS9):c.1309C>T (p.Arg437Trp)	not provided [RCV001034910]	uncertain significance	17	65210507	65210507	Human		name
26918456	CV845954	single nucleotide variant	NM_003835.4(RGS9):c.1409C>T (p.Pro470Leu)	not provided [RCV001043736]	uncertain significance	17	65225003	65225003	Human		name
26920098	CV845955	single nucleotide variant	NM_003835.4(RGS9):c.1457C>T (p.Thr486Ile)	not provided [RCV001046963]	uncertain significance	17	65225051	65225051	Human		name
26888519	CV845956	single nucleotide variant	NM_003835.4(RGS9):c.1475C>T (p.Pro492Leu)	not provided [RCV001057463]	uncertain significance	17	65225069	65225069	Human		name
26920071	CV845957	single nucleotide variant	NM_003835.4(RGS9):c.1561A>G (p.Ile521Val)	not provided [RCV001046927]	uncertain significance	17	65225155	65225155	Human		name
26916851	CV845958	single nucleotide variant	NM_003835.4(RGS9):c.1699C>T (p.Arg567Cys)	Inborn genetic diseases [RCV004958378]\|not provided [RCV001040999]	uncertain significance	17	65225293	65225293	Human	1	name
26913918	CV845959	single nucleotide variant	NM_003835.4(RGS9):c.1714G>A (p.Ala572Thr)	Retinal dystrophy [RCV004818191]\|not provided [RCV001036741]	uncertain significance	17	65225308	65225308	Human	2	name
26885656	CV845960	single nucleotide variant	NM_003835.4(RGS9):c.1868G>T (p.Arg623Leu)	not provided [RCV001053825]	uncertain significance	17	65225462	65225462	Human		name
8636300	CV91523	single nucleotide variant	NM_003835.3(RGS9):c.1726G>A (p.Ala576Thr)	Malignant melanoma [RCV000071621]	not provided	17	65225320	65225320	Human		name
38480141	CV928457	single nucleotide variant	NM_003835.4(RGS9):c.1609G>C (p.Glu537Gln)	not provided [RCV001217412]	uncertain significance	17	65225203	65225203	Human		name
38468578	CV938139	single nucleotide variant	NM_003835.4(RGS9):c.1106A>G (p.Asp369Gly)	not provided [RCV001213165]	uncertain significance	17	65204204	65204204	Human		name
38476973	CV938140	single nucleotide variant	NM_003835.4(RGS9):c.1189A>G (p.Met397Val)	not provided [RCV001204885]	uncertain significance	17	65204287	65204287	Human		name
38457934	CV938141	single nucleotide variant	NM_003835.4(RGS9):c.1217G>A (p.Arg406His)	not provided [RCV001211265]	uncertain significance	17	65207935	65207935	Human		name
38488170	CV938142	single nucleotide variant	NM_003835.4(RGS9):c.1522G>A (p.Ala508Thr)	not provided [RCV001209627]	uncertain significance	17	65225116	65225116	Human		name
38475001	CV938143	single nucleotide variant	NM_003835.4(RGS9):c.1616A>T (p.Lys539Ile)	not provided [RCV001204077]	uncertain significance	17	65225210	65225210	Human		name
38456343	CV938144	single nucleotide variant	NM_003835.4(RGS9):c.1703G>A (p.Ser568Asn)	not provided [RCV001210791]	uncertain significance	17	65225297	65225297	Human		name
38488976	CV938145	single nucleotide variant	NM_003835.4(RGS9):c.2021T>C (p.Leu674Pro)	Inborn genetic diseases [RCV003163594]\|not provided [RCV001209999]	uncertain significance	17	65227403	65227403	Human	1	name
38495601	CV950183	single nucleotide variant	NM_003835.4(RGS9):c.1441A>T (p.Thr481Ser)	not provided [RCV001225822]	uncertain significance	17	65225035	65225035	Human		name
38498469	CV950185	single nucleotide variant	NM_003835.4(RGS9):c.1681C>T (p.Leu561Phe)	not provided [RCV001227775]	uncertain significance	17	65225275	65225275	Human		name
38495354	CV950186	single nucleotide variant	NM_003835.4(RGS9):c.1916T>C (p.Val639Ala)	Inborn genetic diseases [RCV004032546]\|not provided [RCV001225663]	uncertain significance	17	65227298	65227298	Human	1	name
38492381	CV958264	single nucleotide variant	NM_003835.4(RGS9):c.1117A>G (p.Met373Val)	not provided [RCV001240046]	uncertain significance	17	65204215	65204215	Human		name
38493175	CV958265	single nucleotide variant	NM_003835.4(RGS9):c.1762C>T (p.Arg588Ter)	not provided [RCV001240529]	pathogenic\|uncertain significance	17	65225356	65225356	Human		name
38492691	CV958266	single nucleotide variant	NM_003835.4(RGS9):c.1883G>C (p.Arg628Thr)	not provided [RCV001240238]	uncertain significance	17	65225477	65225477	Human		name
38491069	CV958267	single nucleotide variant	NM_003835.4(RGS9):c.1973C>T (p.Ser658Leu)	Inborn genetic diseases [RCV002567929]\|not provided [RCV001239219]	uncertain significance	17	65227355	65227355	Human	1	name
126766625	CV997827	single nucleotide variant	NM_003835.4(RGS9):c.1146C>A (p.His382Gln)	not provided [RCV001301959]	uncertain significance	17	65204244	65204244	Human		name
126747832	CV997828	single nucleotide variant	NM_003835.4(RGS9):c.1637T>C (p.Met546Thr)	Prolonged electroretinal response suppression 1 [RCV004731124]\|not provided [RCV001306318]	likely benign\|uncertain significance	17	65225231	65225231	Human	1	name
