Gpr17 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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More than 1000 records found for search term Gpr17 (Displaying 1000)
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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407479850	CV3436672	single nucleotide variant	NM_001161417.2(GPR17):c.-18T>C	not specified [RCV004632434]	uncertain significance	2	127650718	127650718	Human		name
617149340	CV4021456	single nucleotide variant	NM_001161417.2(GPR17):c.63G>A (p.Glu21=)	not provided [RCV005425425]	likely benign	2	127650798	127650798	Human		name
329376387	CV2438185	single nucleotide variant	NM_001161417.2(GPR17):c.20C>T (p.Ala7Val)	not specified [RCV004256957]	uncertain significance	2	127650755	127650755	Human		name
156273281	CV2344102	single nucleotide variant	NM_001161417.2(GPR17):c.95T>A (p.Met32Lys)	not specified [RCV004195704]	uncertain significance	2	127650830	127650830	Human		name
596947828	CV3547413	single nucleotide variant	NM_001161417.2(GPR17):c.924G>C (p.Leu308=)	not provided [RCV004811717]	likely benign	2	127651659	127651659	Human		name
596945244	CV3547757	single nucleotide variant	NM_001161417.2(GPR17):c.768C>T (p.Ser256=)	not provided [RCV004809088]	likely benign	2	127651503	127651503	Human		name
598129004	CV3886807	single nucleotide variant	NM_001161417.2(GPR17):c.45C>A (p.Phe15Leu)	not provided [RCV005244467]	likely benign	2	127650780	127650780	Human		name
598233843	CV3971151	single nucleotide variant	NM_001161417.2(GPR17):c.49C>G (p.Leu17Val)	not specified [RCV005342816]	uncertain significance	2	127650784	127650784	Human		name
598274398	CV3971153	single nucleotide variant	NM_001161417.2(GPR17):c.28G>A (p.Gly10Ser)	not specified [RCV005351402]	likely benign	2	127650763	127650763	Human		name
15149776	CV707714	single nucleotide variant	NM_001161417.2(GPR17):c.80C>T (p.Thr27Met)	not provided [RCV000967818]	benign	2	127650815	127650815	Human		name
15149782	CV707715	single nucleotide variant	NM_001161417.2(GPR17):c.534G>A (p.Thr178=)	not provided [RCV000967819]	benign	2	127651269	127651269	Human		name
15109667	CV762177	single nucleotide variant	NM_001161417.2(GPR17):c.441C>T (p.Tyr147=)	not provided [RCV000938391]	likely benign	2	127651176	127651176	Human		name
156006969	CV2357835	single nucleotide variant	NM_001161417.2(GPR17):c.179A>T (p.His60Leu)	not specified [RCV004205119]	uncertain significance	2	127650914	127650914	Human		name
597744895	CV3684890	single nucleotide variant	NM_001161417.2(GPR17):c.173G>A (p.Arg58Gln)	not specified [RCV004922356]	uncertain significance	2	127650908	127650908	Human		name
598233836	CV3971149	single nucleotide variant	NM_001161417.2(GPR17):c.106T>G (p.Ser36Ala)	not specified [RCV005342815]	uncertain significance	2	127650841	127650841	Human		name
598274394	CV3971150	single nucleotide variant	NM_001161417.2(GPR17):c.110T>C (p.Phe37Ser)	not specified [RCV005351400]	uncertain significance	2	127650845	127650845	Human		name
156070151	CV2203933	single nucleotide variant	NM_001161417.2(GPR17):c.919G>A (p.Ala307Thr)	not specified [RCV004069981]	uncertain significance	2	127651654	127651654	Human		name
156399189	CV2204968	single nucleotide variant	NM_001161417.2(GPR17):c.557G>A (p.Arg186Gln)	not specified [RCV004077590]	uncertain significance	2	127651292	127651292	Human		name
156306162	CV2252699	single nucleotide variant	NM_001161417.2(GPR17):c.787C>T (p.Arg263Cys)	not specified [RCV004118556]	uncertain significance	2	127651522	127651522	Human		name
156001297	CV2296397	single nucleotide variant	NM_001161417.2(GPR17):c.494C>T (p.Pro165Leu)	not specified [RCV004148144]	uncertain significance	2	127651229	127651229	Human		name
156274314	CV2316365	single nucleotide variant	NM_001161417.2(GPR17):c.678G>C (p.Glu226Asp)	not specified [RCV004169868]	uncertain significance	2	127651413	127651413	Human		name
155902593	CV2386277	single nucleotide variant	NM_001161417.2(GPR17):c.349G>A (p.Ala117Thr)	not specified [RCV004228627]	uncertain significance	2	127651084	127651084	Human		name
156223874	CV2395032	single nucleotide variant	NM_001161417.2(GPR17):c.386G>A (p.Arg129His)	not specified [RCV004236721]	uncertain significance	2	127651121	127651121	Human		name
155996648	CV2398578	single nucleotide variant	NM_001161417.2(GPR17):c.757G>A (p.Val253Ile)	not specified [RCV004237891]	uncertain significance	2	127651492	127651492	Human		name
329396575	CV2459726	single nucleotide variant	NM_001161417.2(GPR17):c.491C>A (p.Ala164Asp)	not specified [RCV004277147]	uncertain significance	2	127651226	127651226	Human		name
401775073	CV2723975	single nucleotide variant	NM_001161417.2(GPR17):c.764G>A (p.Arg255His)	not specified [RCV004326128]	uncertain significance	2	127651499	127651499	Human		name
405738261	CV3255309	single nucleotide variant	NM_001161417.2(GPR17):c.314G>A (p.Arg105His)	not specified [RCV004390936]	uncertain significance	2	127651049	127651049	Human		name
405738267	CV3255310	single nucleotide variant	NM_001161417.2(GPR17):c.358T>C (p.Tyr120His)	not specified [RCV004390937]	uncertain significance	2	127651093	127651093	Human		name
405738280	CV3255312	single nucleotide variant	NM_001161417.2(GPR17):c.625G>A (p.Val209Ile)	not specified [RCV004390939]	uncertain significance	2	127651360	127651360	Human		name
405738285	CV3255313	single nucleotide variant	NM_001161417.2(GPR17):c.650G>A (p.Arg217His)	not specified [RCV004390940]	uncertain significance	2	127651385	127651385	Human		name
405738293	CV3255314	single nucleotide variant	NM_001161417.2(GPR17):c.683G>A (p.Arg228His)	not specified [RCV004390941]	uncertain significance	2	127651418	127651418	Human		name
405738299	CV3255315	single nucleotide variant	NM_001161417.2(GPR17):c.745G>A (p.Val249Met)	not specified [RCV004390942]	uncertain significance	2	127651480	127651480	Human		name
405738307	CV3255316	single nucleotide variant	NM_001161417.2(GPR17):c.775G>A (p.Val259Met)	not specified [RCV004390943]	uncertain significance	2	127651510	127651510	Human		name
407479846	CV3436671	single nucleotide variant	NM_001161417.2(GPR17):c.817C>T (p.Arg273Cys)	not specified [RCV004632433]	uncertain significance	2	127651552	127651552	Human		name
597744901	CV3684891	single nucleotide variant	NM_001161417.2(GPR17):c.838C>T (p.Arg280Cys)	not specified [RCV004922357]	uncertain significance	2	127651573	127651573	Human		name
597744905	CV3684892	single nucleotide variant	NM_001161417.2(GPR17):c.940G>A (p.Gly314Ser)	not specified [RCV004922358]	uncertain significance	2	127651675	127651675	Human		name
597744911	CV3684893	single nucleotide variant	NM_001161417.2(GPR17):c.995C>T (p.Ser332Leu)	not specified [RCV004922359]	uncertain significance	2	127651730	127651730	Human		name
597789862	CV3684894	single nucleotide variant	NM_001161417.2(GPR17):c.520C>A (p.Gln174Lys)	not specified [RCV004933093]	uncertain significance	2	127651255	127651255	Human		name
597744916	CV3684895	single nucleotide variant	NM_001161417.2(GPR17):c.754C>T (p.His252Tyr)	not specified [RCV004922360]	uncertain significance	2	127651489	127651489	Human		name
597744920	CV3684896	single nucleotide variant	NM_001161417.2(GPR17):c.797G>A (p.Gly266Glu)	not specified [RCV004922361]	uncertain significance	2	127651532	127651532	Human		name
598274390	CV3971147	single nucleotide variant	NM_001161417.2(GPR17):c.328C>T (p.Leu110Phe)	not specified [RCV005351398]	uncertain significance	2	127651063	127651063	Human		name
598274396	CV3971152	single nucleotide variant	NM_001161417.2(GPR17):c.434C>T (p.Pro145Leu)	not specified [RCV005351401]	uncertain significance	2	127651169	127651169	Human		name
598233849	CV3971154	single nucleotide variant	NM_001161417.2(GPR17):c.487A>C (p.Met163Leu)	not specified [RCV005342817]	uncertain significance	2	127651222	127651222	Human		name
598233857	CV3971155	single nucleotide variant	NM_001161417.2(GPR17):c.611C>T (p.Pro204Leu)	not specified [RCV005342818]	uncertain significance	2	127651346	127651346	Human		name
150539243	CV1305236	single nucleotide variant	NM_032553.3(GPR174):c.-34C>T	not provided [RCV001766016]	benign	X	79170974	79170974	Human		name
150539245	CV1305238	single nucleotide variant	NM_032553.3(GPR174):c.-17T>C	not provided [RCV001766018]	benign	X	79170991	79170991	Human		name
28903829	CV877329	single nucleotide variant	NM_001004334.4(GPR179):c.*17G>C	Congenital stationary night blindness 1E [RCV001125823]	uncertain significance	17	38326448	38326448	Human	1	name
150459182	CV1269763	single nucleotide variant	NM_001004334.4(GPR179):c.-123C>G	not provided [RCV001693303]	benign	17	38343912	38343912	Human		name
11615136	CV328288	single nucleotide variant	NM_001004334.4(GPR179):c.*554C>T	Congenital stationary night blindness 1E [RCV000283076]	uncertain significance	17	38325911	38325911	Human	1	name
11623794	CV338148	single nucleotide variant	NM_001004334.4(GPR179):c.*613G>C	Congenital stationary night blindness 1E [RCV000377556]	benign\|likely benign	17	38325852	38325852	Human	1	name
11614673	CV338154	single nucleotide variant	NM_001004334.4(GPR179):c.*454G>A	Congenital stationary night blindness 1E [RCV000278748]	uncertain significance	17	38326011	38326011	Human	1	name
11621773	CV338157	single nucleotide variant	NM_001004334.4(GPR179):c.*362G>A	Congenital stationary night blindness 1E [RCV000352388]	benign\|likely benign	17	38326103	38326103	Human	1	name
11664074	CV338167	single nucleotide variant	NM_001004334.4(GPR179):c.*338G>A	Congenital Stationary Night Blindness, Recessive [RCV000402186]	uncertain significance	17	38326127	38326127	Human	1	name
11618334	CV338168	single nucleotide variant	NM_001004334.4(GPR179):c.*304A>G	Congenital stationary night blindness 1E [RCV000312686]	uncertain significance	17	38326161	38326161	Human	1	name
11629429	CV344285	single nucleotide variant	NM_001004334.4(GPR179):c.*824G>A	Congenital stationary night blindness 1E [RCV000323092]	uncertain significance	17	38325641	38325641	Human	1	name
11630009	CV344286	single nucleotide variant	NM_001004334.4(GPR179):c.*523G>A	Congenital stationary night blindness 1E [RCV000338161]	benign\|likely benign	17	38325942	38325942	Human	1	name
11661203	CV344291	single nucleotide variant	NM_001004334.4(GPR179):c.*516T>C	Congenital stationary night blindness 1E [RCV000374147]	uncertain significance	17	38325949	38325949	Human	1	name
28901546	CV877324	single nucleotide variant	NM_001004334.4(GPR179):c.*640G>T	Congenital stationary night blindness 1E [RCV001124842]	uncertain significance	17	38325825	38325825	Human	1	name
28901549	CV877325	single nucleotide variant	NM_001004334.4(GPR179):c.*522C>T	Congenital stationary night blindness 1E [RCV001124843]	uncertain significance	17	38325943	38325943	Human	1	name
28903822	CV877326	single nucleotide variant	NM_001004334.4(GPR179):c.*453C>T	Congenital stationary night blindness 1E [RCV001125820]	uncertain significance	17	38326012	38326012	Human	1	name
28903825	CV877327	single nucleotide variant	NM_001004334.4(GPR179):c.*388A>C	Congenital stationary night blindness 1E [RCV001125821]	uncertain significance	17	38326077	38326077	Human	1	name
28903827	CV877328	single nucleotide variant	NM_001004334.4(GPR179):c.*359C>G	Congenital stationary night blindness 1E [RCV001125822]	uncertain significance	17	38326106	38326106	Human	1	name
127303766	CV1157943	variation	NM_001004334.4(GPR179):c.1891-11=	not provided [RCV001515598]	benign	17	38333408	38333408	Human		name
150450652	CV1254138	single nucleotide variant	NM_001004334.4(GPR179):c.992-107=	not provided [RCV001667776]	benign	17	38337320	38337320	Human		name
150439096	CV1264923	single nucleotide variant	NM_001004334.4(GPR179):c.1646-76=	not provided [RCV001678916]	benign	17	38334918	38334918	Human		name
150489503	CV1268909	single nucleotide variant	NM_001004334.4(GPR179):c.1406+98=	not provided [RCV001687473]	benign	17	38335493	38335493	Human		name
151807335	CV1382336	single nucleotide variant	NM_001004334.4(GPR179):c.991+1G>T	not provided [RCV002028641]	likely pathogenic	17	38337632	38337632	Human		name
151829848	CV1491620	single nucleotide variant	NM_001004334.4(GPR179):c.904-3T>C	not provided [RCV002030691]	uncertain significance	17	38337723	38337723	Human		name
155991238	CV2049617	single nucleotide variant	NM_001004334.4(GPR179):c.992-8C>A	not provided [RCV002819216]	likely benign	17	38337221	38337221	Human		name
405204997	CV3144048	single nucleotide variant	NM_001004334.4(GPR179):c.795-5C>T	not provided [RCV003844838]	likely benign	17	38339530	38339530	Human		name
11622270	CV328318	single nucleotide variant	NM_001004334.4(GPR179):c.991+4T>C	Congenital stationary night blindness 1E [RCV000358219]\|GPR179-related disorder [RCV003922368]\|not provided [RCV002056588]	likely benign\|uncertain significance	17	38337629	38337629	Human	1	name , alternate_id
13525931	CV512958	single nucleotide variant	NM_001004334.4(GPR179):c.795-4G>A	Congenital stationary night blindness 1E [RCV000625280]\|GPR179-related disorder [RCV003905670]\|not provided [RCV002060699]\|not specified [RCV001701130]	benign\|likely benign	17	38339529	38339529	Human	1	name , alternate_id
126751203	CV1033249	single nucleotide variant	NM_001004334.4(GPR179):c.1784+6G>A	not provided [RCV001352394]	uncertain significance	17	38334698	38334698	Human		name
127305593	CV1126175	single nucleotide variant	NM_001004334.4(GPR179):c.794+17A>T	not provided [RCV001462518]	likely benign	17	38342979	38342979	Human		name
127298474	CV1157946	single nucleotide variant	NM_001004334.4(GPR179):c.992-16A>T	not provided [RCV001513272]	benign	17	38337229	38337229	Human		name
150500933	CV1238280	single nucleotide variant	NM_001004334.4(GPR179):c.1784+121=	not provided [RCV001656710]	benign	17	38334583	38334583	Human		name
150446577	CV1250685	single nucleotide variant	NM_001004334.4(GPR179):c.1406+109=	not provided [RCV001667190]	benign	17	38335482	38335482	Human		name
150474283	CV1252544	single nucleotide variant	NM_001004334.4(GPR179):c.991+97G>A	not provided [RCV001671747]	benign	17	38337536	38337536	Human		name
151870960	CV1351678	single nucleotide variant	NM_001004334.4(GPR179):c.1296+3G>C	not provided [RCV002018934]	uncertain significance	17	38336073	38336073	Human		name
151813259	CV1366217	single nucleotide variant	NM_001004334.4(GPR179):c.2037+1G>T	not provided [RCV001933415]	uncertain significance	17	38333250	38333250	Human		name
151858736	CV1398344	single nucleotide variant	NM_001004334.4(GPR179):c.1406+4C>T	not provided [RCV002017495]	uncertain significance	17	38335587	38335587	Human		name
151805149	CV1429846	single nucleotide variant	NM_001004334.4(GPR179):c.1227+3A>G	not provided [RCV001974266]	uncertain significance	17	38336975	38336975	Human		name
151832456	CV1439165	single nucleotide variant	NM_001004334.4(GPR179):c.1296+1G>A	not provided [RCV001976778]	likely pathogenic	17	38336075	38336075	Human		name
152073974	CV1557346	single nucleotide variant	NM_001004334.4(GPR179):c.1228-7T>C	not provided [RCV002129970]	likely benign	17	38336151	38336151	Human		name
152061188	CV1559304	deletion	NM_001004334.4(GPR179):c.794+16del	not provided [RCV002168021]	likely benign	17	38342980	38342980	Human		name
152062586	CV1595192	single nucleotide variant	NM_001004334.4(GPR179):c.1891-9C>T	not provided [RCV002190708]	likely benign	17	38333406	38333406	Human		name
152162738	CV1600595	single nucleotide variant	NM_001004334.4(GPR179):c.1228-9G>A	not provided [RCV002141200]	likely benign	17	38336153	38336153	Human		name
152030437	CV1622181	single nucleotide variant	NM_001004334.4(GPR179):c.795-16C>T	not provided [RCV002186468]	likely benign	17	38339541	38339541	Human		name
152027289	CV1636164	single nucleotide variant	NM_001004334.4(GPR179):c.992-16A>G	not provided [RCV002085084]	likely benign	17	38337229	38337229	Human		name
152152918	CV1664581	single nucleotide variant	NM_001004334.4(GPR179):c.795-13T>C	not provided [RCV002158457]	likely benign	17	38339538	38339538	Human		name
156385732	CV1961221	single nucleotide variant	NM_001004334.4(GPR179):c.992-14C>T	not provided [RCV002583468]	likely benign	17	38337227	38337227	Human		name
156347467	CV1970622	single nucleotide variant	NM_001004334.4(GPR179):c.2038-7C>T	not provided [RCV002601596]	likely benign	17	38331538	38331538	Human		name
156112738	CV1988876	single nucleotide variant	NM_001004334.4(GPR179):c.1785-6C>A	not provided [RCV002622643]	likely benign	17	38334044	38334044	Human		name
156228286	CV2006144	single nucleotide variant	NM_001004334.4(GPR179):c.992-10T>G	not provided [RCV002667481]	likely benign	17	38337223	38337223	Human		name
156089002	CV2017406	single nucleotide variant	NM_001004334.4(GPR179):c.1890+6G>T	not provided [RCV002694874]	uncertain significance	17	38333927	38333927	Human		name
156315008	CV2017928	single nucleotide variant	NM_001004334.4(GPR179):c.1785-6C>T	not provided [RCV002671851]	likely benign	17	38334044	38334044	Human		name
156008956	CV2020045	single nucleotide variant	NM_001004334.4(GPR179):c.1784+3G>C	not provided [RCV002734795]	uncertain significance	17	38334701	38334701	Human		name
155938611	CV2071701	single nucleotide variant	NM_001004334.4(GPR179):c.1645+1G>T	not provided [RCV002839257]	likely pathogenic	17	38335032	38335032	Human		name
156204711	CV2103633	single nucleotide variant	NM_001004334.4(GPR179):c.1296+4A>G	not provided [RCV002931819]	uncertain significance	17	38336072	38336072	Human		name
402476476	CV2857294	single nucleotide variant	NM_001004334.4(GPR179):c.1646-1G>C	not provided [RCV003543457]	likely pathogenic	17	38334843	38334843	Human		name
402499374	CV3015884	single nucleotide variant	NM_001004334.4(GPR179):c.991+19G>T	not provided [RCV003688224]	likely benign	17	38337614	38337614	Human		name
402504713	CV3041851	single nucleotide variant	NM_001004334.4(GPR179):c.1646-5C>A	not provided [RCV003715033]	likely benign	17	38334847	38334847	Human		name
11614765	CV338213	single nucleotide variant	NM_001004334.4(GPR179):c.1784+8C>T	Congenital stationary night blindness 1E [RCV000279321]\|not provided [RCV002056587]	benign\|uncertain significance	17	38334696	38334696	Human	1	name
11631980	CV345752	single nucleotide variant	NM_001004334.4(GPR179):c.1784+9G>A	Congenital stationary night blindness 1E [RCV000394122]	uncertain significance	17	38334695	38334695	Human	1	name
597901457	CV3741359	single nucleotide variant	NM_001004334.4(GPR179):c.1785-7G>A	not provided [RCV005072330]	likely benign	17	38334045	38334045	Human		name
597947834	CV3759034	single nucleotide variant	NM_001004334.4(GPR179):c.1645+5G>C	not provided [RCV005078830]	uncertain significance	17	38335028	38335028	Human		name
597891057	CV3784936	single nucleotide variant	NM_001004334.4(GPR179):c.1297-8C>T	not provided [RCV005125715]	likely benign	17	38335708	38335708	Human		name
597934585	CV3793610	single nucleotide variant	NM_001004334.4(GPR179):c.795-12T>C	not provided [RCV005132266]	likely benign	17	38339537	38339537	Human		name
8568858	CV40160	single nucleotide variant	NM_001004334.4(GPR179):c.1784+1G>A	Congenital stationary night blindness 1E [RCV000024202]	pathogenic	17	38334703	38334703	Human	1	name
28895500	CV880510	single nucleotide variant	NM_001004334.4(GPR179):c.1785-3C>T	Congenital stationary night blindness 1E [RCV001122492]	uncertain significance	17	38334041	38334041	Human	1	name
150494155	CV1226103	single nucleotide variant	NM_001004334.4(GPR179):c.2037+44G>C	not provided [RCV001619322]	benign	17	38333207	38333207	Human		name
150476082	CV1239829	single nucleotide variant	NM_001004334.4(GPR179):c.1890+74G>A	not provided [RCV001652006]	benign	17	38333859	38333859	Human		name
150448667	CV1253585	deletion	NM_001004334.4(GPR179):c.903+203del	not provided [RCV001667513]	benign	17	38339214	38339214	Human		name
150465542	CV1277256	single nucleotide variant	NM_001004334.4(GPR179):c.903+204A>C	not provided [RCV001710550]	benign	17	38339213	38339213	Human		name
152120746	CV1521335	single nucleotide variant	NM_001004334.4(GPR179):c.1785-18G>A	not provided [RCV002135676]	likely benign	17	38334056	38334056	Human		name
152046407	CV1525840	single nucleotide variant	NM_001004334.4(GPR179):c.1891-12C>T	not provided [RCV002126692]	likely benign	17	38333409	38333409	Human		name
152060121	CV1536232	single nucleotide variant	NM_001004334.4(GPR179):c.1785-19C>A	not provided [RCV002146673]	likely benign	17	38334057	38334057	Human		name
152089542	CV1541602	single nucleotide variant	NM_001004334.4(GPR179):c.2038-12G>C	not provided [RCV002171644]	likely benign	17	38331543	38331543	Human		name
152098593	CV1578456	single nucleotide variant	NM_001004334.4(GPR179):c.1785-16C>T	not provided [RCV002151519]	likely benign	17	38334054	38334054	Human		name
152046420	CV1591249	single nucleotide variant	NM_001004334.4(GPR179):c.1296+12G>A	not provided [RCV002188876]	likely benign	17	38336064	38336064	Human		name
152085107	CV1617198	single nucleotide variant	NM_001004334.4(GPR179):c.1890+17C>T	not provided [RCV002076880]	likely benign	17	38333916	38333916	Human		name
152026874	CV1626661	single nucleotide variant	NM_001004334.4(GPR179):c.1646-12G>A	not provided [RCV002185306]	likely benign	17	38334854	38334854	Human		name
152173821	CV1659906	single nucleotide variant	NM_001004334.4(GPR179):c.1227+14C>T	not provided [RCV002162935]	likely benign	17	38336964	38336964	Human		name
156291986	CV1958556	single nucleotide variant	NM_001004334.4(GPR179):c.1407-11A>T	not provided [RCV002577868]	likely benign	17	38335282	38335282	Human		name
156357367	CV1966886	single nucleotide variant	NM_001004334.4(GPR179):c.1227+18C>T	not provided [RCV002581482]	likely benign	17	38336960	38336960	Human		name
156381950	CV2060877	single nucleotide variant	NM_001004334.4(GPR179):c.1297-14C>T	not provided [RCV002815148]	likely benign	17	38335714	38335714	Human		name
156125204	CV2147480	single nucleotide variant	NM_001004334.4(GPR179):c.1227+11C>T	not provided [RCV003021957]	uncertain significance	17	38336967	38336967	Human		name
156060066	CV2154986	single nucleotide variant	NM_001004334.4(GPR179):c.1646-20C>T	not provided [RCV003000172]	likely benign	17	38334862	38334862	Human		name
156344132	CV2176188	single nucleotide variant	NM_001004334.4(GPR179):c.1646-17T>C	not provided [RCV003030462]	likely benign	17	38334859	38334859	Human		name
156014938	CV2177382	single nucleotide variant	NM_001004334.4(GPR179):c.1891-20C>T	not provided [RCV003035436]	likely benign	17	38333417	38333417	Human		name
155964174	CV2179907	single nucleotide variant	NM_001004334.4(GPR179):c.1407-10A>G	not provided [RCV003033085]	uncertain significance	17	38335281	38335281	Human		name
405158646	CV2961140	single nucleotide variant	NM_001004334.4(GPR179):c.1227+10G>A	not provided [RCV003670570]	likely benign	17	38336968	38336968	Human		name
405244919	CV2972614	single nucleotide variant	NM_001004334.4(GPR179):c.1406+18C>A	not provided [RCV003684936]	likely benign	17	38335573	38335573	Human		name
