Gmpr Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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79 records found for search term Gmpr

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405767884	CV3262013	single nucleotide variant	NM_006877.4(GMPR):c.7C>G (p.Arg3Gly)	not specified [RCV004395402]	uncertain significance	6	16238700	16238700	Human		name
407519935	CV3443539	single nucleotide variant	NM_006877.4(GMPR):c.7C>T (p.Arg3Cys)	not specified [RCV004629853]	uncertain significance	6	16238700	16238700	Human		name
407519931	CV3443537	single nucleotide variant	NM_006877.4(GMPR):c.17C>T (p.Ala6Val)	not specified [RCV004629851]	uncertain significance	6	16238710	16238710	Human		name
155901495	CV2274524	single nucleotide variant	NM_006877.4(GMPR):c.36C>A (p.Phe12Leu)	not specified [RCV004138933]	uncertain significance	6	16238729	16238729	Human		name
401781218	CV2681932	single nucleotide variant	NM_006877.4(GMPR):c.56C>T (p.Pro19Leu)	not specified [RCV004296920]	uncertain significance	6	16238749	16238749	Human		name
15176500	CV721869	single nucleotide variant	NM_006877.4(GMPR):c.474C>T (p.Asn158=)	not provided [RCV000884596]	benign	6	16274423	16274423	Human		name
15193591	CV721870	single nucleotide variant	NM_006877.4(GMPR):c.747G>A (p.Thr249=)	not provided [RCV000888989]	benign	6	16290511	16290511	Human		name
156036189	CV2243497	single nucleotide variant	NM_006877.4(GMPR):c.196G>A (p.Val66Met)	not specified [RCV004112458]	uncertain significance	6	16246950	16246950	Human		name
405767862	CV3262009	single nucleotide variant	NM_006877.4(GMPR):c.247G>A (p.Asp83Asn)	not specified [RCV004395398]	uncertain significance	6	16250323	16250323	Human		name
405767866	CV3262010	single nucleotide variant	NM_006877.4(GMPR):c.272A>C (p.Asn91Thr)	not specified [RCV004395399]	uncertain significance	6	16250348	16250348	Human		name
407519925	CV3443534	single nucleotide variant	NM_006877.4(GMPR):c.259C>T (p.Leu87Phe)	not specified [RCV004629848]	uncertain significance	6	16250335	16250335	Human		name
407519937	CV3443540	single nucleotide variant	NM_006877.4(GMPR):c.154G>A (p.Val52Met)	not specified [RCV004629854]	uncertain significance	6	16246908	16246908	Human		name
597788643	CV3678147	single nucleotide variant	NM_006877.4(GMPR):c.266C>T (p.Ala89Val)	not specified [RCV004932716]	uncertain significance	6	16250342	16250342	Human		name
597788633	CV3678154	single nucleotide variant	NM_006877.4(GMPR):c.224C>A (p.Ala75Glu)	not specified [RCV004932719]	uncertain significance	6	16250300	16250300	Human		name
598264034	CV3974321	single nucleotide variant	NM_006877.4(GMPR):c.295G>A (p.Val99Ile)	not specified [RCV005348743]	uncertain significance	6	16254565	16254565	Human		name
155964656	CV2210027	single nucleotide variant	NM_006877.4(GMPR):c.437G>A (p.Arg146His)	not specified [RCV004076459]	uncertain significance	6	16254707	16254707	Human		name
156195538	CV2223437	single nucleotide variant	NM_006877.4(GMPR):c.301G>A (p.Val101Met)	not specified [RCV004106014]	uncertain significance	6	16254571	16254571	Human		name
156180310	CV2245989	single nucleotide variant	NM_006877.4(GMPR):c.637A>G (p.Lys213Glu)	not specified [RCV004113913]	uncertain significance	6	16278873	16278873	Human		name
156171530	CV2286712	single nucleotide variant	NM_006877.4(GMPR):c.695T>G (p.Phe232Cys)	not specified [RCV004142536]	uncertain significance	6	16285833	16285833	Human		name