126742793	CV997829	single nucleotide variant	NM_003835.4(RGS9):c.1852G>T (p.Gly618Cys)	not provided [RCV001305601]	uncertain significance	17	65225446	65225446	Human		name
126750290	CV997830	single nucleotide variant	NM_003835.4(RGS9):c.1918C>A (p.Pro640Thr)	not provided [RCV001297294]	uncertain significance	17	65227300	65227300	Human		name
126735454	CV997831	single nucleotide variant	NM_003835.4(RGS9):c.1982G>A (p.Arg661Gln)	not provided [RCV001295078]	uncertain significance	17	65227364	65227364	Human		name
126731787	CV997832	single nucleotide variant	NM_003835.4(RGS9):c.1984G>A (p.Ala662Thr)	not provided [RCV001303967]	uncertain significance	17	65227366	65227366	Human		name
126748239	CV997833	single nucleotide variant	NM_003835.4(RGS9):c.1999G>A (p.Val667Ile)	not provided [RCV001296892]	uncertain significance	17	65227381	65227381	Human		name
38471301	CV950179	microsatellite	NM_003835.4(RGS9):c.660_663del (p.Thr221fs)	not provided [RCV001231187]	pathogenic\|uncertain significance	17	65189286	65189289	Human		name
126761560	CV1033546	microsatellite	NM_003835.4(RGS9):c.1666AGC[3] (p.Ser557dup)	not provided [RCV001340725]	uncertain significance	17	65225259	65225260	Human		name
126923096	CV1050537	microsatellite	NM_003835.4(RGS9):c.1490CCT[2] (p.Ser499del)	not provided [RCV001365450]	uncertain significance	17	65225082	65225084	Human		name
597972165	CV3794173	deletion	NM_003835.4(RGS9):c.1783_1785del (p.Val595del)	not provided [RCV005142539]	uncertain significance	17	65225377	65225379	Human		name
10052505	CV194917	indel	NM_003835.4(RGS9):c.313_314delinsGG (p.Thr105Gly)	Retinal dystrophy [RCV004816295]\|not provided [RCV000724351]	conflicting interpretations of pathogenicity\|uncertain significance	17	65160536	65160537	Human		name
38492721	CV958263	deletion	NM_003835.4(RGS9):c.607_618del (p.Tyr203_Asp206del)	not provided [RCV001240271]	uncertain significance	17	65177750	65177761	Human		name
156153148	CV2070546	indel	NM_003835.4(RGS9):c.2014_2017delinsAAGGTCATCT (p.Glu672_Ser673delinsLysValIleCys)	not provided [RCV002850938]	uncertain significance	17	65227396	65227399	Human		name
9688784	CV178017	single nucleotide variant	NM_207391.3(RGS9BP):c.*2G>A	not provided [RCV004717072]\|not specified [RCV000153842]	benign	19	32676973	32676973	Human		name
329351173	CV2477959	insertion	RGS9BP, 1-BP INS, 607G	Prolonged electroretinal response suppression 2 [RCV003224070]	drug response				Human		name
127234041	CV1084555	single nucleotide variant	NM_207391.3(RGS9BP):c.540G>A (p.Ala180=)	RGS9BP-related disorder [RCV003938708]\|not provided [RCV001414124]	likely benign	19	32676803	32676803	Human	1	name , trait , alternate_id
127290292	CV1127731	single nucleotide variant	NM_207391.3(RGS9BP):c.588C>A (p.Val196=)	RGS9BP-related disorder [RCV003930949]\|not provided [RCV001451186]	likely benign	19	32676851	32676851	Human	1	name , trait , alternate_id
11640457	CV272548	single nucleotide variant	NM_207391.3(RGS9BP):c.311C>T (p.Pro104Leu)	RGS9BP-related disorder [RCV004757193]\|not provided [RCV000338080]	likely benign\|uncertain significance	19	32676574	32676574	Human	1	name , trait , alternate_id
405262455	CV3194424	single nucleotide variant	NM_207391.3(RGS9BP):c.48G>A (p.Thr16=)	RGS9BP-related disorder [RCV003896453]	likely benign	19	32676311	32676311	Human		name , trait , alternate_id
15180406	CV728095	single nucleotide variant	NM_207391.3(RGS9BP):c.30G>A (p.Leu10=)	RGS9BP-related disorder [RCV003895426]\|not provided [RCV000885520]	benign\|likely benign	19	32676293	32676293	Human	1	name , trait , alternate_id
152027936	CV1642573	single nucleotide variant	NM_207391.3(RGS9BP):c.15G>A (p.Glu5=)	not provided [RCV002185668]	likely benign	19	32676278	32676278	Human		name
127235115	CV1106329	single nucleotide variant	NM_207391.3(RGS9BP):c.72G>A (p.Val24=)	not provided [RCV001422206]	likely benign	19	32676335	32676335	Human		name
152065793	CV1646898	single nucleotide variant	NM_207391.3(RGS9BP):c.36G>A (p.Gly12=)	not provided [RCV002128956]	likely benign	19	32676299	32676299	Human		name
405233367	CV3144986	single nucleotide variant	NM_207391.3(RGS9BP):c.51T>G (p.Thr17=)	not provided [RCV003853243]	likely benign	19	32676314	32676314	Human		name
13519043	CV490053	single nucleotide variant	NM_207391.3(RGS9BP):c.39C>G (p.Leu13=)	not provided [RCV001514784]\|not specified [RCV000597742]	benign	19	32676302	32676302	Human		name
127233492	CV1106330	single nucleotide variant	NM_207391.3(RGS9BP):c.180T>C (p.Ala60=)	not provided [RCV001421781]	likely benign	19	32676443	32676443	Human		name