405032238	CV3130303	single nucleotide variant	NM_001004334.4(GPR179):c.1785-19C>T	not provided [RCV003830710]	likely benign	17	38334057	38334057	Human		name
405230250	CV3153847	single nucleotide variant	NM_001004334.4(GPR179):c.1891-18C>G	not provided [RCV003848714]	likely benign	17	38333415	38333415	Human		name
405209993	CV3162644	single nucleotide variant	NM_001004334.4(GPR179):c.1407-16A>G	not provided [RCV003861943]	likely benign	17	38335287	38335287	Human		name
596942589	CV3408512	single nucleotide variant	NM_001004334.4(GPR179):c.1891-11A>G	Retinal dystrophy [RCV004816183]	likely benign	17	38333408	38333408	Human	2	name
597930160	CV3745812	single nucleotide variant	NM_001004334.4(GPR179):c.1646-10C>T	not provided [RCV005075797]	likely benign	17	38334852	38334852	Human		name
597969202	CV3821423	single nucleotide variant	NM_001004334.4(GPR179):c.1646-13T>C	not provided [RCV005166065]	likely benign	17	38334855	38334855	Human		name
597883219	CV3834147	single nucleotide variant	NM_001004334.4(GPR179):c.1407-19T>C	not provided [RCV005178466]	likely benign	17	38335290	38335290	Human		name
150515140	CV1217393	single nucleotide variant	NM_001004334.4(GPR179):c.1890+210C>G	not provided [RCV001608298]	benign	17	38333723	38333723	Human		name
150503508	CV1223764	single nucleotide variant	NM_001004334.4(GPR179):c.2038-202G>C	not provided [RCV001621413]	benign	17	38331733	38331733	Human		name
150460383	CV1231331	single nucleotide variant	NM_001004334.4(GPR179):c.1891-221C>G	not provided [RCV001640896]	benign	17	38333618	38333618	Human		name
150474011	CV1272265	single nucleotide variant	NM_001004334.4(GPR179):c.1891-107G>A	not provided [RCV001695803]	benign	17	38333504	38333504	Human		name
150509600	CV1284586	single nucleotide variant	NM_001004334.4(GPR179):c.1785-237G>A	not provided [RCV001720694]	benign	17	38334275	38334275	Human		name
150509854	CV1284677	single nucleotide variant	NM_001004334.4(GPR179):c.1407-157G>T	not provided [RCV001720785]	benign	17	38335428	38335428	Human		name
152115906	CV1553306	microsatellite	NM_001004334.4(GPR179):c.1646-23_1646-20del	not provided [RCV002080889]	likely benign	17	38334862	38334865	Human		name
156019826	CV2058875	deletion	NM_001004334.4(GPR179):c.1891-24_1891-15del	not provided [RCV002820561]	uncertain significance	17	38333412	38333421	Human		name
127306355	CV1157939	single nucleotide variant	NM_001004334.4(GPR179):c.5089T>G (p.Leu1697Val)	GPR179-related disorder [RCV003956175]\|not provided [RCV001516598]	benign\|likely benign	17	38328480	38328480	Human	1	alternate_id
151754274	CV1343131	single nucleotide variant	NM_001004334.4(GPR179):c.2357T>C (p.Leu786Pro)	GPR179-related disorder [RCV004756343]\|not provided [RCV002043597]	uncertain significance	17	38331212	38331212	Human	1	name , alternate_id
151880437	CV1436908	deletion	NM_001004334.4(GPR179):c.2695_2696del (p.Leu899fs)	GPR179-related disorder [RCV004756339]\|not provided [RCV001999483]	uncertain significance	17	38330873	38330874	Human	1	alternate_id
151792397	CV1471183	single nucleotide variant	NM_001004334.4(GPR179):c.1429C>T (p.Arg477Ter)	GPR179-related disorder [RCV003395297]\|not provided [RCV001931545]	pathogenic\|likely pathogenic	17	38335249	38335249	Human	1	name , alternate_id
151769396	CV1481646	single nucleotide variant	NM_001004334.4(GPR179):c.814G>A (p.Val272Ile)	GPR179-related disorder [RCV004756335]\|Inborn genetic diseases [RCV004045235]\|not provided [RCV002008699]	likely benign\|uncertain significance	17	38339506	38339506	Human	2	name , alternate_id
152122323	CV1521595	single nucleotide variant	NM_001004334.4(GPR179):c.3287G>A (p.Arg1096His)	GPR179-related disorder [RCV003923779]\|not provided [RCV002135868]	likely benign	17	38330282	38330282	Human	1	alternate_id
152121928	CV1541310	single nucleotide variant	NM_001004334.4(GPR179):c.2337G>A (p.Arg779=)	GPR179-related disorder [RCV003926280]\|not provided [RCV002175693]	likely benign	17	38331232	38331232	Human	1	name , alternate_id
152106188	CV1560041	single nucleotide variant	NM_001004334.4(GPR179):c.4881G>A (p.Ser1627=)	GPR179-related disorder [RCV003958873]\|not provided [RCV002133881]	likely benign	17	38328688	38328688	Human	1	name , alternate_id
152050482	CV1585737	single nucleotide variant	NM_001004334.4(GPR179):c.2583G>A (p.Glu861=)	GPR179-related disorder [RCV003903444]\|not provided [RCV002145628]	likely benign	17	38330986	38330986	Human	1	name , alternate_id
152037409	CV1605612	single nucleotide variant	NM_001004334.4(GPR179):c.5403G>A (p.Val1801=)	GPR179-related disorder [RCV003893101]\|not provided [RCV002087449]	likely benign	17	38328166	38328166	Human	1	name , alternate_id
152156146	CV1615715	single nucleotide variant	NM_001004334.4(GPR179):c.1617C>T (p.His539=)	GPR179-related disorder [RCV003951289]\|not provided [RCV002158877]	likely benign	17	38335061	38335061	Human	1	name , alternate_id
152098064	CV1616382	single nucleotide variant	NM_001004334.4(GPR179):c.2035C>T (p.Arg679Trp)	GPR179-related disorder [RCV003971033]\|not provided [RCV002132898]	benign	17	38333253	38333253	Human	1	name , alternate_id
152148327	CV1618878	single nucleotide variant	NM_001004334.4(GPR179):c.1558G>T (p.Ala520Ser)	GPR179-related disorder [RCV003923742]\|Inborn genetic diseases [RCV003161596]\|not provided [RCV002121396]	likely benign\|uncertain significance	17	38335120	38335120	Human	2	name , alternate_id
152107936	CV1634723	single nucleotide variant	NM_001004334.4(GPR179):c.7014G>A (p.Ser2338=)	GPR179-related disorder [RCV003911163]\|not provided [RCV002079858]	benign\|likely benign	17	38326555	38326555	Human	1	name , alternate_id
152115417	CV1653545	single nucleotide variant	NM_001004334.4(GPR179):c.5457C>T (p.Pro1819=)	GPR179-related disorder [RCV003916321]\|not provided [RCV002153593]	likely benign	17	38328112	38328112	Human	1	name , alternate_id
152064536	CV1654280	single nucleotide variant	NM_001004334.4(GPR179):c.1113G>A (p.Pro371=)	GPR179-related disorder [RCV003960912]\|not provided [RCV002190967]	likely benign	17	38337092	38337092	Human	1	name , alternate_id
10047703	CV190984	single nucleotide variant	NM_001004334.4(GPR179):c.5563C>G (p.Leu1855Val)	Congenital stationary night blindness 1E [RCV000347999]\|GPR179-related disorder [RCV003927592]\|not provided [RCV001523321]\|not specified [RCV000174022]	benign\|likely benign\|uncertain significance	17	38328006	38328006	Human	1	alternate_id
10049819	CV190988	single nucleotide variant	NM_001004334.4(GPR179):c.2410C>T (p.Arg804Trp)	Congenital stationary night blindness 1E [RCV001126138]\|GPR179-related disorder [RCV003947469]\|not provided [RCV000174026]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	17	38331159	38331159	Human	1	name , alternate_id
10051478	CV193454	single nucleotide variant	NM_001004334.4(GPR179):c.959G>A (p.Arg320Gln)	Congenital stationary night blindness 1E [RCV000765348]\|GPR179-related disorder [RCV003977447]\|not provided [RCV000177095]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	17	38337665	38337665	Human	1	name , alternate_id
405061172	CV3029998	single nucleotide variant	NM_001004334.4(GPR179):c.930T>C (p.Phe310=)	GPR179-related disorder [RCV003929297]\|not provided [RCV003697672]	likely benign	17	38337694	38337694	Human	1	name , alternate_id
405262892	CV3189383	single nucleotide variant	NM_032553.3(GPR174):c.546C>T (p.Ser182=)	GPR174-related disorder [RCV003896617]	likely benign	X	79171553	79171553	Human		name , trait , alternate_id
405292362	CV3192389	single nucleotide variant	NM_032553.3(GPR174):c.263C>A (p.Pro88His)	GPR174-related disorder [RCV003929659]	likely benign	X	79171270	79171270	Human		name , trait , alternate_id
405284173	CV3196621	single nucleotide variant	NM_032553.3(GPR174):c.484T>C (p.Ser162Pro)	GPR174-related disorder [RCV003979534]	benign	X	79171491	79171491	Human		name , trait , alternate_id
405276679	CV3198572	single nucleotide variant	NM_001004334.4(GPR179):c.1110A>C (p.Thr370=)	GPR179-related disorder [RCV003903901]	likely benign	17	38337095	38337095	Human		name , trait , alternate_id
405258224	CV3208281	single nucleotide variant	NM_032553.3(GPR174):c.606A>G (p.Leu202=)	GPR174-related disorder [RCV003941710]	benign	X	79171613	79171613	Human		name , trait , alternate_id
405255705	CV3210804	single nucleotide variant	NM_032553.3(GPR174):c.222G>A (p.Leu74=)	GPR174-related disorder [RCV003939316]	likely benign	X	79171229	79171229	Human		name , trait , alternate_id
405268444	CV3219623	single nucleotide variant	NM_001004334.4(GPR179):c.5574C>T (p.Asp1858=)	GPR179-related disorder [RCV003969823]	likely benign	17	38327995	38327995	Human		name , trait , alternate_id
11613555	CV328292	single nucleotide variant	NM_001004334.4(GPR179):c.6798T>G (p.Phe2266Leu)	Congenital stationary night blindness 1E [RCV000269557]\|GPR179-related disorder [RCV003910227]\|not provided [RCV002056577]	benign\|uncertain significance	17	38326771	38326771	Human	1	alternate_id
11615907	CV328306	single nucleotide variant	NM_001004334.4(GPR179):c.3726G>A (p.Glu1242=)	Congenital stationary night blindness 1E [RCV000289908]\|GPR179-related disorder [RCV003910229]\|not provided [RCV002056583]	benign\|likely benign\|uncertain significance	17	38329843	38329843	Human	1	name , alternate_id
11625513	CV338188	single nucleotide variant	NM_001004334.4(GPR179):c.4888G>C (p.Glu1630Gln)	Congenital stationary night blindness 1E [RCV000399884]\|GPR179-related disorder [RCV003922366]\|not provided [RCV001523242]\|not specified [RCV000731892]	benign\|likely benign\|uncertain significance	17	38328681	38328681	Human	1	alternate_id
11617454	CV338194	single nucleotide variant	NM_001004334.4(GPR179):c.4888G>A (p.Glu1630Lys)	Congenital stationary night blindness 1E [RCV000304495]\|GPR179-related disorder [RCV003910228]\|not provided [RCV002056580]	likely benign\|uncertain significance	17	38328681	38328681	Human	1	alternate_id
11619832	CV338197	single nucleotide variant	NM_001004334.4(GPR179):c.3819C>G (p.Ala1273=)	Congenital stationary night blindness 1E [RCV000329746]\|GPR179-related disorder [RCV003950100]\|not provided [RCV002056582]	benign\|likely benign\|uncertain significance	17	38329750	38329750	Human	1	name , alternate_id
11626258	CV344341	single nucleotide variant	NM_001004334.4(GPR179):c.61G>C (p.Val21Leu)	Congenital stationary night blindness 1E [RCV000260831]\|GPR179-related disorder [RCV003969915]\|not provided [RCV001523683]	benign\|likely benign\|uncertain significance	17	38343729	38343729	Human	1	name , alternate_id
11629805	CV345715	single nucleotide variant	NM_001004334.4(GPR179):c.3900A>T (p.Ile1300=)	Congenital stationary night blindness 1E [RCV000333372]\|GPR179-related disorder [RCV003940270]\|not provided [RCV002056581]	benign\|likely benign\|uncertain significance	17	38329669	38329669	Human	1	name , alternate_id
11632176	CV345728	single nucleotide variant	NM_001004334.4(GPR179):c.3426C>T (p.Ala1142=)	Congenital stationary night blindness 1E [RCV000399377]\|GPR179-related disorder [RCV003910230]\|not provided [RCV001520255]	benign\|likely benign\|uncertain significance	17	38330143	38330143	Human	1	name , alternate_id
11626806	CV345748	single nucleotide variant	NM_001004334.4(GPR179):c.2604G>C (p.Glu868Asp)	Congenital stationary night blindness 1E [RCV000270668]\|GPR179-related disorder [RCV003940271]\|not provided [RCV001512531]	benign\|likely benign\|uncertain significance	17	38330965	38330965	Human	1	name , alternate_id
11632235	CV345755	single nucleotide variant	NM_001004334.4(GPR179):c.1417C>T (p.Leu473=)	Congenital stationary night blindness 1E [RCV000401589]\|GPR179-related disorder [RCV003922367]\|not provided [RCV002522950]	likely benign\|uncertain significance	17	38335261	38335261	Human	1	name , alternate_id
11630142	CV345768	single nucleotide variant	NM_001004334.4(GPR179):c.627C>T (p.Leu209=)	Congenital stationary night blindness 1E [RCV000341327]\|GPR179-related disorder [RCV003910231]\|not provided [RCV002056589]	benign\|likely benign\|uncertain significance	17	38343163	38343163	Human	1	name , alternate_id
408366711	CV3515140	single nucleotide variant	NM_001004334.4(GPR179):c.2692C>T (p.Pro898Ser)	GPR179-related disorder [RCV004756957]	uncertain significance	17	38330877	38330877	Human		trait , alternate_id
13525930	CV512957	single nucleotide variant	NM_001004334.4(GPR179):c.3441C>T (p.Ser1147=)	Congenital stationary night blindness 1E [RCV000625278]\|GPR179-related disorder [RCV003917989]\|not provided [RCV002060698]\|not specified [RCV001701129]	benign\|likely benign	17	38330128	38330128	Human	1	name , alternate_id
15154342	CV729717	single nucleotide variant	NM_032553.3(GPR174):c.483C>T (p.Thr161=)	GPR174-related disorder [RCV003948300]\|not provided [RCV000880196]	benign	X	79171490	79171490	Human		name , alternate_id
15184206	CV774255	single nucleotide variant	NM_032553.3(GPR174):c.423C>T (p.Gly141=)	GPR174-related disorder [RCV003942901]\|not provided [RCV000930757]	likely benign	X	79171430	79171430	Human		name , alternate_id
28894615	CV877332	single nucleotide variant	NM_001004334.4(GPR179):c.5905G>A (p.Val1969Ile)	Congenital stationary night blindness 1E [RCV001122171]\|GPR179-related disorder [RCV003938472]\|not provided [RCV002069987]	benign\|likely benign\|uncertain significance	17	38327664	38327664	Human	1	alternate_id
28908164	CV877342	single nucleotide variant	NM_001004334.4(GPR179):c.4381G>C (p.Glu1461Gln)	Congenital stationary night blindness 1E [RCV001128030]\|GPR179-related disorder [RCV003938481]\|not provided [RCV002070489]	likely benign	17	38329188	38329188	Human	1	alternate_id
28894875	CV877343	single nucleotide variant	NM_001004334.4(GPR179):c.4188A>G (p.Gln1396=)	Congenital stationary night blindness 1E [RCV001122267]\|GPR179-related disorder [RCV003938473]\|not provided [RCV002069988]	benign\|likely benign\|uncertain significance	17	38329381	38329381	Human	1	name , alternate_id
15156152	CV720251	single nucleotide variant	NM_013308.4(GPR171):c.15G>A (p.Ser5=)	not provided [RCV000880566]	benign	3	151199372	151199372	Human		name
156294566	CV2293209	single nucleotide variant	NM_007223.3(GPR176):c.26C>T (p.Ser9Phe)	not specified [RCV004150717]	uncertain significance	15	39920001	39920001	Human		name
155999802	CV2396476	single nucleotide variant	NM_018969.6(GPR173):c.19G>A (p.Glu7Lys)	not specified [RCV004242186]	uncertain significance	X	53076640	53076640	Human		name
407526431	CV3436675	single nucleotide variant	NM_018969.6(GPR173):c.16G>A (p.Gly6Arg)	not specified [RCV004632437]	uncertain significance	X	53076637	53076637	Human		name
8630644	CV85799	single nucleotide variant	NM_013308.3(GPR171):c.177C>T (p.Ala59=)	Malignant melanoma [RCV000065882]	not provided	3	151199210	151199210	Human		name
152067611	CV1529392	single nucleotide variant	NM_001004334.4(GPR179):c.18G>A (p.Ala6=)	not provided [RCV002168878]	likely benign	17	38343772	38343772	Human		name
152056027	CV1582248	single nucleotide variant	NM_001004334.4(GPR179):c.18G>C (p.Ala6=)	not provided [RCV002089718]	likely benign	17	38343772	38343772	Human		name
156054639	CV2137352	deletion	NM_001004334.4(GPR179):c.9del (p.Arg4fs)	not provided [RCV002999990]	pathogenic	17	38343781	38343781	Human		name
156149834	CV2201043	single nucleotide variant	NM_032553.3(GPR174):c.74C>T (p.Thr25Ile)	not specified [RCV004074805]	uncertain significance	X	79171081	79171081	Human		name
401876236	CV2777718	single nucleotide variant	NM_007223.3(GPR176):c.28C>T (p.Pro10Ser)	not specified [RCV004345554]	uncertain significance	15	39919999	39919999	Human		name
401896636	CV2791839	single nucleotide variant	NM_013308.4(GPR171):c.28G>A (p.Val10Ile)	not specified [RCV004359286]	uncertain significance	3	151199359	151199359	Human		name
401923059	CV2825013	single nucleotide variant	NM_013308.4(GPR171):c.879C>T (p.Arg293=)	not provided [RCV003434774]	likely benign	3	151198508	151198508	Human		name
401929056	CV2826565	single nucleotide variant	NM_032553.3(GPR174):c.675A>G (p.Lys225=)	not provided [RCV003439704]	likely benign	X	79171682	79171682	Human		name
401944692	CV2840484	single nucleotide variant	NM_013308.4(GPR171):c.735G>A (p.Pro245=)	not provided [RCV003457398]	likely benign	3	151198652	151198652	Human		name
407479860	CV3436674	single nucleotide variant	NM_013308.4(GPR171):c.43G>A (p.Glu15Lys)	not specified [RCV004632436]	uncertain significance	3	151199344	151199344	Human		name
407526445	CV3436679	single nucleotide variant	NM_007223.3(GPR176):c.39C>G (p.Ser13Arg)	not specified [RCV004632441]	uncertain significance	15	39919988	39919988	Human		name
407526452	CV3436681	single nucleotide variant	NM_007223.3(GPR176):c.82C>G (p.Arg28Gly)	not specified [RCV004632443]	uncertain significance	15	39919945	39919945	Human		name
597744971	CV3684914	single nucleotide variant	NM_007223.3(GPR176):c.29C>T (p.Pro10Leu)	not specified [RCV004922372]	uncertain significance	15	39919998	39919998	Human		name
10048470	CV193455	single nucleotide variant	NM_001004334.4(GPR179):c.909= (p.Val303=)	Congenital stationary night blindness 1E [RCV000317577]\|not provided [RCV001518129]\|not specified [RCV000177096]	benign	17	38337715	38337715	Human	1	name
156088772	CV2008882	single nucleotide variant	NM_001004334.4(GPR179):c.81G>T (p.Gly27=)	not provided [RCV002706237]	likely benign	17	38343709	38343709	Human		name
156175225	CV2071967	single nucleotide variant	NM_001004334.4(GPR179):c.63C>A (p.Val21=)	not provided [RCV002851659]	likely benign	17	38343727	38343727	Human		name
156050090	CV2271854	single nucleotide variant	NM_032553.3(GPR174):c.114A>G (p.Ile38Met)	not specified [RCV004130678]	uncertain significance	X	79171121	79171121	Human		name
155999857	CV2287319	single nucleotide variant	NM_013308.4(GPR171):c.168G>C (p.Leu56Phe)	not specified [RCV004146944]	uncertain significance	3	151199219	151199219	Human		name
156039045	CV2332677	single nucleotide variant	NM_018969.6(GPR173):c.220G>A (p.Val74Ile)	not specified [RCV004189354]	uncertain significance	X	53076841	53076841	Human		name
156188425	CV2342210	single nucleotide variant	NM_032553.3(GPR174):c.177A>G (p.Ile59Met)	not specified [RCV004191793]	uncertain significance	X	79171184	79171184	Human		name
156007342	CV2365146	single nucleotide variant	NM_007223.3(GPR176):c.202C>T (p.Arg68Cys)	not specified [RCV004205168]	uncertain significance	15	39807229	39807229	Human		name
156108801	CV2390287	single nucleotide variant	NM_007223.3(GPR176):c.181A>T (p.Met61Leu)	not specified [RCV004240654]	uncertain significance	15	39807250	39807250	Human		name
329389809	CV2441347	single nucleotide variant	NM_018969.6(GPR173):c.152G>A (p.Arg51His)	not specified [RCV004257156]	uncertain significance	X	53076773	53076773	Human		name
329372313	CV2455157	single nucleotide variant	NM_018969.6(GPR173):c.253C>T (p.His85Tyr)	not specified [RCV004274397]	uncertain significance	X	53076874	53076874	Human		name
401775180	CV2692285	single nucleotide variant	NM_032553.3(GPR174):c.148G>A (p.Glu50Lys)	not specified [RCV004310283]	uncertain significance	X	79171155	79171155	Human		name
401873184	CV2779767	single nucleotide variant	NM_007223.3(GPR176):c.125A>T (p.Gln42Leu)	not specified [RCV004353403]	uncertain significance	15	39919902	39919902	Human		name
405187362	CV2964193	single nucleotide variant	NM_001004334.4(GPR179):c.45G>A (p.Leu15=)	not provided [RCV003676879]	likely benign	17	38343745	38343745	Human		name
405738312	CV3255317	single nucleotide variant	NM_013308.4(GPR171):c.122A>G (p.Gln41Arg)	not specified [RCV004390944]	uncertain significance	3	151199265	151199265	Human		name
405738337	CV3255320	single nucleotide variant	NM_018969.6(GPR173):c.145A>C (p.Lys49Gln)	not specified [RCV004390947]	uncertain significance	X	53076766	53076766	Human		name
407479855	CV3436673	single nucleotide variant	NM_013308.4(GPR171):c.229G>A (p.Val77Met)	not specified [RCV004632435]	uncertain significance	3	151199158	151199158	Human		name
597744925	CV3684898	single nucleotide variant	NM_013308.4(GPR171):c.113C>T (p.Ala38Val)	not specified [RCV004922362]	uncertain significance	3	151199274	151199274	Human		name
597789870	CV3684903	single nucleotide variant	NM_018969.6(GPR173):c.251G>A (p.Arg84His)	not specified [RCV004933095]	uncertain significance	X	53076872	53076872	Human		name
597789874	CV3684905	single nucleotide variant	NM_018969.6(GPR173):c.244T>G (p.Ser82Ala)	not specified [RCV004933096]	uncertain significance	X	53076865	53076865	Human		name
597744952	CV3684908	single nucleotide variant	NM_032553.3(GPR174):c.276G>A (p.Met92Ile)	not specified [RCV004922368]	uncertain significance	X	79171283	79171283	Human		name
597789881	CV3684910	single nucleotide variant	NM_007223.3(GPR176):c.211G>A (p.Val71Met)	not specified [RCV004933098]	uncertain significance	15	39807220	39807220	Human		name
597744984	CV3684917	single nucleotide variant	NM_007223.3(GPR176):c.178T>C (p.Phe60Leu)	not specified [RCV004922375]	uncertain significance	15	39807253	39807253	Human		name
598233871	CV3971160	single nucleotide variant	NM_018969.6(GPR173):c.250C>T (p.Arg84Cys)	not specified [RCV005342820]	uncertain significance	X	53076871	53076871	Human		name
8630645	CV85800	single nucleotide variant	NM_013308.3(GPR171):c.176C>T (p.Ala59Val)	Malignant melanoma [RCV000065883]	not provided	3	151199211	151199211	Human		name
151754015	CV1343061	single nucleotide variant	NM_001004334.4(GPR179):c.14G>T (p.Gly5Val)	not provided [RCV002043575]	uncertain significance	17	38343776	38343776	Human		name
151843183	CV1418404	single nucleotide variant	NM_001004334.4(GPR179):c.17C>T (p.Ala6Val)	Inborn genetic diseases [RCV002555245]\|not provided [RCV001903099]	likely benign\|uncertain significance	17	38343773	38343773	Human	1	name
151755987	CV1498958	single nucleotide variant	NM_001004334.4(GPR179):c.19G>T (p.Val7Phe)	not provided [RCV002023851]	uncertain significance	17	38343771	38343771	Human		name
151794896	CV1506275	single nucleotide variant	NM_001004334.4(GPR179):c.14G>A (p.Gly5Glu)	not provided [RCV001917166]	uncertain significance	17	38343776	38343776	Human		name
152160403	CV1522845	single nucleotide variant	NM_001004334.4(GPR179):c.243A>G (p.Glu81=)	not provided [RCV002140820]	likely benign	17	38343547	38343547	Human		name
152095046	CV1533928	single nucleotide variant	NM_001004334.4(GPR179):c.285A>G (p.Leu95=)	not provided [RCV002151093]	likely benign	17	38343505	38343505	Human		name
152091858	CV1602931	single nucleotide variant	NM_001004334.4(GPR179):c.204C>G (p.Ala68=)	not provided [RCV002194403]	likely benign	17	38343586	38343586	Human		name
152126722	CV1641963	single nucleotide variant	NM_001004334.4(GPR179):c.297G>A (p.Ala99=)	not provided [RCV002176268]	likely benign	17	38343493	38343493	Human		name
152033103	CV1657762	single nucleotide variant	NM_001004334.4(GPR179):c.171G>A (p.Glu57=)	not provided [RCV002187024]	likely benign	17	38343619	38343619	Human		name
10049070	CV195602	single nucleotide variant	NM_001004334.4(GPR179):c.1478= (p.His493=)	Congenital stationary night blindness 1E [RCV000365567]\|not provided [RCV001515685]\|not specified [RCV000179792]	benign\|likely benign	17	38335200	38335200	Human	1	name