156103948	CV2291659	single nucleotide variant	NM_006877.4(GMPR):c.786G>C (p.Lys262Asn)	not specified [RCV004155945]	uncertain significance	6	16290550	16290550	Human		name
155997354	CV2393300	single nucleotide variant	NM_006877.4(GMPR):c.530A>G (p.Lys177Arg)	not specified [RCV004228810]	uncertain significance	6	16274479	16274479	Human		name
329351564	CV2462110	single nucleotide variant	NM_006877.4(GMPR):c.778G>A (p.Gly260Arg)	not specified [RCV004266137]	uncertain significance	6	16290542	16290542	Human		name
401766815	CV2680158	single nucleotide variant	NM_006877.4(GMPR):c.649A>G (p.Ile217Val)	not specified [RCV004286641]	uncertain significance	6	16278885	16278885	Human		name
401778566	CV2709281	single nucleotide variant	NM_006877.4(GMPR):c.355G>T (p.Ala119Ser)	not specified [RCV004316439]	uncertain significance	6	16254625	16254625	Human		name
401887391	CV2773423	single nucleotide variant	NM_006877.4(GMPR):c.868G>C (p.Gly290Arg)	not specified [RCV004354063]	uncertain significance	6	16295016	16295016	Human		name
401897028	CV2785514	single nucleotide variant	NM_006877.4(GMPR):c.858A>T (p.Arg286Ser)	not specified [RCV004363039]	uncertain significance	6	16295006	16295006	Human		name
8565334	CV31000	single nucleotide variant	NM_006877.4(GMPR):c.766T>A (p.Phe256Ile)	GMPR POLYMORPHISM [RCV000017331]\|not provided [RCV001610292]	benign	6	16290530	16290530	Human	13	name , trait
8565334	CV31000	single nucleotide variant	NM_006877.4(GMPR):c.766T>A (p.Phe256Ile)	GMPR POLYMORPHISM [RCV000017331]\|not provided [RCV001610292]	benign	6	16290530	16290531	Human	13	name , trait
405767873	CV3262011	single nucleotide variant	NM_006877.4(GMPR):c.331G>A (p.Glu111Lys)	not specified [RCV004395400]	uncertain significance	6	16254601	16254601	Human		name
405767877	CV3262012	single nucleotide variant	NM_006877.4(GMPR):c.460A>G (p.Ile154Val)	not specified [RCV004395401]	uncertain significance	6	16254730	16254730	Human		name
407519927	CV3443535	single nucleotide variant	NM_006877.4(GMPR):c.590C>T (p.Pro197Leu)	not specified [RCV004629849]	uncertain significance	6	16278826	16278826	Human		name
407519929	CV3443536	single nucleotide variant	NM_006877.4(GMPR):c.798C>A (p.Phe266Leu)	not specified [RCV004629850]	uncertain significance	6	16290562	16290562	Human		name
597730087	CV3678146	single nucleotide variant	NM_006877.4(GMPR):c.464T>C (p.Met155Thr)	not specified [RCV004919783]	uncertain significance	6	16254734	16254734	Human		name
597730108	CV3678149	single nucleotide variant	NM_006877.4(GMPR):c.485G>A (p.Gly162Glu)	not specified [RCV004919785]	uncertain significance	6	16274434	16274434	Human		name
597788639	CV3678150	single nucleotide variant	NM_006877.4(GMPR):c.802G>A (p.Gly268Arg)	not specified [RCV004932717]	uncertain significance	6	16290566	16290566	Human		name
597730116	CV3678151	single nucleotide variant	NM_006877.4(GMPR):c.761A>G (p.Glu254Gly)	not specified [RCV004919786]	uncertain significance	6	16290525	16290525	Human		name
597730127	CV3678152	single nucleotide variant	NM_006877.4(GMPR):c.898G>C (p.Asp300His)	not specified [RCV004919787]	uncertain significance	6	16295046	16295046	Human		name
597788636	CV3678153	single nucleotide variant	NM_006877.4(GMPR):c.668C>T (p.Thr223Met)	not specified [RCV004932718]	uncertain significance	6	16285806	16285806	Human		name
598264028	CV3974319	single nucleotide variant	NM_006877.4(GMPR):c.521A>T (p.Asp174Val)	not specified [RCV005348741]	uncertain significance	6	16274470	16274470	Human		name
