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46 records found for search term Adcyap1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598244407CV3944753single nucleotide variantNM_001099733.2(ADCYAP1):c.267C>T (p.Asn89=)not specified [RCV005322046]likely benign18908289908289Humanname
401770801CV2707423single nucleotide variantNM_001099733.2(ADCYAP1):c.86C>T (p.Ala29Val)not specified [RCV004312810]uncertain significance18905472905472Humanname
401873197CV2779756single nucleotide variantNM_001099733.2(ADCYAP1):c.70A>C (p.Ser24Arg)not specified [RCV004353394]uncertain significance18905456905456Humanname
156230712CV2264213single nucleotide variantNM_001099733.2(ADCYAP1):c.277C>T (p.Arg93Cys)not specified [RCV004136359]uncertain significance18908299908299Humanname
156152053CV2307602single nucleotide variantNM_001099733.2(ADCYAP1):c.284T>C (p.Val95Ala)not specified [RCV004168026]uncertain significance18908306908306Humanname
156296393CV2318137single nucleotide variantNM_001099733.2(ADCYAP1):c.218C>T (p.Ala73Val)not specified [RCV004177548]uncertain significance18907766907766Humanname
156182749CV2382156single nucleotide variantNM_001099733.2(ADCYAP1):c.176C>G (p.Pro59Arg)not specified [RCV004228113]uncertain significance18907724907724Humanname
405705742CV3244019single nucleotide variantNM_001099733.2(ADCYAP1):c.154G>A (p.Asp52Asn)not specified [RCV004375884]uncertain significance18907702907702Humanname
405705816CV3244029single nucleotide variantNM_001099733.2(ADCYAP1):c.280A>C (p.Lys94Gln)not specified [RCV004375894]uncertain significance18908302908302Humanname
597804356CV3657137single nucleotide variantNM_001099733.2(ADCYAP1):c.172C>A (p.Pro58Thr)not specified [RCV004907937]uncertain significance18907720907720Humanname
597804360CV3657140single nucleotide variantNM_001099733.2(ADCYAP1):c.181G>T (p.Ala61Ser)not specified [RCV004907939]uncertain significance18907729907729Humanname
598244336CV3944743single nucleotide variantNM_001099733.2(ADCYAP1):c.267C>A (p.Asn89Lys)not specified [RCV005322036]uncertain significance18908289908289Humanname
401883664CV2764459single nucleotide variantNM_001099733.2(ADCYAP1):c.320C>T (p.Ser107Leu)not specified [RCV004339024]uncertain significance18908342908342Humanname
597804358CV3657139single nucleotide variantNM_001099733.2(ADCYAP1):c.369C>A (p.Asp123Glu)not specified [RCV004907938]likely benign18909473909473Humanname
15133943CV779426single nucleotide variantNM_001118.5(ADCYAP1R1):c.52-6C>Tnot provided [RCV000965040]benign73106482531064825Humanname
405705971CV3244050single nucleotide variantNM_001118.5(ADCYAP1R1):c.1047-3076C>Tnot specified [RCV004375915]uncertain significance73110016131100161Humanname
15158067CV700035single nucleotide variantNM_001118.5(ADCYAP1R1):c.186G>A (p.Thr62=)not provided [RCV000947004]benign73107801931078019Humanname
401757749CV2675490single nucleotide variantNM_001118.5(ADCYAP1R1):c.143A>G (p.Asn48Ser)not specified [RCV004292281]uncertain significance73106492231064922Humanname
407465245CV3429969single nucleotide variantNM_001118.5(ADCYAP1R1):c.170T>C (p.Met57Thr)not specified [RCV004613656]uncertain significance73107800331078003Humanname
597804364CV3657143single nucleotide variantNM_001118.5(ADCYAP1R1):c.221T>G (p.Leu74Arg)not specified [RCV004907941]uncertain significance73107805431078054Humanname
597804375CV3657169single nucleotide variantNM_001118.5(ADCYAP1R1):c.149C>T (p.Ser50Phe)not specified [RCV004907947]uncertain significance73106492831064928Humanname
598264600CV3944760single nucleotide variantNM_001118.5(ADCYAP1R1):c.292T>A (p.Ser98Thr)not specified [RCV005326166]uncertain significance73108171831081718Humanname
156262019CV2201065single nucleotide variantNM_001118.5(ADCYAP1R1):c.529C>T (p.Arg177Cys)not specified [RCV004075189]uncertain significance73108482731084827Humanname
