Gpr18 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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100 records found for search term Gpr18

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597744989	CV3684930	single nucleotide variant	NM_001098200.2(GPR18):c.8C>T (p.Thr3Ile)	not specified [RCV004922376]	uncertain significance	13	99255865	99255865	Human		name
401723894	CV2725076	single nucleotide variant	NM_001098200.2(GPR18):c.77T>C (p.Leu26Pro)	not specified [RCV004319827]	uncertain significance	13	99255796	99255796	Human		name
156303617	CV2258879	single nucleotide variant	NM_001098200.2(GPR18):c.216A>G (p.Ile72Met)	not specified [RCV004118086]	uncertain significance	13	99255657	99255657	Human		name
156303624	CV2258880	single nucleotide variant	NM_001098200.2(GPR18):c.218T>C (p.Met73Thr)	not specified [RCV004118087]	uncertain significance	13	99255655	99255655	Human		name
156347813	CV2315470	single nucleotide variant	NM_001098200.2(GPR18):c.161G>T (p.Arg54Ile)	not specified [RCV004167419]	uncertain significance	13	99255712	99255712	Human		name
401885529	CV2768226	single nucleotide variant	NM_001098200.2(GPR18):c.104T>C (p.Ile35Thr)	not specified [RCV004350224]	uncertain significance	13	99255769	99255769	Human		name
156236525	CV2193487	single nucleotide variant	NM_001098200.2(GPR18):c.656C>T (p.Thr219Met)	not specified [RCV004072971]	uncertain significance	13	99255217	99255217	Human		name
155932364	CV2232065	single nucleotide variant	NM_001098200.2(GPR18):c.443T>C (p.Met148Thr)	not specified [RCV004093109]	uncertain significance	13	99255430	99255430	Human		name
156059783	CV2239368	single nucleotide variant	NM_001098200.2(GPR18):c.794A>T (p.Asn265Ile)	not specified [RCV004114103]	uncertain significance	13	99255079	99255079	Human		name
156278165	CV2284909	single nucleotide variant	NM_001098200.2(GPR18):c.628A>G (p.Ile210Val)	not specified [RCV004143357]	uncertain significance	13	99255245	99255245	Human		name
156259871	CV2305007	single nucleotide variant	NM_001098200.2(GPR18):c.421G>C (p.Ala141Pro)	not specified [RCV004168898]	uncertain significance	13	99255452	99255452	Human		name
156287162	CV2327298	single nucleotide variant	NM_001098200.2(GPR18):c.932G>T (p.Arg311Leu)	not specified [RCV004174742]	uncertain significance	13	99254941	99254941	Human		name
329380027	CV2444154	single nucleotide variant	NM_001098200.2(GPR18):c.649G>A (p.Gly217Ser)	not specified [RCV004260891]	uncertain significance	13	99255224	99255224	Human		name
401759284	CV2701472	single nucleotide variant	NM_001098200.2(GPR18):c.988A>C (p.Met330Leu)	not specified [RCV004312141]	uncertain significance	13	99254885	99254885	Human		name
401867711	CV2767063	single nucleotide variant	NM_001098200.2(GPR18):c.947G>T (p.Arg316Leu)	not specified [RCV004347469]	uncertain significance	13	99254926	99254926	Human		name
405738493	CV3255344	single nucleotide variant	NM_001098200.2(GPR18):c.331C>T (p.Leu111Phe)	not specified [RCV004390971]	uncertain significance	13	99255542	99255542	Human		name
405738499	CV3255345	single nucleotide variant	NM_001098200.2(GPR18):c.427G>A (p.Val143Met)	not specified [RCV004390972]	uncertain significance	13	99255446	99255446	Human		name
405738504	CV3255346	single nucleotide variant	NM_001098200.2(GPR18):c.691A>C (p.Ile231Leu)	not specified [RCV004390973]	uncertain significance	13	99255182	99255182	Human		name
405738515	CV3255347	single nucleotide variant	NM_001098200.2(GPR18):c.839G>C (p.Cys280Ser)	not specified [RCV004390974]	uncertain significance	13	99255034	99255034	Human		name