156383141	CV1975305	single nucleotide variant	NM_001004334.4(GPR179):c.174C>T (p.Ala58=)	not provided [RCV002604110]	likely benign	17	38343616	38343616	Human		name
156282495	CV2001480	single nucleotide variant	NM_001004334.4(GPR179):c.270G>T (p.Gly90=)	not provided [RCV002646891]	likely benign	17	38343520	38343520	Human		name
156008329	CV2010009	single nucleotide variant	NM_001004334.4(GPR179):c.195T>G (p.Ser65=)	not provided [RCV002734764]	likely benign	17	38343595	38343595	Human		name
155958149	CV2033553	single nucleotide variant	NM_001004334.4(GPR179):c.24G>A (p.Met8Ile)	not provided [RCV002731040]	uncertain significance	17	38343766	38343766	Human		name
156136381	CV2048111	single nucleotide variant	NM_001004334.4(GPR179):c.240T>C (p.Tyr80=)	not provided [RCV002800798]	likely benign	17	38343550	38343550	Human		name
156124935	CV2090092	single nucleotide variant	NM_001004334.4(GPR179):c.117T>A (p.Ser39=)	not provided [RCV002889713]	likely benign	17	38343673	38343673	Human		name
156027287	CV2096661	single nucleotide variant	NM_001004334.4(GPR179):c.108C>G (p.Pro36=)	not provided [RCV002885240]	likely benign	17	38343682	38343682	Human		name
156029372	CV2125382	single nucleotide variant	NM_001004334.4(GPR179):c.144C>G (p.Pro48=)	not provided [RCV002949158]	likely benign	17	38343646	38343646	Human		name
156264941	CV2198614	single nucleotide variant	NM_007223.3(GPR176):c.545A>G (p.Asn182Ser)	not specified [RCV004075632]	uncertain significance	15	39802135	39802135	Human		name
155917497	CV2198954	single nucleotide variant	NM_032553.3(GPR174):c.629T>C (p.Leu210Ser)	not specified [RCV004080370]	uncertain significance	X	79171636	79171636	Human		name
156399579	CV2205203	single nucleotide variant	NM_013308.4(GPR171):c.722T>C (p.Ile241Thr)	not specified [RCV004079837]	uncertain significance	3	151198665	151198665	Human		name
156191669	CV2206192	single nucleotide variant	NM_007223.3(GPR176):c.638C>T (p.Thr213Met)	not specified [RCV004080630]	uncertain significance	15	39802042	39802042	Human		name
155939086	CV2225330	single nucleotide variant	NM_018969.6(GPR173):c.484G>A (p.Val162Met)	not specified [RCV004100755]	uncertain significance	X	53077105	53077105	Human		name
155933740	CV2228993	single nucleotide variant	NM_007223.3(GPR176):c.795C>G (p.His265Gln)	not specified [RCV004098780]	uncertain significance	15	39801885	39801885	Human		name
156278112	CV2252056	single nucleotide variant	NM_007223.3(GPR176):c.976T>G (p.Ser326Ala)	not specified [RCV004122090]	uncertain significance	15	39801704	39801704	Human		name
156312341	CV2256856	single nucleotide variant	NM_007223.3(GPR176):c.796G>A (p.Ala266Thr)	not specified [RCV004121067]	uncertain significance	15	39801884	39801884	Human		name
156238342	CV2265401	single nucleotide variant	NM_013308.4(GPR171):c.552T>G (p.Cys184Trp)	not specified [RCV004128278]	uncertain significance	3	151198835	151198835	Human		name
155998456	CV2287153	single nucleotide variant	NM_013308.4(GPR171):c.593C>G (p.Ser198Cys)	not specified [RCV004146806]	uncertain significance	3	151198794	151198794	Human		name
156148668	CV2292787	single nucleotide variant	NM_032553.3(GPR174):c.560C>G (p.Thr187Ser)	not specified [RCV004154448]	uncertain significance	X	79171567	79171567	Human		name
156068262	CV2317976	single nucleotide variant	NM_013308.4(GPR171):c.821C>T (p.Ala274Val)	not specified [RCV004177095]	uncertain significance	3	151198566	151198566	Human		name
156077368	CV2318541	single nucleotide variant	NM_032553.3(GPR174):c.473G>C (p.Ser158Thr)	not specified [RCV004173449]	uncertain significance	X	79171480	79171480	Human		name
156078211	CV2318692	single nucleotide variant	NM_007223.3(GPR176):c.542C>G (p.Thr181Ser)	not specified [RCV004173586]	uncertain significance	15	39802138	39802138	Human		name
156148066	CV2358059	single nucleotide variant	NM_007223.3(GPR176):c.620T>C (p.Leu207Pro)	not specified [RCV004209825]	uncertain significance	15	39802060	39802060	Human		name
156009797	CV2362040	single nucleotide variant	NM_013308.4(GPR171):c.775A>G (p.Thr259Ala)	not specified [RCV004209852]	uncertain significance	3	151198612	151198612	Human		name
156262917	CV2368570	single nucleotide variant	NM_018969.6(GPR173):c.658G>A (p.Val220Met)	not provided [RCV003435961]\|not specified [RCV004221356]	likely benign\|uncertain significance	X	53077279	53077279	Human		name
155938686	CV2380893	single nucleotide variant	NM_007223.3(GPR176):c.646G>A (p.Val216Met)	not specified [RCV004218439]	uncertain significance	15	39802034	39802034	Human		name
329386837	CV2452586	single nucleotide variant	NM_018969.6(GPR173):c.943T>C (p.Cys315Arg)	not specified [RCV004275169]	uncertain significance	X	53077564	53077564	Human		name
329358024	CV2453863	single nucleotide variant	NM_013308.4(GPR171):c.436A>T (p.Met146Leu)	not specified [RCV004271259]	uncertain significance	3	151198951	151198951	Human		name
329397685	CV2463910	single nucleotide variant	NM_013308.4(GPR171):c.764C>G (p.Thr255Ser)	not specified [RCV004279979]	likely benign	3	151198623	151198623	Human		name
401732264	CV2698265	single nucleotide variant	NM_007223.3(GPR176):c.853C>A (p.Leu285Met)	not specified [RCV004304819]	uncertain significance	15	39801827	39801827	Human		name
401765004	CV2701696	single nucleotide variant	NM_007223.3(GPR176):c.725T>C (p.Ile242Thr)	not specified [RCV004314104]	uncertain significance	15	39801955	39801955	Human		name
401778431	CV2709114	single nucleotide variant	NM_007223.3(GPR176):c.698G>C (p.Ser233Thr)	not specified [RCV004314445]	uncertain significance	15	39801982	39801982	Human		name
401856881	CV2755148	single nucleotide variant	NM_007223.3(GPR176):c.659T>C (p.Val220Ala)	not specified [RCV004335297]	uncertain significance	15	39802021	39802021	Human		name
401892878	CV2758179	single nucleotide variant	NM_013308.4(GPR171):c.545T>A (p.Phe182Tyr)	not specified [RCV004341549]	uncertain significance	3	151198842	151198842	Human		name
401892205	CV2777323	single nucleotide variant	NM_007223.3(GPR176):c.961C>G (p.Leu321Val)	not specified [RCV004354336]	uncertain significance	15	39801719	39801719	Human		name
401888327	CV2788334	single nucleotide variant	NM_013308.4(GPR171):c.841G>T (p.Asp281Tyr)	not specified [RCV004352913]	uncertain significance	3	151198546	151198546	Human		name
401888360	CV2788387	single nucleotide variant	NM_032553.3(GPR174):c.553A>G (p.Met185Val)	not specified [RCV004354924]	uncertain significance	X	79171560	79171560	Human		name
401926551	CV2825014	single nucleotide variant	NM_013308.4(GPR171):c.520A>G (p.Arg174Gly)	not provided [RCV003437969]	uncertain significance	3	151198867	151198867	Human		name
401929053	CV2826564	single nucleotide variant	NM_032553.3(GPR174):c.374G>A (p.Arg125His)	not provided [RCV003439703]	likely benign	X	79171381	79171381	Human		name
405738328	CV3255319	single nucleotide variant	NM_013308.4(GPR171):c.860A>G (p.His287Arg)	not specified [RCV004390946]	uncertain significance	3	151198527	151198527	Human		name
405738352	CV3255322	single nucleotide variant	NM_018969.6(GPR173):c.401G>A (p.Arg134His)	not specified [RCV004390949]	uncertain significance	X	53077022	53077022	Human		name
405738359	CV3255323	single nucleotide variant	NM_018969.6(GPR173):c.752G>A (p.Arg251His)	not specified [RCV004390950]	uncertain significance	X	53077373	53077373	Human		name
405738370	CV3255325	single nucleotide variant	NM_032553.3(GPR174):c.841G>T (p.Ala281Ser)	not specified [RCV004390952]	uncertain significance	X	79171848	79171848	Human		name
405738378	CV3255326	single nucleotide variant	NM_032553.3(GPR174):c.873A>G (p.Ile291Met)	not specified [RCV004390953]	uncertain significance	X	79171880	79171880	Human		name
405738386	CV3255327	single nucleotide variant	NM_032553.3(GPR174):c.937C>A (p.Gln313Lys)	not specified [RCV004390954]	uncertain significance	X	79171944	79171944	Human		name
405738391	CV3255328	single nucleotide variant	NM_032553.3(GPR174):c.997T>C (p.Cys333Arg)	not specified [RCV004390955]	uncertain significance	X	79172004	79172004	Human		name
407526435	CV3436676	single nucleotide variant	NM_018969.6(GPR173):c.806G>A (p.Ser269Asn)	not specified [RCV004632438]	uncertain significance	X	53077427	53077427	Human		name
407526438	CV3436677	single nucleotide variant	NM_032553.3(GPR174):c.623C>T (p.Thr208Met)	not specified [RCV004632439]	uncertain significance	X	79171630	79171630	Human		name
407526441	CV3436678	single nucleotide variant	NM_032553.3(GPR174):c.389A>G (p.Lys130Arg)	not specified [RCV004632440]	uncertain significance	X	79171396	79171396	Human		name
11630812	CV344329	single nucleotide variant	NM_001004334.4(GPR179):c.180C>T (p.Leu60=)	Congenital stationary night blindness 1E [RCV000359189]\|not provided [RCV002056591]	likely benign\|uncertain significance	17	38343610	38343610	Human	1	name
597744929	CV3684899	single nucleotide variant	NM_013308.4(GPR171):c.796G>T (p.Ala266Ser)	not specified [RCV004922363]	uncertain significance	3	151198591	151198591	Human		name
597744934	CV3684900	single nucleotide variant	NM_013308.4(GPR171):c.596A>G (p.Asn199Ser)	not specified [RCV004922364]	uncertain significance	3	151198791	151198791	Human		name
597744939	CV3684901	single nucleotide variant	NM_013308.4(GPR171):c.899T>C (p.Phe300Ser)	not specified [RCV004922365]	uncertain significance	3	151198488	151198488	Human		name
597789866	CV3684902	single nucleotide variant	NM_013308.4(GPR171):c.578C>T (p.Ala193Val)	not specified [RCV004933094]	uncertain significance	3	151198809	151198809	Human		name
597744947	CV3684906	single nucleotide variant	NM_032553.3(GPR174):c.706G>T (p.Ala236Ser)	not specified [RCV004922367]	uncertain significance	X	79171713	79171713	Human		name
597789877	CV3684907	single nucleotide variant	NM_032553.3(GPR174):c.397T>C (p.Tyr133His)	not specified [RCV004933097]	uncertain significance	X	79171404	79171404	Human		name
597744957	CV3684909	single nucleotide variant	NM_032553.3(GPR174):c.341T>C (p.Val114Ala)	not specified [RCV004922369]	uncertain significance	X	79171348	79171348	Human		name
597744976	CV3684915	single nucleotide variant	NM_007223.3(GPR176):c.358G>A (p.Val120Ile)	not specified [RCV004922373]	uncertain significance	15	39807073	39807073	Human		name
597744980	CV3684916	single nucleotide variant	NM_007223.3(GPR176):c.659T>G (p.Val220Gly)	not specified [RCV004922374]	uncertain significance	15	39802021	39802021	Human		name
597870524	CV3749926	single nucleotide variant	NM_001004334.4(GPR179):c.246G>A (p.Ala82=)	not provided [RCV005068607]	likely benign	17	38343544	38343544	Human		name
597955401	CV3796225	single nucleotide variant	NM_001004334.4(GPR179):c.16G>A (p.Ala6Thr)	not provided [RCV005137042]	uncertain significance	17	38343774	38343774	Human		name
598274400	CV3971156	single nucleotide variant	NM_013308.4(GPR171):c.956C>T (p.Ala319Val)	not specified [RCV005351403]	uncertain significance	3	151198431	151198431	Human		name
598274403	CV3971157	single nucleotide variant	NM_013308.4(GPR171):c.689C>T (p.Thr230Met)	not specified [RCV005351404]	uncertain significance	3	151198698	151198698	Human		name
598274405	CV3971158	single nucleotide variant	NM_013308.4(GPR171):c.410T>C (p.Val137Ala)	not specified [RCV005351405]	uncertain significance	3	151198977	151198977	Human		name
598274408	CV3971161	single nucleotide variant	NM_018969.6(GPR173):c.926G>A (p.Arg309Gln)	not specified [RCV005351406]	uncertain significance	X	53077547	53077547	Human		name
598274414	CV3971164	single nucleotide variant	NM_032553.3(GPR174):c.706G>A (p.Ala236Thr)	not specified [RCV005351409]	uncertain significance	X	79171713	79171713	Human		name
598233879	CV3971165	single nucleotide variant	NM_032553.3(GPR174):c.463C>T (p.Leu155Phe)	not specified [RCV005342821]	uncertain significance	X	79171470	79171470	Human		name
598233886	CV3971167	single nucleotide variant	NM_007223.3(GPR176):c.412A>G (p.Ile138Val)	not specified [RCV005342822]	uncertain significance	15	39807019	39807019	Human		name
598274418	CV3971168	single nucleotide variant	NM_007223.3(GPR176):c.347T>G (p.Phe116Cys)	not specified [RCV005351411]	uncertain significance	15	39807084	39807084	Human		name
598274420	CV3971169	single nucleotide variant	NM_007223.3(GPR176):c.617T>C (p.Val206Ala)	not specified [RCV005351412]	uncertain significance	15	39802063	39802063	Human		name
598274422	CV3971170	single nucleotide variant	NM_007223.3(GPR176):c.331A>G (p.Ile111Val)	not specified [RCV005351413]	uncertain significance	15	39807100	39807100	Human		name
127253276	CV1082964	single nucleotide variant	NM_001004334.4(GPR179):c.672G>A (p.Thr224=)	not provided [RCV001400495]	likely benign	17	38343118	38343118	Human		name
127295603	CV1157947	single nucleotide variant	NM_001004334.4(GPR179):c.909C>T (p.Val303=)	Retinal dystrophy [RCV004815541]\|not provided [RCV001512255]	benign\|likely benign	17	38337715	38337715	Human	2	name
151842799	CV1339109	single nucleotide variant	NM_001004334.4(GPR179):c.70T>C (p.Trp24Arg)	not provided [RCV001977903]	uncertain significance	17	38343720	38343720	Human		name
151782248	CV1360511	single nucleotide variant	NM_001004334.4(GPR179):c.88C>T (p.Arg30Trp)	not provided [RCV001865075]	uncertain significance	17	38343702	38343702	Human		name
151750048	CV1360697	single nucleotide variant	NM_001004334.4(GPR179):c.97C>T (p.Arg33Cys)	not provided [RCV001894242]	uncertain significance	17	38343693	38343693	Human		name
151729609	CV1410149	single nucleotide variant	NM_001004334.4(GPR179):c.89G>A (p.Arg30Gln)	Inborn genetic diseases [RCV003247167]\|not provided [RCV001910725]	uncertain significance	17	38343701	38343701	Human	1	name
151875307	CV1461221	single nucleotide variant	NM_001004334.4(GPR179):c.35T>C (p.Met12Thr)	not provided [RCV001925738]	uncertain significance	17	38343755	38343755	Human		name
151741662	CV1504287	single nucleotide variant	NM_001004334.4(GPR179):c.83G>A (p.Gly28Asp)	not provided [RCV002022378]	uncertain significance	17	38343707	38343707	Human		name
152174879	CV1536127	single nucleotide variant	NM_001004334.4(GPR179):c.414C>T (p.Ala138=)	not provided [RCV002163301]	likely benign	17	38343376	38343376	Human		name
152060652	CV1559229	single nucleotide variant	NM_001004334.4(GPR179):c.510G>A (p.Gly170=)	not provided [RCV002167961]	likely benign	17	38343280	38343280	Human		name
152156473	CV1573065	single nucleotide variant	NM_001004334.4(GPR179):c.957C>T (p.Cys319=)	not provided [RCV002180209]	likely benign	17	38337667	38337667	Human		name
152106099	CV1612721	single nucleotide variant	NM_001004334.4(GPR179):c.468G>A (p.Gly156=)	not provided [RCV002173737]	likely benign	17	38343322	38343322	Human		name
152052172	CV1622579	single nucleotide variant	NM_001004334.4(GPR179):c.315C>A (p.Ala105=)	not provided [RCV002207657]	likely benign	17	38343475	38343475	Human		name
152038679	CV1625350	single nucleotide variant	NM_001004334.4(GPR179):c.408C>T (p.Ser136=)	not provided [RCV002206007]	likely benign	17	38343382	38343382	Human		name
152075432	CV1635411	single nucleotide variant	NM_001004334.4(GPR179):c.813C>T (p.Asp271=)	not provided [RCV002092159]	likely benign	17	38339507	38339507	Human		name
152142986	CV1651410	single nucleotide variant	NM_001004334.4(GPR179):c.636C>T (p.Pro212=)	not provided [RCV002138410]	likely benign	17	38343154	38343154	Human		name
156283076	CV1968048	single nucleotide variant	NM_001004334.4(GPR179):c.597G>A (p.Lys199=)	not provided [RCV002598460]	likely benign	17	38343193	38343193	Human		name
156130852	CV1977030	single nucleotide variant	NM_001004334.4(GPR179):c.450C>T (p.Thr150=)	not provided [RCV002593489]	likely benign	17	38343340	38343340	Human		name
156220914	CV1981290	single nucleotide variant	NM_001004334.4(GPR179):c.972C>T (p.Tyr324=)	not provided [RCV002626443]	likely benign	17	38337652	38337652	Human		name
156109531	CV2002220	single nucleotide variant	NM_001004334.4(GPR179):c.504G>A (p.Arg168=)	not provided [RCV002639882]	likely benign	17	38343286	38343286	Human		name
156140466	CV2002719	single nucleotide variant	NM_001004334.4(GPR179):c.399G>A (p.Leu133=)	not provided [RCV002663549]	likely benign	17	38343391	38343391	Human		name
156292628	CV2009814	single nucleotide variant	NM_001004334.4(GPR179):c.36G>A (p.Met12Ile)	not provided [RCV002715716]	uncertain significance	17	38343754	38343754	Human		name
156336845	CV2095836	single nucleotide variant	NM_001004334.4(GPR179):c.354C>T (p.Ile118=)	not provided [RCV002900250]	likely benign	17	38343436	38343436	Human		name
156012559	CV2122998	single nucleotide variant	NM_001004334.4(GPR179):c.336G>T (p.Leu112=)	not provided [RCV002975725]	likely benign	17	38343454	38343454	Human		name
156020761	CV2148006	single nucleotide variant	NM_001004334.4(GPR179):c.37T>A (p.Trp13Arg)	not provided [RCV003018217]	uncertain significance	17	38343753	38343753	Human		name
156093804	CV2167220	single nucleotide variant	NM_001004334.4(GPR179):c.618A>G (p.Leu206=)	not provided [RCV003038316]	likely benign	17	38343172	38343172	Human		name
156330231	CV2171698	deletion	NM_001004334.4(GPR179):c.166del (p.Ala56fs)	not provided [RCV003029728]	pathogenic	17	38343624	38343624	Human		name
156371628	CV2174609	single nucleotide variant	NM_001004334.4(GPR179):c.465A>C (p.Pro155=)	not provided [RCV003049746]	likely benign	17	38343325	38343325	Human		name
155956403	CV2182467	single nucleotide variant	NM_001004334.4(GPR179):c.753C>T (p.Ala251=)	not provided [RCV003032704]	likely benign	17	38343037	38343037	Human		name
156377629	CV2217080	single nucleotide variant	NM_007223.3(GPR176):c.1307C>T (p.Pro436Leu)	not specified [RCV004085758]	uncertain significance	15	39801373	39801373	Human		name
156029324	CV2238305	single nucleotide variant	NM_007223.3(GPR176):c.1503G>A (p.Met501Ile)	not specified [RCV004113383]	uncertain significance	15	39801177	39801177	Human		name
156238233	CV2285869	single nucleotide variant	NM_007223.3(GPR176):c.1429C>T (p.Pro477Ser)	not specified [RCV004143805]	uncertain significance	15	39801251	39801251	Human		name
156149714	CV2293009	single nucleotide variant	NM_007223.3(GPR176):c.1114A>G (p.Met372Val)	not specified [RCV004148484]	uncertain significance	15	39801566	39801566	Human		name
156103062	CV2386881	single nucleotide variant	NM_007223.3(GPR176):c.1013T>C (p.Leu338Pro)	not specified [RCV004233515]	uncertain significance	15	39801667	39801667	Human		name
329353667	CV2467030	single nucleotide variant	NM_007223.3(GPR176):c.1151C>T (p.Thr384Ile)	not specified [RCV004282773]	uncertain significance	15	39801529	39801529	Human		name
401754688	CV2682271	single nucleotide variant	NM_007223.3(GPR176):c.1495C>T (p.Arg499Trp)	not specified [RCV004297225]	uncertain significance	15	39801185	39801185	Human		name
401752864	CV2682962	single nucleotide variant	NM_007223.3(GPR176):c.1022G>A (p.Arg341Gln)	not specified [RCV004283752]	uncertain significance	15	39801658	39801658	Human		name
401884927	CV2766343	single nucleotide variant	NM_007223.3(GPR176):c.1430C>T (p.Pro477Leu)	not specified [RCV004342595]	uncertain significance	15	39801250	39801250	Human		name
401871449	CV2783506	single nucleotide variant	NM_007223.3(GPR176):c.1488G>C (p.Arg496Ser)	not specified [RCV004365839]	uncertain significance	15	39801192	39801192	Human		name
402495047	CV2875047	single nucleotide variant	NM_001004334.4(GPR179):c.612T>C (p.Asn204=)	not provided [RCV003545310]	likely benign	17	38343178	38343178	Human		name
402469546	CV2931020	single nucleotide variant	NM_001004334.4(GPR179):c.951C>T (p.Cys317=)	not provided [RCV003570131]	likely benign	17	38337673	38337673	Human		name
405173183	CV3026824	duplication	NM_001004334.4(GPR179):c.280dup (p.Ser94fs)	not provided [RCV003704864]	pathogenic	17	38343509	38343510	Human		name
402511748	CV3042605	single nucleotide variant	NM_001004334.4(GPR179):c.672G>T (p.Thr224=)	not provided [RCV003715684]	likely benign	17	38343118	38343118	Human		name
405210184	CV3117352	single nucleotide variant	NM_001004334.4(GPR179):c.72G>C (p.Trp24Cys)	not provided [RCV003823139]	uncertain significance	17	38343718	38343718	Human		name
405229190	CV3180389	single nucleotide variant	NM_001004334.4(GPR179):c.369G>A (p.Val123=)	not provided [RCV003864810]	likely benign	17	38343421	38343421	Human		name
405738397	CV3255329	single nucleotide variant	NM_007223.3(GPR176):c.1252T>C (p.Phe418Leu)	not specified [RCV004390956]	uncertain significance	15	39801428	39801428	Human		name
405738403	CV3255330	single nucleotide variant	NM_007223.3(GPR176):c.1433C>G (p.Pro478Arg)	not specified [RCV004390957]	uncertain significance	15	39801247	39801247	Human		name
11615916	CV328320	single nucleotide variant	NM_001004334.4(GPR179):c.663G>T (p.Val221=)	Congenital stationary night blindness 1E [RCV000289986]\|not provided [RCV002522952]	likely benign\|uncertain significance	17	38343127	38343127	Human	1	name
11621876	CV328336	single nucleotide variant	NM_001004334.4(GPR179):c.74C>A (p.Ala25Asp)	Congenital stationary night blindness 1E [RCV000353416]\|not provided [RCV001516533]	benign\|likely benign	17	38343716	38343716	Human	1	name
11651809	CV338241	single nucleotide variant	NM_001004334.4(GPR179):c.98G>A (p.Arg33His)	Congenital stationary night blindness 1E [RCV000300941]	uncertain significance	17	38343692	38343692	Human	1	name
407526448	CV3436680	single nucleotide variant	NM_007223.3(GPR176):c.1343A>G (p.Lys448Arg)	not specified [RCV004632442]	uncertain significance	15	39801337	39801337	Human		name
11628728	CV344328	single nucleotide variant	NM_001004334.4(GPR179):c.645G>A (p.Pro215=)	Congenital stationary night blindness 1E [RCV000307518]\|not provided [RCV001513439]	benign\|uncertain significance	17	38343145	38343145	Human	1	name
11629552	CV345722	single nucleotide variant	NM_001004334.4(GPR179):c.3699= (p.Leu1233=)	Congenital stationary night blindness 1E [RCV000326088]\|not provided [RCV001518134]	benign	17	38329870	38329870	Human	1	name
11631804	CV345764	single nucleotide variant	NM_001004334.4(GPR179):c.880C>T (p.Leu294=)	Congenital stationary night blindness 1E [RCV000388457]\|not provided [RCV001513350]	benign\|likely benign	17	38339440	38339440	Human	1	name
11630343	CV345766	single nucleotide variant	NM_001004334.4(GPR179):c.657A>T (p.Gly219=)	Congenital stationary night blindness 1E [RCV000347175]\|not provided [RCV001516670]	benign\|likely benign\|uncertain significance	17	38343133	38343133	Human	1	name
11632256	CV345771	single nucleotide variant	NM_001004334.4(GPR179):c.522C>T (p.Ile174=)	Congenital stationary night blindness 1E [RCV000402255]\|not provided [RCV002056590]	likely benign\|uncertain significance	17	38343268	38343268	Human	1	name
597744943	CV3684904	single nucleotide variant	NM_018969.6(GPR173):c.1085G>A (p.Gly362Asp)	not specified [RCV004922366]	uncertain significance	X	53077706	53077706	Human		name
597789885	CV3684911	single nucleotide variant	NM_007223.3(GPR176):c.1030C>T (p.Arg344Cys)	not specified [RCV004933099]	uncertain significance	15	39801650	39801650	Human		name
