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60 records found for search term Trpv2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15176400CV778319single nucleotide variantNM_016113.5(TRPV2):c.1351-4G>Anot provided [RCV000950816]benign171642831316428313Humanname
407527899CV3488927single nucleotide variantNM_016113.5(TRPV2):c.58G>A (p.Glu20Lys)not specified [RCV004680191]uncertain significance171641772616417726Humanname
155925613CV2207993single nucleotide variantNM_016113.5(TRPV2):c.187G>A (p.Gly63Arg)not specified [RCV004086696]uncertain significance171641785516417855Humanname
155924936CV2248903single nucleotide variantNM_016113.5(TRPV2):c.148T>C (p.Phe50Leu)not specified [RCV004115911]uncertain significance171641781616417816Humanname
156119543CV2275826single nucleotide variantNM_016113.5(TRPV2):c.218G>A (p.Arg73Gln)not specified [RCV004139493]uncertain significance171642013216420132Humanname
155974800CV2318054single nucleotide variantNM_016113.5(TRPV2):c.248T>G (p.Val83Gly)not specified [RCV004177155]uncertain significance171642016216420162Humanname
156085102CV2366131single nucleotide variantNM_016113.5(TRPV2):c.142C>T (p.Arg48Trp)not specified [RCV004210164]uncertain significance171641781016417810Humanname
156349013CV2376392single nucleotide variantNM_016113.5(TRPV2):c.254G>A (p.Arg85Gln)not specified [RCV004220581]uncertain significance171642016816420168Humanname
329382606CV2465285single nucleotide variantNM_016113.5(TRPV2):c.206C>T (p.Pro69Leu)not specified [RCV004281083]uncertain significance171642012016420120Humanname
405777307CV3344491single nucleotide variantNM_016113.5(TRPV2):c.143G>A (p.Arg48Gln)not specified [RCV004471336]uncertain significance171641781116417811Humanname
407461782CV3488928single nucleotide variantNM_016113.5(TRPV2):c.103G>A (p.Gly35Arg)not specified [RCV004687744]uncertain significance171641777116417771Humanname
597681335CV3621328single nucleotide variantNM_016113.5(TRPV2):c.193G>A (p.Gly65Ser)not specified [RCV004883614]uncertain significance171641786116417861Humanname
597681343CV3621329single nucleotide variantNM_016113.5(TRPV2):c.136G>A (p.Glu46Lys)not specified [RCV004883615]uncertain significance171641780416417804Humanname
597681407CV3621338single nucleotide variantNM_016113.5(TRPV2):c.245C>A (p.Ala82Glu)not specified [RCV004883623]uncertain significance171642015916420159Humanname
598237051CV3932276single nucleotide variantNM_016113.5(TRPV2):c.137A>G (p.Glu46Gly)not specified [RCV005296167]uncertain significance171641780516417805Humanname
598237060CV3932279single nucleotide variantNM_016113.5(TRPV2):c.151G>A (p.Ala51Thr)not specified [RCV005296169]uncertain significance171641781916417819Humanname
598215486CV3932283single nucleotide variantNM_016113.5(TRPV2):c.296G>C (p.Ser99Thr)not specified [RCV005292735]uncertain significance171642021016420210Humanname
156108646CV2211018single nucleotide variantNM_016113.5(TRPV2):c.749A>G (p.His250Arg)not specified [RCV004088208]uncertain significance171642359216423592Humanname
155979821CV2215270single nucleotide variantNM_016113.5(TRPV2):c.868C>T (p.Arg290Cys)not specified [RCV004086971]uncertain significance171642371116423711Humanname
156229050CV2234940single nucleotide variantNM_016113.5(TRPV2):c.889C>A (p.Pro297Thr)not specified [RCV004113143]uncertain significance171642373216423732Humanname
155921462CV2340459single nucleotide variantNM_016113.5(TRPV2):c.706G>T (p.Ala236Ser)not specified [RCV004197186]uncertain significance171642354916423549Humanname
156193996CV2350664single nucleotide variantNM_016113.5(TRPV2):c.505A>G (p.Ile169Val)not specified [RCV004204996]uncertain significance171642276916422769Humanname
401861687CV2756414single nucleotide variantNM_016113.5(TRPV2):c.706G>A (p.Ala236Thr)not specified [RCV004342954]uncertain significance171642354916423549Humanname
405777334CV3344496single nucleotide variantNM_016113.5(TRPV2):c.424G>C (p.Asp142His)not specified [RCV004471341]uncertain significance171642268816422688Humanname
405777342CV3344497single nucleotide variantNM_016113.5(TRPV2):c.922G>A (p.Glu308Lys)not specified [RCV004471342]uncertain significance171642376516423765Humanname
597681317CV3621326single nucleotide variantNM_016113.5(TRPV2):c.475G>A (p.Asp159Asn)not specified [RCV004883612]uncertain significance171642273916422739Humanname
597681384CV3621335single nucleotide variantNM_016113.5(TRPV2):c.600G>C (p.Lys200Asn)not specified [RCV004883620]uncertain significance171642286416422864Humanname
597681391CV3621336single nucleotide variantNM_016113.5(TRPV2):c.937A>G (p.Ile313Val)not specified [RCV004883621]uncertain significance171642611116426111Humanname
597681399CV3621337single nucleotide variantNM_016113.5(TRPV2):c.977G>A (p.Arg326Gln)not specified [RCV004883622]uncertain significance171642615116426151Humanname
598237047CV3932275single nucleotide variantNM_016113.5(TRPV2):c.716A>G (p.Gln239Arg)not specified [RCV005296166]uncertain significance171642355916423559Humanname