405738519	CV3255348	single nucleotide variant	NM_001098200.2(GPR18):c.887G>A (p.Arg296Gln)	not specified [RCV004390975]	uncertain significance	13	99254986	99254986	Human		name
405738528	CV3255349	single nucleotide variant	NM_001098200.2(GPR18):c.903G>A (p.Met301Ile)	not specified [RCV004390976]	uncertain significance	13	99254970	99254970	Human		name
407479133	CV3436695	single nucleotide variant	NM_001098200.2(GPR18):c.776C>T (p.Thr259Met)	not specified [RCV004623989]	uncertain significance	13	99255097	99255097	Human		name
597789894	CV3684931	single nucleotide variant	NM_001098200.2(GPR18):c.889G>A (p.Val297Ile)	not specified [RCV004933101]	uncertain significance	13	99254984	99254984	Human		name
597789897	CV3684932	single nucleotide variant	NM_001098200.2(GPR18):c.781G>C (p.Glu261Gln)	not specified [RCV004933102]	uncertain significance	13	99255092	99255092	Human		name
597744994	CV3684933	single nucleotide variant	NM_001098200.2(GPR18):c.883G>A (p.Ala295Thr)	not specified [RCV004922377]	uncertain significance	13	99254990	99254990	Human		name
597744999	CV3684934	single nucleotide variant	NM_001098200.2(GPR18):c.863T>A (p.Ile288Asn)	not specified [RCV004922378]	uncertain significance	13	99255010	99255010	Human		name
597745003	CV3684935	single nucleotide variant	NM_001098200.2(GPR18):c.757G>A (p.Ala253Thr)	not specified [RCV004922379]	uncertain significance	13	99255116	99255116	Human		name
598274439	CV3971182	single nucleotide variant	NM_001098200.2(GPR18):c.961C>T (p.Arg321Trp)	not specified [RCV005351423]	uncertain significance	13	99254912	99254912	Human		name
598233903	CV3971183	single nucleotide variant	NM_001098200.2(GPR18):c.733T>C (p.Phe245Leu)	not specified [RCV005342825]	uncertain significance	13	99255140	99255140	Human		name
15170028	CV702753	single nucleotide variant	NM_001098200.2(GPR18):c.559C>A (p.Leu187Met)	not provided [RCV000949574]	likely benign	13	99255314	99255314	Human		name
405257847	CV3207912	single nucleotide variant	NM_180989.6(GPR180):c.145+9G>C	GPR180-related disorder [RCV003941386]	likely benign	13	94602081	94602081	Human		name , trait , alternate_id
405279828	CV3191491	single nucleotide variant	NM_180989.6(GPR180):c.926A>G (p.Asp309Gly)	GPR180-related disorder [RCV003919643]	benign	13	94623140	94623140	Human		name , trait , alternate_id
405276987	CV3193557	single nucleotide variant	NM_180989.6(GPR180):c.852G>A (p.Thr284=)	GPR180-related disorder [RCV003974725]	benign	13	94621193	94621193	Human		name , trait , alternate_id
405284468	CV3196839	single nucleotide variant	NM_180989.6(GPR180):c.459A>G (p.Pro153=)	GPR180-related disorder [RCV003979709]	benign	13	94612344	94612344	Human		name , trait , alternate_id
405267851	CV3198474	single nucleotide variant	NM_180989.6(GPR180):c.813G>C (p.Met271Ile)	GPR180-related disorder [RCV003911839]	benign	13	94621154	94621154	Human		name , trait , alternate_id
405276806	CV3198625	single nucleotide variant	NM_180989.6(GPR180):c.1155A>G (p.Gln385=)	GPR180-related disorder [RCV003903952]	likely benign	13	94626034	94626034	Human		name , trait , alternate_id
405280403	CV3200729	single nucleotide variant	NM_180989.6(GPR180):c.465C>T (p.Ala155=)	GPR180-related disorder [RCV003977354]	benign	13	94612350	94612350	Human		name , trait , alternate_id
405294778	CV3211819	single nucleotide variant	NM_180989.6(GPR180):c.574T>C (p.Leu192=)	GPR180-related disorder [RCV003934674]	likely benign	13	94619218	94619218	Human		name , trait , alternate_id
405278356	CV3216517	single nucleotide variant	NM_180989.6(GPR180):c.1049G>A (p.Ser350Asn)	GPR180-related disorder [RCV003954439]	benign	13	94623263	94623263	Human		name , trait , alternate_id