127305589	CV1127727	single nucleotide variant	NM_207391.3(RGS9BP):c.105C>T (p.Asn35=)	not provided [RCV001455290]	likely benign	19	32676368	32676368	Human		name
127334273	CV1127728	single nucleotide variant	NM_207391.3(RGS9BP):c.199C>T (p.Leu67=)	not provided [RCV001473483]	likely benign	19	32676462	32676462	Human		name
127310920	CV1127729	single nucleotide variant	NM_207391.3(RGS9BP):c.294G>A (p.Glu98=)	not provided [RCV001456726]	likely benign	19	32676557	32676557	Human		name
127335164	CV1127730	single nucleotide variant	NM_207391.3(RGS9BP):c.297G>C (p.Leu99=)	not provided [RCV001474051]	likely benign	19	32676560	32676560	Human		name
152142972	CV1533297	single nucleotide variant	NM_207391.3(RGS9BP):c.169C>A (p.Arg57=)	not provided [RCV002157010]	likely benign	19	32676432	32676432	Human		name
152174322	CV1536300	single nucleotide variant	NM_207391.3(RGS9BP):c.118C>T (p.Leu40=)	not provided [RCV002144398]	likely benign	19	32676381	32676381	Human		name
152079828	CV1612599	single nucleotide variant	NM_207391.3(RGS9BP):c.144G>A (p.Gln48=)	not provided [RCV002170394]	likely benign	19	32676407	32676407	Human		name
156141932	CV1921962	single nucleotide variant	NM_207391.3(RGS9BP):c.288G>A (p.Ala96=)	not provided [RCV002623691]	likely benign	19	32676551	32676551	Human		name
155909279	CV1980011	single nucleotide variant	NM_207391.3(RGS9BP):c.207C>T (p.Ala69=)	not provided [RCV002613870]	likely benign	19	32676470	32676470	Human		name
155957107	CV2066326	single nucleotide variant	NM_207391.3(RGS9BP):c.280C>A (p.Arg94=)	not provided [RCV002816576]	uncertain significance	19	32676543	32676543	Human		name
155985486	CV2136876	single nucleotide variant	NM_207391.3(RGS9BP):c.153G>A (p.Ala51=)	not provided [RCV002996312]	likely benign	19	32676416	32676416	Human		name
156302670	CV2146402	single nucleotide variant	NM_207391.3(RGS9BP):c.249G>A (p.Ser83=)	not provided [RCV003028169]	likely benign	19	32676512	32676512	Human		name
156301093	CV2170214	single nucleotide variant	NM_207391.3(RGS9BP):c.249G>C (p.Ser83=)	not provided [RCV003045554]	likely benign	19	32676512	32676512	Human		name
402519693	CV3136012	single nucleotide variant	NM_207391.3(RGS9BP):c.120G>T (p.Leu40=)	not provided [RCV003824638]	likely benign	19	32676383	32676383	Human		name
15172374	CV704903	single nucleotide variant	NM_207391.3(RGS9BP):c.138G>A (p.Lys46=)	not provided [RCV000950013]	likely benign	19	32676401	32676401	Human		name
38481981	CV928912	deletion	NM_207391.3(RGS9BP):c.47del (p.Thr16fs)	not provided [RCV001218255]	uncertain significance	19	32676310	32676310	Human		name
127269410	CV1106331	single nucleotide variant	NM_207391.3(RGS9BP):c.336G>C (p.Leu112=)	not provided [RCV001441065]	likely benign	19	32676599	32676599	Human		name
127276740	CV1106332	single nucleotide variant	NM_207391.3(RGS9BP):c.375G>A (p.Ala125=)	not provided [RCV001432944]	likely benign	19	32676638	32676638	Human		name
127261516	CV1106333	single nucleotide variant	NM_207391.3(RGS9BP):c.387G>C (p.Leu129=)	not provided [RCV001438781]	likely benign	19	32676650	32676650	Human		name
127301658	CV1127732	single nucleotide variant	NM_207391.3(RGS9BP):c.609G>C (p.Gly203=)	not provided [RCV001454218]	likely benign	19	32676872	32676872	Human		name
127300787	CV1127733	single nucleotide variant	NM_207391.3(RGS9BP):c.612G>C (p.Gly204=)	not provided [RCV001461174]	likely benign	19	32676875	32676875	Human		name
127302401	CV1148674	single nucleotide variant	NM_207391.3(RGS9BP):c.585G>T (p.Ser195=)	not provided [RCV001499075]	likely benign	19	32676848	32676848	Human		name
127298253	CV1148675	single nucleotide variant	NM_207391.3(RGS9BP):c.609G>T (p.Gly203=)	not provided [RCV001497988]	likely benign	19	32676872	32676872	Human		name
151852254	CV1409202	single nucleotide variant	NM_207391.3(RGS9BP):c.35G>T (p.Gly12Val)	not provided [RCV001937517]	uncertain significance	19	32676298	32676298	Human		name
152159085	CV1522551	single nucleotide variant	NM_207391.3(RGS9BP):c.657C>T (p.Ala219=)	not provided [RCV002140604]	likely benign	19	32676920	32676920	Human		name
152115855	CV1526359	single nucleotide variant	NM_207391.3(RGS9BP):c.453G>A (p.Glu151=)	not provided [RCV002174917]	likely benign	19	32676716	32676716	Human		name
152162014	CV1534914	single nucleotide variant	NM_207391.3(RGS9BP):c.444G>A (p.Arg148=)	not provided [RCV002141080]	likely benign	19	32676707	32676707	Human		name
152150000	CV1545495	single nucleotide variant	NM_207391.3(RGS9BP):c.573C>T (p.Ala191=)	not provided [RCV002121606]	likely benign	19	32676836	32676836	Human		name
152031463	CV1546652	single nucleotide variant	NM_207391.3(RGS9BP):c.408C>G (p.Leu136=)	not provided [RCV002124559]	likely benign	19	32676671	32676671	Human		name