597744962	CV3684912	single nucleotide variant	NM_007223.3(GPR176):c.1167G>T (p.Glu389Asp)	not specified [RCV004922370]	uncertain significance	15	39801513	39801513	Human		name
597744966	CV3684913	single nucleotide variant	NM_007223.3(GPR176):c.1433C>A (p.Pro478His)	not specified [RCV004922371]	uncertain significance	15	39801247	39801247	Human		name
597965311	CV3751062	single nucleotide variant	NM_001004334.4(GPR179):c.744A>C (p.Thr248=)	not provided [RCV005082624]	likely benign	17	38343046	38343046	Human		name
597921604	CV3774981	single nucleotide variant	NM_001004334.4(GPR179):c.927C>A (p.Gly309=)	not provided [RCV005115327]	likely benign	17	38337697	38337697	Human		name
597963191	CV3819553	single nucleotide variant	NM_001004334.4(GPR179):c.657A>G (p.Gly219=)	not provided [RCV005164269]	likely benign	17	38343133	38343133	Human		name
598233863	CV3971159	single nucleotide variant	NM_018969.6(GPR173):c.1072T>C (p.Trp358Arg)	not specified [RCV005342819]	uncertain significance	X	53077693	53077693	Human		name
598274410	CV3971162	single nucleotide variant	NM_018969.6(GPR173):c.1024C>G (p.Leu342Val)	not specified [RCV005351407]	uncertain significance	X	53077645	53077645	Human		name
598274412	CV3971163	single nucleotide variant	NM_018969.6(GPR173):c.1057A>G (p.Thr353Ala)	not specified [RCV005351408]	uncertain significance	X	53077678	53077678	Human		name
598274427	CV3971174	single nucleotide variant	NM_001004334.4(GPR179):c.56G>T (p.Cys19Phe)	Inborn genetic diseases [RCV005351416]	uncertain significance	17	38343734	38343734	Human	1	name
8568856	CV40158	deletion	NM_001004334.4(GPR179):c.278del (p.Pro93fs)	Congenital stationary night blindness 1E [RCV000024200]\|not provided [RCV003556084]	pathogenic	17	38343512	38343512	Human	1	name
8568860	CV40162	deletion	NM_001004334.4(GPR179):c.187del (p.Leu63fs)	Congenital stationary night blindness 1E [RCV000024204]	pathogenic	17	38343603	38343603	Human	1	name
13834606	CV585855	single nucleotide variant	NM_001004334.4(GPR179):c.582C>A (p.Thr194=)	not provided [RCV000730167]	conflicting interpretations of pathogenicity\|uncertain significance	17	38343208	38343208	Human		name
14693589	CV620586	duplication	NM_001004334.4(GPR179):c.278dup (p.Ser94fs)	Congenital stationary night blindness 1E [RCV000779219]	uncertain significance	17	38343511	38343512	Human		name
8627627	CV82771	single nucleotide variant	NM_007223.2(GPR176):c.1462C>T (p.Gln488Ter)	Malignant melanoma [RCV000062851]	not provided	15	39801218	39801218	Human		name
8627628	CV82772	single nucleotide variant	NM_007223.2(GPR176):c.1096G>A (p.Gly366Ser)	Malignant melanoma [RCV000062852]	not provided	15	39801584	39801584	Human		name
28908668	CV877385	single nucleotide variant	NM_001004334.4(GPR179):c.858A>G (p.Pro286=)	Congenital stationary night blindness 1E [RCV001128302]\|not provided [RCV003708575]	likely benign\|uncertain significance	17	38339462	38339462	Human	1	name
28898750	CV877388	single nucleotide variant	NM_001004334.4(GPR179):c.489C>T (p.Ala163=)	Congenital stationary night blindness 1E [RCV001123665]\|not provided [RCV002070018]	likely benign\|uncertain significance	17	38343301	38343301	Human	1	name
126744549	CV1012722	single nucleotide variant	NM_001004334.4(GPR179):c.1812G>A (p.Pro604=)	not provided [RCV001325774]	likely benign\|uncertain significance	17	38334011	38334011	Human		name
126738379	CV1012723	single nucleotide variant	NM_001004334.4(GPR179):c.247C>T (p.Arg83Cys)	not provided [RCV001324915]	uncertain significance	17	38343543	38343543	Human		name
127265769	CV1064160	deletion	NM_001004334.4(GPR179):c.800del (p.Gln267fs)	not provided [RCV001388539]	pathogenic	17	38339520	38339520	Human		name
127283207	CV1082963	single nucleotide variant	NM_001004334.4(GPR179):c.1866G>C (p.Thr622=)	not provided [RCV001411613]	likely benign	17	38333957	38333957	Human		name
127273389	CV1104757	single nucleotide variant	NM_001004334.4(GPR179):c.1464G>C (p.Gly488=)	not provided [RCV001442501]	likely benign	17	38335214	38335214	Human		name
127239423	CV1104758	single nucleotide variant	NM_001004334.4(GPR179):c.1023G>A (p.Gly341=)	not provided [RCV001433969]	likely benign	17	38337182	38337182	Human		name
127233882	CV1104759	single nucleotide variant	NM_001004334.4(GPR179):c.164G>A (p.Gly55Glu)	not provided [RCV001421897]	likely benign	17	38343626	38343626	Human		name
127326446	CV1126174	single nucleotide variant	NM_001004334.4(GPR179):c.2907T>C (p.Ala969=)	not provided [RCV001468742]	likely benign	17	38330662	38330662	Human		name
127329481	CV1147075	single nucleotide variant	NM_001004334.4(GPR179):c.2838G>A (p.Gly946=)	not provided [RCV001487434]	likely benign	17	38330731	38330731	Human		name
127305751	CV1147076	single nucleotide variant	NM_001004334.4(GPR179):c.1419G>A (p.Leu473=)	not provided [RCV001499981]	likely benign	17	38335259	38335259	Human		name
150488415	CV1274219	single nucleotide variant	NM_001004334.4(GPR179):c.1839C>T (p.Phe613=)	not provided [RCV001727928]\|not specified [RCV001699850]	benign\|likely benign	17	38333984	38333984	Human		name
150547011	CV1291834	single nucleotide variant	NM_001004334.4(GPR179):c.274C>A (p.Pro92Thr)	Congenital stationary night blindness 1E [RCV001733520]\|not provided [RCV005094915]	uncertain significance	17	38343516	38343516	Human	1	name
150542420	CV1314778	single nucleotide variant	NM_001004334.4(GPR179):c.148C>T (p.Gln50Ter)	Congenital stationary night blindness 1E [RCV001782229]	likely pathogenic	17	38343642	38343642	Human	1	name
151754646	CV1343286	single nucleotide variant	NM_001004334.4(GPR179):c.2688G>T (p.Gly896=)	not provided [RCV002043633]	likely benign\|uncertain significance	17	38330881	38330881	Human		name
151827022	CV1400512	single nucleotide variant	NM_001004334.4(GPR179):c.181G>A (p.Ala61Thr)	not provided [RCV001976274]	uncertain significance	17	38343609	38343609	Human		name
151731462	CV1421342	single nucleotide variant	NM_001004334.4(GPR179):c.277C>A (p.Pro93Thr)	not provided [RCV001892294]	uncertain significance	17	38343513	38343513	Human		name
151824617	CV1429385	deletion	NM_001004334.4(GPR179):c.857del (p.Pro286fs)	not provided [RCV001993116]	pathogenic	17	38339463	38339463	Human		name
151818118	CV1436125	single nucleotide variant	NM_001004334.4(GPR179):c.181G>T (p.Ala61Ser)	Inborn genetic diseases [RCV005350807]\|not provided [RCV001975459]	uncertain significance	17	38343609	38343609	Human	1	name
151847911	CV1439755	single nucleotide variant	NM_001004334.4(GPR179):c.1212C>G (p.Arg404=)	not provided [RCV002016184]	likely benign\|uncertain significance	17	38336993	38336993	Human		name
151723068	CV1442768	single nucleotide variant	NM_001004334.4(GPR179):c.175G>A (p.Ala59Thr)	Inborn genetic diseases [RCV002545527]\|Retinal dystrophy [RCV004816915]\|not provided [RCV002040337]	uncertain significance	17	38343615	38343615	Human	3	name
151768110	CV1445363	single nucleotide variant	NM_001004334.4(GPR179):c.225T>A (p.Asn75Lys)	Inborn genetic diseases [RCV004042475]\|not provided [RCV002025096]	uncertain significance	17	38343565	38343565	Human	1	name
151867076	CV1447637	single nucleotide variant	NM_001004334.4(GPR179):c.1707G>A (p.Ser569=)	not provided [RCV001924738]	likely benign\|uncertain significance	17	38334781	38334781	Human		name
151724361	CV1459273	single nucleotide variant	NM_001004334.4(GPR179):c.248G>A (p.Arg83His)	not provided [RCV002020595]	uncertain significance	17	38343542	38343542	Human		name
151862865	CV1474366	single nucleotide variant	NM_001004334.4(GPR179):c.289G>C (p.Gly97Arg)	not provided [RCV001884159]	uncertain significance	17	38343501	38343501	Human		name
151730530	CV1489497	single nucleotide variant	NM_001004334.4(GPR179):c.236G>A (p.Arg79His)	not provided [RCV001910825]	uncertain significance	17	38343554	38343554	Human		name
151718133	CV1513414	single nucleotide variant	NM_001004334.4(GPR179):c.2475G>A (p.Val825=)	not provided [RCV001890654]	likely benign\|uncertain significance	17	38331094	38331094	Human		name
151889581	CV1516316	single nucleotide variant	NM_001004334.4(GPR179):c.2472G>A (p.Thr824=)	not provided [RCV002038631]	likely benign\|uncertain significance	17	38331097	38331097	Human		name
152055310	CV1522027	single nucleotide variant	NM_001004334.4(GPR179):c.1146C>T (p.Ala382=)	not provided [RCV002189888]	likely benign	17	38337059	38337059	Human		name
152132399	CV1522077	single nucleotide variant	NM_001004334.4(GPR179):c.1062G>C (p.Leu354=)	not provided [RCV002199494]	likely benign	17	38337143	38337143	Human		name
152126201	CV1532453	single nucleotide variant	NM_001004334.4(GPR179):c.2229C>T (p.His743=)	not provided [RCV002118484]	likely benign	17	38331340	38331340	Human		name
152145888	CV1543341	single nucleotide variant	NM_001004334.4(GPR179):c.1153C>T (p.Leu385=)	not provided [RCV002178715]	likely benign	17	38337052	38337052	Human		name
152169800	CV1546583	single nucleotide variant	NM_001004334.4(GPR179):c.1956C>T (p.Asp652=)	not provided [RCV002142907]	likely benign	17	38333332	38333332	Human		name
152081284	CV1548239	single nucleotide variant	NM_001004334.4(GPR179):c.2286C>T (p.Pro762=)	not provided [RCV002076402]	likely benign	17	38331283	38331283	Human		name
152084097	CV1554838	single nucleotide variant	NM_001004334.4(GPR179):c.1374C>T (p.Ile458=)	not provided [RCV002211807]	likely benign	17	38335623	38335623	Human		name
152066155	CV1556953	single nucleotide variant	NM_001004334.4(GPR179):c.1138C>T (p.Leu380=)	not provided [RCV002191199]	likely benign	17	38337067	38337067	Human		name
152079448	CV1557889	single nucleotide variant	NM_001004334.4(GPR179):c.1824C>T (p.Leu608=)	not provided [RCV002170346]	likely benign	17	38333999	38333999	Human		name
152114052	CV1559256	single nucleotide variant	NM_001004334.4(GPR179):c.2340G>A (p.Glu780=)	not provided [RCV002174694]	likely benign	17	38331229	38331229	Human		name
152114112	CV1559298	single nucleotide variant	NM_001004334.4(GPR179):c.2172G>A (p.Ala724=)	not provided [RCV002174701]	likely benign	17	38331397	38331397	Human		name
152176089	CV1562297	single nucleotide variant	NM_001004334.4(GPR179):c.1134G>A (p.Ala378=)	not provided [RCV002164229]	likely benign	17	38337071	38337071	Human		name
152110631	CV1564087	single nucleotide variant	NM_001004334.4(GPR179):c.2841C>A (p.Gly947=)	not provided [RCV002174290]	likely benign	17	38330728	38330728	Human		name
152166690	CV1566554	single nucleotide variant	NM_001004334.4(GPR179):c.1914C>T (p.Pro638=)	not provided [RCV002160700]	likely benign	17	38333374	38333374	Human		name
152173752	CV1567175	single nucleotide variant	NM_001004334.4(GPR179):c.2721G>A (p.Lys907=)	not provided [RCV002144216]	likely benign	17	38330848	38330848	Human		name
152087099	CV1578278	single nucleotide variant	NM_001004334.4(GPR179):c.2784G>A (p.Leu928=)	not provided [RCV002171319]	likely benign	17	38330785	38330785	Human		name
152128567	CV1583770	single nucleotide variant	NM_001004334.4(GPR179):c.1935G>A (p.Glu645=)	not provided [RCV002199015]	likely benign	17	38333353	38333353	Human		name
152129716	CV1584345	single nucleotide variant	NM_001004334.4(GPR179):c.2502C>A (p.Pro834=)	not provided [RCV002082694]	likely benign	17	38331067	38331067	Human		name
152081583	CV1589435	single nucleotide variant	NM_001004334.4(GPR179):c.2517G>A (p.Lys839=)	not provided [RCV002112824]	likely benign	17	38331052	38331052	Human		name
152061004	CV1597139	single nucleotide variant	NM_001004334.4(GPR179):c.2520G>A (p.Ser840=)	Retinal dystrophy [RCV004816973]\|not provided [RCV002208650]	likely benign\|uncertain significance	17	38331049	38331049	Human	2	name
152094850	CV1599406	single nucleotide variant	NM_001004334.4(GPR179):c.1152G>T (p.Val384=)	not provided [RCV002094699]	likely benign	17	38337053	38337053	Human		name
152096524	CV1599724	single nucleotide variant	NM_001004334.4(GPR179):c.1866G>A (p.Thr622=)	not provided [RCV002151271]	likely benign	17	38333957	38333957	Human		name
152164579	CV1605084	single nucleotide variant	NM_001004334.4(GPR179):c.2409C>T (p.Ser803=)	not provided [RCV002204068]	likely benign	17	38331160	38331160	Human		name
152147317	CV1608176	single nucleotide variant	NM_001004334.4(GPR179):c.1057C>T (p.Leu353=)	not provided [RCV002178921]	likely benign	17	38337148	38337148	Human		name
152087392	CV1608527	single nucleotide variant	NM_001004334.4(GPR179):c.2574C>T (p.Tyr858=)	not provided [RCV002212233]	likely benign	17	38330995	38330995	Human		name
152165868	CV1612744	single nucleotide variant	NM_001004334.4(GPR179):c.2892G>A (p.Leu964=)	not provided [RCV002160533]	likely benign	17	38330677	38330677	Human		name
152156819	CV1615824	single nucleotide variant	NM_001004334.4(GPR179):c.1323T>C (p.Ser441=)	not provided [RCV002158952]	likely benign	17	38335674	38335674	Human		name
152157987	CV1616040	single nucleotide variant	NM_001004334.4(GPR179):c.1992C>T (p.Ile664=)	not provided [RCV002159123]	likely benign	17	38333296	38333296	Human		name
152085147	CV1617210	single nucleotide variant	NM_001004334.4(GPR179):c.1233C>T (p.Ile411=)	not provided [RCV002076885]	likely benign	17	38336139	38336139	Human		name
152163429	CV1619007	single nucleotide variant	NM_001004334.4(GPR179):c.1485G>T (p.Gly495=)	not provided [RCV002123607]	likely benign	17	38335193	38335193	Human		name
152163436	CV1619008	single nucleotide variant	NM_001004334.4(GPR179):c.1434G>T (p.Thr478=)	not provided [RCV002123608]	likely benign	17	38335244	38335244	Human		name
152159201	CV1621085	single nucleotide variant	NM_001004334.4(GPR179):c.1557C>T (p.His519=)	not provided [RCV002203141]	likely benign	17	38335121	38335121	Human		name
152042525	CV1624258	single nucleotide variant	NM_001004334.4(GPR179):c.1326A>G (p.Val442=)	not provided [RCV002126273]	likely benign	17	38335671	38335671	Human		name
152026896	CV1626677	single nucleotide variant	NM_001004334.4(GPR179):c.2122C>A (p.Arg708=)	not provided [RCV002185314]	likely benign	17	38331447	38331447	Human		name
152157852	CV1630637	single nucleotide variant	NM_001004334.4(GPR179):c.1140G>A (p.Leu380=)	not provided [RCV002122679]	benign\|likely benign	17	38337065	38337065	Human		name
152162435	CV1635742	single nucleotide variant	NM_001004334.4(GPR179):c.1536C>T (p.Ala512=)	not provided [RCV002203668]	likely benign	17	38335142	38335142	Human		name
152040024	CV1644049	single nucleotide variant	NM_001004334.4(GPR179):c.2457C>T (p.Ser819=)	not provided [RCV002125951]	likely benign	17	38331112	38331112	Human		name
152142447	CV1654312	single nucleotide variant	NM_001004334.4(GPR179):c.1764C>T (p.Ser588=)	not provided [RCV002200752]	likely benign	17	38334724	38334724	Human		name
152165359	CV1654512	single nucleotide variant	NM_001004334.4(GPR179):c.1017T>C (p.Thr339=)	not provided [RCV002181718]	likely benign	17	38337188	38337188	Human		name
152052491	CV1659093	single nucleotide variant	NM_001004334.4(GPR179):c.2652G>A (p.Arg884=)	not provided [RCV002189584]	likely benign	17	38330917	38330917	Human		name
152066490	CV1659931	single nucleotide variant	NM_001004334.4(GPR179):c.2991C>T (p.Asn997=)	not provided [RCV002147494]	likely benign	17	38330578	38330578	Human		name
152054363	CV1665421	single nucleotide variant	NM_001004334.4(GPR179):c.1344T>G (p.Leu448=)	not provided [RCV002089527]	likely benign	17	38335653	38335653	Human		name
152133231	CV1666230	single nucleotide variant	NM_001004334.4(GPR179):c.2811T>C (p.Val937=)	not provided [RCV002099767]	likely benign	17	38330758	38330758	Human		name
155709151	CV1775724	single nucleotide variant	NM_001004334.4(GPR179):c.295G>A (p.Ala99Thr)	not provided [RCV002296116]	uncertain significance	17	38343495	38343495	Human		name
156250308	CV1953836	single nucleotide variant	NM_001004334.4(GPR179):c.2598A>G (p.Ala866=)	not provided [RCV002576517]	likely benign	17	38330971	38330971	Human		name
156408739	CV1954498	single nucleotide variant	NM_001004334.4(GPR179):c.2292G>C (p.Gly764=)	not provided [RCV002586602]	likely benign	17	38331277	38331277	Human		name
156080205	CV1959881	single nucleotide variant	NM_001004334.4(GPR179):c.1252C>T (p.Leu418=)	not provided [RCV002569885]	likely benign	17	38336120	38336120	Human		name
156415741	CV1966218	single nucleotide variant	NM_001004334.4(GPR179):c.2730C>T (p.Ser910=)	not provided [RCV002589340]	likely benign	17	38330839	38330839	Human		name
156158755	CV1967772	single nucleotide variant	NM_001004334.4(GPR179):c.2565C>T (p.Ser855=)	not provided [RCV002594392]	likely benign	17	38331004	38331004	Human		name
156270381	CV1970920	single nucleotide variant	NM_001004334.4(GPR179):c.2112G>A (p.Leu704=)	not provided [RCV002598071]	likely benign	17	38331457	38331457	Human		name
156178657	CV1978705	single nucleotide variant	NM_001004334.4(GPR179):c.2349G>A (p.Pro783=)	not provided [RCV002594996]	likely benign	17	38331220	38331220	Human		name
156413594	CV1979069	single nucleotide variant	NM_001004334.4(GPR179):c.2820C>A (p.Pro940=)	not provided [RCV002608889]	likely benign	17	38330749	38330749	Human		name
156400687	CV1981907	single nucleotide variant	NM_001004334.4(GPR179):c.1083G>A (p.Glu361=)	not provided [RCV002605573]	likely benign	17	38337122	38337122	Human		name
156416098	CV1983965	single nucleotide variant	NM_001004334.4(GPR179):c.2799C>A (p.Ile933=)	not provided [RCV002609995]	likely benign	17	38330770	38330770	Human		name
156089730	CV1983983	single nucleotide variant	NM_001004334.4(GPR179):c.2394C>T (p.Ala798=)	not provided [RCV002621817]	likely benign	17	38331175	38331175	Human		name
156157410	CV1987914	single nucleotide variant	NM_001004334.4(GPR179):c.1804C>T (p.Leu602=)	not provided [RCV002642280]	likely benign	17	38334019	38334019	Human		name
156402740	CV1988697	single nucleotide variant	NM_001004334.4(GPR179):c.100T>C (p.Ser34Pro)	not provided [RCV002605766]	uncertain significance	17	38343690	38343690	Human		name
156321518	CV1992003	single nucleotide variant	NM_001004334.4(GPR179):c.2871C>T (p.Thr957=)	not provided [RCV002649276]	likely benign	17	38330698	38330698	Human		name
156401868	CV1992248	single nucleotide variant	NM_001004334.4(GPR179):c.2181C>T (p.Pro727=)	not provided [RCV002605684]	likely benign	17	38331388	38331388	Human		name
156403311	CV1993199	single nucleotide variant	NM_001004334.4(GPR179):c.2926C>T (p.Leu976=)	not provided [RCV002657826]	likely benign	17	38330643	38330643	Human		name
156094361	CV2004478	single nucleotide variant	NM_001004334.4(GPR179):c.2418G>C (p.Ser806=)	not provided [RCV002639338]	likely benign	17	38331151	38331151	Human		name
156102524	CV2009872	single nucleotide variant	NM_001004334.4(GPR179):c.2232C>T (p.Gly744=)	not provided [RCV002706725]	likely benign	17	38331337	38331337	Human		name
156175219	CV2010330	single nucleotide variant	NM_001004334.4(GPR179):c.1608C>T (p.Leu536=)	not provided [RCV002710607]	likely benign	17	38335070	38335070	Human		name
156092563	CV2014057	single nucleotide variant	NM_001004334.4(GPR179):c.2217A>T (p.Gly739=)	not provided [RCV002694996]	likely benign	17	38331352	38331352	Human		name
156011969	CV2016804	single nucleotide variant	NM_001004334.4(GPR179):c.1977C>T (p.Tyr659=)	not provided [RCV002734942]	likely benign	17	38333311	38333311	Human		name
156317704	CV2018114	single nucleotide variant	NM_001004334.4(GPR179):c.257G>A (p.Gly86Glu)	not provided [RCV002671998]	uncertain significance	17	38343533	38343533	Human		name
155948346	CV2029099	single nucleotide variant	NM_001004334.4(GPR179):c.278C>T (p.Pro93Leu)	not provided [RCV002730537]	uncertain significance	17	38343512	38343512	Human		name
156232201	CV2048769	single nucleotide variant	NM_001004334.4(GPR179):c.1338C>T (p.Ile446=)	not provided [RCV002791039]	likely benign	17	38335659	38335659	Human		name
156102656	CV2051185	single nucleotide variant	NM_001004334.4(GPR179):c.2106C>T (p.Pro702=)	not provided [RCV002824614]	likely benign	17	38331463	38331463	Human		name
156118110	CV2055168	single nucleotide variant	NM_001004334.4(GPR179):c.1431A>G (p.Arg477=)	not provided [RCV002825191]	likely benign	17	38335247	38335247	Human		name
155996782	CV2064087	single nucleotide variant	NM_001004334.4(GPR179):c.119C>G (p.Ser40Cys)	not provided [RCV002843221]	uncertain significance	17	38343671	38343671	Human		name
156176481	CV2072042	single nucleotide variant	NM_001004334.4(GPR179):c.206A>G (p.Gln69Arg)	not provided [RCV002851698]	uncertain significance	17	38343584	38343584	Human		name
155952181	CV2076461	single nucleotide variant	NM_001004334.4(GPR179):c.2238G>A (p.Leu746=)	not provided [RCV002862407]	likely benign	17	38331331	38331331	Human		name
156227320	CV2088837	single nucleotide variant	NM_001004334.4(GPR179):c.1395C>T (p.Leu465=)	not provided [RCV002876102]	likely benign	17	38335602	38335602	Human		name
156263534	CV2100785	single nucleotide variant	NM_001004334.4(GPR179):c.2379G>A (p.Lys793=)	not provided [RCV002877355]	likely benign	17	38331190	38331190	Human		name
156024766	CV2112323	deletion	NM_001004334.4(GPR179):c.416del (p.Glu139fs)	not provided [RCV002909783]	pathogenic	17	38343374	38343374	Human		name
155907324	CV2148253	single nucleotide variant	NM_001004334.4(GPR179):c.161A>C (p.Glu54Ala)	not provided [RCV003012000]	uncertain significance	17	38343629	38343629	Human		name
156191999	CV2150006	single nucleotide variant	NM_001004334.4(GPR179):c.1404C>T (p.Tyr468=)	not provided [RCV003006032]	likely benign	17	38335593	38335593	Human		name
155970940	CV2152580	single nucleotide variant	NM_001004334.4(GPR179):c.109C>T (p.Pro37Ser)	not provided [RCV003015933]	uncertain significance	17	38343681	38343681	Human		name
156360287	CV2162458	duplication	NM_001004334.4(GPR179):c.416dup (p.Asp141fs)	not provided [RCV003031517]	pathogenic	17	38343373	38343374	Human		name
155998064	CV2167858	single nucleotide variant	NM_001004334.4(GPR179):c.1020C>T (p.Thr340=)	not provided [RCV003034640]	likely benign	17	38337185	38337185	Human		name
156333330	CV2172028	single nucleotide variant	NM_001004334.4(GPR179):c.1593C>T (p.Gly531=)	not provided [RCV003029891]	likely benign	17	38335085	38335085	Human		name
156087445	CV2184574	single nucleotide variant	NM_001004334.4(GPR179):c.1890G>A (p.Lys630=)	not provided [RCV003054239]	uncertain significance	17	38333933	38333933	Human		name
156338486	CV2188234	single nucleotide variant	NM_001004334.4(GPR179):c.2601G>A (p.Lys867=)	not provided [RCV003064102]	likely benign	17	38330968	38330968	Human		name
156402999	CV2189679	single nucleotide variant	NM_001004334.4(GPR179):c.1722A>G (p.Pro574=)	not provided [RCV003052507]	likely benign	17	38334766	38334766	Human		name
156076718	CV2230233	single nucleotide variant	NM_001004334.4(GPR179):c.220G>A (p.Val74Met)	Inborn genetic diseases [RCV002737678]	uncertain significance	17	38343570	38343570	Human	1	name
329397888	CV2466406	single nucleotide variant	NM_001004334.4(GPR179):c.271C>T (p.Leu91Phe)	Inborn genetic diseases [RCV003195781]	uncertain significance	17	38343519	38343519	Human	1	name
