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108 records found for search term Gpr37
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405739289CV3252003single nucleotide variantNM_005302.5(GPR37):c.8C>T (p.Ala3Val)not specified [RCV004391087]uncertain significance7124764969124764969Humanname
15111192CV717953single nucleotide variantNM_005302.5(GPR37):c.240T>C (p.Phe80=)not provided [RCV000961055]benign7124764737124764737Humanname
156120785CV2275949single nucleotide variantNM_005302.5(GPR37):c.79G>A (p.Ala27Thr)not specified [RCV004139598]uncertain significance7124764898124764898Humanname
156143979CV2383895single nucleotide variantNM_005302.5(GPR37):c.33G>T (p.Met11Ile)not specified [RCV004231753]uncertain significance7124764944124764944Humanname
405739252CV3251997single nucleotide variantNM_005302.5(GPR37):c.31A>G (p.Met11Val)not specified [RCV004391081]uncertain significance7124764946124764946Humanname
405739272CV3252000single nucleotide variantNM_005302.5(GPR37):c.52C>G (p.Leu18Val)not specified [RCV004391084]uncertain significance7124764925124764925Humanname
597745232CV3685025single nucleotide variantNM_005302.5(GPR37):c.29G>T (p.Arg10Leu)not specified [RCV004922430]uncertain significance7124764948124764948Humanname
598274557CV3967312single nucleotide variantNM_005302.5(GPR37):c.67T>A (p.Ser23Thr)not specified [RCV005351477]uncertain significance7124764910124764910Humanname
598234008CV3967316single nucleotide variantNM_005302.5(GPR37):c.97G>A (p.Ala33Thr)not specified [RCV005342842]uncertain significance7124764880124764880Humanname
15183765CV706407single nucleotide variantNM_005302.5(GPR37):c.723G>T (p.Thr241=)not provided [RCV000952541]benign7124764254124764254Humanname
15163391CV743553single nucleotide variantNM_005302.5(GPR37):c.822C>T (p.Thr274=)not provided [RCV000903763]benign7124764155124764155Humanname
401772763CV2719751single nucleotide variantNM_005302.5(GPR37):c.133G>A (p.Ala45Thr)not specified [RCV004329186]uncertain significance7124764844124764844Humanname
598274561CV3967314single nucleotide variantNM_005302.5(GPR37):c.265C>A (p.Pro89Thr)not specified [RCV005351479]uncertain significance7124764712124764712Humanname
15097890CV729801single nucleotide variantNM_005302.5(GPR37):c.1011G>T (p.Val337=)not provided [RCV000891606]likely benign7124763966124763966Humanname
15183342CV729802single nucleotide variantNM_005302.5(GPR37):c.1281A>G (p.Leu427=)not provided [RCV000886205]benign7124747086124747086Humanname
15190480CV729803single nucleotide variantNM_005302.5(GPR37):c.1728A>C (p.Ser576=)not provided [RCV000888110]benign7124746639124746639Humanname
155924208CV2217835single nucleotide variantNM_005302.5(GPR37):c.407G>A (p.Arg136Lys)not specified [RCV004084008]uncertain significance7124764570124764570Humanname
156126566CV2223693single nucleotide variantNM_005302.5(GPR37):c.629G>T (p.Trp210Leu)not specified [RCV004093797]uncertain significance7124764348124764348Humanname
156303962CV2255485single nucleotide variantNM_005302.5(GPR37):c.626G>A (p.Gly209Glu)not specified [RCV004118137]uncertain significance7124764351124764351Humanname
156163677CV2319651single nucleotide variantNM_005302.5(GPR37):c.767A>G (p.Gln256Arg)not specified [RCV004185196]uncertain significance7124764210124764210Humanname
156355892CV2320682single nucleotide variantNM_005302.5(GPR37):c.521C>G (p.Pro174Arg)not specified [RCV004179043]uncertain significance7124764456124764456Humanname
156125492CV2350196single nucleotide variantNM_005302.5(GPR37):c.467C>T (p.Pro156Leu)not specified [RCV004200110]uncertain significance7124764510124764510Humanname