152106637	CV1577669	single nucleotide variant	NM_207391.3(RGS9BP):c.357C>A (p.Gly119=)	not provided [RCV002096261]	likely benign	19	32676620	32676620	Human		name
152100357	CV1595732	single nucleotide variant	NM_207391.3(RGS9BP):c.483C>T (p.Ile161=)	not provided [RCV002213923]	likely benign	19	32676746	32676746	Human		name
152036611	CV1605492	single nucleotide variant	NM_207391.3(RGS9BP):c.693G>A (p.Val231=)	not provided [RCV002107090]	likely benign	19	32676956	32676956	Human		name
152094366	CV1609328	single nucleotide variant	NM_207391.3(RGS9BP):c.429C>T (p.Asp143=)	not provided [RCV002172251]	likely benign	19	32676692	32676692	Human		name
152054139	CV1609953	single nucleotide variant	NM_207391.3(RGS9BP):c.366C>A (p.Ser122=)	not provided [RCV002167226]	likely benign	19	32676629	32676629	Human		name
152085223	CV1617229	single nucleotide variant	NM_207391.3(RGS9BP):c.417G>A (p.Glu139=)	not provided [RCV002076894]	likely benign	19	32676680	32676680	Human		name
152085079	CV1623010	single nucleotide variant	NM_207391.3(RGS9BP):c.669G>A (p.Ala223=)	not provided [RCV002113272]	likely benign	19	32676932	32676932	Human		name
152163129	CV1635852	single nucleotide variant	NM_207391.3(RGS9BP):c.531C>T (p.Ala177=)	not provided [RCV002203779]	likely benign	19	32676794	32676794	Human		name
152065559	CV1641264	single nucleotide variant	NM_207391.3(RGS9BP):c.369C>T (p.Gly123=)	not provided [RCV002209284]	likely benign	19	32676632	32676632	Human		name
9688783	CV178016	single nucleotide variant	NM_207391.3(RGS9BP):c.696G>A (p.Ala232=)	not provided [RCV001523354]\|not specified [RCV000153841]	benign	19	32676959	32676959	Human		name
8557023	CV17870	duplication	NM_207391.3(RGS9BP):c.193dup (p.Arg65fs)	Bradyopsia [RCV000002965]	pathogenic	19	32676454	32676455	Human	2	name
156414937	CV1983092	single nucleotide variant	NM_207391.3(RGS9BP):c.552G>A (p.Glu184=)	not provided [RCV002609435]	likely benign	19	32676815	32676815	Human		name
156319698	CV2014388	single nucleotide variant	NM_207391.3(RGS9BP):c.684C>T (p.Ala228=)	not provided [RCV002672107]	likely benign	19	32676947	32676947	Human		name
156020095	CV2029220	single nucleotide variant	NM_207391.3(RGS9BP):c.510G>A (p.Val170=)	not provided [RCV002735336]	likely benign	19	32676773	32676773	Human		name
156242450	CV2053161	deletion	NM_207391.3(RGS9BP):c.162del (p.Cys55fs)	not provided [RCV002791401]	uncertain significance	19	32676424	32676424	Human		name
156068091	CV2054643	single nucleotide variant	NM_207391.3(RGS9BP):c.29T>C (p.Leu10Pro)	not provided [RCV002797317]	uncertain significance	19	32676292	32676292	Human		name
155991370	CV2066827	single nucleotide variant	NM_207391.3(RGS9BP):c.537G>A (p.Gln179=)	not provided [RCV002842972]	uncertain significance	19	32676800	32676800	Human		name
156211317	CV2074256	single nucleotide variant	NM_207391.3(RGS9BP):c.663G>A (p.Leu221=)	not provided [RCV002829308]	uncertain significance	19	32676926	32676926	Human		name
156228503	CV2121924	single nucleotide variant	NM_207391.3(RGS9BP):c.360C>T (p.Ala120=)	not provided [RCV002958418]	likely benign	19	32676623	32676623	Human		name
156388284	CV2122198	single nucleotide variant	NM_207391.3(RGS9BP):c.360C>G (p.Ala120=)	not provided [RCV002943660]	likely benign	19	32676623	32676623	Human		name
155978651	CV2157093	single nucleotide variant	NM_207391.3(RGS9BP):c.327G>A (p.Arg109=)	not provided [RCV003016267]	likely benign	19	32676590	32676590	Human		name
156198094	CV2157415	single nucleotide variant	NM_207391.3(RGS9BP):c.669G>T (p.Ala223=)	not provided [RCV003006230]	likely benign	19	32676932	32676932	Human		name
155951816	CV2169652	duplication	NM_207391.3(RGS9BP):c.264dup (p.Leu89fs)	not provided [RCV003014892]	uncertain significance	19	32676526	32676527	Human		name
156369169	CV2190600	single nucleotide variant	NM_207391.3(RGS9BP):c.408C>T (p.Leu136=)	not provided [RCV003066160]	uncertain significance	19	32676671	32676671	Human		name
401928657	CV2811951	single nucleotide variant	NM_207391.3(RGS9BP):c.606C>T (p.Arg202=)	not provided [RCV003406926]	likely benign	19	32676869	32676869	Human		name
402482501	CV2940783	single nucleotide variant	NM_207391.3(RGS9BP):c.654C>T (p.Gly218=)	not provided [RCV003659703]	likely benign	19	32676917	32676917	Human		name
405104541	CV3120097	single nucleotide variant	NM_207391.3(RGS9BP):c.345A>G (p.Thr115=)	not provided [RCV003812167]	likely benign	19	32676608	32676608	Human		name
405132377	CV3163714	single nucleotide variant	NM_207391.3(RGS9BP):c.555C>G (p.Leu185=)	not provided [RCV003854702]	likely benign	19	32676818	32676818	Human		name