11633582	CV270659	duplication	NM_001004334.4(GPR179):c.647dup (p.Ala217fs)	not provided [RCV000349499]	pathogenic	17	38343142	38343143	Human		name
405081165	CV2864778	single nucleotide variant	NM_001004334.4(GPR179):c.2463C>T (p.His821=)	not provided [RCV003549243]	likely benign	17	38331106	38331106	Human		name
402518324	CV2870860	single nucleotide variant	NM_001004334.4(GPR179):c.1134G>C (p.Ala378=)	not provided [RCV003547567]	likely benign	17	38337071	38337071	Human		name
402473185	CV2908699	single nucleotide variant	NM_001004334.4(GPR179):c.2277C>T (p.Leu759=)	not provided [RCV003570864]	likely benign	17	38331292	38331292	Human		name
405221136	CV2912837	single nucleotide variant	NM_001004334.4(GPR179):c.1797T>A (p.Val599=)	not provided [RCV003568449]	likely benign	17	38334026	38334026	Human		name
402466464	CV2914779	single nucleotide variant	NM_001004334.4(GPR179):c.1476G>T (p.Arg492=)	not provided [RCV003569457]	likely benign	17	38335202	38335202	Human		name
402464677	CV2916381	single nucleotide variant	NM_001004334.4(GPR179):c.1470G>A (p.Leu490=)	not provided [RCV003569070]	likely benign	17	38335208	38335208	Human		name
405068551	CV2924052	single nucleotide variant	NM_001004334.4(GPR179):c.2184G>A (p.Glu728=)	not provided [RCV003580976]	likely benign	17	38331385	38331385	Human		name
405036865	CV2932876	single nucleotide variant	NM_001004334.4(GPR179):c.2940A>G (p.Pro980=)	not provided [RCV003578795]	likely benign	17	38330629	38330629	Human		name
404981777	CV2986239	single nucleotide variant	NM_001004334.4(GPR179):c.2820C>T (p.Pro940=)	not provided [RCV003691328]	likely benign	17	38330749	38330749	Human		name
405239803	CV2993501	single nucleotide variant	NM_001004334.4(GPR179):c.2475G>C (p.Val825=)	not provided [RCV003718956]	likely benign	17	38331094	38331094	Human		name
405249264	CV3003900	single nucleotide variant	NM_001004334.4(GPR179):c.2661A>C (p.Ser887=)	not provided [RCV003721253]	likely benign	17	38330908	38330908	Human		name
405219870	CV3035085	single nucleotide variant	NM_001004334.4(GPR179):c.1455G>A (p.Leu485=)	not provided [RCV003709753]	likely benign	17	38335223	38335223	Human		name
405208327	CV3037168	single nucleotide variant	NM_001004334.4(GPR179):c.2895G>T (p.Leu965=)	not provided [RCV003708301]	likely benign	17	38330674	38330674	Human		name
405208612	CV3037224	single nucleotide variant	NM_001004334.4(GPR179):c.2241C>T (p.Pro747=)	not provided [RCV003708336]	likely benign	17	38331328	38331328	Human		name
404999303	CV3120158	single nucleotide variant	NM_001004334.4(GPR179):c.2835T>G (p.Ser945=)	not provided [RCV003827948]	likely benign	17	38330734	38330734	Human		name
405194631	CV3128603	single nucleotide variant	NM_001004334.4(GPR179):c.1693C>A (p.Arg565=)	not provided [RCV003821340]	likely benign	17	38334795	38334795	Human		name
405029683	CV3129922	single nucleotide variant	NM_001004334.4(GPR179):c.2076C>T (p.His692=)	not provided [RCV003830520]	likely benign	17	38331493	38331493	Human		name
405112138	CV3133563	single nucleotide variant	NM_001004334.4(GPR179):c.1038A>T (p.Pro346=)	not provided [RCV003836356]	likely benign	17	38337167	38337167	Human		name
405091863	CV3134528	single nucleotide variant	NM_001004334.4(GPR179):c.1713C>T (p.Phe571=)	not provided [RCV003834874]	likely benign	17	38334775	38334775	Human		name
405055790	CV3138604	single nucleotide variant	NM_001004334.4(GPR179):c.1461C>T (p.Ser487=)	not provided [RCV003832449]	likely benign	17	38335217	38335217	Human		name
405198596	CV3168214	single nucleotide variant	NM_001004334.4(GPR179):c.1737C>T (p.Ile579=)	not provided [RCV003860346]	likely benign	17	38334751	38334751	Human		name
405000359	CV3183564	single nucleotide variant	NM_001004334.4(GPR179):c.2316C>T (p.Arg772=)	not provided [RCV003882441]	likely benign	17	38331253	38331253	Human		name
11617179	CV328327	single nucleotide variant	NM_001004334.4(GPR179):c.296C>T (p.Ala99Val)	Congenital stationary night blindness 1E [RCV000302010]	uncertain significance	17	38343494	38343494	Human	1	name
11629056	CV344314	single nucleotide variant	NM_001004334.4(GPR179):c.2988G>A (p.Glu996=)	Congenital stationary night blindness 1E [RCV000313951]\|not provided [RCV001519324]	benign\|likely benign	17	38330581	38330581	Human	1	name
11629544	CV344319	single nucleotide variant	NM_001004334.4(GPR179):c.2556C>T (p.Leu852=)	Congenital stationary night blindness 1E [RCV000325746]\|not provided [RCV001448662]	likely benign\|uncertain significance	17	38331013	38331013	Human	1	name
11644836	CV344331	single nucleotide variant	NM_001004334.4(GPR179):c.134G>T (p.Gly45Val)	Congenital stationary night blindness 1E [RCV000261865]	uncertain significance	17	38343656	38343656	Human	1	name
11627033	CV345738	single nucleotide variant	NM_001004334.4(GPR179):c.2895G>A (p.Leu965=)	Congenital stationary night blindness 1E [RCV000274012]\|not provided [RCV002056585]	benign\|uncertain significance	17	38330674	38330674	Human	1	name
11631436	CV345750	single nucleotide variant	NM_001004334.4(GPR179):c.2040C>T (p.Asp680=)	Congenital stationary night blindness 1E [RCV000377369]\|not provided [RCV001522895]	benign\|likely benign	17	38331529	38331529	Human	1	name
11627367	CV345751	single nucleotide variant	NM_001004334.4(GPR179):c.2022C>T (p.Asp674=)	Congenital stationary night blindness 1E [RCV000625279]\|not provided [RCV001523759]\|not specified [RCV001699315]	benign\|uncertain significance	17	38333266	38333266	Human	1	name
597918769	CV3737881	single nucleotide variant	NM_001004334.4(GPR179):c.2715T>A (p.Pro905=)	not provided [RCV005074480]	likely benign	17	38330854	38330854	Human		name
597880986	CV3744791	single nucleotide variant	NM_001004334.4(GPR179):c.2289G>A (p.Glu763=)	not provided [RCV005069816]	likely benign	17	38331280	38331280	Human		name
597856617	CV3748071	single nucleotide variant	NM_001004334.4(GPR179):c.1149T>C (p.Ala383=)	not provided [RCV005066893]	likely benign	17	38337056	38337056	Human		name
597832205	CV3751300	single nucleotide variant	NM_001004334.4(GPR179):c.2061C>A (p.Ala687=)	not provided [RCV005084846]	likely benign	17	38331508	38331508	Human		name
597844364	CV3752603	single nucleotide variant	NM_001004334.4(GPR179):c.1380C>T (p.Tyr460=)	not provided [RCV005087009]	likely benign	17	38335617	38335617	Human		name
597905318	CV3772876	single nucleotide variant	NM_001004334.4(GPR179):c.1812G>C (p.Pro604=)	not provided [RCV005112941]	likely benign	17	38334011	38334011	Human		name
597895193	CV3806300	single nucleotide variant	NM_001004334.4(GPR179):c.2421G>T (p.Val807=)	not provided [RCV005151883]	likely benign	17	38331148	38331148	Human		name
597895260	CV3806310	single nucleotide variant	NM_001004334.4(GPR179):c.2562C>T (p.Ala854=)	not provided [RCV005151893]	likely benign	17	38331007	38331007	Human		name
597944217	CV3812507	single nucleotide variant	NM_001004334.4(GPR179):c.1845C>T (p.Thr615=)	not provided [RCV005159717]	likely benign	17	38333978	38333978	Human		name
597860966	CV3813466	single nucleotide variant	NM_001004334.4(GPR179):c.1564C>T (p.Leu522=)	not provided [RCV005146728]	likely benign	17	38335114	38335114	Human		name
597832239	CV3830944	single nucleotide variant	NM_001004334.4(GPR179):c.2376G>A (p.Arg792=)	not provided [RCV005170341]	likely benign	17	38331193	38331193	Human		name
597883431	CV3857918	single nucleotide variant	NM_001004334.4(GPR179):c.2430C>T (p.Pro810=)	not provided [RCV005199346]	likely benign	17	38331139	38331139	Human		name
598274424	CV3971172	single nucleotide variant	NM_001004334.4(GPR179):c.147G>A (p.Met49Ile)	Inborn genetic diseases [RCV005351414]	uncertain significance	17	38343643	38343643	Human	1	name
8568859	CV40161	deletion	NM_001004334.4(GPR179):c.984del (p.Ser329fs)	Congenital stationary night blindness 1E [RCV000024203]\|Congenital stationary night blindness [RCV000505034]\|Optic atrophy [RCV004814924]\|Retinal dystrophy [RCV001073427]\|not provided [RCV000309713]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	17	38337640	38337640	Human	7	name
28908502	CV877373	single nucleotide variant	NM_001004334.4(GPR179):c.1947C>T (p.Asp649=)	Congenital stationary night blindness 1E [RCV001128224]\|not provided [RCV002070493]	likely benign\|uncertain significance	17	38333341	38333341	Human	1	name
28895502	CV877374	single nucleotide variant	NM_001004334.4(GPR179):c.1533C>T (p.Gly511=)	Congenital stationary night blindness 1E [RCV001122493]\|not provided [RCV002069998]	likely benign\|uncertain significance	17	38335145	38335145	Human	1	name
28904847	CV877381	single nucleotide variant	NM_001004334.4(GPR179):c.1029C>T (p.Phe343=)	Congenital stationary night blindness 1E [RCV001126250]\|not provided [RCV001513426]	benign\|likely benign	17	38337176	38337176	Human	1	name
28898748	CV877389	single nucleotide variant	NM_001004334.4(GPR179):c.272T>C (p.Leu91Pro)	Congenital stationary night blindness 1E [RCV001123666]	uncertain significance	17	38343518	38343518	Human	1	name
28898670	CV877390	single nucleotide variant	NM_001004334.4(GPR179):c.131C>A (p.Pro44Gln)	Congenital stationary night blindness 1E [RCV001123667]\|Inborn genetic diseases [RCV003259108]\|not provided [RCV001856631]	uncertain significance	17	38343659	38343659	Human	2	name
126731028	CV1021634	deletion	NM_001004334.4(GPR179):c.1368del (p.Phe456fs)	not provided [RCV001960675]	pathogenic	17	38335629	38335629	Human		name
126730157	CV1033251	single nucleotide variant	NM_001004334.4(GPR179):c.403C>T (p.Arg135Cys)	not provided [RCV001349221]	uncertain significance	17	38343387	38343387	Human		name
126916877	CV1050219	single nucleotide variant	NM_001004334.4(GPR179):c.761A>G (p.Tyr254Cys)	Inborn genetic diseases [RCV004980401]\|not provided [RCV001371756]	uncertain significance	17	38343029	38343029	Human	1	name
127242997	CV1082962	single nucleotide variant	NM_001004334.4(GPR179):c.5898A>G (p.Ala1966=)	not provided [RCV001416048]	likely benign	17	38327671	38327671	Human		name
127331419	CV1147074	single nucleotide variant	NM_001004334.4(GPR179):c.5931T>C (p.Pro1977=)	not provided [RCV001488772]	likely benign	17	38327638	38327638	Human		name
127299800	CV1157940	single nucleotide variant	NM_001004334.4(GPR179):c.4260G>A (p.Pro1420=)	not provided [RCV001513837]	benign	17	38329309	38329309	Human		name
127295616	CV1157942	single nucleotide variant	NM_001004334.4(GPR179):c.3699G>C (p.Leu1233=)	Retinal dystrophy [RCV004815543]\|not provided [RCV001512257]	benign\|likely benign	17	38329870	38329870	Human	2	name
150546077	CV1291836	single nucleotide variant	NM_001004334.4(GPR179):c.619G>C (p.Gly207Arg)	Congenital stationary night blindness 1E [RCV001732863]\|not provided [RCV005094917]	likely benign\|uncertain significance	17	38343171	38343171	Human	1	name
150542419	CV1314777	single nucleotide variant	NM_001004334.4(GPR179):c.481C>T (p.Gln161Ter)	Congenital stationary night blindness 1E [RCV004797250]	likely pathogenic	17	38343309	38343309	Human	1	name
151858517	CV1347658	single nucleotide variant	NM_001004334.4(GPR179):c.553G>A (p.Glu185Lys)	not provided [RCV002034076]	uncertain significance	17	38343237	38343237	Human		name
151843075	CV1357839	single nucleotide variant	NM_001004334.4(GPR179):c.301A>C (p.Thr101Pro)	not provided [RCV001881596]	uncertain significance	17	38343489	38343489	Human		name
151839802	CV1364340	single nucleotide variant	NM_001004334.4(GPR179):c.724C>T (p.Arg242Ter)	not provided [RCV001994599]	pathogenic	17	38343066	38343066	Human		name
151866263	CV1392901	single nucleotide variant	NM_001004334.4(GPR179):c.561C>G (p.Asn187Lys)	Inborn genetic diseases [RCV002562013]\|not provided [RCV001939197]	uncertain significance	17	38343229	38343229	Human	1	name
151889101	CV1402555	single nucleotide variant	NM_001004334.4(GPR179):c.440C>T (p.Ala147Val)	not provided [RCV001942728]	uncertain significance	17	38343350	38343350	Human		name
151847536	CV1409684	single nucleotide variant	NM_001004334.4(GPR179):c.940C>T (p.Arg314Cys)	not provided [RCV001882155]	uncertain significance	17	38337684	38337684	Human		name
151769622	CV1410685	single nucleotide variant	NM_001004334.4(GPR179):c.671C>T (p.Thr224Met)	Inborn genetic diseases [RCV003289330]\|not provided [RCV001971052]	likely benign\|uncertain significance	17	38343119	38343119	Human	1	name
151773665	CV1414558	single nucleotide variant	NM_001004334.4(GPR179):c.850A>G (p.Ser284Gly)	not provided [RCV001874690]	uncertain significance	17	38339470	38339470	Human		name
151846812	CV1431813	single nucleotide variant	NM_001004334.4(GPR179):c.953G>A (p.Arg318His)	not provided [RCV001957445]	uncertain significance	17	38337671	38337671	Human		name
151724136	CV1437008	single nucleotide variant	NM_001004334.4(GPR179):c.757T>C (p.Phe253Leu)	not provided [RCV002004058]	uncertain significance	17	38343033	38343033	Human		name
151835108	CV1446942	single nucleotide variant	NM_001004334.4(GPR179):c.611A>G (p.Asn204Ser)	not provided [RCV002031201]	uncertain significance	17	38343179	38343179	Human		name
151777169	CV1450166	single nucleotide variant	NM_001004334.4(GPR179):c.719G>A (p.Arg240Gln)	not provided [RCV001864627]	uncertain significance	17	38343071	38343071	Human		name
151746915	CV1455874	single nucleotide variant	NM_001004334.4(GPR179):c.436A>G (p.Arg146Gly)	not provided [RCV002022931]	uncertain significance	17	38343354	38343354	Human		name
151803899	CV1462821	single nucleotide variant	NM_001004334.4(GPR179):c.3699G>A (p.Leu1233=)	not provided [RCV002028349]	uncertain significance	17	38329870	38329870	Human		name
151826228	CV1467251	single nucleotide variant	NM_001004334.4(GPR179):c.740T>G (p.Ile247Ser)	not provided [RCV001901357]	uncertain significance	17	38343050	38343050	Human		name
151882138	CV1484477	single nucleotide variant	NM_001004334.4(GPR179):c.4167C>T (p.Gly1389=)	not provided [RCV001941226]	likely benign\|uncertain significance	17	38329402	38329402	Human		name
151838273	CV1487359	single nucleotide variant	NM_001004334.4(GPR179):c.325C>G (p.Leu109Val)	not provided [RCV001935795]	uncertain significance	17	38343465	38343465	Human		name
151819023	CV1488163	single nucleotide variant	NM_001004334.4(GPR179):c.599G>T (p.Arg200Leu)	not provided [RCV001975545]	uncertain significance	17	38343191	38343191	Human		name
151807167	CV1505294	single nucleotide variant	NM_001004334.4(GPR179):c.307G>C (p.Ala103Pro)	not provided [RCV002048513]	uncertain significance	17	38343483	38343483	Human		name
151719665	CV1505902	single nucleotide variant	NM_001004334.4(GPR179):c.941G>A (p.Arg314His)	Inborn genetic diseases [RCV002545738]\|not provided [RCV002039885]	likely benign\|uncertain significance	17	38337683	38337683	Human	1	name
151730268	CV1515954	single nucleotide variant	NM_001004334.4(GPR179):c.988G>T (p.Gly330Trp)	not provided [RCV001984126]	uncertain significance	17	38337636	38337636	Human		name
151867883	CV1516543	single nucleotide variant	NM_001004334.4(GPR179):c.473G>A (p.Ser158Asn)	not provided [RCV001980928]	uncertain significance	17	38343317	38343317	Human		name
152048288	CV1519891	single nucleotide variant	NM_001004334.4(GPR179):c.4944C>T (p.Val1648=)	not provided [RCV002145343]	benign	17	38328625	38328625	Human		name
152037222	CV1521906	single nucleotide variant	NM_001004334.4(GPR179):c.5008A>C (p.Arg1670=)	not provided [RCV002187710]	likely benign	17	38328561	38328561	Human		name
152038714	CV1524221	single nucleotide variant	NM_001004334.4(GPR179):c.6100A>C (p.Arg2034=)	not provided [RCV002125760]	likely benign	17	38327469	38327469	Human		name
152168134	CV1524720	single nucleotide variant	NM_001004334.4(GPR179):c.5127G>A (p.Val1709=)	not provided [RCV002182341]	likely benign	17	38328442	38328442	Human		name
152065301	CV1525949	single nucleotide variant	NM_001004334.4(GPR179):c.4617G>A (p.Glu1539=)	not provided [RCV002128889]	likely benign	17	38328952	38328952	Human		name
152123901	CV1527588	single nucleotide variant	NM_001004334.4(GPR179):c.5910T>G (p.Ser1970=)	not provided [RCV002081945]	likely benign	17	38327659	38327659	Human		name
152090994	CV1528627	single nucleotide variant	NM_001004334.4(GPR179):c.5988C>T (p.Asp1996=)	not provided [RCV002094174]	likely benign	17	38327581	38327581	Human		name
152169759	CV1529347	single nucleotide variant	NM_001004334.4(GPR179):c.4623G>A (p.Thr1541=)	not provided [RCV002161549]	likely benign	17	38328946	38328946	Human		name
152107566	CV1529873	single nucleotide variant	NM_001004334.4(GPR179):c.5295G>A (p.Gly1765=)	not provided [RCV002196354]	likely benign	17	38328274	38328274	Human		name
152127136	CV1530236	single nucleotide variant	NM_001004334.4(GPR179):c.4710G>A (p.Thr1570=)	not provided [RCV002198829]	likely benign	17	38328859	38328859	Human		name
152050818	CV1533312	single nucleotide variant	NM_001004334.4(GPR179):c.6135A>G (p.Lys2045=)	not provided [RCV002166857]	likely benign	17	38327434	38327434	Human		name
152094919	CV1533891	single nucleotide variant	NM_001004334.4(GPR179):c.5904C>T (p.Ser1968=)	not provided [RCV002151074]	likely benign	17	38327665	38327665	Human		name
152162472	CV1535056	single nucleotide variant	NM_001004334.4(GPR179):c.4287A>G (p.Pro1429=)	not provided [RCV002141156]	likely benign	17	38329282	38329282	Human		name
152121791	CV1547637	single nucleotide variant	NM_001004334.4(GPR179):c.5226G>A (p.Glu1742=)	not provided [RCV002081653]	likely benign	17	38328343	38328343	Human		name
152089758	CV1550460	single nucleotide variant	NM_001004334.4(GPR179):c.718C>T (p.Arg240Trp)	Inborn genetic diseases [RCV003061789]\|not provided [RCV002131896]	likely benign\|uncertain significance	17	38343072	38343072	Human	1	name
152109063	CV1550890	single nucleotide variant	NM_001004334.4(GPR179):c.4191G>A (p.Glu1397=)	not provided [RCV002152796]	likely benign	17	38329378	38329378	Human		name
152067188	CV1557189	single nucleotide variant	NM_001004334.4(GPR179):c.4776C>T (p.Ile1592=)	not provided [RCV002191318]	likely benign	17	38328793	38328793	Human		name
152106197	CV1560042	single nucleotide variant	NM_001004334.4(GPR179):c.4575G>A (p.Val1525=)	not provided [RCV002133882]	likely benign	17	38328994	38328994	Human		name
152103329	CV1560670	single nucleotide variant	NM_001004334.4(GPR179):c.4227C>A (p.Thr1409=)	not provided [RCV002152074]	likely benign	17	38329342	38329342	Human		name
152176045	CV1562207	single nucleotide variant	NM_001004334.4(GPR179):c.5721C>T (p.Ser1907=)	not provided [RCV002164185]	likely benign	17	38327848	38327848	Human		name
152152231	CV1565097	single nucleotide variant	NM_001004334.4(GPR179):c.3132G>A (p.Glu1044=)	not provided [RCV002102402]	likely benign	17	38330437	38330437	Human		name
152093952	CV1565665	single nucleotide variant	NM_001004334.4(GPR179):c.3474C>T (p.Asn1158=)	not provided [RCV002150951]	likely benign	17	38330095	38330095	Human		name
152057362	CV1567279	single nucleotide variant	NM_001004334.4(GPR179):c.4656T>C (p.Asn1552=)	not provided [RCV002146390]	likely benign	17	38328913	38328913	Human		name
152174556	CV1567288	single nucleotide variant	NM_001004334.4(GPR179):c.5529G>A (p.Arg1843=)	not provided [RCV002163194]	likely benign	17	38328040	38328040	Human		name
152081190	CV1578354	single nucleotide variant	NM_001004334.4(GPR179):c.4740G>A (p.Pro1580=)	not provided [RCV002149331]	likely benign	17	38328829	38328829	Human		name
152080021	CV1579957	single nucleotide variant	NM_001004334.4(GPR179):c.4050G>A (p.Gly1350=)	not provided [RCV002076244]	likely benign	17	38329519	38329519	Human		name
152127565	CV1581127	single nucleotide variant	NM_001004334.4(GPR179):c.4899A>G (p.Thr1633=)	not provided [RCV002099031]	likely benign	17	38328670	38328670	Human		name
152107244	CV1581853	single nucleotide variant	NM_001004334.4(GPR179):c.6924T>G (p.Gly2308=)	not provided [RCV002079773]	likely benign	17	38326645	38326645	Human		name
152044519	CV1584340	single nucleotide variant	NM_001004334.4(GPR179):c.4917G>A (p.Glu1639=)	not provided [RCV002071435]	likely benign	17	38328652	38328652	Human		name
152044562	CV1584353	single nucleotide variant	NM_001004334.4(GPR179):c.3861A>G (p.Gln1287=)	not provided [RCV002071440]	likely benign	17	38329708	38329708	Human		name
152162578	CV1584882	single nucleotide variant	NM_001004334.4(GPR179):c.5295G>C (p.Gly1765=)	not provided [RCV002123471]	likely benign	17	38328274	38328274	Human		name
152090821	CV1602763	single nucleotide variant	NM_001004334.4(GPR179):c.6471T>C (p.Leu2157=)	not provided [RCV002194274]	likely benign	17	38327098	38327098	Human		name
152077443	CV1604754	single nucleotide variant	NM_001004334.4(GPR179):c.3816A>G (p.Gly1272=)	not provided [RCV002092414]	likely benign	17	38329753	38329753	Human		name
152162085	CV1606263	single nucleotide variant	NM_001004334.4(GPR179):c.6045G>A (p.Lys2015=)	not provided [RCV002181107]	likely benign	17	38327524	38327524	Human		name
152119812	CV1612109	single nucleotide variant	NM_001004334.4(GPR179):c.3231C>T (p.Ala1077=)	not provided [RCV002135565]	likely benign	17	38330338	38330338	Human		name
152140851	CV1613920	single nucleotide variant	NM_001004334.4(GPR179):c.4314C>T (p.Pro1438=)	not provided [RCV002084136]	likely benign	17	38329255	38329255	Human		name
152042166	CV1618007	single nucleotide variant	NM_001004334.4(GPR179):c.3930A>G (p.Pro1310=)	not provided [RCV002206490]	likely benign	17	38329639	38329639	Human		name
152057077	CV1618814	single nucleotide variant	NM_001004334.4(GPR179):c.5563C>T (p.Leu1855=)	not provided [RCV002127910]	likely benign	17	38328006	38328006	Human		name
152163950	CV1619134	single nucleotide variant	NM_001004334.4(GPR179):c.3807G>A (p.Thr1269=)	not provided [RCV002123704]	likely benign	17	38329762	38329762	Human		name
152164070	CV1619620	single nucleotide variant	NM_001004334.4(GPR179):c.4407T>C (p.Asp1469=)	not provided [RCV002181462]	likely benign	17	38329162	38329162	Human		name
152147880	CV1623670	single nucleotide variant	NM_001004334.4(GPR179):c.4599G>A (p.Glu1533=)	not provided [RCV002157712]	likely benign	17	38328970	38328970	Human		name
152150085	CV1625677	single nucleotide variant	NM_001004334.4(GPR179):c.4140G>A (p.Pro1380=)	not provided [RCV002139385]	benign	17	38329429	38329429	Human		name
152104033	CV1625696	single nucleotide variant	NM_001004334.4(GPR179):c.3678C>T (p.Pro1226=)	not provided [RCV002152157]	likely benign	17	38329891	38329891	Human		name
152087951	CV1626046	single nucleotide variant	NM_001004334.4(GPR179):c.3480C>T (p.His1160=)	not provided [RCV002131682]	likely benign	17	38330089	38330089	Human		name
152152217	CV1626840	single nucleotide variant	NM_001004334.4(GPR179):c.5526G>A (p.Gln1842=)	not provided [RCV002202144]	likely benign	17	38328043	38328043	Human		name
152146413	CV1631649	single nucleotide variant	NM_001004334.4(GPR179):c.4650A>G (p.Leu1550=)	not provided [RCV002157503]	likely benign	17	38328919	38328919	Human		name
152030611	CV1632235	single nucleotide variant	NM_001004334.4(GPR179):c.3186C>T (p.Asp1062=)	not provided [RCV002124370]	likely benign	17	38330383	38330383	Human		name
152075828	CV1635477	single nucleotide variant	NM_001004334.4(GPR179):c.3144C>T (p.Asp1048=)	not provided [RCV002092205]	likely benign	17	38330425	38330425	Human		name