156074914CV2365561single nucleotide variantNM_005302.5(GPR37):c.414C>A (p.Asn138Lys)not specified [RCV004211675]uncertain significance7124764563124764563Humanname
156067963CV2381131single nucleotide variantNM_005302.5(GPR37):c.797G>T (p.Cys266Phe)not specified [RCV004225161]uncertain significance7124764180124764180Humanname
329386672CV2428376single nucleotide variantNM_005302.5(GPR37):c.308A>C (p.Glu103Ala)not specified [RCV004253184]uncertain significance7124764669124764669Humanname
401775422CV2692369single nucleotide variantNM_005302.5(GPR37):c.869A>G (p.Tyr290Cys)not specified [RCV004310350]uncertain significance7124764108124764108Humanname
401764865CV2701474single nucleotide variantNM_005302.5(GPR37):c.791T>A (p.Val264Asp)not specified [RCV004312143]uncertain significance7124764186124764186Humanname
401885726CV2774487single nucleotide variantNM_005302.5(GPR37):c.524G>A (p.Gly175Glu)not specified [RCV004349979]uncertain significance7124764453124764453Humanname
401883013CV2788712single nucleotide variantNM_005302.5(GPR37):c.847A>G (p.Met283Val)not specified [RCV004361189]uncertain significance7124764130124764130Humanname
405739265CV3251999single nucleotide variantNM_005302.5(GPR37):c.424C>A (p.Leu142Ile)not specified [RCV004391083]uncertain significance7124764553124764553Humanname
405739277CV3252001single nucleotide variantNM_005302.5(GPR37):c.548C>G (p.Pro183Arg)not specified [RCV004391085]uncertain significance7124764429124764429Humanname
405739281CV3252002single nucleotide variantNM_005302.5(GPR37):c.605A>G (p.Asn202Ser)not specified [RCV004391086]likely benign7124764372124764372Humanname
407526602CV3436745single nucleotide variantNM_005302.5(GPR37):c.325C>T (p.Pro109Ser)not specified [RCV004632497]uncertain significance7124764652124764652Humanname
407526606CV3436746single nucleotide variantNM_005302.5(GPR37):c.785A>G (p.Tyr262Cys)not specified [RCV004632498]uncertain significance7124764192124764192Humanname
407526610CV3436747single nucleotide variantNM_005302.5(GPR37):c.554G>A (p.Arg185Lys)not specified [RCV004632499]uncertain significance7124764423124764423Humanname
597745229CV3685024single nucleotide variantNM_005302.5(GPR37):c.630G>T (p.Trp210Cys)not specified [RCV004922429]uncertain significance7124764347124764347Humanname
598274559CV3967313single nucleotide variantNM_005302.5(GPR37):c.836A>G (p.Asn279Ser)not specified [RCV005351478]uncertain significance7124764141124764141Humanname
598274563CV3967315single nucleotide variantNM_005302.5(GPR37):c.319G>A (p.Ala107Thr)not specified [RCV005351480]uncertain significance7124764658124764658Humanname
15151324CV717954single nucleotide variantNM_005302.5(GPR37):c.683G>T (p.Gly228Val)not provided [RCV000968114]benign7124764294124764294Humanname
156140416CV2202976single nucleotide variantNM_005302.5(GPR37):c.1315G>A (p.Asp439Asn)not specified [RCV004069237]uncertain significance7124747052124747052Humanname
156239912CV2286009single nucleotide variantNM_005302.5(GPR37):c.1462A>G (p.Ser488Gly)not specified [RCV004143918]uncertain significance7124746905124746905Humanname
156360979CV2329747single nucleotide variantNM_005302.5(GPR37):c.1519C>A (p.Pro507Thr)not specified [RCV004180841]uncertain significance7124746848124746848Humanname
156163199CV2389545single nucleotide variantNM_005302.5(GPR37):c.1579A>G (p.Met527Val)not specified [RCV004243616]uncertain significance7124746788124746788Humanname