405289920	CV3218946	single nucleotide variant	NM_180989.6(GPR180):c.321C>T (p.Thr107=)	GPR180-related disorder [RCV003962019]	likely benign	13	94612206	94612206	Human		name , trait , alternate_id
156338684	CV2351463	single nucleotide variant	NM_180989.6(GPR180):c.8G>T (p.Gly3Val)	not specified [RCV004193148]	uncertain significance	13	94601935	94601935	Human		name
597789903	CV3684936	single nucleotide variant	NM_180989.6(GPR180):c.8G>C (p.Gly3Ala)	not specified [RCV004933103]	uncertain significance	13	94601935	94601935	Human		name
155965689	CV2395988	single nucleotide variant	NM_004951.5(GPR183):c.16G>A (p.Ala6Thr)	not specified [RCV004237536]	uncertain significance	13	99296130	99296130	Human		name
156281598	CV2338473	single nucleotide variant	NM_004951.5(GPR183):c.86C>T (p.Thr29Met)	not specified [RCV004188515]	uncertain significance	13	99296060	99296060	Human		name
401883793	CV2785767	single nucleotide variant	NM_004951.5(GPR183):c.52G>A (p.Gly18Arg)	not specified [RCV004365016]	uncertain significance	13	99296094	99296094	Human		name
597745051	CV3684950	single nucleotide variant	NM_004951.5(GPR183):c.98T>C (p.Val33Ala)	not specified [RCV004922390]	uncertain significance	13	99296048	99296048	Human		name
15199604	CV702436	single nucleotide variant	NM_007264.4(GPR182):c.543G>A (p.Ser181=)	not provided [RCV000957086]	benign	12	56995752	56995752	Human		name
156277346	CV2328234	single nucleotide variant	NM_004951.5(GPR183):c.101T>C (p.Met34Thr)	not specified [RCV004173323]	uncertain significance	13	99296045	99296045	Human		name
329401435	CV2460824	single nucleotide variant	NM_004951.5(GPR183):c.121G>A (p.Val41Ile)	not specified [RCV004271138]	uncertain significance	13	99296025	99296025	Human		name
405738557	CV3255353	single nucleotide variant	NM_180989.6(GPR180):c.157C>T (p.Leu53Phe)	not specified [RCV004390980]	uncertain significance	13	94605402	94605402	Human		name
405738590	CV3255358	single nucleotide variant	NM_004951.5(GPR183):c.139G>A (p.Val47Met)	not specified [RCV004390985]	uncertain significance	13	99296007	99296007	Human		name
405738594	CV3255359	single nucleotide variant	NM_004951.5(GPR183):c.202C>T (p.Leu68Phe)	not specified [RCV004390986]	uncertain significance	13	99295944	99295944	Human		name
405738602	CV3255360	single nucleotide variant	NM_004951.5(GPR183):c.269A>T (p.Tyr90Phe)	not specified [RCV004390987]	uncertain significance	13	99295877	99295877	Human		name
405738616	CV3255362	single nucleotide variant	NM_004951.5(GPR183):c.295A>T (p.Ile99Phe)	not specified [RCV004390989]	uncertain significance	13	99295851	99295851	Human		name
597789905	CV3684938	single nucleotide variant	NM_180989.6(GPR180):c.254G>A (p.Ser85Asn)	not specified [RCV004933104]	uncertain significance	13	94605499	94605499	Human		name
598274441	CV3971185	single nucleotide variant	NM_180989.6(GPR180):c.286T>C (p.Ser96Pro)	not specified [RCV005351424]	uncertain significance	13	94605531	94605531	Human		name
156089889	CV2206528	single nucleotide variant	NM_180989.6(GPR180):c.431T>C (p.Ile144Thr)	not specified [RCV004080880]	uncertain significance	13	94612316	94612316	Human		name
156037381	CV2313492	single nucleotide variant	NM_180989.6(GPR180):c.968G>A (p.Gly323Glu)	not specified [RCV004163798]	uncertain significance	13	94623182	94623182	Human		name
156290191	CV2324883	single nucleotide variant	NM_180989.6(GPR180):c.888G>T (p.Met296Ile)	not specified [RCV004175151]	likely benign	13	94621229	94621229	Human		name