152162512	CV1635753	single nucleotide variant	NM_001004334.4(GPR179):c.6441A>G (p.Arg2147=)	not provided [RCV002203679]	likely benign	17	38327128	38327128	Human		name
152134986	CV1638476	single nucleotide variant	NM_001004334.4(GPR179):c.4125C>T (p.Ile1375=)	not provided [RCV002083382]	likely benign	17	38329444	38329444	Human		name
152142504	CV1639245	single nucleotide variant	NM_001004334.4(GPR179):c.3897C>T (p.Pro1299=)	not provided [RCV002178243]	likely benign	17	38329672	38329672	Human		name
152125481	CV1640623	single nucleotide variant	NM_001004334.4(GPR179):c.4692T>C (p.Asn1564=)	not provided [RCV002176124]	likely benign	17	38328877	38328877	Human		name
152039234	CV1643890	single nucleotide variant	NM_001004334.4(GPR179):c.3387G>A (p.Ser1129=)	not provided [RCV002125834]	benign	17	38330182	38330182	Human		name
152117963	CV1643978	single nucleotide variant	NM_001004334.4(GPR179):c.6723C>T (p.Ile2241=)	not provided [RCV002135341]	likely benign	17	38326846	38326846	Human		name
152167905	CV1644915	single nucleotide variant	NM_001004334.4(GPR179):c.6381A>G (p.Lys2127=)	not provided [RCV002142277]	likely benign	17	38327188	38327188	Human		name
152085645	CV1645244	single nucleotide variant	NM_001004334.4(GPR179):c.4023C>A (p.Gly1341=)	not provided [RCV002131392]	likely benign	17	38329546	38329546	Human		name
152065556	CV1646849	single nucleotide variant	NM_001004334.4(GPR179):c.3345C>T (p.Asn1115=)	not provided [RCV002128923]	likely benign	17	38330224	38330224	Human		name
152144032	CV1651593	single nucleotide variant	NM_001004334.4(GPR179):c.4458C>T (p.Asn1486=)	not provided [RCV002138543]	likely benign	17	38329111	38329111	Human		name
152148117	CV1653870	single nucleotide variant	NM_001004334.4(GPR179):c.3444T>C (p.Asp1148=)	not provided [RCV002139108]	likely benign	17	38330125	38330125	Human		name
152169112	CV1661024	single nucleotide variant	NM_001004334.4(GPR179):c.6495G>A (p.Thr2165=)	not provided [RCV002142678]	likely benign	17	38327074	38327074	Human		name
152169314	CV1661291	single nucleotide variant	NM_001004334.4(GPR179):c.4749G>A (p.Gln1583=)	not provided [RCV002142748]	likely benign	17	38328820	38328820	Human		name
152133212	CV1666226	single nucleotide variant	NM_001004334.4(GPR179):c.3759G>A (p.Thr1253=)	not provided [RCV002099765]	likely benign	17	38329810	38329810	Human		name
10044986	CV188881	single nucleotide variant	NM_001004334.4(GPR179):c.349G>A (p.Asp117Asn)	Congenital stationary night blindness 1E [RCV003989479]\|not provided [RCV000171255]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	17	38343441	38343441	Human	1	name
156333543	CV1954271	single nucleotide variant	NM_001004334.4(GPR179):c.6972A>G (p.Leu2324=)	not provided [RCV002580130]	likely benign	17	38326597	38326597	Human		name
156174906	CV1956515	single nucleotide variant	NM_001004334.4(GPR179):c.4914T>C (p.Pro1638=)	not provided [RCV002573927]	likely benign	17	38328655	38328655	Human		name
156407945	CV1957661	single nucleotide variant	NM_001004334.4(GPR179):c.599G>A (p.Arg200Gln)	not provided [RCV002586371]	uncertain significance	17	38343191	38343191	Human		name
156136208	CV1962931	single nucleotide variant	NM_001004334.4(GPR179):c.3543G>A (p.Arg1181=)	not provided [RCV002572404]	likely benign	17	38330026	38330026	Human		name
156252648	CV1963909	single nucleotide variant	NM_001004334.4(GPR179):c.4104A>C (p.Pro1368=)	not provided [RCV002576591]	likely benign	17	38329465	38329465	Human		name
156350921	CV1965416	single nucleotide variant	NM_001004334.4(GPR179):c.958C>T (p.Arg320Ter)	Congenital stationary night blindness 1E [RCV005412425]\|Retinal dystrophy [RCV004817053]\|not provided [RCV002581055]	pathogenic\|likely pathogenic	17	38337666	38337666	Human	3	name
156412528	CV1968715	single nucleotide variant	NM_001004334.4(GPR179):c.3657T>C (p.Pro1219=)	not provided [RCV002608569]	likely benign	17	38329912	38329912	Human		name
156417062	CV1970183	single nucleotide variant	NM_001004334.4(GPR179):c.751G>A (p.Ala251Thr)	Inborn genetic diseases [RCV003289539]\|not provided [RCV002590011]	uncertain significance	17	38343039	38343039	Human	1	name
156270001	CV1970906	single nucleotide variant	NM_001004334.4(GPR179):c.3333C>T (p.Pro1111=)	not provided [RCV002598059]	likely benign	17	38330236	38330236	Human		name
156411983	CV1972948	single nucleotide variant	NM_001004334.4(GPR179):c.749C>A (p.Ser250Tyr)	not provided [RCV002587668]	uncertain significance	17	38343041	38343041	Human		name
156053170	CV1974454	single nucleotide variant	NM_001004334.4(GPR179):c.5724G>A (p.Leu1908=)	not provided [RCV002590727]	likely benign	17	38327845	38327845	Human		name
156191627	CV1974480	single nucleotide variant	NM_001004334.4(GPR179):c.5679C>T (p.Asp1893=)	not provided [RCV002625438]	likely benign	17	38327890	38327890	Human		name
156315956	CV1974784	single nucleotide variant	NM_001004334.4(GPR179):c.3081C>G (p.Ala1027=)	not provided [RCV002630063]	likely benign	17	38330488	38330488	Human		name
156382814	CV1975244	single nucleotide variant	NM_001004334.4(GPR179):c.4941G>A (p.Ala1647=)	not provided [RCV002604088]	likely benign	17	38328628	38328628	Human		name
156130702	CV1977022	single nucleotide variant	NM_001004334.4(GPR179):c.5706G>A (p.Val1902=)	not provided [RCV002593484]	likely benign	17	38327863	38327863	Human		name
156059106	CV1978870	single nucleotide variant	NM_001004334.4(GPR179):c.4713G>A (p.Gln1571=)	not provided [RCV002590916]	likely benign	17	38328856	38328856	Human		name
156413557	CV1979054	single nucleotide variant	NM_001004334.4(GPR179):c.382G>A (p.Glu128Lys)	not provided [RCV002608877]	uncertain significance	17	38343408	38343408	Human		name
155910102	CV1980074	single nucleotide variant	NM_001004334.4(GPR179):c.4308G>C (p.Arg1436=)	not provided [RCV002613923]	likely benign	17	38329261	38329261	Human		name
155999643	CV1987093	single nucleotide variant	NM_001004334.4(GPR179):c.3183G>A (p.Val1061=)	not provided [RCV002618385]	likely benign	17	38330386	38330386	Human		name
156415731	CV1987465	single nucleotide variant	NM_001004334.4(GPR179):c.4461G>A (p.Val1487=)	not provided [RCV002609806]	likely benign	17	38329108	38329108	Human		name
156107624	CV1988509	single nucleotide variant	NM_001004334.4(GPR179):c.431T>C (p.Val144Ala)	Inborn genetic diseases [RCV002605725]\|not provided [RCV002622448]	likely benign\|uncertain significance	17	38343359	38343359	Human	1	name
156391433	CV1990180	single nucleotide variant	NM_001004334.4(GPR179):c.5511T>C (p.Ser1837=)	not provided [RCV002604705]	likely benign	17	38328058	38328058	Human		name
156127132	CV1993067	single nucleotide variant	NM_001004334.4(GPR179):c.4662A>C (p.Ser1554=)	not provided [RCV002623170]	likely benign	17	38328907	38328907	Human		name
156404535	CV1993388	single nucleotide variant	NM_001004334.4(GPR179):c.6813T>C (p.Pro2271=)	not provided [RCV002658076]	likely benign	17	38326756	38326756	Human		name
156030131	CV2001094	single nucleotide variant	NM_001004334.4(GPR179):c.3936G>A (p.Arg1312=)	not provided [RCV002658625]	likely benign	17	38329633	38329633	Human		name
156108271	CV2002143	single nucleotide variant	NM_001004334.4(GPR179):c.5391G>A (p.Arg1797=)	not provided [RCV002639838]	likely benign	17	38328178	38328178	Human		name
156087172	CV2008811	single nucleotide variant	NM_001004334.4(GPR179):c.4971C>A (p.Gly1657=)	not provided [RCV002706184]	likely benign	17	38328598	38328598	Human		name
156200662	CV2010888	single nucleotide variant	NM_001004334.4(GPR179):c.4902T>A (p.Ala1634=)	not provided [RCV002700268]	likely benign	17	38328667	38328667	Human		name
156278873	CV2011497	single nucleotide variant	NM_001004334.4(GPR179):c.3078A>C (p.Arg1026=)	not provided [RCV002715231]	likely benign	17	38330491	38330491	Human		name
156271586	CV2018329	single nucleotide variant	NM_001004334.4(GPR179):c.4359G>C (p.Gly1453=)	not provided [RCV002714999]	likely benign	17	38329210	38329210	Human		name
156210068	CV2018827	single nucleotide variant	NM_001004334.4(GPR179):c.988G>C (p.Gly330Arg)	not provided [RCV002700593]	uncertain significance	17	38337636	38337636	Human		name
156163378	CV2019565	single nucleotide variant	NM_001004334.4(GPR179):c.962C>G (p.Pro321Arg)	not provided [RCV002710255]	uncertain significance	17	38337662	38337662	Human		name
156367561	CV2021029	single nucleotide variant	NM_001004334.4(GPR179):c.5739G>A (p.Lys1913=)	not provided [RCV002721285]	likely benign	17	38327830	38327830	Human		name
155980546	CV2025098	single nucleotide variant	NM_001004334.4(GPR179):c.825G>C (p.Gln275His)	not provided [RCV002755306]	uncertain significance	17	38339495	38339495	Human		name
156320125	CV2025280	single nucleotide variant	NM_001004334.4(GPR179):c.3438C>T (p.Pro1146=)	not provided [RCV002717035]	likely benign	17	38330131	38330131	Human		name
156047896	CV2030974	single nucleotide variant	NM_001004334.4(GPR179):c.7056G>A (p.Gln2352=)	not provided [RCV002736412]	likely benign	17	38326513	38326513	Human		name
156032505	CV2037026	single nucleotide variant	NM_001004334.4(GPR179):c.3669G>A (p.Gln1223=)	not provided [RCV002781168]	likely benign	17	38329900	38329900	Human		name
156258802	CV2037576	single nucleotide variant	NM_001004334.4(GPR179):c.6924T>C (p.Gly2308=)	not provided [RCV002806255]	likely benign	17	38326645	38326645	Human		name
156136821	CV2040523	single nucleotide variant	NM_001004334.4(GPR179):c.6885C>G (p.Pro2295=)	not provided [RCV002786378]	likely benign	17	38326684	38326684	Human		name
156010424	CV2051385	single nucleotide variant	NM_001004334.4(GPR179):c.3402G>A (p.Arg1134=)	not provided [RCV002820093]	likely benign	17	38330167	38330167	Human		name
155939939	CV2054871	single nucleotide variant	NM_001004334.4(GPR179):c.487G>A (p.Ala163Thr)	not provided [RCV002815624]	uncertain significance	17	38343303	38343303	Human		name
156268611	CV2059727	single nucleotide variant	NM_001004334.4(GPR179):c.4113T>C (p.His1371=)	not provided [RCV002806581]	likely benign	17	38329456	38329456	Human		name
156019026	CV2061813	single nucleotide variant	NM_001004334.4(GPR179):c.5220C>G (p.Pro1740=)	not provided [RCV002820522]	likely benign	17	38328349	38328349	Human		name
155973471	CV2062615	single nucleotide variant	NM_001004334.4(GPR179):c.4116C>T (p.Thr1372=)	not provided [RCV002842185]	likely benign	17	38329453	38329453	Human		name
155933813	CV2067517	single nucleotide variant	NM_001004334.4(GPR179):c.958C>G (p.Arg320Gly)	not provided [RCV002838932]	uncertain significance	17	38337666	38337666	Human		name
156303132	CV2070054	duplication	NM_001004334.4(GPR179):c.2523dup (p.Ser842fs)	not provided [RCV002833722]	uncertain significance	17	38331045	38331046	Human		name
156218049	CV2070757	single nucleotide variant	NM_001004334.4(GPR179):c.6108T>C (p.Asp2036=)	not provided [RCV002829576]	likely benign	17	38327461	38327461	Human		name
156109220	CV2072585	single nucleotide variant	NM_001004334.4(GPR179):c.6945T>C (p.Pro2315=)	not provided [RCV002870827]	likely benign	17	38326624	38326624	Human		name
156205773	CV2076701	single nucleotide variant	NM_001004334.4(GPR179):c.4803A>G (p.Thr1601=)	not provided [RCV002852634]	likely benign	17	38328766	38328766	Human		name
156209729	CV2076891	single nucleotide variant	NM_001004334.4(GPR179):c.5007G>A (p.Glu1669=)	not provided [RCV002852779]	likely benign	17	38328562	38328562	Human		name
156140113	CV2082275	single nucleotide variant	NM_001004334.4(GPR179):c.6528C>A (p.Pro2176=)	not provided [RCV002871952]	likely benign	17	38327041	38327041	Human		name
156009846	CV2083345	single nucleotide variant	NM_001004334.4(GPR179):c.4920G>A (p.Gly1640=)	not provided [RCV002866045]	likely benign	17	38328649	38328649	Human		name
156226678	CV2088792	single nucleotide variant	NM_001004334.4(GPR179):c.5160A>G (p.Gly1720=)	not provided [RCV002876079]	likely benign	17	38328409	38328409	Human		name
156049549	CV2093449	single nucleotide variant	NM_001004334.4(GPR179):c.6528C>G (p.Pro2176=)	not provided [RCV002867740]	likely benign	17	38327041	38327041	Human		name
156227093	CV2097487	single nucleotide variant	NM_001004334.4(GPR179):c.5961G>C (p.Leu1987=)	not provided [RCV002894410]	likely benign	17	38327608	38327608	Human		name
156234313	CV2108765	single nucleotide variant	NM_001004334.4(GPR179):c.548T>C (p.Val183Ala)	not provided [RCV002932960]	uncertain significance	17	38343242	38343242	Human		name
156166824	CV2133408	deletion	NM_001004334.4(GPR179):c.1250del (p.Val417fs)	not provided [RCV003005262]	pathogenic	17	38336122	38336122	Human		name
155904819	CV2137636	single nucleotide variant	NM_001004334.4(GPR179):c.640T>C (p.Trp214Arg)	not provided [RCV003011855]	uncertain significance	17	38343150	38343150	Human		name
156316952	CV2137780	single nucleotide variant	NM_001004334.4(GPR179):c.5322G>A (p.Gln1774=)	not provided [RCV002962959]	likely benign	17	38328247	38328247	Human		name
156104271	CV2139818	single nucleotide variant	NM_001004334.4(GPR179):c.5877A>G (p.Pro1959=)	not provided [RCV003002334]	likely benign	17	38327692	38327692	Human		name
156093363	CV2143146	single nucleotide variant	NM_001004334.4(GPR179):c.3255C>T (p.Arg1085=)	not provided [RCV002979695]	likely benign	17	38330314	38330314	Human		name
156246318	CV2145464	single nucleotide variant	NM_001004334.4(GPR179):c.6540G>A (p.Glu2180=)	not provided [RCV003008282]	likely benign	17	38327029	38327029	Human		name
156058020	CV2151384	duplication	NM_001004334.4(GPR179):c.357dup (p.Glu120Ter)	not provided [RCV003019629]	pathogenic	17	38343432	38343433	Human		name
156325819	CV2159889	single nucleotide variant	NM_001004334.4(GPR179):c.3624G>A (p.Arg1208=)	not provided [RCV003029481]	likely benign	17	38329945	38329945	Human		name
156142018	CV2163798	single nucleotide variant	NM_001004334.4(GPR179):c.5973G>T (p.Gly1991=)	not provided [RCV003022555]	likely benign	17	38327596	38327596	Human		name
156208866	CV2165170	single nucleotide variant	NM_001004334.4(GPR179):c.5346T>C (p.Asp1782=)	not provided [RCV003024728]	likely benign	17	38328223	38328223	Human		name
156095355	CV2167327	single nucleotide variant	NM_001004334.4(GPR179):c.926G>C (p.Gly309Ala)	not provided [RCV003038370]	uncertain significance	17	38337698	38337698	Human		name
156344212	CV2176200	single nucleotide variant	NM_001004334.4(GPR179):c.4572A>G (p.Ala1524=)	not provided [RCV003030466]	likely benign	17	38328997	38328997	Human		name
156253788	CV2185136	single nucleotide variant	NM_001004334.4(GPR179):c.5491T>C (p.Leu1831=)	not provided [RCV003043886]	likely benign	17	38328078	38328078	Human		name
156147277	CV2188424	single nucleotide variant	NM_001004334.4(GPR179):c.3324G>A (p.Glu1108=)	not provided [RCV003056404]	likely benign	17	38330245	38330245	Human		name
156292069	CV2192436	single nucleotide variant	NM_001004334.4(GPR179):c.6438A>G (p.Glu2146=)	not provided [RCV003045182]	likely benign	17	38327131	38327131	Human		name
156250398	CV2232167	single nucleotide variant	NM_001004334.4(GPR179):c.472A>G (p.Ser158Gly)	Inborn genetic diseases [RCV002713940]	uncertain significance	17	38343318	38343318	Human	1	name
329399955	CV2444426	single nucleotide variant	NM_001004334.4(GPR179):c.316G>T (p.Ala106Ser)	Inborn genetic diseases [RCV003196961]	uncertain significance	17	38343474	38343474	Human	1	name
11639041	CV267422	single nucleotide variant	NM_001004334.4(GPR179):c.5019C>G (p.Thr1673=)	Congenital stationary night blindness 1E [RCV001128027]\|not provided [RCV001523386]\|not specified [RCV000313135]	benign\|likely benign	17	38328550	38328550	Human	1	name
401781875	CV2689975	single nucleotide variant	NM_001004334.4(GPR179):c.449C>T (p.Thr150Ile)	Inborn genetic diseases [RCV003265436]	uncertain significance	17	38343341	38343341	Human	1	name
11637677	CV269509	single nucleotide variant	NM_001004334.4(GPR179):c.415G>A (p.Glu139Lys)	Inborn genetic diseases [RCV003243042]\|not provided [RCV000290054]	uncertain significance	17	38343375	38343375	Human	1	name
11579979	CV272088	single nucleotide variant	NM_001004334.4(GPR179):c.673C>T (p.Gln225Ter)	not provided [RCV000319046]	pathogenic	17	38343117	38343117	Human		name
11643141	CV272089	single nucleotide variant	NM_001004334.4(GPR179):c.320A>G (p.Asn107Ser)	not provided [RCV000387552]	uncertain significance	17	38343470	38343470	Human		name
401773915	CV2727672	single nucleotide variant	NM_001004334.4(GPR179):c.964G>A (p.Gly322Arg)	Inborn genetic diseases [RCV003305124]	uncertain significance	17	38337660	38337660	Human	1	name
401881670	CV2783916	single nucleotide variant	NM_001004334.4(GPR179):c.965G>A (p.Gly322Glu)	Inborn genetic diseases [RCV003385437]	uncertain significance	17	38337659	38337659	Human	1	name
405207616	CV2909084	single nucleotide variant	NM_001004334.4(GPR179):c.5241T>A (p.Ala1747=)	not provided [RCV003566708]	likely benign	17	38328328	38328328	Human		name
402480602	CV2910966	single nucleotide variant	NM_001004334.4(GPR179):c.4380T>A (p.Ala1460=)	not provided [RCV003572035]	likely benign	17	38329189	38329189	Human		name
402506038	CV2927824	deletion	NM_001004334.4(GPR179):c.2056del (p.Tyr686fs)	not provided [RCV003574466]	uncertain significance	17	38331513	38331513	Human		name
402490441	CV2949000	single nucleotide variant	NM_001004334.4(GPR179):c.5307A>G (p.Pro1769=)	not provided [RCV003660496]	likely benign	17	38328262	38328262	Human		name
405119122	CV2949599	single nucleotide variant	NM_001004334.4(GPR179):c.5790C>T (p.Thr1930=)	not provided [RCV003667074]	likely benign	17	38327779	38327779	Human		name
405246759	CV2966442	deletion	NM_001004334.4(GPR179):c.1005del (p.Ser335fs)	not provided [RCV003685503]	pathogenic	17	38337200	38337200	Human		name
405244219	CV2968101	single nucleotide variant	NM_001004334.4(GPR179):c.580A>G (p.Thr194Ala)	not provided [RCV003684787]	uncertain significance	17	38343210	38343210	Human		name
405197390	CV2972810	single nucleotide variant	NM_001004334.4(GPR179):c.6015A>G (p.Ala2005=)	not provided [RCV003677813]	likely benign	17	38327554	38327554	Human		name
405063868	CV3020697	single nucleotide variant	NM_001004334.4(GPR179):c.4875A>G (p.Gly1625=)	not provided [RCV003697886]	likely benign	17	38328694	38328694	Human		name
405159607	CV3021347	single nucleotide variant	NM_001004334.4(GPR179):c.3234T>C (p.Pro1078=)	not provided [RCV003703867]	likely benign	17	38330335	38330335	Human		name
405219159	CV3035008	single nucleotide variant	NM_001004334.4(GPR179):c.4461G>T (p.Val1487=)	not provided [RCV003709713]	likely benign	17	38329108	38329108	Human		name
405221787	CV3038631	single nucleotide variant	NM_001004334.4(GPR179):c.595A>T (p.Lys199Ter)	not provided [RCV003710083]	pathogenic	17	38343195	38343195	Human		name
405103180	CV3119576	single nucleotide variant	NM_001004334.4(GPR179):c.4695A>C (p.Gly1565=)	not provided [RCV003811838]	likely benign	17	38328874	38328874	Human		name
405011048	CV3128049	single nucleotide variant	NM_001004334.4(GPR179):c.3018T>C (p.Asn1006=)	not provided [RCV003828929]	likely benign	17	38330551	38330551	Human		name
405119992	CV3131389	single nucleotide variant	NM_001004334.4(GPR179):c.6405G>A (p.Ala2135=)	not provided [RCV003837253]	likely benign	17	38327164	38327164	Human		name
405123204	CV3131716	single nucleotide variant	NM_001004334.4(GPR179):c.6729T>G (p.Pro2243=)	not provided [RCV003837580]	likely benign	17	38326840	38326840	Human		name
405110436	CV3136890	single nucleotide variant	NM_001004334.4(GPR179):c.4449G>A (p.Leu1483=)	not provided [RCV003836044]	likely benign	17	38329120	38329120	Human		name
405217664	CV3143748	single nucleotide variant	NM_001004334.4(GPR179):c.506C>G (p.Thr169Ser)	not provided [RCV003846718]	uncertain significance	17	38343284	38343284	Human		name
405057217	CV3147772	single nucleotide variant	NM_001004334.4(GPR179):c.5691C>T (p.Ser1897=)	not provided [RCV003850002]	likely benign	17	38327878	38327878	Human		name
405159641	CV3152931	single nucleotide variant	NM_001004334.4(GPR179):c.3270G>A (p.Ala1090=)	not provided [RCV003840666]	likely benign	17	38330299	38330299	Human		name
405191821	CV3157129	single nucleotide variant	NM_001004334.4(GPR179):c.3828G>A (p.Ser1276=)	not provided [RCV003859817]	likely benign	17	38329741	38329741	Human		name
405223114	CV3158306	single nucleotide variant	NM_001004334.4(GPR179):c.5916A>G (p.Leu1972=)	not provided [RCV003863802]	likely benign	17	38327653	38327653	Human		name
405237453	CV3169230	single nucleotide variant	NM_001004334.4(GPR179):c.4818A>G (p.Thr1606=)	not provided [RCV003866509]	likely benign	17	38328751	38328751	Human		name
405000061	CV3173128	deletion	NM_001004334.4(GPR179):c.1000del (p.Glu334fs)	not provided [RCV003882411]	pathogenic	17	38337205	38337205	Human		name
405738470	CV3255340	single nucleotide variant	NM_001004334.4(GPR179):c.644C>T (p.Pro215Leu)	Inborn genetic diseases [RCV004390967]	uncertain significance	17	38343146	38343146	Human	1	name
11624509	CV328319	single nucleotide variant	NM_001004334.4(GPR179):c.691C>T (p.Pro231Ser)	Congenital stationary night blindness 1E [RCV000386648]\|not provided [RCV001522219]	benign\|uncertain significance	17	38343099	38343099	Human	1	name
11625532	CV328324	single nucleotide variant	NM_001004334.4(GPR179):c.654T>G (p.Asp218Glu)	Congenital stationary night blindness 1E [RCV000399798]\|not provided [RCV001516531]	benign\|likely benign	17	38343136	38343136	Human	1	name
11618701	CV338178	single nucleotide variant	NM_001004334.4(GPR179):c.5982C>T (p.Ala1994=)	Congenital stationary night blindness 1E [RCV000316820]\|Retinal dystrophy [RCV004816566]\|not provided [RCV000733442]	conflicting interpretations of pathogenicity\|uncertain significance	17	38327587	38327587	Human	3	name
11612508	CV338237	single nucleotide variant	NM_001004334.4(GPR179):c.921T>A (p.Ser307Arg)	Congenital stationary night blindness 1E [RCV000259989]\|not provided [RCV001512248]	benign\|uncertain significance	17	38337703	38337703	Human	1	name
11650960	CV338239	single nucleotide variant	NM_001004334.4(GPR179):c.810G>A (p.Met270Ile)	Congenital Stationary Night Blindness, Recessive [RCV000295948]	uncertain significance	17	38339510	38339510	Human	1	name
405855273	CV3394035	deletion	NM_001004334.4(GPR179):c.1144del (p.Ala382fs)	Congenital stationary night blindness 1B [RCV004547261]	likely pathogenic	17	38337061	38337061	Human	1	name
596942061	CV3408419	single nucleotide variant	NM_001004334.4(GPR179):c.349G>T (p.Asp117Tyr)	Retinal dystrophy [RCV004816090]	uncertain significance	17	38343441	38343441	Human	2	name
596944570	CV3408896	single nucleotide variant	NM_001004334.4(GPR179):c.362C>T (p.Ser121Phe)	Optic atrophy [RCV004817549]\|not provided [RCV005059580]	uncertain significance	17	38343428	38343428	Human	2	name
11631958	CV344293	single nucleotide variant	NM_001004334.4(GPR179):c.7035C>T (p.Gly2345=)	Congenital stationary night blindness 1E [RCV000393492]\|not provided [RCV002056575]	likely benign\|uncertain significance	17	38326534	38326534	Human	1	name