402514983	CV3178756	single nucleotide variant	NM_207391.3(RGS9BP):c.600G>A (p.Gln200=)	not provided [RCV003879189]	likely benign	19	32676863	32676863	Human		name
13516812	CV489871	single nucleotide variant	NM_207391.3(RGS9BP):c.96C>G (p.Asp32Glu)	not provided [RCV000595992]	conflicting interpretations of pathogenicity\|uncertain significance	19	32676359	32676359	Human		name
15108363	CV772571	single nucleotide variant	NM_207391.3(RGS9BP):c.699G>A (p.Lys233=)	not provided [RCV000938141]	likely benign	19	32676962	32676962	Human		name
38465740	CV950733	single nucleotide variant	NM_207391.3(RGS9BP):c.29T>A (p.Leu10Gln)	not provided [RCV001230189]	uncertain significance	19	32676292	32676292	Human		name
38481644	CV950734	single nucleotide variant	NM_207391.3(RGS9BP):c.67C>A (p.Leu23Met)	not provided [RCV001235227]	uncertain significance	19	32676330	32676330	Human		name
126756204	CV1013641	single nucleotide variant	NM_207391.3(RGS9BP):c.194G>C (p.Arg65Pro)	not provided [RCV001317126]\|not specified [RCV004847798]	uncertain significance	19	32676457	32676457	Human		name
8643586	CV102569	single nucleotide variant	NM_207391.3(RGS9BP):c.286G>T (p.Ala96Ser)	not provided [RCV000986208]\|not specified [RCV000082841]	benign	19	32676549	32676549	Human		name
126738205	CV1034200	single nucleotide variant	NM_207391.3(RGS9BP):c.191A>T (p.Asp64Val)	not provided [RCV001350448]	uncertain significance	19	32676454	32676454	Human		name
126911011	CV1051195	single nucleotide variant	NM_207391.3(RGS9BP):c.173T>A (p.Leu58Gln)	not provided [RCV001369021]	uncertain significance	19	32676436	32676436	Human		name
151802568	CV1354380	deletion	NM_207391.3(RGS9BP):c.695del (p.Ala232fs)	not provided [RCV001867260]	uncertain significance	19	32676958	32676958	Human		name
151843473	CV1408766	single nucleotide variant	NM_207391.3(RGS9BP):c.112C>G (p.Gln38Glu)	not provided [RCV002015621]	uncertain significance	19	32676375	32676375	Human		name
151722456	CV1414013	single nucleotide variant	NM_207391.3(RGS9BP):c.181G>A (p.Val61Met)	not provided [RCV002020382]	uncertain significance	19	32676444	32676444	Human		name
151731293	CV1419224	single nucleotide variant	NM_207391.3(RGS9BP):c.135G>C (p.Gln45His)	not provided [RCV001946073]	uncertain significance	19	32676398	32676398	Human		name
151738558	CV1437433	single nucleotide variant	NM_207391.3(RGS9BP):c.226G>A (p.Glu76Lys)	not provided [RCV001870781]	uncertain significance	19	32676489	32676489	Human		name
151865660	CV1484239	deletion	NM_207391.3(RGS9BP):c.614del (p.Gly205fs)	not provided [RCV001959791]	uncertain significance	19	32676870	32676870	Human		name
151828737	CV1510209	single nucleotide variant	NM_207391.3(RGS9BP):c.193C>T (p.Arg65Trp)	not provided [RCV001920282]	uncertain significance	19	32676456	32676456	Human		name
156336638	CV1963978	single nucleotide variant	NM_207391.3(RGS9BP):c.145G>A (p.Glu49Lys)	not provided [RCV002580280]	uncertain significance	19	32676408	32676408	Human		name
156239071	CV1973125	single nucleotide variant	NM_207391.3(RGS9BP):c.169C>T (p.Arg57Trp)	not provided [RCV002597083]	uncertain significance	19	32676432	32676432	Human		name
156116031	CV1993927	single nucleotide variant	NM_207391.3(RGS9BP):c.220G>T (p.Glu74Ter)	not provided [RCV002662669]	uncertain significance	19	32676483	32676483	Human		name
156219876	CV1995702	single nucleotide variant	NM_207391.3(RGS9BP):c.190G>C (p.Asp64His)	not provided [RCV002667186]	uncertain significance	19	32676453	32676453	Human		name
155902387	CV1999261	single nucleotide variant	NM_207391.3(RGS9BP):c.245T>C (p.Phe82Ser)	not provided [RCV002681183]	uncertain significance	19	32676508	32676508	Human		name
155906067	CV2027594	single nucleotide variant	NM_207391.3(RGS9BP):c.187C>T (p.Arg63Cys)	not provided [RCV002726477]	uncertain significance	19	32676450	32676450	Human		name
156293842	CV2152810	single nucleotide variant	NM_207391.3(RGS9BP):c.100C>T (p.Gln34Ter)	not provided [RCV003010078]	uncertain significance	19	32676363	32676363	Human		name
402520923	CV3002615	deletion	NM_207391.3(RGS9BP):c.445del (p.Glu149fs)	not provided [RCV003690291]	uncertain significance	19	32676706	32676706	Human		name
405048067	CV3071762	single nucleotide variant	NM_207391.3(RGS9BP):c.139G>T (p.Ala47Ser)	not provided [RCV003740338]	uncertain significance	19	32676402	32676402	Human		name
407474388	CV3472860	single nucleotide variant	NM_207391.3(RGS9BP):c.220G>A (p.Glu74Lys)	not specified [RCV004662988]	uncertain significance	19	32676483	32676483	Human		name
407474398	CV3472862	single nucleotide variant	NM_207391.3(RGS9BP):c.182T>G (p.Val61Gly)	not specified [RCV004662990]	uncertain significance	19	32676445	32676445	Human		name