156336349	CV2333659	single nucleotide variant	NM_180989.6(GPR180):c.598G>A (p.Gly200Arg)	not specified [RCV004192499]	uncertain significance	13	94619242	94619242	Human		name
155905622	CV2349817	single nucleotide variant	NM_004951.5(GPR183):c.751G>A (p.Val251Ile)	not specified [RCV004204225]	uncertain significance	13	99295395	99295395	Human		name
401740682	CV2679780	single nucleotide variant	NM_180989.6(GPR180):c.919T>C (p.Phe307Leu)	not specified [RCV004282244]	uncertain significance	13	94623133	94623133	Human		name
401762437	CV2714139	single nucleotide variant	NM_180989.6(GPR180):c.328A>C (p.Asn110His)	not specified [RCV004317391]	uncertain significance	13	94612213	94612213	Human		name
401889280	CV2759758	single nucleotide variant	NM_004951.5(GPR183):c.413G>A (p.Arg138His)	not specified [RCV004342803]	uncertain significance	13	99295733	99295733	Human		name
401877242	CV2769386	single nucleotide variant	NM_004951.5(GPR183):c.929T>C (p.Phe310Ser)	not specified [RCV004357375]	uncertain significance	13	99295217	99295217	Human		name
405738621	CV3255363	single nucleotide variant	NM_004951.5(GPR183):c.566A>T (p.Glu189Val)	not specified [RCV004390990]	uncertain significance	13	99295580	99295580	Human		name
405738629	CV3255364	single nucleotide variant	NM_004951.5(GPR183):c.801T>A (p.His267Gln)	not specified [RCV004390991]	uncertain significance	13	99295345	99295345	Human		name
407526479	CV3436696	single nucleotide variant	NM_180989.6(GPR180):c.722G>A (p.Gly241Glu)	not specified [RCV004632453]	uncertain significance	13	94619503	94619503	Human		name
407526486	CV3436698	single nucleotide variant	NM_180989.6(GPR180):c.475C>A (p.Pro159Thr)	not specified [RCV004632455]	uncertain significance	13	94612360	94612360	Human		name
407526489	CV3436699	single nucleotide variant	NM_007264.4(GPR182):c.770G>A (p.Cys257Tyr)	not specified [RCV004632456]	uncertain significance	12	56995979	56995979	Human		name
407526493	CV3436700	single nucleotide variant	NM_007264.4(GPR182):c.821A>G (p.Tyr274Cys)	not specified [RCV004632457]	uncertain significance	12	56996030	56996030	Human		name
407479865	CV3436703	single nucleotide variant	NM_004951.5(GPR183):c.490C>T (p.Leu164Phe)	not specified [RCV004632460]	uncertain significance	13	99295656	99295656	Human		name
597745007	CV3684937	single nucleotide variant	NM_180989.6(GPR180):c.380C>G (p.Ala127Gly)	not specified [RCV004922380]	uncertain significance	13	94612265	94612265	Human		name
597745017	CV3684941	single nucleotide variant	NM_180989.6(GPR180):c.768A>T (p.Leu256Phe)	not specified [RCV004922382]	uncertain significance	13	94621109	94621109	Human		name
597745025	CV3684943	single nucleotide variant	NM_007264.4(GPR182):c.532T>G (p.Trp178Gly)	not specified [RCV004922384]	uncertain significance	12	56995741	56995741	Human		name
597790134	CV3684944	single nucleotide variant	NM_007264.4(GPR182):c.784G>C (p.Ala262Pro)	not specified [RCV004933106]	uncertain significance	12	56995993	56995993	Human		name
597745030	CV3684945	single nucleotide variant	NM_007264.4(GPR182):c.343C>G (p.Leu115Val)	not specified [RCV004922385]	uncertain significance	12	56995552	56995552	Human		name
597745035	CV3684946	single nucleotide variant	NM_007264.4(GPR182):c.845C>A (p.Thr282Lys)	not specified [RCV004922386]	uncertain significance	12	56996054	56996054	Human		name
597745040	CV3684947	single nucleotide variant	NM_004951.5(GPR183):c.323C>T (p.Ala108Val)	not specified [RCV004922387]	uncertain significance	13	99295823	99295823	Human		name
597745042	CV3684948	single nucleotide variant	NM_004951.5(GPR183):c.973C>T (p.Arg325Trp)	not specified [RCV004922388]	uncertain significance	13	99295173	99295173	Human		name