401756985CV2678168single nucleotide variantNM_005302.5(GPR37):c.1261A>G (p.Ile421Val)not specified [RCV004296676]uncertain significance7124747106124747106Humanname
401731851CV2712184single nucleotide variantNM_005302.5(GPR37):c.1113A>C (p.Glu371Asp)not specified [RCV004311903]uncertain significance7124747254124747254Humanname
405739248CV3251996single nucleotide variantNM_005302.5(GPR37):c.1777C>T (p.Leu593Phe)not specified [RCV004391080]uncertain significance7124746590124746590Humanname
407526596CV3436743single nucleotide variantNM_005302.5(GPR37):c.1475G>A (p.Cys492Tyr)not specified [RCV004632495]uncertain significance7124746892124746892Humanname
407526599CV3436744single nucleotide variantNM_005302.5(GPR37):c.1606T>C (p.Phe536Leu)not specified [RCV004632496]uncertain significance7124746761124746761Humanname
407526613CV3436748single nucleotide variantNM_005302.5(GPR37):c.1450A>C (p.Ile484Leu)not specified [RCV004632500]uncertain significance7124746917124746917Humanname
597745236CV3685026single nucleotide variantNM_005302.5(GPR37):c.1580T>G (p.Met527Arg)not specified [RCV004922431]uncertain significance7124746787124746787Humanname
597745242CV3685027single nucleotide variantNM_005302.5(GPR37):c.1789A>G (p.Ser597Gly)not specified [RCV004922432]uncertain significance7124746578124746578Humanname
405739338CV3252010single nucleotide variantNM_004767.5(GPR37L1):c.165C>T (p.Gly55=)not specified [RCV004391094]likely benign1202123128202123128Humanname
329355316CV2449318single nucleotide variantNM_004767.5(GPR37L1):c.63G>C (p.Arg21Ser)not specified [RCV004257447]uncertain significance1202123026202123026Humanname
8629230CV84375single nucleotide variantNM_004767.3(GPR37L1):c.71G>A (p.Gly24Glu)Malignant melanoma [RCV000064457]not provided1202123034202123034Humanname
329357621CV2427783single nucleotide variantNM_004767.5(GPR37L1):c.166G>A (p.Val56Met)not specified [RCV004252562]uncertain significance1202123129202123129Humanname
329353121CV2468086single nucleotide variantNM_004767.5(GPR37L1):c.205C>T (p.Arg69Trp)not specified [RCV004275692]uncertain significance1202123168202123168Humanname
405739345CV3252011single nucleotide variantNM_004767.5(GPR37L1):c.181C>T (p.Pro61Ser)not specified [RCV004391095]uncertain significance1202123144202123144Humanname
407526616CV3436750single nucleotide variantNM_004767.5(GPR37L1):c.202C>T (p.Pro68Ser)not specified [RCV004632501]uncertain significance1202123165202123165Humanname
156398651CV2194701single nucleotide variantNM_004767.5(GPR37L1):c.879C>A (p.Ser293Arg)not specified [RCV004075258]uncertain significance1202127989202127989Humanname
155970512CV2217836single nucleotide variantNM_004767.5(GPR37L1):c.325G>A (p.Ala109Thr)not specified [RCV004084009]likely benign1202123288202123288Humanname
156172513CV2267910single nucleotide variantNM_004767.5(GPR37L1):c.365C>G (p.Pro122Arg)not specified [RCV004136202]uncertain significance1202123328202123328Humanname
156238253CV2285870single nucleotide variantNM_004767.5(GPR37L1):c.976G>A (p.Val326Ile)not specified [RCV004143806]uncertain significance1202128086202128086Humanname
156277801CV2352104single nucleotide variantNM_004767.5(GPR37L1):c.444C>A (p.Asn148Lys)not specified [RCV004191196]uncertain significance1202123407202123407Humanname
156190213CV2391044single nucleotide variantNM_004767.5(GPR37L1):c.886G>A (p.Glu296Lys)not specified [RCV004235039]uncertain significance1202127996202127996Humanname
401735742CV2672730single nucleotide variantNM_004767.5(GPR37L1):c.614C>T (p.Ala205Val)not specified [RCV004287742]uncertain significance1202123577202123577Humanname