13835947	CV587212	single nucleotide variant	NM_207391.3(RGS9BP):c.126G>C (p.Lys42Asn)	not provided [RCV000731893]	uncertain significance	19	32676389	32676389	Human		name
38490300	CV950735	duplication	NM_207391.3(RGS9BP):c.614dup (p.Cys206fs)	Prolonged electroretinal response suppression 2 [RCV003229031]\|not provided [RCV001238773]	conflicting interpretations of pathogenicity\|drug response\|uncertain significance	19	32676869	32676870	Human	1	name
126744936	CV998486	single nucleotide variant	NM_207391.3(RGS9BP):c.272C>A (p.Ala91Glu)	not provided [RCV001305910]\|not specified [RCV004034078]	uncertain significance	19	32676535	32676535	Human		name
126731975	CV1013642	single nucleotide variant	NM_207391.3(RGS9BP):c.506A>G (p.Asn169Ser)	not provided [RCV001313131]	uncertain significance	19	32676769	32676769	Human		name
126750103	CV1013643	single nucleotide variant	NM_207391.3(RGS9BP):c.583T>G (p.Ser195Ala)	Prolonged electroretinal response suppression 2 [RCV005394947]\|Retinal dystrophy [RCV004815380]\|not provided [RCV001326666]	uncertain significance	19	32676846	32676846	Human	3	name
126766095	CV1013644	single nucleotide variant	NM_207391.3(RGS9BP):c.589G>T (p.Val197Leu)	not provided [RCV001320305]	uncertain significance	19	32676852	32676852	Human		name
126754600	CV1013645	single nucleotide variant	NM_207391.3(RGS9BP):c.625A>G (p.Arg209Gly)	not provided [RCV001316749]	uncertain significance	19	32676888	32676888	Human		name
126746218	CV1034201	single nucleotide variant	NM_207391.3(RGS9BP):c.571G>A (p.Ala191Thr)	not provided [RCV001351494]	uncertain significance	19	32676834	32676834	Human		name
126753454	CV1034202	single nucleotide variant	NM_207391.3(RGS9BP):c.649T>C (p.Phe217Leu)	not provided [RCV001338596]	uncertain significance	19	32676912	32676912	Human		name
126909153	CV1051196	single nucleotide variant	NM_207391.3(RGS9BP):c.305C>T (p.Ala102Val)	not provided [RCV001368250]	uncertain significance	19	32676568	32676568	Human		name
127261909	CV1106334	single nucleotide variant	NM_207391.3(RGS9BP):c.467A>G (p.Gln156Arg)	not provided [RCV001438829]	likely benign	19	32676730	32676730	Human		name
127295259	CV1127734	single nucleotide variant	NM_207391.3(RGS9BP):c.637G>T (p.Ala213Ser)	not provided [RCV001477055]	likely benign	19	32676900	32676900	Human		name
151863952	CV1346424	single nucleotide variant	NM_207391.3(RGS9BP):c.574G>C (p.Gly192Arg)	not provided [RCV001959591]	uncertain significance	19	32676837	32676837	Human		name
151750696	CV1370505	single nucleotide variant	NM_207391.3(RGS9BP):c.403C>T (p.Arg135Trp)	not provided [RCV001872226]	uncertain significance	19	32676666	32676666	Human		name
151836190	CV1375008	single nucleotide variant	NM_207391.3(RGS9BP):c.380G>C (p.Arg127Pro)	not provided [RCV001921002]	uncertain significance	19	32676643	32676643	Human		name
151801588	CV1378786	single nucleotide variant	NM_207391.3(RGS9BP):c.390C>G (p.Ser130Arg)	not provided [RCV001877420]\|not specified [RCV004040599]	uncertain significance	19	32676653	32676653	Human		name
151866127	CV1381300	single nucleotide variant	NM_207391.3(RGS9BP):c.646C>A (p.Leu216Ile)	not provided [RCV001905903]	uncertain significance	19	32676909	32676909	Human		name
151826424	CV1400445	single nucleotide variant	NM_207391.3(RGS9BP):c.557T>G (p.Leu186Arg)	not provided [RCV001976224]	uncertain significance	19	32676820	32676820	Human		name
151762985	CV1407474	single nucleotide variant	NM_207391.3(RGS9BP):c.395G>T (p.Arg132Leu)	not provided [RCV002044494]	uncertain significance	19	32676658	32676658	Human		name
151773035	CV1414339	single nucleotide variant	NM_207391.3(RGS9BP):c.361T>G (p.Ser121Ala)	not provided [RCV001874636]	uncertain significance	19	32676624	32676624	Human		name
151766242	CV1418824	single nucleotide variant	NM_207391.3(RGS9BP):c.349G>A (p.Val117Met)	not provided [RCV001929076]\|not specified [RCV004044209]	uncertain significance	19	32676612	32676612	Human		name
151731366	CV1436156	single nucleotide variant	NM_207391.3(RGS9BP):c.613G>A (p.Gly205Ser)	not provided [RCV002004806]	uncertain significance	19	32676876	32676876	Human		name
151881105	CV1437302	single nucleotide variant	NM_207391.3(RGS9BP):c.592T>A (p.Ser198Thr)	not provided [RCV001999587]	uncertain significance	19	32676855	32676855	Human		name
151731701	CV1454275	single nucleotide variant	NM_207391.3(RGS9BP):c.508G>A (p.Val170Met)	not provided [RCV001967176]	uncertain significance	19	32676771	32676771	Human		name
151743586	CV1466908	single nucleotide variant	NM_207391.3(RGS9BP):c.343A>G (p.Thr115Ala)	not provided [RCV001871265]	uncertain significance	19	32676606	32676606	Human		name