11628654	CV344297	single nucleotide variant	NM_001004334.4(GPR179):c.6621C>T (p.Ser2207=)	Congenital stationary night blindness 1E [RCV000306010]\|not provided [RCV005055880]	likely benign\|uncertain significance	17	38326948	38326948	Human	1	name
11628288	CV344308	single nucleotide variant	NM_001004334.4(GPR179):c.3357G>A (p.Ala1119=)	Congenital stationary night blindness 1E [RCV000298512]\|not provided [RCV002056584]	likely benign\|uncertain significance	17	38330212	38330212	Human	1	name
11626563	CV344327	single nucleotide variant	NM_001004334.4(GPR179):c.989G>T (p.Gly330Val)	Congenital stationary night blindness 1E [RCV000265836]\|Inborn genetic diseases [RCV004021701]\|not provided [RCV001338272]	uncertain significance	17	38337635	38337635	Human	2	name
11630422	CV345700	single nucleotide variant	NM_001004334.4(GPR179):c.7080T>G (p.Thr2360=)	Congenital stationary night blindness 1E [RCV000349058]\|not provided [RCV001522894]	benign\|likely benign	17	38326489	38326489	Human	1	name
11631374	CV345761	single nucleotide variant	NM_001004334.4(GPR179):c.973G>A (p.Gly325Arg)	Congenital stationary night blindness 1E [RCV000375619]\|Inborn genetic diseases [RCV002522951]\|not provided [RCV001795942]	likely benign\|uncertain significance	17	38337651	38337651	Human	2	name
11630370	CV345765	single nucleotide variant	NM_001004334.4(GPR179):c.725G>A (p.Arg242Gln)	Congenital stationary night blindness 1E [RCV000348476]\|not provided [RCV001397404]	likely benign\|uncertain significance	17	38343065	38343065	Human	1	name
408387315	CV3527019	single nucleotide variant	NM_001004334.4(GPR179):c.562C>A (p.Pro188Thr)	not provided [RCV004773321]	uncertain significance	17	38343228	38343228	Human		name
596925651	CV3542158	single nucleotide variant	NM_001004334.4(GPR179):c.951C>A (p.Cys317Ter)	Congenital stationary night blindness 1E [RCV004795876]	likely pathogenic	17	38337673	38337673	Human	1	name
596925654	CV3542159	single nucleotide variant	NM_001004334.4(GPR179):c.955T>C (p.Cys319Arg)	Congenital stationary night blindness 1E [RCV004795877]	uncertain significance	17	38337669	38337669	Human	1	name
597680892	CV3684920	single nucleotide variant	NM_001004334.4(GPR179):c.644C>A (p.Pro215Gln)	Inborn genetic diseases [RCV004982743]	uncertain significance	17	38343146	38343146	Human	1	name
597683779	CV3684929	single nucleotide variant	NM_001004334.4(GPR179):c.837C>G (p.Ile279Met)	Inborn genetic diseases [RCV004983770]	uncertain significance	17	38339483	38339483	Human	1	name
597932513	CV3742561	single nucleotide variant	NM_001004334.4(GPR179):c.4887C>T (p.Ile1629=)	not provided [RCV005076000]	likely benign	17	38328682	38328682	Human		name
597860296	CV3748658	single nucleotide variant	NM_001004334.4(GPR179):c.6375C>G (p.Ala2125=)	not provided [RCV005067290]	likely benign	17	38327194	38327194	Human		name
597909574	CV3749546	single nucleotide variant	NM_001004334.4(GPR179):c.5973G>A (p.Gly1991=)	not provided [RCV005073394]	likely benign	17	38327596	38327596	Human		name
597965212	CV3751115	single nucleotide variant	NM_001004334.4(GPR179):c.5547G>A (p.Lys1849=)	not provided [RCV005082677]	likely benign	17	38328022	38328022	Human		name
597966155	CV3751511	single nucleotide variant	NM_001004334.4(GPR179):c.5919C>T (p.Asp1973=)	not provided [RCV005082880]	likely benign	17	38327650	38327650	Human		name
597966803	CV3751668	single nucleotide variant	NM_001004334.4(GPR179):c.5493G>A (p.Leu1831=)	not provided [RCV005083038]	likely benign	17	38328076	38328076	Human		name
597841433	CV3752831	single nucleotide variant	NM_001004334.4(GPR179):c.4770A>G (p.Thr1590=)	not provided [RCV005086560]	likely benign	17	38328799	38328799	Human		name
597962280	CV3753642	single nucleotide variant	NM_001004334.4(GPR179):c.3705C>T (p.Ser1235=)	not provided [RCV005081946]	likely benign	17	38329864	38329864	Human		name
597962510	CV3753673	single nucleotide variant	NM_001004334.4(GPR179):c.502C>T (p.Arg168Trp)	not provided [RCV005081977]	uncertain significance	17	38343288	38343288	Human		name
597950456	CV3759697	single nucleotide variant	NM_001004334.4(GPR179):c.4392G>A (p.Leu1464=)	not provided [RCV005079297]	likely benign	17	38329177	38329177	Human		name
597945014	CV3776757	single nucleotide variant	NM_001004334.4(GPR179):c.5133T>G (p.Ala1711=)	not provided [RCV005119613]	likely benign	17	38328436	38328436	Human		name
597900936	CV3796381	single nucleotide variant	NM_001004334.4(GPR179):c.6132G>A (p.Glu2044=)	not provided [RCV005152464]	likely benign	17	38327437	38327437	Human		name
597892240	CV3803829	single nucleotide variant	NM_001004334.4(GPR179):c.6318T>C (p.Ser2106=)	not provided [RCV005151390]	likely benign	17	38327251	38327251	Human		name
597950629	CV3815179	single nucleotide variant	NM_001004334.4(GPR179):c.5598G>A (p.Leu1866=)	not provided [RCV005161129]	likely benign	17	38327971	38327971	Human		name
597946756	CV3817761	single nucleotide variant	NM_001004334.4(GPR179):c.3339G>A (p.Gly1113=)	not provided [RCV005160228]	likely benign	17	38330230	38330230	Human		name
597863752	CV3823046	single nucleotide variant	NM_001004334.4(GPR179):c.6159G>A (p.Glu2053=)	not provided [RCV005175396]	likely benign	17	38327410	38327410	Human		name
597972546	CV3823397	duplication	NM_001004334.4(GPR179):c.1874dup (p.Ile626fs)	not provided [RCV005167493]	pathogenic	17	38333948	38333949	Human		name
597975289	CV3832319	single nucleotide variant	NM_001004334.4(GPR179):c.6981G>A (p.Glu2327=)	not provided [RCV005169056]	likely benign	17	38326588	38326588	Human		name
597886317	CV3854928	single nucleotide variant	NM_001004334.4(GPR179):c.3060C>T (p.His1020=)	not provided [RCV005199774]	likely benign	17	38330509	38330509	Human		name
597869714	CV3858479	single nucleotide variant	NM_001004334.4(GPR179):c.6861T>C (p.Phe2287=)	not provided [RCV005197222]	likely benign	17	38326708	38326708	Human		name
8568857	CV40159	single nucleotide variant	NM_001004334.4(GPR179):c.598C>T (p.Arg200Ter)	Congenital stationary night blindness 1E [RCV000024201]	pathogenic	17	38343192	38343192	Human	1	name
8568861	CV40163	single nucleotide variant	NM_001004334.4(GPR179):c.659A>G (p.Tyr220Cys)	Congenital stationary night blindness 1E [RCV000024205]\|not provided [RCV000059655]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	17	38343131	38343131	Human	1	name
12906221	CV415553	duplication	NM_001004334.4(GPR179):c.2427dup (p.Pro810fs)	not provided [RCV000488964]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	17	38331141	38331142	Human		name
13515260	CV488915	single nucleotide variant	NM_001004334.4(GPR179):c.5058C>T (p.Ala1686=)	Congenital stationary night blindness 1E [RCV001125926]\|not provided [RCV000594060]	conflicting interpretations of pathogenicity\|uncertain significance	17	38328511	38328511	Human	1	name
13525925	CV512954	single nucleotide variant	NM_001004334.4(GPR179):c.6336G>A (p.Ala2112=)	Congenital stationary night blindness 1E [RCV000625274]\|not provided [RCV001519808]\|not specified [RCV001700419]	benign\|likely benign	17	38327233	38327233	Human	1	name
13525929	CV512956	single nucleotide variant	NM_001004334.4(GPR179):c.5385C>T (p.Gly1795=)	Congenital stationary night blindness 1E [RCV000625277]\|not provided [RCV001512454]	benign\|likely benign	17	38328184	38328184	Human	1	name
14396348	CV612106	deletion	NM_001004334.4(GPR179):c.1727del (p.Tyr576fs)	Congenital stationary night blindness 1E [RCV000761283]\|not provided [RCV001869039]	pathogenic\|likely pathogenic	17	38334761	38334761	Human	1	name
8624539	CV79650	single nucleotide variant	NM_001004334.4(GPR179):c.376G>C (p.Asp126His)	not provided [RCV000059654]	not provided	17	38343414	38343414	Human		name
28901780	CV877333	single nucleotide variant	NM_001004334.4(GPR179):c.5868C>T (p.Ser1956=)	Congenital stationary night blindness 1E [RCV001124946]\|not provided [RCV001469156]	likely benign\|uncertain significance	17	38327701	38327701	Human	1	name
28901783	CV877334	single nucleotide variant	NM_001004334.4(GPR179):c.5859G>A (p.Glu1953=)	Congenital stationary night blindness 1E [RCV001124947]\|not provided [RCV002070035]	likely benign\|uncertain significance	17	38327710	38327710	Human	1	name
28901787	CV877335	single nucleotide variant	NM_001004334.4(GPR179):c.5769T>C (p.Gly1923=)	Congenital stationary night blindness 1E [RCV001124948]	uncertain significance	17	38327800	38327800	Human	1	name
28894890	CV877348	single nucleotide variant	NM_001004334.4(GPR179):c.4071G>A (p.Lys1357=)	Congenital stationary night blindness 1E [RCV001122272]	uncertain significance	17	38329498	38329498	Human	1	name
28894891	CV877349	single nucleotide variant	NM_001004334.4(GPR179):c.4047G>A (p.Ala1349=)	Congenital stationary night blindness 1E [RCV001122273]\|not provided [RCV002069990]	likely benign\|uncertain significance	17	38329522	38329522	Human	1	name
28902002	CV877350	single nucleotide variant	NM_001004334.4(GPR179):c.3876G>A (p.Glu1292=)	Congenital stationary night blindness 1E [RCV001125047]	uncertain significance	17	38329693	38329693	Human	1	name
28902006	CV877351	single nucleotide variant	NM_001004334.4(GPR179):c.3846C>T (p.Asp1282=)	Congenital stationary night blindness 1E [RCV001125048]	uncertain significance	17	38329723	38329723	Human	1	name
28904295	CV877352	single nucleotide variant	NM_001004334.4(GPR179):c.3699G>T (p.Leu1233=)	Congenital stationary night blindness 1E [RCV001126026]	uncertain significance	17	38329870	38329870	Human	1	name
28908337	CV877357	single nucleotide variant	NM_001004334.4(GPR179):c.3447C>T (p.Asp1149=)	Congenital stationary night blindness 1E [RCV001128127]\|not provided [RCV004694803]	uncertain significance	17	38330122	38330122	Human	1	name
28895177	CV877359	single nucleotide variant	NM_001004334.4(GPR179):c.3411G>A (p.Ala1137=)	Congenital stationary night blindness 1E [RCV001122379]\|not provided [RCV002069993]	likely benign\|uncertain significance	17	38330158	38330158	Human	1	name
28895193	CV877363	single nucleotide variant	NM_001004334.4(GPR179):c.3348C>T (p.Ser1116=)	Congenital stationary night blindness 1E [RCV001122383]\|not provided [RCV002069994]	likely benign\|uncertain significance	17	38330221	38330221	Human	1	name
28904850	CV877382	single nucleotide variant	NM_001004334.4(GPR179):c.983C>T (p.Pro328Leu)	Congenital stationary night blindness 1E [RCV001126251]\|not provided [RCV002556741]	uncertain significance	17	38337641	38337641	Human	1	name
28904854	CV877383	single nucleotide variant	NM_001004334.4(GPR179):c.976G>A (p.Ala326Thr)	Congenital stationary night blindness 1E [RCV001126252]\|not provided [RCV002070063]	likely benign\|uncertain significance	17	38337648	38337648	Human	1	name
28908666	CV877384	single nucleotide variant	NM_001004334.4(GPR179):c.952C>T (p.Arg318Cys)	Congenital stationary night blindness 1E [RCV001128301]	uncertain significance	17	38337672	38337672	Human	1	name
28895749	CV877386	single nucleotide variant	NM_001004334.4(GPR179):c.628G>A (p.Gly210Ser)	Congenital stationary night blindness 1E [RCV001122585]\|not provided [RCV001519513]	benign	17	38343162	38343162	Human	1	name
28898668	CV877387	single nucleotide variant	NM_001004334.4(GPR179):c.508G>C (p.Gly170Arg)	Congenital stationary night blindness 1E [RCV001123664]\|not provided [RCV001516532]	benign	17	38343282	38343282	Human	1	name
126740177	CV1012720	single nucleotide variant	NM_001004334.4(GPR179):c.2583G>T (p.Glu861Asp)	not provided [RCV001325160]	likely benign\|uncertain significance	17	38330986	38330986	Human		name
126731041	CV1021631	deletion	NM_001004334.4(GPR179):c.4867del (p.Met1623fs)	Congenital stationary night blindness, type 1E [RCV001333606]	pathogenic	17	38328702	38328702	Human		name
126731037	CV1021632	duplication	NM_001004334.4(GPR179):c.4550dup (p.Met1517fs)	Congenital stationary night blindness 1E [RCV001808083]\|not provided [RCV001885287]	pathogenic\|likely pathogenic\|uncertain significance	17	38329018	38329019	Human	1	name
126731033	CV1021633	duplication	NM_001004334.4(GPR179):c.3473dup (p.Asn1158fs)	not provided [RCV001994316]	pathogenic\|uncertain significance	17	38330095	38330096	Human		name
126748130	CV1033240	duplication	NM_001004334.4(GPR179):c.5457dup (p.Trp1820fs)	not provided [RCV001337593]	uncertain significance	17	38328111	38328112	Human		name
126759639	CV1033247	single nucleotide variant	NM_001004334.4(GPR179):c.2981C>T (p.Pro994Leu)	Inborn genetic diseases [RCV003246904]\|not provided [RCV001340189]	uncertain significance	17	38330588	38330588	Human	1	name
126728251	CV1033248	single nucleotide variant	NM_001004334.4(GPR179):c.2573A>G (p.Tyr858Cys)	not provided [RCV001348879]	uncertain significance	17	38330996	38330996	Human		name
126747427	CV1033250	single nucleotide variant	NM_001004334.4(GPR179):c.1694G>A (p.Arg565Gln)	not provided [RCV001351668]	uncertain significance	17	38334794	38334794	Human		name
126911037	CV1038522	single nucleotide variant	NM_001004334.4(GPR179):c.1024C>A (p.Gln342Lys)	not provided [RCV001354945]	uncertain significance	17	38337181	38337181	Human		name
126916638	CV1050216	single nucleotide variant	NM_001004334.4(GPR179):c.2584A>C (p.Thr862Pro)	not provided [RCV001360696]	uncertain significance	17	38330985	38330985	Human		name
126910633	CV1050217	single nucleotide variant	NM_001004334.4(GPR179):c.2063A>G (p.Gln688Arg)	not provided [RCV001368892]	uncertain significance	17	38331506	38331506	Human		name
126911030	CV1050218	single nucleotide variant	NM_001004334.4(GPR179):c.1430G>A (p.Arg477Gln)	not provided [RCV001369030]	uncertain significance	17	38335248	38335248	Human		name
127295609	CV1157944	single nucleotide variant	NM_001004334.4(GPR179):c.1478A>G (p.His493Arg)	Retinal dystrophy [RCV004815542]\|not provided [RCV001512256]	benign\|likely benign	17	38335200	38335200	Human	2	name
127314183	CV1157945	single nucleotide variant	NM_001004334.4(GPR179):c.1210C>T (p.Arg404Cys)	Inborn genetic diseases [RCV004037949]\|not provided [RCV001519519]	benign\|uncertain significance	17	38336995	38336995	Human	1	name
150339409	CV1174859	single nucleotide variant	NM_001004334.4(GPR179):c.1818G>A (p.Trp606Ter)	not provided [RCV001543489]	pathogenic\|likely pathogenic	17	38334005	38334005	Human		name
151777792	CV1337017	single nucleotide variant	NM_001004334.4(GPR179):c.2545A>C (p.Lys849Gln)	not provided [RCV002025968]	uncertain significance	17	38331024	38331024	Human		name
151777897	CV1337029	single nucleotide variant	NM_001004334.4(GPR179):c.1751A>C (p.Glu584Ala)	not provided [RCV002025978]	uncertain significance	17	38334737	38334737	Human		name
151881745	CV1339850	single nucleotide variant	NM_001004334.4(GPR179):c.2908C>A (p.Pro970Thr)	Congenital stationary night blindness 1E [RCV005017065]\|not provided [RCV001999692]	uncertain significance	17	38330661	38330661	Human	1	name
151805798	CV1340121	single nucleotide variant	NM_001004334.4(GPR179):c.2662G>A (p.Ala888Thr)	Inborn genetic diseases [RCV002551030]\|not provided [RCV001867541]	uncertain significance	17	38330907	38330907	Human	1	name
151767598	CV1341230	single nucleotide variant	NM_001004334.4(GPR179):c.2611G>A (p.Glu871Lys)	not provided [RCV001863765]	uncertain significance	17	38330958	38330958	Human		name
151775895	CV1342534	single nucleotide variant	NM_001004334.4(GPR179):c.1339G>A (p.Ala447Thr)	not provided [RCV001988682]	uncertain significance	17	38335658	38335658	Human		name
151811263	CV1345286	single nucleotide variant	NM_001004334.4(GPR179):c.2521C>T (p.Leu841Phe)	Inborn genetic diseases [RCV002547948]\|not provided [RCV001878292]	uncertain significance	17	38331048	38331048	Human	1	name
151856734	CV1347815	single nucleotide variant	NM_001004334.4(GPR179):c.1990A>G (p.Ile664Val)	not provided [RCV001979617]	uncertain significance	17	38333298	38333298	Human		name
151829579	CV1348479	single nucleotide variant	NM_001004334.4(GPR179):c.2678G>A (p.Arg893Gln)	not provided [RCV001870401]	uncertain significance	17	38330891	38330891	Human		name
151785858	CV1348841	deletion	NM_001004334.4(GPR179):c.5723del (p.Leu1908fs)	not provided [RCV001897680]	uncertain significance	17	38327846	38327846	Human		name
151852660	CV1349098	single nucleotide variant	NM_001004334.4(GPR179):c.2351C>G (p.Pro784Arg)	not provided [RCV001923005]	uncertain significance	17	38331218	38331218	Human		name
151716292	CV1349756	deletion	NM_001004334.4(GPR179):c.6439del (p.Arg2147fs)	not provided [RCV001965277]	uncertain significance	17	38327130	38327130	Human		name
151778530	CV1351958	single nucleotide variant	NM_001004334.4(GPR179):c.1693C>T (p.Arg565Trp)	not provided [RCV002009519]	uncertain significance	17	38334795	38334795	Human		name
151802535	CV1352069	single nucleotide variant	NM_001004334.4(GPR179):c.2458G>A (p.Ala820Thr)	not provided [RCV002048113]	likely benign\|uncertain significance	17	38331111	38331111	Human		name
151722541	CV1352371	single nucleotide variant	NM_001004334.4(GPR179):c.1100T>C (p.Met367Thr)	Inborn genetic diseases [RCV005350867]\|not provided [RCV002040278]	uncertain significance	17	38337105	38337105	Human	1	name
151861945	CV1353939	single nucleotide variant	NM_001004334.4(GPR179):c.1544G>A (p.Arg515Gln)	Inborn genetic diseases [RCV002571185]\|not provided [RCV001959329]	uncertain significance	17	38335134	38335134	Human	1	name
151763322	CV1357072	duplication	NM_001004334.4(GPR179):c.5693dup (p.Met1898fs)	not provided [RCV001970439]	uncertain significance	17	38327875	38327876	Human		name
151852652	CV1357290	single nucleotide variant	NM_001004334.4(GPR179):c.1994C>T (p.Ala665Val)	not provided [RCV001904302]	uncertain significance	17	38333294	38333294	Human		name
151748336	CV1362520	single nucleotide variant	NM_001004334.4(GPR179):c.1519G>T (p.Val507Leu)	not provided [RCV001968904]	uncertain significance	17	38335159	38335159	Human		name
151830206	CV1362600	single nucleotide variant	NM_001004334.4(GPR179):c.1525A>G (p.Thr509Ala)	Inborn genetic diseases [RCV004044645]\|not provided [RCV001993643]	uncertain significance	17	38335153	38335153	Human	1	name
151820059	CV1363266	single nucleotide variant	NM_001004334.4(GPR179):c.2731G>A (p.Val911Met)	Inborn genetic diseases [RCV003289412]\|not provided [RCV002049701]	likely benign\|uncertain significance	17	38330838	38330838	Human	1	name
151803556	CV1364726	single nucleotide variant	NM_001004334.4(GPR179):c.1234T>C (p.Trp412Arg)	not provided [RCV001991169]	uncertain significance	17	38336138	38336138	Human		name
151862771	CV1365139	single nucleotide variant	NM_001004334.4(GPR179):c.1132G>A (p.Ala378Thr)	not provided [RCV002017963]	uncertain significance	17	38337073	38337073	Human		name
151717306	CV1368339	single nucleotide variant	NM_001004334.4(GPR179):c.2207G>A (p.Arg736Gln)	Inborn genetic diseases [RCV004631848]\|not provided [RCV001965417]	uncertain significance	17	38331362	38331362	Human	1	name
151802166	CV1368908	single nucleotide variant	NM_001004334.4(GPR179):c.2965C>A (p.Leu989Ile)	not provided [RCV002028199]	uncertain significance	17	38330604	38330604	Human		name
151801177	CV1369301	single nucleotide variant	NM_001004334.4(GPR179):c.1224C>G (p.Asn408Lys)	not provided [RCV002028104]	uncertain significance	17	38336981	38336981	Human		name
151879969	CV1370425	single nucleotide variant	NM_001004334.4(GPR179):c.1030G>A (p.Gly344Arg)	not provided [RCV001961513]	uncertain significance	17	38337175	38337175	Human		name
151844031	CV1375854	deletion	NM_001004334.4(GPR179):c.3907del (p.Val1303fs)	not provided [RCV001995103]	uncertain significance	17	38329662	38329662	Human		name
151709618	CV1375944	single nucleotide variant	NM_001004334.4(GPR179):c.1141C>T (p.Arg381Trp)	Inborn genetic diseases [RCV002569303]\|not provided [RCV001964021]	uncertain significance	17	38337064	38337064	Human	1	name
151830958	CV1377858	single nucleotide variant	NM_001004334.4(GPR179):c.2171C>T (p.Ala724Val)	Inborn genetic diseases [RCV003161206]\|not provided [RCV002014307]	uncertain significance	17	38331398	38331398	Human	1	name
151819876	CV1378289	single nucleotide variant	NM_001004334.4(GPR179):c.1123G>A (p.Glu375Lys)	not provided [RCV002029785]	uncertain significance	17	38337082	38337082	Human		name
151801385	CV1378759	single nucleotide variant	NM_001004334.4(GPR179):c.1844C>T (p.Thr615Ile)	not provided [RCV001877403]	uncertain significance	17	38333979	38333979	Human		name
151852637	CV1378966	single nucleotide variant	NM_001004334.4(GPR179):c.1574G>A (p.Arg525Gln)	not provided [RCV001882948]	uncertain significance	17	38335104	38335104	Human		name
151831614	CV1379447	deletion	NM_001004334.4(GPR179):c.5586del (p.Met1863fs)	not provided [RCV001935107]	uncertain significance	17	38327983	38327983	Human		name
151842430	CV1379668	single nucleotide variant	NM_001004334.4(GPR179):c.2050A>C (p.Lys684Gln)	not provided [RCV001936280]	uncertain significance	17	38331519	38331519	Human		name
151837696	CV1382656	single nucleotide variant	NM_001004334.4(GPR179):c.2947C>G (p.Pro983Ala)	not provided [RCV002031463]	uncertain significance	17	38330622	38330622	Human		name
151817817	CV1385657	single nucleotide variant	NM_001004334.4(GPR179):c.2734G>A (p.Asp912Asn)	Inborn genetic diseases [RCV004631913]\|not provided [RCV002013076]	uncertain significance	17	38330835	38330835	Human	1	name
151741297	CV1386637	single nucleotide variant	NM_001004334.4(GPR179):c.1001A>C (p.Glu334Ala)	not provided [RCV001893295]	uncertain significance	17	38337204	38337204	Human		name
151846792	CV1386708	single nucleotide variant	NM_001004334.4(GPR179):c.1381G>A (p.Gly461Ser)	Inborn genetic diseases [RCV004041435]\|not provided [RCV001882048]	uncertain significance	17	38335616	38335616	Human	1	name
151742766	CV1389376	single nucleotide variant	NM_001004334.4(GPR179):c.1474C>T (p.Arg492Trp)	not provided [RCV002042398]	uncertain significance	17	38335204	38335204	Human		name
151818691	CV1390617	single nucleotide variant	NM_001004334.4(GPR179):c.2581G>C (p.Glu861Gln)	not provided [RCV001954541]	uncertain significance	17	38330988	38330988	Human		name
151854676	CV1390997	single nucleotide variant	NM_001004334.4(GPR179):c.1847A>C (p.His616Pro)	not provided [RCV001958442]	uncertain significance	17	38333976	38333976	Human		name
151766716	CV1391477	single nucleotide variant	NM_001004334.4(GPR179):c.2933C>A (p.Pro978Gln)	not provided [RCV001970774]	uncertain significance	17	38330636	38330636	Human		name
151830688	CV1391785	deletion	NM_001004334.4(GPR179):c.3636del (p.Lys1213fs)	not provided [RCV002050697]	uncertain significance	17	38329933	38329933	Human		name
151778782	CV1392432	single nucleotide variant	NM_001004334.4(GPR179):c.2353C>G (p.Leu785Val)	not provided [RCV001897045]	uncertain significance	17	38331216	38331216	Human		name
151835122	CV1394412	single nucleotide variant	NM_001004334.4(GPR179):c.2632G>C (p.Ala878Pro)	not provided [RCV002051121]	uncertain significance	17	38330937	38330937	Human		name
151711252	CV1394996	single nucleotide variant	NM_001004334.4(GPR179):c.2559G>A (p.Met853Ile)	not provided [RCV001964343]	uncertain significance	17	38331010	38331010	Human		name