401773819CV2702451single nucleotide variantNM_004767.5(GPR37L1):c.932G>T (p.Trp311Leu)not specified [RCV004316963]uncertain significance1202128042202128042Humanname
401866003CV2762486single nucleotide variantNM_004767.5(GPR37L1):c.745C>G (p.Leu249Val)not specified [RCV004338022]uncertain significance1202127855202127855Humanname
405739352CV3252012single nucleotide variantNM_004767.5(GPR37L1):c.583C>G (p.Gln195Glu)not specified [RCV004391096]uncertain significance1202123546202123546Humanname
405739360CV3252013single nucleotide variantNM_004767.5(GPR37L1):c.748G>A (p.Ala250Thr)not specified [RCV004391097]uncertain significance1202127858202127858Humanname
407504604CV3436749single nucleotide variantNM_004767.5(GPR37L1):c.601G>A (p.Val201Ile)not specified [RCV004623995]uncertain significance1202123564202123564Humanname
407526620CV3436751single nucleotide variantNM_004767.5(GPR37L1):c.829G>A (p.Ala277Thr)not specified [RCV004632502]uncertain significance1202127939202127939Humanname
407526625CV3436754single nucleotide variantNM_004767.5(GPR37L1):c.977T>G (p.Val326Gly)not specified [RCV004632504]uncertain significance1202128087202128087Humanname
597745247CV3685029single nucleotide variantNM_004767.5(GPR37L1):c.764T>C (p.Ile255Thr)not specified [RCV004922433]uncertain significance1202127874202127874Humanname
597790149CV3685030single nucleotide variantNM_004767.5(GPR37L1):c.410C>T (p.Ala137Val)not specified [RCV004933142]uncertain significance1202123373202123373Humanname
597745252CV3685031single nucleotide variantNM_004767.5(GPR37L1):c.502A>G (p.Ile168Val)not specified [RCV004922434]uncertain significance1202123465202123465Humanname
597769644CV3685033single nucleotide variantNM_004767.5(GPR37L1):c.481C>G (p.Leu161Val)not specified [RCV004928113]uncertain significance1202123444202123444Humanname
597745257CV3685034single nucleotide variantNM_004767.5(GPR37L1):c.490G>A (p.Ala164Thr)not specified [RCV004922435]uncertain significance1202123453202123453Humanname
598234014CV3967318single nucleotide variantNM_004767.5(GPR37L1):c.463G>A (p.Val155Met)not specified [RCV005342843]uncertain significance1202123426202123426Humanname
598274567CV3967319single nucleotide variantNM_004767.5(GPR37L1):c.782C>T (p.Thr261Met)not specified [RCV005351482]uncertain significance1202127892202127892Humanname
598274571CV3967321single nucleotide variantNM_004767.5(GPR37L1):c.907A>G (p.Met303Val)not specified [RCV005351484]uncertain significance1202128017202128017Humanname
598274573CV3967322single nucleotide variantNM_004767.5(GPR37L1):c.631G>A (p.Val211Ile)not specified [RCV005351485]uncertain significance1202127741202127741Humanname
598274576CV3967323single nucleotide variantNM_004767.5(GPR37L1):c.362A>G (p.Tyr121Cys)not specified [RCV005351486]uncertain significance1202123325202123325Humanname
598274578CV3967324single nucleotide variantNM_004767.5(GPR37L1):c.481C>A (p.Leu161Met)not specified [RCV005351487]uncertain significance1202123444202123444Humanname
598274583CV3967327single nucleotide variantNM_004767.5(GPR37L1):c.650C>T (p.Thr217Met)not specified [RCV005351489]uncertain significance1202127760202127760Humanname
156051894CV2320261single nucleotide variantNM_004767.5(GPR37L1):c.1328C>T (p.Ser443Leu)not specified [RCV004178430]uncertain significance1202128438202128438Humanname
156037558CV2332547single nucleotide variantNM_004767.5(GPR37L1):c.1240G>T (p.Val414Leu)not specified [RCV004196263]uncertain significance1202128350202128350Humanname
155977596CV2338794single nucleotide variantNM_004767.5(GPR37L1):c.1081G>A (p.Val361Met)not specified [RCV004182352]uncertain significance1202128191202128191Humanname