151742125	CV1470207	single nucleotide variant	NM_207391.3(RGS9BP):c.658G>T (p.Val220Leu)	not provided [RCV001871119]	uncertain significance	19	32676921	32676921	Human		name
151790398	CV1475291	single nucleotide variant	NM_207391.3(RGS9BP):c.550G>A (p.Glu184Lys)	not provided [RCV001972996]	uncertain significance	19	32676813	32676813	Human		name
151874326	CV1510368	single nucleotide variant	NM_207391.3(RGS9BP):c.409G>C (p.Glu137Gln)	not provided [RCV001940204]\|not specified [RCV004043308]	uncertain significance	19	32676672	32676672	Human		name
151716176	CV1513010	single nucleotide variant	NM_207391.3(RGS9BP):c.397A>C (p.Ser133Arg)	not provided [RCV001890365]	uncertain significance	19	32676660	32676660	Human		name
9688782	CV177034	single nucleotide variant	NM_207391.3(RGS9BP):c.668C>T (p.Ala223Val)	not provided [RCV001518431]\|not specified [RCV000153840]	benign	19	32676931	32676931	Human	3	name
9688782	CV177034	single nucleotide variant	NM_207391.3(RGS9BP):c.668C>T (p.Ala223Val)	not provided [RCV001518431]\|not specified [RCV000153840]	benign	19	32676931	32676932	Human	3	name
155664444	CV1773253	single nucleotide variant	NM_207391.3(RGS9BP):c.586G>A (p.Val196Ile)	not provided [RCV002296965]	uncertain significance	19	32676849	32676849	Human		name
155693807	CV1775341	single nucleotide variant	NM_207391.3(RGS9BP):c.362C>T (p.Ser121Phe)	not provided [RCV002299466]	uncertain significance	19	32676625	32676625	Human		name
156363119	CV1895451	single nucleotide variant	NM_207391.3(RGS9BP):c.611G>T (p.Gly204Val)	not provided [RCV003091848]	uncertain significance	19	32676874	32676874	Human		name
156266945	CV1957017	single nucleotide variant	NM_207391.3(RGS9BP):c.449T>C (p.Leu150Pro)	not provided [RCV002577036]	uncertain significance	19	32676712	32676712	Human		name
156090477	CV1963126	single nucleotide variant	NM_207391.3(RGS9BP):c.445G>C (p.Glu149Gln)	not provided [RCV002570205]	uncertain significance	19	32676708	32676708	Human		name
156318885	CV1965905	single nucleotide variant	NM_207391.3(RGS9BP):c.668C>A (p.Ala223Glu)	not provided [RCV002600107]	uncertain significance	19	32676931	32676931	Human		name
156412929	CV1968876	single nucleotide variant	NM_207391.3(RGS9BP):c.356G>A (p.Gly119Asp)	not provided [RCV002608685]\|not specified [RCV005266319]	uncertain significance	19	32676619	32676619	Human		name
156290166	CV1998156	single nucleotide variant	NM_207391.3(RGS9BP):c.418G>A (p.Gly140Ser)	not provided [RCV002647160]	uncertain significance	19	32676681	32676681	Human		name
156087426	CV2007323	single nucleotide variant	NM_207391.3(RGS9BP):c.448C>G (p.Leu150Val)	not provided [RCV002694819]	uncertain significance	19	32676711	32676711	Human		name
155943743	CV2032518	single nucleotide variant	NM_207391.3(RGS9BP):c.590T>C (p.Val197Ala)	not provided [RCV002730283]	uncertain significance	19	32676853	32676853	Human		name
155981056	CV2097959	single nucleotide variant	NM_207391.3(RGS9BP):c.601G>T (p.Glu201Ter)	not provided [RCV002907708]	uncertain significance	19	32676864	32676864	Human		name
156334436	CV2112997	single nucleotide variant	NM_207391.3(RGS9BP):c.631G>T (p.Ala211Ser)	not provided [RCV002938548]	uncertain significance	19	32676894	32676894	Human		name
156022612	CV2138961	single nucleotide variant	NM_207391.3(RGS9BP):c.685G>C (p.Val229Leu)	not provided [RCV002998752]	uncertain significance	19	32676948	32676948	Human		name
155940733	CV2142914	single nucleotide variant	NM_207391.3(RGS9BP):c.581C>T (p.Ser194Phe)	not provided [RCV002994035]	uncertain significance	19	32676844	32676844	Human		name
155938100	CV2146403	single nucleotide variant	NM_207391.3(RGS9BP):c.368G>A (p.Gly123Asp)	not provided [RCV003014081]	uncertain significance	19	32676631	32676631	Human		name
156057015	CV2151319	single nucleotide variant	NM_207391.3(RGS9BP):c.386T>C (p.Leu129Pro)	not provided [RCV003019592]	uncertain significance	19	32676649	32676649	Human		name
156214056	CV2176477	single nucleotide variant	NM_207391.3(RGS9BP):c.688T>G (p.Cys230Gly)	not provided [RCV003024923]	uncertain significance	19	32676951	32676951	Human		name
156022615	CV2184678	single nucleotide variant	NM_207391.3(RGS9BP):c.436G>A (p.Asp146Asn)	not provided [RCV003035805]	uncertain significance	19	32676699	32676699	Human		name
156059277	CV2322996	single nucleotide variant	NM_207391.3(RGS9BP):c.498G>T (p.Met166Ile)	not specified [RCV004185430]	uncertain significance	19	32676761	32676761	Human		name
156174660	CV2326973	single nucleotide variant	NM_207391.3(RGS9BP):c.536A>C (p.Gln179Pro)	not specified [RCV004176781]	uncertain significance	19	32676799	32676799	Human		name