598237056CV3932278single nucleotide variantNM_016113.5(TRPV2):c.320A>G (p.Asp107Gly)not specified [RCV005296168]uncertain significance171642023416420234Humanname
8636030CV91253single nucleotide variantNM_016113.4(TRPV2):c.815G>A (p.Gly272Glu)Malignant melanoma [RCV000071351]not provided171642365816423658Humanname
155915844CV2239581single nucleotide variantNM_016113.5(TRPV2):c.1317C>G (p.Ile439Met)not specified [RCV004108148]uncertain significance171642751416427514Humanname
156171746CV2247466single nucleotide variantNM_016113.5(TRPV2):c.1850A>G (p.His617Arg)not specified [RCV004108790]likely benign171643216116432161Humanname
155988487CV2251220single nucleotide variantNM_016113.5(TRPV2):c.1046G>A (p.Cys349Tyr)not specified [RCV004115445]uncertain significance171642622016426220Humanname
155926552CV2258811single nucleotide variantNM_016113.5(TRPV2):c.1280T>C (p.Val427Ala)not specified [RCV004118032]likely benign171642747716427477Humanname
156042059CV2275814single nucleotide variantNM_016113.5(TRPV2):c.1538A>G (p.Tyr513Cys)not specified [RCV004139483]uncertain significance171642893316428933Humanname
155993549CV2281332single nucleotide variantNM_016113.5(TRPV2):c.1648G>A (p.Ala550Thr)not specified [RCV004147559]uncertain significance171643184416431844Humanname
155958522CV2282214single nucleotide variantNM_016113.5(TRPV2):c.2033G>A (p.Cys678Tyr)not specified [RCV004132796]uncertain significance171643361716433617Humanname
156346926CV2305550single nucleotide variantNM_016113.5(TRPV2):c.1858G>A (p.Gly620Ser)not specified [RCV004165250]uncertain significance171643216916432169Humanname
156257197CV2322046single nucleotide variantNM_016113.5(TRPV2):c.1734G>A (p.Met578Ile)not specified [RCV004173795]uncertain significance171643204516432045Humanname
156262842CV2391619single nucleotide variantNM_016113.5(TRPV2):c.1288T>C (p.Ser430Pro)not specified [RCV004241783]uncertain significance171642748516427485Humanname
329376380CV2465132single nucleotide variantNM_016113.5(TRPV2):c.1540A>G (p.Thr514Ala)not specified [RCV004287186]uncertain significance171642893516428935Humanname
401894532CV2788344single nucleotide variantNM_016113.5(TRPV2):c.1278G>C (p.Glu426Asp)not specified [RCV004352923]uncertain significance171642747516427475Humanname
405777302CV3344490single nucleotide variantNM_016113.5(TRPV2):c.1342G>A (p.Val448Met)not specified [RCV004471335]uncertain significance171642753916427539Humanname
405777314CV3344492single nucleotide variantNM_016113.5(TRPV2):c.1774G>A (p.Gly592Ser)not specified [RCV004471337]uncertain significance171643208516432085Humanname
405777318CV3344493single nucleotide variantNM_016113.5(TRPV2):c.2097T>A (p.Asp699Glu)not specified [RCV004471338]uncertain significance171643368116433681Humanname
405777323CV3344494single nucleotide variantNM_016113.5(TRPV2):c.2256G>T (p.Glu752Asp)not specified [RCV004471339]uncertain significance171643685016436850Humanname
405777328CV3344495single nucleotide variantNM_016113.5(TRPV2):c.2272G>A (p.Val758Ile)not specified [RCV004471340]uncertain significance171643686616436866Humanname
407527902CV3488929single nucleotide variantNM_016113.5(TRPV2):c.1363T>A (p.Trp455Arg)not specified [RCV004680192]uncertain significance171642832916428329Humanname
597681326CV3621327single nucleotide variantNM_016113.5(TRPV2):c.1750G>A (p.Glu584Lys)not specified [RCV004883613]uncertain significance171643206116432061Humanname
597681351CV3621330single nucleotide variantNM_016113.5(TRPV2):c.2009A>C (p.Glu670Ala)not specified [RCV004883616]uncertain significance171643359316433593Humanname
597681359CV3621331single nucleotide variantNM_016113.5(TRPV2):c.1504G>A (p.Ala502Thr)not specified [RCV004883617]uncertain significance171642889916428899Humanname
597681367CV3621332single nucleotide variantNM_016113.5(TRPV2):c.1676A>G (p.Glu559Gly)not specified [RCV004883618]uncertain significance171643198716431987Humanname
597681374CV3621333single nucleotide variantNM_016113.5(TRPV2):c.1496T>G (p.Leu499Arg)not specified [RCV004883619]uncertain significance171642889116428891Humanname
598215472CV3932277single nucleotide variantNM_016113.5(TRPV2):c.1391C>T (p.Ser464Leu)not specified [RCV005292732]uncertain significance171642835716428357Humanname
598215477CV3932280single nucleotide variantNM_016113.5(TRPV2):c.2010G>T (p.Glu670Asp)not specified [RCV005292733]uncertain significance171643359416433594Humanname
598237065CV3932281single nucleotide variantNM_016113.5(TRPV2):c.1739G>A (p.Gly580Glu)not specified [RCV005296170]uncertain significance171643205016432050Humanname
598215481CV3932282single nucleotide variantNM_016113.5(TRPV2):c.1339C>T (p.Leu447Phe)not specified [RCV005292734]uncertain significance171642753616427536Humanname
598215492CV3932284single nucleotide variantNM_016113.5(TRPV2):c.1597C>T (p.Arg533Trp)not specified [RCV005292736]uncertain significance171643179316431793Humanname