156184490CV2349941single nucleotide variantNM_004767.5(GPR37L1):c.1339G>A (p.Ala447Thr)not specified [RCV004206353]uncertain significance1202128449202128449Humanname
155919302CV2360218single nucleotide variantNM_004767.5(GPR37L1):c.1347T>A (p.Asn449Lys)not specified [RCV004208567]uncertain significance1202128457202128457Humanname
156343263CV2364087single nucleotide variantNM_004767.5(GPR37L1):c.1178C>T (p.Thr393Ile)not specified [RCV004221469]uncertain significance1202128288202128288Humanname
156064088CV2375937single nucleotide variantNM_004767.5(GPR37L1):c.1327T>C (p.Ser443Pro)not specified [RCV004218147]uncertain significance1202128437202128437Humanname
329355990CV2442426single nucleotide variantNM_004767.5(GPR37L1):c.1169C>T (p.Thr390Ile)not specified [RCV004266672]uncertain significance1202128279202128279Humanname
401722003CV2680780single nucleotide variantNM_004767.5(GPR37L1):c.1039G>T (p.Ala347Ser)not specified [RCV004293430]uncertain significance1202128149202128149Humanname
401730665CV2711438single nucleotide variantNM_004767.5(GPR37L1):c.1205A>G (p.Gln402Arg)not specified [RCV004313184]uncertain significance1202128315202128315Humanname
401778146CV2718515single nucleotide variantNM_004767.5(GPR37L1):c.1418C>T (p.Pro473Leu)not specified [RCV004318322]uncertain significance1202128528202128528Humanname
405739295CV3252004single nucleotide variantNM_004767.5(GPR37L1):c.1129G>A (p.Val377Ile)not specified [RCV004391088]uncertain significance1202128239202128239Humanname
405739303CV3252005single nucleotide variantNM_004767.5(GPR37L1):c.1141G>A (p.Val381Met)not specified [RCV004391089]uncertain significance1202128251202128251Humanname
405739309CV3252006single nucleotide variantNM_004767.5(GPR37L1):c.1162G>A (p.Glu388Lys)not specified [RCV004391090]uncertain significance1202128272202128272Humanname
405739317CV3252007single nucleotide variantNM_004767.5(GPR37L1):c.1346A>G (p.Asn449Ser)not specified [RCV004391091]likely benign1202128456202128456Humanname
405739324CV3252008single nucleotide variantNM_004767.5(GPR37L1):c.1352C>T (p.Ser451Leu)not specified [RCV004391092]uncertain significance1202128462202128462Humanname
405739331CV3252009single nucleotide variantNM_004767.5(GPR37L1):c.1420C>T (p.Leu474Phe)not specified [RCV004391093]uncertain significance1202128530202128530Humanname
597790145CV3685028single nucleotide variantNM_004767.5(GPR37L1):c.1318G>A (p.Gly440Ser)not specified [RCV004933141]uncertain significance1202128428202128428Humanname
597790153CV3685032single nucleotide variantNM_004767.5(GPR37L1):c.1031A>G (p.Glu344Gly)not specified [RCV004933143]uncertain significance1202128141202128141Humanname
597769647CV3685035single nucleotide variantNM_004767.5(GPR37L1):c.1418C>G (p.Pro473Arg)not specified [RCV004928114]uncertain significance1202128528202128528Humanname
598274569CV3967320single nucleotide variantNM_004767.5(GPR37L1):c.1265C>T (p.Pro422Leu)not specified [RCV005351483]uncertain significance1202128375202128375Humanname
598234021CV3967325single nucleotide variantNM_004767.5(GPR37L1):c.1012C>T (p.Pro338Ser)not specified [RCV005342844]uncertain significance1202128122202128122Humanname
598274581CV3967326single nucleotide variantNM_004767.5(GPR37L1):c.1297T>C (p.Cys433Arg)not specified [RCV005351488]uncertain significance1202128407202128407Humanname
13526917CV513204single nucleotide variantNM_004767.5(GPR37L1):c.1047G>T (p.Lys349Asn)not provided [RCV000625728]uncertain significance1202128157202128157Humanname