407474392	CV3472861	single nucleotide variant	NM_207391.3(RGS9BP):c.401T>G (p.Leu134Arg)	not specified [RCV004662989]	uncertain significance	19	32676664	32676664	Human		name
597788193	CV3586429	single nucleotide variant	NM_207391.3(RGS9BP):c.431T>C (p.Val144Ala)	not specified [RCV004855434]	uncertain significance	19	32676694	32676694	Human		name
597775948	CV3586430	single nucleotide variant	NM_207391.3(RGS9BP):c.374C>T (p.Ala125Val)	not specified [RCV004852389]	uncertain significance	19	32676637	32676637	Human		name
597775952	CV3586431	single nucleotide variant	NM_207391.3(RGS9BP):c.403C>G (p.Arg135Gly)	not specified [RCV004852390]	uncertain significance	19	32676666	32676666	Human		name
598189474	CV3902624	single nucleotide variant	NM_207391.3(RGS9BP):c.613G>T (p.Gly205Cys)	not specified [RCV005266718]	uncertain significance	19	32676876	32676876	Human		name
13528885	CV513659	single nucleotide variant	NM_207391.3(RGS9BP):c.365C>G (p.Ser122Cys)	Bradyopsia [RCV000626144]\|Retinal dystrophy [RCV004817829]\|not provided [RCV001701422]	likely pathogenic\|uncertain significance	19	32676628	32676628	Human	4	name
26890491	CV847488	single nucleotide variant	NM_207391.3(RGS9BP):c.323C>T (p.Pro108Leu)	not provided [RCV001059366]	uncertain significance	19	32676586	32676586	Human		name
26885543	CV847489	single nucleotide variant	NM_207391.3(RGS9BP):c.352G>A (p.Ala118Thr)	not provided [RCV001053654]	uncertain significance	19	32676615	32676615	Human		name
26890290	CV847490	single nucleotide variant	NM_207391.3(RGS9BP):c.542C>T (p.Ala181Val)	not provided [RCV001059105]	uncertain significance	19	32676805	32676805	Human		name
38456263	CV938629	single nucleotide variant	NM_207391.3(RGS9BP):c.578C>T (p.Pro193Leu)	not provided [RCV001210759]\|not specified [RCV004033804]	uncertain significance	19	32676841	32676841	Human		name
38497712	CV950736	single nucleotide variant	NM_207391.3(RGS9BP):c.691G>A (p.Val231Met)	not provided [RCV001227260]\|not specified [RCV004032598]	uncertain significance	19	32676954	32676954	Human		name
38457615	CV958591	single nucleotide variant	NM_207391.3(RGS9BP):c.488A>G (p.Asn163Ser)	not provided [RCV001246097]	uncertain significance	19	32676751	32676751	Human		name
38493785	CV958592	single nucleotide variant	NM_207391.3(RGS9BP):c.548C>T (p.Ala183Val)	not provided [RCV001240895]	uncertain significance	19	32676811	32676811	Human		name
126745163	CV998487	single nucleotide variant	NM_207391.3(RGS9BP):c.298G>A (p.Gly100Ser)	not provided [RCV001305943]	uncertain significance	19	32676561	32676561	Human		name
401946829	CV2831832	deletion	NM_207391.3(RGS9BP):c.277_278del (p.Met93fs)	Prolonged electroretinal response suppression 2 [RCV003445475]	drug response	19	32676540	32676541	Human	1	name
156205908	CV1922810	deletion	NM_207391.3(RGS9BP):c.389_419del (p.Ser130fs)	not provided [RCV002643806]	uncertain significance	19	32676652	32676682	Human		name
405707693	CV3225355	deletion	NM_207391.3(RGS9BP):c.330_342del (p.Pro111fs)	Prolonged electroretinal response suppression 2 [RCV003990409]	pathogenic	19	32676593	32676605	Human	1	name
26901249	CV847487	deletion	NM_207391.3(RGS9BP):c.307_326del (p.Phe103fs)	not provided [RCV001068405]	uncertain significance	19	32676562	32676581	Human		name
151721304	CV1494709	indel	NM_207391.3(RGS9BP):c.262_263delinsAA (p.Leu88Lys)	not provided [RCV001966021]	uncertain significance	19	32676525	32676526	Human		name
329351172	CV2477958	deletion	NM_207391.3(RGS9BP):c.94_102del (p.Asp32_Gln34del)	Prolonged electroretinal response suppression 2 [RCV003224069]	drug response	19	32676356	32676364	Human	1	name
126766914	CV1034203	indel	NM_207391.3(RGS9BP):c.650_651delinsAA (p.Phe217Ter)	not provided [RCV001342612]	uncertain significance	19	32676913	32676914	Human		name
151770646	CV1504363	duplication	NM_207391.3(RGS9BP):c.111_131dup (p.Glu39_Gln45dup)	not provided [RCV002045211]	uncertain significance	19	32676370	32676371	Human		name
156081977	CV2098722	indel	NM_207391.3(RGS9BP):c.380_381delinsTT (p.Arg127Leu)	not provided [RCV002912734]	uncertain significance	19	32676643	32676644	Human		name
151797743	CV1439572	deletion	NM_207391.3(RGS9BP):c.371_382del (p.Val124_Arg127del)	not provided [RCV002011282]	uncertain significance	19	32676631	32676642	Human		name
41408235	CV980965	indel	NM_207391.3(RGS9BP):c.323_342delinsACCGGCG (p.Pro108fs)	Bradyopsia [RCV001283837]	pathogenic	19	32676586	32676605	Human		name
126912542	CV1051197	duplication	NM_207391.3(RGS9BP):c.674_702dup (p.Ser235delinsTrpProTer)	not provided [RCV001369772]	uncertain significance	19	32676932	32676933	Human		name

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