598264032	CV3974320	single nucleotide variant	NM_006877.4(GMPR):c.487G>A (p.Glu163Lys)	not specified [RCV005348742]	uncertain significance	6	16274436	16274436	Human		name
598264037	CV3974322	single nucleotide variant	NM_006877.4(GMPR):c.997T>C (p.Phe333Leu)	not specified [RCV005348744]	uncertain significance	6	16295145	16295145	Human		name
15199987	CV721871	single nucleotide variant	NM_006877.4(GMPR):c.899A>T (p.Asp300Val)	not provided [RCV000890787]	benign	6	16295047	16295047	Human		name
597730098	CV3678148	single nucleotide variant	NM_006877.4(GMPR):c.1018C>T (p.His340Tyr)	not specified [RCV004919784]	uncertain significance	6	16295166	16295166	Human		name
15199990	CV721872	duplication	NM_006877.4(GMPR):c.970_973dup (p.Lys325fs)	not provided [RCV000890788]	benign	6	16295116	16295117	Human		name
15174063	CV735524	duplication	NM_006877.4(GMPR):c.855_856dup (p.Arg286fs)	not provided [RCV000905921]	likely benign	6	16290617	16290618	Human		name
598232686	CV3974325	single nucleotide variant	NM_001002002.3(GMPR2):c.-14C>G	not specified [RCV005342637]	uncertain significance	14	24233240	24233240	Human		name
405767900	CV3262016	single nucleotide variant	NM_001002002.3(GMPR2):c.-35-4C>A	not specified [RCV004395405]	uncertain significance	14	24233215	24233215	Human		name
598264047	CV3974326	single nucleotide variant	NM_001002002.3(GMPR2):c.2T>C (p.Met1Thr)	not specified [RCV005348747]	uncertain significance	14	24233255	24233255	Human		name
8635191	CV90413	single nucleotide variant	NM_001002000.2(GMPR2):c.840G>A (p.Gly280=)	Malignant melanoma [RCV000070511]	not provided	14	24238388	24238388	Human		name
156042896	CV2261494	single nucleotide variant	NM_001002002.3(GMPR2):c.166G>A (p.Asp56Asn)	not specified [RCV004130113]	uncertain significance	14	24233557	24233557	Human		name
155925377	CV2277296	single nucleotide variant	NM_001002002.3(GMPR2):c.269G>T (p.Gly90Val)	not specified [RCV004142910]	uncertain significance	14	24235798	24235798	Human		name
156154819	CV2328696	single nucleotide variant	NM_001002002.3(GMPR2):c.131C>T (p.Thr44Ile)	not specified [RCV004177935]	uncertain significance	14	24233522	24233522	Human		name
329388801	CV2469582	single nucleotide variant	NM_001002002.3(GMPR2):c.203G>T (p.Cys68Phe)	not specified [RCV004283015]	uncertain significance	14	24233594	24233594	Human		name
597730148	CV3678159	single nucleotide variant	NM_001002002.3(GMPR2):c.124A>G (p.Lys42Glu)	not specified [RCV004919789]	uncertain significance	14	24233515	24233515	Human		name
597730177	CV3678163	single nucleotide variant	NM_001002002.3(GMPR2):c.152T>C (p.Ile51Thr)	not specified [RCV004919792]	uncertain significance	14	24233543	24233543	Human		name
598264044	CV3974324	single nucleotide variant	NM_001002002.3(GMPR2):c.196G>A (p.Val66Ile)	not specified [RCV005348746]	uncertain significance	14	24233587	24233587	Human		name
156113115	CV2212660	single nucleotide variant	NM_001002002.3(GMPR2):c.563C>T (p.Thr188Ile)	not specified [RCV004085177]	uncertain significance	14	24237260	24237260	Human		name
156296689	CV2233864	single nucleotide variant	NM_001002002.3(GMPR2):c.415G>A (p.Val139Ile)	not specified [RCV004102076]	uncertain significance	14	24236090	24236090	Human		name
156279902	CV2315930	single nucleotide variant	NM_001002002.3(GMPR2):c.365A>G (p.Gln122Arg)	not specified [RCV004172008]	uncertain significance	14	24236040	24236040	Human		name
156275029	CV2330645	single nucleotide variant	NM_001002002.3(GMPR2):c.848C>T (p.Ala283Val)	not specified [RCV004183674]	uncertain significance	14	24238396	24238396	Human		name