151879286	CV1395563	single nucleotide variant	NM_001004334.4(GPR179):c.1049C>A (p.Ser350Tyr)	not provided [RCV001999324]	uncertain significance	17	38337156	38337156	Human		name
151752493	CV1398046	single nucleotide variant	NM_001004334.4(GPR179):c.1196T>C (p.Met399Thr)	not provided [RCV001969333]	uncertain significance	17	38337009	38337009	Human		name
151776308	CV1398978	single nucleotide variant	NM_001004334.4(GPR179):c.1508G>A (p.Gly503Asp)	not provided [RCV001930007]	uncertain significance	17	38335170	38335170	Human		name
151776381	CV1399007	single nucleotide variant	NM_001004334.4(GPR179):c.1331G>A (p.Arg444His)	not provided [RCV001930015]	uncertain significance	17	38335666	38335666	Human		name
151892018	CV1399642	single nucleotide variant	NM_001004334.4(GPR179):c.1475G>A (p.Arg492Gln)	not provided [RCV001943672]	uncertain significance	17	38335203	38335203	Human		name
151745884	CV1401814	single nucleotide variant	NM_001004334.4(GPR179):c.1442G>A (p.Arg481Gln)	not provided [RCV002042723]	uncertain significance	17	38335236	38335236	Human		name
151746702	CV1402922	single nucleotide variant	NM_001004334.4(GPR179):c.2056T>A (p.Tyr686Asn)	not provided [RCV001912509]	uncertain significance	17	38331513	38331513	Human		name
151890533	CV1405217	single nucleotide variant	NM_001004334.4(GPR179):c.2306A>G (p.His769Arg)	not provided [RCV001888434]	uncertain significance	17	38331263	38331263	Human		name
151839046	CV1407654	single nucleotide variant	NM_001004334.4(GPR179):c.1778C>T (p.Thr593Ile)	not provided [RCV002051537]	uncertain significance	17	38334710	38334710	Human		name
151768700	CV1409586	single nucleotide variant	NM_001004334.4(GPR179):c.2123G>A (p.Arg708Gln)	Inborn genetic diseases [RCV003264198]\|not provided [RCV001896119]	uncertain significance	17	38331446	38331446	Human	1	name
151729682	CV1410157	single nucleotide variant	NM_001004334.4(GPR179):c.1948G>A (p.Glu650Lys)	not provided [RCV001910732]	uncertain significance	17	38333340	38333340	Human		name
151823078	CV1415217	duplication	NM_001004334.4(GPR179):c.6928dup (p.Arg2310fs)	not provided [RCV001954957]	uncertain significance	17	38326640	38326641	Human		name
151809291	CV1418021	single nucleotide variant	NM_001004334.4(GPR179):c.1846C>G (p.His616Asp)	not provided [RCV001867843]	uncertain significance	17	38333977	38333977	Human		name
151730252	CV1420462	single nucleotide variant	NM_001004334.4(GPR179):c.2975T>G (p.Ile992Ser)	not provided [RCV002041121]	uncertain significance	17	38330594	38330594	Human		name
151731177	CV1420737	deletion	NM_001004334.4(GPR179):c.4967del (p.Pro1656fs)	not provided [RCV002021312]	uncertain significance	17	38328602	38328602	Human		name
151796369	CV1421555	single nucleotide variant	NM_001004334.4(GPR179):c.2197C>T (p.Gln733Ter)	not provided [RCV001917297]	uncertain significance	17	38331372	38331372	Human		name
151781503	CV1422123	single nucleotide variant	NM_001004334.4(GPR179):c.1906G>C (p.Ala636Pro)	not provided [RCV001972124]	uncertain significance	17	38333382	38333382	Human		name
151775282	CV1424243	single nucleotide variant	NM_001004334.4(GPR179):c.1403A>T (p.Tyr468Phe)	not provided [RCV002025749]	uncertain significance	17	38335594	38335594	Human		name
151823395	CV1425185	single nucleotide variant	NM_001004334.4(GPR179):c.1354C>T (p.Arg452Trp)	not provided [RCV001919798]	uncertain significance	17	38335643	38335643	Human		name
151804384	CV1429719	single nucleotide variant	NM_001004334.4(GPR179):c.1915C>T (p.Arg639Trp)	not provided [RCV001974204]	uncertain significance	17	38333373	38333373	Human		name
151742220	CV1431595	deletion	NM_001004334.4(GPR179):c.4019del (p.Pro1340fs)	not provided [RCV001926575]	uncertain significance	17	38329550	38329550	Human		name
151804531	CV1432353	single nucleotide variant	NM_001004334.4(GPR179):c.2768A>C (p.Glu923Ala)	not provided [RCV001991256]	uncertain significance	17	38330801	38330801	Human		name
151816494	CV1433112	single nucleotide variant	NM_001004334.4(GPR179):c.2983T>C (p.Trp995Arg)	not provided [RCV001954334]	uncertain significance	17	38330586	38330586	Human		name
151738016	CV1437335	single nucleotide variant	NM_001004334.4(GPR179):c.2606G>A (p.Arg869Gln)	not provided [RCV001870730]	uncertain significance	17	38330963	38330963	Human		name
151738383	CV1437394	single nucleotide variant	NM_001004334.4(GPR179):c.1474C>G (p.Arg492Gly)	Inborn genetic diseases [RCV004988828]\|not provided [RCV001870763]	uncertain significance	17	38335204	38335204	Human	1	name
151833657	CV1439427	single nucleotide variant	NM_001004334.4(GPR179):c.2041G>T (p.Glu681Ter)	not provided [RCV001976900]	uncertain significance	17	38331528	38331528	Human		name
151833681	CV1439433	single nucleotide variant	NM_001004334.4(GPR179):c.2458G>C (p.Ala820Pro)	not provided [RCV001976903]	uncertain significance	17	38331111	38331111	Human		name
151723422	CV1442942	single nucleotide variant	NM_001004334.4(GPR179):c.1133C>A (p.Ala378Glu)	not provided [RCV002040382]	uncertain significance	17	38337072	38337072	Human		name
151711251	CV1443808	single nucleotide variant	NM_001004334.4(GPR179):c.1933G>A (p.Glu645Lys)	not provided [RCV001908055]	uncertain significance	17	38333355	38333355	Human		name
151799364	CV1445895	single nucleotide variant	NM_001004334.4(GPR179):c.2605C>T (p.Arg869Trp)	Congenital stationary night blindness 1E [RCV003483879]\|Inborn genetic diseases [RCV004046658]\|not provided [RCV002011423]	uncertain significance\|not provided	17	38330964	38330964	Human	2	name
151764611	CV1447676	single nucleotide variant	NM_001004334.4(GPR179):c.1622G>T (p.Arg541Leu)	not provided [RCV001895728]	uncertain significance	17	38335056	38335056	Human		name
151769119	CV1450914	single nucleotide variant	NM_001004334.4(GPR179):c.1037C>T (p.Pro346Leu)	not provided [RCV001929344]	uncertain significance	17	38337168	38337168	Human		name
151734587	CV1453122	single nucleotide variant	NM_001004334.4(GPR179):c.2519C>T (p.Ser840Leu)	not provided [RCV002041558]	uncertain significance	17	38331050	38331050	Human		name
151741126	CV1455409	single nucleotide variant	NM_001004334.4(GPR179):c.1528G>A (p.Val510Met)	not provided [RCV002005828]	uncertain significance	17	38335150	38335150	Human		name
151854511	CV1455761	duplication	NM_001004334.4(GPR179):c.5236dup (p.Thr1746fs)	not provided [RCV002017009]	uncertain significance	17	38328332	38328333	Human		name
151853524	CV1457053	single nucleotide variant	NM_001004334.4(GPR179):c.2206C>T (p.Arg736Trp)	not provided [RCV001883047]	uncertain significance	17	38331363	38331363	Human		name
151851869	CV1459387	single nucleotide variant	NM_001004334.4(GPR179):c.2866C>A (p.Pro956Thr)	Inborn genetic diseases [RCV002545339]\|not provided [RCV002033284]	uncertain significance	17	38330703	38330703	Human	1	name
151840406	CV1462958	single nucleotide variant	NM_001004334.4(GPR179):c.1561C>A (p.Pro521Thr)	Inborn genetic diseases [RCV002551217]\|not provided [RCV002031752]	uncertain significance	17	38335117	38335117	Human	1	name
151815267	CV1463373	single nucleotide variant	NM_001004334.4(GPR179):c.1706C>T (p.Ser569Leu)	not provided [RCV001900351]	uncertain significance	17	38334782	38334782	Human		name
151827959	CV1465324	single nucleotide variant	NM_001004334.4(GPR179):c.2923G>C (p.Ala975Pro)	not provided [RCV002014023]	uncertain significance	17	38330646	38330646	Human		name
151798984	CV1467202	single nucleotide variant	NM_001004334.4(GPR179):c.2624C>T (p.Ala875Val)	not provided [RCV001898882]	uncertain significance	17	38330945	38330945	Human		name
151781811	CV1468949	single nucleotide variant	NM_001004334.4(GPR179):c.2192C>T (p.Ala731Val)	not provided [RCV002026332]	uncertain significance	17	38331377	38331377	Human		name
151862873	CV1474368	single nucleotide variant	NM_001004334.4(GPR179):c.2335A>G (p.Arg779Gly)	not provided [RCV001884160]	uncertain significance	17	38331234	38331234	Human		name
151864536	CV1478749	single nucleotide variant	NM_001004334.4(GPR179):c.2252G>A (p.Arg751His)	not provided [RCV002018173]	uncertain significance	17	38331317	38331317	Human		name
151769958	CV1481712	single nucleotide variant	NM_001004334.4(GPR179):c.1465C>T (p.Arg489Trp)	not provided [RCV002008749]	uncertain significance	17	38335213	38335213	Human		name
151848373	CV1484175	single nucleotide variant	NM_001004334.4(GPR179):c.2336G>A (p.Arg779Lys)	not provided [RCV001903758]	uncertain significance	17	38331233	38331233	Human		name
151720388	CV1491521	single nucleotide variant	NM_001004334.4(GPR179):c.2710T>C (p.Ser904Pro)	not provided [RCV002003578]	uncertain significance	17	38330859	38330859	Human		name
151720623	CV1491562	single nucleotide variant	NM_001004334.4(GPR179):c.1916G>A (p.Arg639Gln)	Congenital stationary night blindness 1E [RCV003130661]\|not provided [RCV002003609]	uncertain significance	17	38333372	38333372	Human	1	name
151783404	CV1491858	single nucleotide variant	NM_001004334.4(GPR179):c.2639C>A (p.Ala880Asp)	not provided [RCV002026480]	uncertain significance	17	38330930	38330930	Human		name
151838520	CV1501405	single nucleotide variant	NM_001004334.4(GPR179):c.1637T>C (p.Met546Thr)	not provided [RCV001977410]	uncertain significance	17	38335041	38335041	Human		name
151745319	CV1502526	single nucleotide variant	NM_001004334.4(GPR179):c.2914C>G (p.Pro972Ala)	not provided [RCV001912351]	uncertain significance	17	38330655	38330655	Human		name
151762821	CV1503101	single nucleotide variant	NM_001004334.4(GPR179):c.1091C>T (p.Thr364Ile)	not provided [RCV001914189]	uncertain significance	17	38337114	38337114	Human		name
151891836	CV1503107	single nucleotide variant	NM_001004334.4(GPR179):c.2740T>C (p.Ser914Pro)	Inborn genetic diseases [RCV003264268]\|not provided [RCV001943514]	uncertain significance	17	38330829	38330829	Human	1	name
151730451	CV1505506	single nucleotide variant	NM_001004334.4(GPR179):c.1433C>A (p.Thr478Lys)	not provided [RCV002021240]	uncertain significance	17	38335245	38335245	Human		name
151730761	CV1505556	single nucleotide variant	NM_001004334.4(GPR179):c.2036G>A (p.Arg679Gln)	not provided [RCV002021275]	uncertain significance	17	38333252	38333252	Human		name
151743644	CV1507625	single nucleotide variant	NM_001004334.4(GPR179):c.2713C>T (p.Pro905Ser)	not provided [RCV001968398]	uncertain significance	17	38330856	38330856	Human		name
151750902	CV1508314	single nucleotide variant	NM_001004334.4(GPR179):c.1375G>A (p.Val459Ile)	not provided [RCV001986271]	uncertain significance	17	38335622	38335622	Human		name
151783691	CV1508324	single nucleotide variant	NM_001004334.4(GPR179):c.1534G>A (p.Ala512Thr)	not provided [RCV002009971]	uncertain significance	17	38335144	38335144	Human		name
151783784	CV1508339	single nucleotide variant	NM_001004334.4(GPR179):c.2684G>A (p.Arg895Gln)	not provided [RCV002009978]	uncertain significance	17	38330885	38330885	Human		name
151889059	CV1509435	single nucleotide variant	NM_001004334.4(GPR179):c.1236G>C (p.Trp412Cys)	not provided [RCV001888099]	uncertain significance	17	38336136	38336136	Human		name
151874315	CV1510364	single nucleotide variant	NM_001004334.4(GPR179):c.2206C>G (p.Arg736Gly)	Inborn genetic diseases [RCV005343139]\|not provided [RCV001940203]	uncertain significance	17	38331363	38331363	Human	1	name
151731624	CV1512168	single nucleotide variant	NM_001004334.4(GPR179):c.2792C>T (p.Pro931Leu)	Inborn genetic diseases [RCV002548886]\|not provided [RCV002021358]	uncertain significance	17	38330777	38330777	Human	1	name
151734398	CV1512562	single nucleotide variant	NM_001004334.4(GPR179):c.2590C>T (p.Arg864Trp)	not provided [RCV002021631]	uncertain significance	17	38330979	38330979	Human		name
151765510	CV1517219	single nucleotide variant	NM_001004334.4(GPR179):c.1224C>A (p.Asn408Lys)	Inborn genetic diseases [RCV004976184]\|not provided [RCV002024848]	uncertain significance	17	38336981	38336981	Human	1	name
152051029	CV1523393	single nucleotide variant	NM_001004334.4(GPR179):c.1021G>A (p.Gly341Arg)	not provided [RCV002127256]	benign	17	38337184	38337184	Human		name
152086489	CV1578117	single nucleotide variant	NM_001004334.4(GPR179):c.2992G>A (p.Ala998Thr)	Optic atrophy [RCV004816963]\|not provided [RCV002171236]	benign\|uncertain significance	17	38330577	38330577	Human	2	name
152127286	CV1596369	single nucleotide variant	NM_001004334.4(GPR179):c.1211G>A (p.Arg404His)	not provided [RCV002118623]	likely benign	17	38336994	38336994	Human		name
152095768	CV1597388	single nucleotide variant	NM_001004334.4(GPR179):c.2614C>T (p.Arg872Trp)	not provided [RCV002114676]	likely benign	17	38330955	38330955	Human		name
155267827	CV1701388	single nucleotide variant	NM_001004334.4(GPR179):c.1667G>A (p.Trp556Ter)	Congenital stationary night blindness 1E [RCV002283613]	pathogenic	17	38334821	38334821	Human	1	name
155670596	CV1771013	single nucleotide variant	NM_001004334.4(GPR179):c.2379G>T (p.Lys793Asn)	not provided [RCV002297329]	uncertain significance	17	38331190	38331190	Human		name
155744425	CV1771272	single nucleotide variant	NM_001004334.4(GPR179):c.1096T>G (p.Cys366Gly)	not provided [RCV002303167]	uncertain significance	17	38337109	38337109	Human		name
155694944	CV1771966	single nucleotide variant	NM_001004334.4(GPR179):c.2092G>C (p.Ala698Pro)	not provided [RCV002299542]	uncertain significance	17	38331477	38331477	Human		name
10047706	CV190989	single nucleotide variant	NM_001004334.4(GPR179):c.2392G>A (p.Ala798Thr)	Congenital stationary night blindness 1E [RCV000380390]\|not provided [RCV001516530]\|not specified [RCV000174027]	benign\|likely benign	17	38331177	38331177	Human	1	name
10052106	CV194331	single nucleotide variant	NM_001004334.4(GPR179):c.1220G>A (p.Arg407Gln)	Congenital stationary night blindness 1E [RCV000364314]\|Inborn genetic diseases [RCV002516766]\|not provided [RCV000178134]	likely benign\|uncertain significance	17	38336985	38336985	Human	2	name
10052465	CV194861	single nucleotide variant	NM_001004334.4(GPR179):c.1228A>G (p.Arg410Gly)	not provided [RCV000178812]	uncertain significance	17	38336144	38336144	Human		name
10052971	CV195601	single nucleotide variant	NM_001004334.4(GPR179):c.1484G>A (p.Gly495Glu)	not provided [RCV000179791]	uncertain significance	17	38335194	38335194	Human		name
155910119	CV1980075	deletion	NM_001004334.4(GPR179):c.3434del (p.Ile1145fs)	not provided [RCV002613924]	uncertain significance	17	38330135	38330135	Human		name
155998770	CV1987050	single nucleotide variant	NM_001004334.4(GPR179):c.2615G>A (p.Arg872Gln)	Inborn genetic diseases [RCV004065846]\|not provided [RCV002618348]	uncertain significance	17	38330954	38330954	Human	1	name
156112359	CV1993681	single nucleotide variant	NM_001004334.4(GPR179):c.1105G>A (p.Ala369Thr)	not provided [RCV002662539]	uncertain significance	17	38337100	38337100	Human		name
156112449	CV1993684	single nucleotide variant	NM_001004334.4(GPR179):c.2503G>A (p.Ala835Thr)	Inborn genetic diseases [RCV004632042]\|not provided [RCV002662542]	uncertain significance	17	38331066	38331066	Human	1	name
156038524	CV1998899	single nucleotide variant	NM_001004334.4(GPR179):c.1216C>A (p.Arg406Ser)	Inborn genetic diseases [RCV003167604]\|not provided [RCV002658943]	uncertain significance	17	38336989	38336989	Human	1	name
156013214	CV2008975	deletion	NM_001004334.4(GPR179):c.4452del (p.Asp1484fs)	not provided [RCV002690628]	uncertain significance	17	38329117	38329117	Human		name
156122149	CV2015995	single nucleotide variant	NM_001004334.4(GPR179):c.2855G>A (p.Arg952Lys)	not provided [RCV002696078]	uncertain significance	17	38330714	38330714	Human		name
156018011	CV2019177	single nucleotide variant	NM_001004334.4(GPR179):c.2041G>A (p.Glu681Lys)	not provided [RCV002690861]	uncertain significance	17	38331528	38331528	Human		name
155995535	CV2023595	single nucleotide variant	NM_001004334.4(GPR179):c.1184T>C (p.Ile395Thr)	Inborn genetic diseases [RCV004067862]\|not provided [RCV002755942]	uncertain significance	17	38337021	38337021	Human	1	name
156084934	CV2023784	single nucleotide variant	NM_001004334.4(GPR179):c.2474T>C (p.Val825Ala)	not provided [RCV002760747]	uncertain significance	17	38331095	38331095	Human		name
156095565	CV2030908	single nucleotide variant	NM_001004334.4(GPR179):c.2651G>A (p.Arg884Gln)	not provided [RCV002761112]	uncertain significance	17	38330918	38330918	Human		name
155940382	CV2054914	single nucleotide variant	NM_001004334.4(GPR179):c.2618A>C (p.Lys873Thr)	not provided [RCV002815654]	uncertain significance	17	38330951	38330951	Human		name
155958717	CV2066639	single nucleotide variant	NM_001004334.4(GPR179):c.1528G>T (p.Val510Leu)	not provided [RCV002816660]	uncertain significance	17	38335150	38335150	Human		name
155925527	CV2073899	single nucleotide variant	NM_001004334.4(GPR179):c.1082A>T (p.Glu361Val)	not provided [RCV002838511]	uncertain significance	17	38337123	38337123	Human		name
156086002	CV2080046	deletion	NM_001004334.4(GPR179):c.5817del (p.Glu1940fs)	not provided [RCV002847547]	uncertain significance	17	38327752	38327752	Human		name
155943570	CV2115156	single nucleotide variant	NM_001004334.4(GPR179):c.2489C>G (p.Pro830Arg)	not provided [RCV002904633]	uncertain significance	17	38331080	38331080	Human		name
155933619	CV2138531	duplication	NM_001004334.4(GPR179):c.4920dup (p.Gln1641fs)	not provided [RCV002993559]	uncertain significance	17	38328648	38328649	Human		name
156024414	CV2145545	single nucleotide variant	NM_001004334.4(GPR179):c.1709C>A (p.Ala570Asp)	not provided [RCV003018385]	uncertain significance	17	38334779	38334779	Human		name
156189155	CV2148610	single nucleotide variant	NM_001004334.4(GPR179):c.2557A>G (p.Met853Val)	not provided [RCV003005946]	uncertain significance	17	38331012	38331012	Human		name
156104127	CV2164578	single nucleotide variant	NM_001004334.4(GPR179):c.1321A>C (p.Ser441Arg)	Inborn genetic diseases [RCV003038695]\|not provided [RCV003038694]	uncertain significance	17	38335676	38335676	Human	1	name
156104260	CV2164589	single nucleotide variant	NM_001004334.4(GPR179):c.1913C>A (p.Pro638His)	not provided [RCV003038700]	uncertain significance	17	38333375	38333375	Human		name
156010898	CV2170597	single nucleotide variant	NM_001004334.4(GPR179):c.2564G>T (p.Ser855Ile)	not provided [RCV003017735]	uncertain significance	17	38331005	38331005	Human		name
156014059	CV2177291	single nucleotide variant	NM_001004334.4(GPR179):c.1448C>T (p.Ala483Val)	not provided [RCV003035393]	uncertain significance	17	38335230	38335230	Human		name
155939479	CV2225538	single nucleotide variant	NM_001004334.4(GPR179):c.2182G>A (p.Glu728Lys)	Inborn genetic diseases [RCV002751737]	uncertain significance	17	38331387	38331387	Human	1	name
156062055	CV2316430	single nucleotide variant	NM_001004334.4(GPR179):c.1002G>C (p.Glu334Asp)	Inborn genetic diseases [RCV002911849]	uncertain significance	17	38337203	38337203	Human	1	name
11638250	CV274551	duplication	NM_001004334.4(GPR179):c.4217dup (p.Gln1407fs)	not provided [RCV000298643]	uncertain significance	17	38329351	38329352	Human		name
11615522	CV328316	single nucleotide variant	NM_001004334.4(GPR179):c.2332C>T (p.Arg778Cys)	Congenital stationary night blindness 1E [RCV000286479]\|not provided [RCV002521104]	uncertain significance	17	38331237	38331237	Human	1	name
11619025	CV338208	single nucleotide variant	NM_001004334.4(GPR179):c.2248T>A (p.Ser750Thr)	Congenital stationary night blindness 1E [RCV000320453]\|not provided [RCV002056586]	likely benign\|uncertain significance	17	38331321	38331321	Human	1	name
11620539	CV338210	single nucleotide variant	NM_001004334.4(GPR179):c.1837T>A (p.Phe613Ile)	Congenital Stationary Night Blindness, Recessive [RCV000337901]\|Inborn genetic diseases [RCV005338143]\|not provided [RCV001859914]	uncertain significance	17	38333986	38333986	Human	2	name
11624745	CV338217	single nucleotide variant	NM_001004334.4(GPR179):c.1595G>A (p.Arg532His)	Congenital stationary night blindness 1E [RCV000390007]\|not provided [RCV001512599]	benign\|likely benign	17	38335083	38335083	Human	1	name
11613352	CV338228	single nucleotide variant	NM_001004334.4(GPR179):c.1217G>A (p.Arg406His)	Congenital stationary night blindness 1E [RCV000267367]\|not provided [RCV001367852]	uncertain significance	17	38336988	38336988	Human	1	name
11617579	CV338229	single nucleotide variant	NM_001004334.4(GPR179):c.1070T>C (p.Leu357Pro)	Congenital stationary night blindness 1E [RCV000305732]	uncertain significance	17	38337135	38337135	Human	1	name
11631133	CV344318	single nucleotide variant	NM_001004334.4(GPR179):c.2924C>A (p.Ala975Asp)	Congenital stationary night blindness 1E [RCV000368519]\|not provided [RCV001523376]	benign\|likely benign	17	38330645	38330645	Human	1	name
11629649	CV345739	single nucleotide variant	NM_001004334.4(GPR179):c.2809G>A (p.Val937Ile)	Congenital stationary night blindness 1E [RCV000329168]\|Inborn genetic diseases [RCV002522949]\|not provided [RCV001850723]	uncertain significance	17	38330760	38330760	Human	2	name
11631030	CV345744	single nucleotide variant	NM_001004334.4(GPR179):c.2650C>T (p.Arg884Trp)	Congenital stationary night blindness 1E [RCV000365115]\|not provided [RCV001522297]	benign\|likely benign	17	38330919	38330919	Human	1	name
11630571	CV345753	single nucleotide variant	NM_001004334.4(GPR179):c.1723C>T (p.Arg575Cys)	Congenital stationary night blindness 1E [RCV000352780]\|not provided [RCV001519733]	benign\|uncertain significance	17	38334765	38334765	Human	1	name
11629022	CV345754	single nucleotide variant	NM_001004334.4(GPR179):c.1589G>A (p.Ser530Asn)	Congenital stationary night blindness 1E [RCV000313185]\|Inborn genetic diseases [RCV003168476]\|not provided [RCV001850724]	uncertain significance	17	38335089	38335089	Human	2	name
11652870	CV345760	single nucleotide variant	NM_001004334.4(GPR179):c.1388T>A (p.Ile463Asn)	Congenital stationary night blindness 1E [RCV000307344]	uncertain significance	17	38335609	38335609	Human	1	name
12900970	CV409916	deletion	NM_001004334.4(GPR179):c.6789del (p.Arg2264fs)	not provided [RCV000483601]	uncertain significance	17	38326780	38326780	Human		name
13832964	CV584191	single nucleotide variant	NM_001004334.4(GPR179):c.1304T>C (p.Ile435Thr)	not provided [RCV000728081]	uncertain significance	17	38335693	38335693	Human		name
13837885	CV589181	single nucleotide variant	NM_001004334.4(GPR179):c.1543C>T (p.Arg515Ter)	not provided [RCV000734439]	pathogenic	17	38335135	38335135	Human		name
126762178	CV997518	single nucleotide variant	NM_001004334.4(GPR179):c.1724G>A (p.Arg575His)	not provided [RCV001309810]	uncertain significance	17	38334764	38334764	Human		name
126746464	CV997519	single nucleotide variant	NM_001004334.4(GPR179):c.1709C>T (p.Ala570Val)	not provided [RCV001306107]	uncertain significance	17	38334779	38334779	Human		name
126752940	CV997520	single nucleotide variant	NM_001004334.4(GPR179):c.1622G>A (p.Arg541His)	not provided [RCV001297814]	uncertain significance	17	38335056	38335056	Human		name

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