156402169CV2368101single nucleotide variantNM_001118.5(ADCYAP1R1):c.550A>C (p.Thr184Pro)not specified [RCV004216451]uncertain significance73108532331085323Humanname
156000101CV2383171single nucleotide variantNM_001118.5(ADCYAP1R1):c.895A>T (p.Met299Leu)not specified [RCV004220185]uncertain significance73108763731087637Humanname
401758332CV2704433single nucleotide variantNM_001118.5(ADCYAP1R1):c.371C>T (p.Ser124Leu)not specified [RCV004311395]uncertain significance73108418331084183Humanname
401752281CV2723182single nucleotide variantNM_001118.5(ADCYAP1R1):c.556A>G (p.Asn186Asp)not specified [RCV004329426]uncertain significance73108532931085329Humanname
401879487CV2772992single nucleotide variantNM_001118.5(ADCYAP1R1):c.985G>T (p.Val329Phe)not specified [RCV004351446]uncertain significance73109267431092674Humanname
405706162CV3244075single nucleotide variantNM_001118.5(ADCYAP1R1):c.520A>G (p.Ile174Val)not specified [RCV004375940]uncertain significance73108481831084818Humanname
405706221CV3244083single nucleotide variantNM_001118.5(ADCYAP1R1):c.533T>G (p.Phe178Cys)not specified [RCV004375948]uncertain significance73108483131084831Humanname
405706280CV3244092single nucleotide variantNM_001118.5(ADCYAP1R1):c.641A>G (p.Gln214Arg)not specified [RCV004375957]uncertain significance73108541431085414Humanname
405706297CV3244094single nucleotide variantNM_001118.5(ADCYAP1R1):c.857C>T (p.Thr286Met)not specified [RCV004375959]uncertain significance73108697631086976Humanname
597804369CV3657161single nucleotide variantNM_001118.5(ADCYAP1R1):c.570G>A (p.Met190Ile)not specified [RCV004907944]uncertain significance73108534331085343Humanname
597804371CV3657163single nucleotide variantNM_001118.5(ADCYAP1R1):c.442T>G (p.Tyr148Asp)not specified [RCV004907945]uncertain significance73108474031084740Humanname
329360732CV2439650single nucleotide variantNM_001118.5(ADCYAP1R1):c.1292G>A (p.Arg431Gln)not specified [RCV004255665]uncertain significance73110656931106569Humanname
329359098CV2450841single nucleotide variantNM_001118.5(ADCYAP1R1):c.1030G>A (p.Glu344Lys)not specified [RCV004267755]uncertain significance73109271931092719Humanname
401768433CV2675332single nucleotide variantNM_001118.5(ADCYAP1R1):c.1296C>A (p.His432Gln)not specified [RCV004292140]uncertain significance73110657331106573Humanname
401768436CV2675333single nucleotide variantNM_001118.5(ADCYAP1R1):c.1297C>G (p.Pro433Ala)not specified [RCV004292141]uncertain significance73110657431106574Humanname
405705914CV3244042single nucleotide variantNM_001118.5(ADCYAP1R1):c.1018A>G (p.Met340Val)not specified [RCV004375907]uncertain significance73109270731092707Humanname
405706009CV3244055single nucleotide variantNM_001118.5(ADCYAP1R1):c.1058G>A (p.Arg353Gln)not specified [RCV004375920]uncertain significance73110324831103248Humanname
405706049CV3244060single nucleotide variantNM_001118.5(ADCYAP1R1):c.1294C>T (p.His432Tyr)not specified [RCV004375925]uncertain significance73110657131106571Humanname
405706099CV3244066single nucleotide variantNM_001118.5(ADCYAP1R1):c.1303C>G (p.Leu435Val)not specified [RCV004375931]uncertain significance73110658031106580Humanname
597804366CV3657146single nucleotide variantNM_001118.5(ADCYAP1R1):c.1298C>T (p.Pro433Leu)not specified [RCV004907942]uncertain significance73110657531106575Humanname
597804367CV3657155single nucleotide variantNM_001118.5(ADCYAP1R1):c.1204T>A (p.Phe402Ile)not specified [RCV004907943]uncertain significance73110489531104895Humanname
597804373CV3657166single nucleotide variantNM_001118.5(ADCYAP1R1):c.1295A>G (p.His432Arg)not specified [RCV004907946]uncertain significance73110657231106572Humanname
8632545CV87753single nucleotide variantNM_001199635.1(ADCYAP1R1):c.1322G>A (p.Arg441Gln)Malignant melanoma [RCV000067845]not provided73110651531106515Humanname