156279630	CV2348356	single nucleotide variant	NM_001002002.3(GMPR2):c.437G>A (p.Arg146Gln)	not specified [RCV004193551]	uncertain significance	14	24236112	24236112	Human		name
329377782	CV2450084	single nucleotide variant	NM_001002002.3(GMPR2):c.989G>A (p.Arg330Lys)	not specified [RCV004269130]	uncertain significance	14	24238720	24238720	Human		name
401735367	CV2706766	single nucleotide variant	NM_001002002.3(GMPR2):c.720G>C (p.Met240Ile)	not specified [RCV004319325]	uncertain significance	14	24238268	24238268	Human		name
401776012	CV2706849	single nucleotide variant	NM_001002002.3(GMPR2):c.854A>C (p.Tyr285Ser)	not specified [RCV004321479]	uncertain significance	14	24238402	24238402	Human		name
405767887	CV3262014	single nucleotide variant	NM_001002002.3(GMPR2):c.973A>G (p.Lys325Glu)	not specified [RCV004395403]	uncertain significance	14	24238704	24238704	Human		name
405767907	CV3262017	single nucleotide variant	NM_001002002.3(GMPR2):c.712T>C (p.Phe238Leu)	not specified [RCV004395406]	uncertain significance	14	24238260	24238260	Human		name
407519940	CV3443541	single nucleotide variant	NM_001002002.3(GMPR2):c.427A>G (p.Lys143Glu)	not specified [RCV004629855]	uncertain significance	14	24236102	24236102	Human		name
407519942	CV3443542	single nucleotide variant	NM_001002002.3(GMPR2):c.869G>A (p.Gly290Glu)	not specified [RCV004629856]	uncertain significance	14	24238600	24238600	Human		name
407519944	CV3443543	single nucleotide variant	NM_001002002.3(GMPR2):c.904G>C (p.Glu302Gln)	not specified [RCV004629857]	uncertain significance	14	24238635	24238635	Human		name
597730137	CV3678156	single nucleotide variant	NM_001002002.3(GMPR2):c.376A>G (p.Ile126Val)	not specified [RCV004919788]	uncertain significance	14	24236051	24236051	Human		name
597788626	CV3678157	single nucleotide variant	NM_001002002.3(GMPR2):c.443G>A (p.Arg148His)	not specified [RCV004932721]	uncertain significance	14	24236118	24236118	Human		name
597788622	CV3678158	single nucleotide variant	NM_001002002.3(GMPR2):c.583G>A (p.Gly195Arg)	not specified [RCV004932722]	uncertain significance	14	24237280	24237280	Human		name
597730158	CV3678160	single nucleotide variant	NM_001002002.3(GMPR2):c.361C>T (p.Pro121Ser)	not specified [RCV004919790]	uncertain significance	14	24236036	24236036	Human		name
597730168	CV3678161	single nucleotide variant	NM_001002002.3(GMPR2):c.326A>G (p.Asp109Gly)	not specified [RCV004919791]	uncertain significance	14	24236001	24236001	Human		name
597788618	CV3678162	single nucleotide variant	NM_001002002.3(GMPR2):c.769G>A (p.Glu257Lys)	not specified [RCV004932723]	uncertain significance	14	24238317	24238317	Human		name
598264051	CV3974327	single nucleotide variant	NM_001002002.3(GMPR2):c.539T>A (p.Ile180Asn)	not specified [RCV005348748]	uncertain significance	14	24237144	24237144	Human		name
8689309	CV97396	single nucleotide variant	NM_001002002.3(GMPR2):c.812C>T (p.Ser271Phe)	not provided [RCV000122475]	uncertain significance	14	24238360	24238360	Human		name
405767894	CV3262015	single nucleotide variant	NM_001002002.3(GMPR2):c.1004G>A (p.Arg335Gln)	not specified [RCV004395404]	uncertain significance	14	24238735	24238735	Human		name
598264041	CV3974323	single nucleotide variant	NM_001002002.3(GMPR2):c.1027A>G (p.Ile343Val)	not specified [RCV005348745]	uncertain significance	14	24238758	24238758	Human		name

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