597745056	CV3684951	single nucleotide variant	NM_004951.5(GPR183):c.944A>G (p.Tyr315Cys)	not specified [RCV004922391]	uncertain significance	13	99295202	99295202	Human		name
597745062	CV3684952	single nucleotide variant	NM_004951.5(GPR183):c.966G>C (p.Met322Ile)	not specified [RCV004922392]	uncertain significance	13	99295180	99295180	Human		name
598233909	CV3971184	single nucleotide variant	NM_180989.6(GPR180):c.442A>G (p.Met148Val)	not specified [RCV005342826]	uncertain significance	13	94612327	94612327	Human		name
598233915	CV3971186	single nucleotide variant	NM_007264.4(GPR182):c.982C>T (p.Arg328Trp)	not specified [RCV005342827]	uncertain significance	12	56996191	56996191	Human		name
598233923	CV3971187	single nucleotide variant	NM_004951.5(GPR183):c.817C>T (p.Arg273Cys)	not specified [RCV005342828]	uncertain significance	13	99295329	99295329	Human		name
598274443	CV3971188	single nucleotide variant	NM_004951.5(GPR183):c.913C>T (p.Pro305Ser)	not specified [RCV005351425]	uncertain significance	13	99295233	99295233	Human		name
156098899	CV2306499	single nucleotide variant	NM_004951.5(GPR183):c.1073C>T (p.Ser358Leu)	not specified [RCV004157115]	likely benign	13	99295073	99295073	Human		name
156085961	CV2340897	single nucleotide variant	NM_180989.6(GPR180):c.1310G>A (p.Arg437His)	not specified [RCV004181395]	uncertain significance	13	94627158	94627158	Human		name
401892207	CV2777324	single nucleotide variant	NM_004951.5(GPR183):c.1031G>A (p.Arg344His)	not specified [RCV004354337]	uncertain significance	13	99295115	99295115	Human		name
405738535	CV3255350	single nucleotide variant	NM_180989.6(GPR180):c.1145G>A (p.Ser382Asn)	not specified [RCV004390977]	likely benign	13	94626024	94626024	Human		name
405738543	CV3255351	single nucleotide variant	NM_180989.6(GPR180):c.1270G>T (p.Val424Leu)	not specified [RCV004390978]	uncertain significance	13	94627118	94627118	Human		name
405738581	CV3255357	single nucleotide variant	NM_004951.5(GPR183):c.1045A>G (p.Thr349Ala)	not specified [RCV004390984]	uncertain significance	13	99295101	99295101	Human		name
407526482	CV3436697	single nucleotide variant	NM_180989.6(GPR180):c.1205T>C (p.Met402Thr)	not specified [RCV004632454]	uncertain significance	13	94627053	94627053	Human		name
407526496	CV3436701	single nucleotide variant	NM_007264.4(GPR182):c.1147T>C (p.Phe383Leu)	not specified [RCV004632458]	uncertain significance	12	56996356	56996356	Human		name
597745012	CV3684939	single nucleotide variant	NM_180989.6(GPR180):c.1138A>G (p.Ile380Val)	not specified [RCV004922381]	uncertain significance	13	94626017	94626017	Human		name
597789909	CV3684940	single nucleotide variant	NM_180989.6(GPR180):c.1084A>G (p.Lys362Glu)	not specified [RCV004933105]	uncertain significance	13	94623298	94623298	Human		name
597745022	CV3684942	single nucleotide variant	NM_180989.6(GPR180):c.1050T>A (p.Ser350Arg)	not specified [RCV004922383]	uncertain significance	13	94623264	94623264	Human		name
597745046	CV3684949	single nucleotide variant	NM_004951.5(GPR183):c.1058T>C (p.Ile353Thr)	not specified [RCV004922389]	uncertain significance	13	99295088	99295088	Human		name
598274447	CV3971190	single nucleotide variant	NM_004951.5(GPR183):c.1051A>G (p.Met351Val)	not specified [RCV005351427]	uncertain significance	13	99295095	99295095	Human		name
8634805	CV90025	single nucleotide variant	NM_007264.3(GPR182):c.1145G>A (p.Ser382Asn)	Malignant melanoma [RCV000070122]	not provided	12	56996354	56996354	Human		name

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