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Variants search result for All species
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52 records found for search term Camkk1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401729694CV2690445single nucleotide variantNM_032294.3(CAMKK1):c.13C>A (p.Pro5Thr)not specified [RCV004304217]uncertain significance1738856753885675Humanname
156273161CV2320161single nucleotide variantNM_032294.3(CAMKK1):c.70G>A (p.Asp24Asn)not specified [RCV004169786]uncertain significance1738856183885618Humanname
405767223CV3302641single nucleotide variantNM_032294.3(CAMKK1):c.38G>A (p.Arg13Gln)not specified [RCV004434655]uncertain significance1738856503885650Humanname
598204015CV3942973single nucleotide variantNM_032294.3(CAMKK1):c.32A>G (p.Asp11Gly)not specified [RCV005314719]uncertain significance1738856563885656Humanname
156247433CV2276867single nucleotide variantNM_032294.3(CAMKK1):c.170G>C (p.Ser57Thr)not specified [RCV004140210]uncertain significance1738855183885518Humanname
329361859CV2468385single nucleotide variantNM_032294.3(CAMKK1):c.140G>A (p.Arg47Gln)not specified [RCV004275918]uncertain significance1738855483885548Humanname
401775564CV2710617single nucleotide variantNM_032294.3(CAMKK1):c.137C>G (p.Pro46Arg)not specified [RCV004319533]uncertain significance1738855513885551Humanname
401935628CV2814720single nucleotide variantNM_032294.3(CAMKK1):c.1182C>T (p.Pro394=)not provided [RCV003413085]likely benign1738698313869831Humanname
407474535CV3424480single nucleotide variantNM_032294.3(CAMKK1):c.289A>G (p.Ser97Gly)not specified [RCV004600642]uncertain significance1738853993885399Humanname
407474540CV3424481single nucleotide variantNM_032294.3(CAMKK1):c.130C>G (p.Pro44Ala)not specified [RCV004600643]uncertain significance1738855583885558Humanname
597763967CV3647435single nucleotide variantNM_032294.3(CAMKK1):c.134C>G (p.Pro45Arg)not specified [RCV004895504]uncertain significance1738855543885554Humanname
597750773CV3647444single nucleotide variantNM_032294.3(CAMKK1):c.194G>A (p.Arg65Gln)not specified [RCV004892629]uncertain significance1738854943885494Humanname
156375118CV2213501single nucleotide variantNM_032294.3(CAMKK1):c.814G>A (p.Val272Ile)not specified [RCV004087467]likely benign1738764053876405Humanname
156025262CV2242218single nucleotide variantNM_032294.3(CAMKK1):c.367G>A (p.Val123Met)not specified [RCV004111250]uncertain significance1738844213884421Humanname
155978437CV2266517single nucleotide variantNM_032294.3(CAMKK1):c.943G>A (p.Ala315Thr)not specified [RCV004131078]uncertain significance1738762763876276Humanname
156277521CV2352059single nucleotide variantNM_032294.3(CAMKK1):c.864C>A (p.His288Gln)not specified [RCV004191154]uncertain significance1738763553876355Humanname
155968818CV2391503single nucleotide variantNM_032294.3(CAMKK1):c.298T>A (p.Ser100Thr)not specified [RCV004239889]uncertain significance1738853903885390Humanname
401863843CV2773480single nucleotide variantNM_032294.3(CAMKK1):c.727T>C (p.Cys243Arg)not specified [RCV004354113]uncertain significance1738804153880415Humanname
405767229CV3302642single nucleotide variantNM_032294.3(CAMKK1):c.440A>G (p.Asn147Ser)not specified [RCV004434656]uncertain significance1738839063883906Humanname
405767235CV3302643single nucleotide variantNM_032294.3(CAMKK1):c.457C>T (p.His153Tyr)not specified [RCV004434657]uncertain significance1738838893883889Humanname
405767241CV3302644single nucleotide variantNM_032294.3(CAMKK1):c.584G>A (p.Arg195Gln)not specified [RCV004434658]uncertain significance1738831063883106Humanname
405767249CV3302645single nucleotide variantNM_032294.3(CAMKK1):c.719A>G (p.Glu240Gly)not specified [RCV004434659]uncertain significance1738804233880423Humanname
405767254CV3302646single nucleotide variantNM_032294.3(CAMKK1):c.929C>T (p.Thr310Met)not specified [RCV004434660]uncertain significance1738762903876290Humanname
407474520CV3424477single nucleotide variantNM_032294.3(CAMKK1):c.758G>A (p.Arg253His)not specified [RCV004600639]uncertain significance1738803843880384Humanname
407474527CV3424478single nucleotide variantNM_032294.3(CAMKK1):c.757C>T (p.Arg253Cys)not specified [RCV004600640]uncertain significance1738803853880385Humanname
597763963CV3647433single nucleotide variantNM_032294.3(CAMKK1):c.719A>C (p.Glu240Ala)not specified [RCV004895503]uncertain significance1738804233880423Humanname
597763975CV3647437single nucleotide variantNM_032294.3(CAMKK1):c.418G>A (p.Gly140Ser)not specified [RCV004895506]uncertain significance1738839283883928Humanname
597763983CV3647440single nucleotide variantNM_032294.3(CAMKK1):c.363C>G (p.Asp121Glu)not specified [RCV004895508]uncertain significance1738844253884425Humanname
597763987CV3647441single nucleotide variantNM_032294.3(CAMKK1):c.727T>A (p.Cys243Ser)not specified [RCV004895509]uncertain significance1738804153880415Humanname
597763991CV3647442single nucleotide variantNM_032294.3(CAMKK1):c.559G>C (p.Ala187Pro)not specified [RCV004895510]uncertain significance1738831313883131Humanname
597763995CV3647443single nucleotide variantNM_032294.3(CAMKK1):c.992G>C (p.Gly331Ala)not specified [RCV004895511]uncertain significance1738762273876227Humanname
156069332CV2237122single nucleotide variantNM_032294.3(CAMKK1):c.1066G>A (p.Asp356Asn)not specified [RCV004114875]uncertain significance1738726123872612Humanname
156048531CV2391014single nucleotide variantNM_032294.3(CAMKK1):c.1305G>T (p.Lys435Asn)not specified [RCV004235014]uncertain significance1738695233869523Humanname
156049271CV2391075single nucleotide variantNM_032294.3(CAMKK1):c.1276G>A (p.Val426Met)not specified [RCV004235066]uncertain significance1738695523869552Humanname
329373720CV2434564single nucleotide variantNM_032294.3(CAMKK1):c.1266G>C (p.Glu422Asp)not specified [RCV004254264]uncertain significance1738695623869562Humanname
329396373CV2462562single nucleotide variantNM_032294.3(CAMKK1):c.1183G>C (p.Glu395Gln)not specified [RCV004278513]uncertain significance1738698303869830Humanname
401733818CV2687842single nucleotide variantNM_032294.3(CAMKK1):c.1400C>A (p.Ala467Glu)not specified [RCV004303150]uncertain significance1738659533865953Humanname
401877263CV2764565single nucleotide variantNM_032294.3(CAMKK1):c.1403G>A (p.Arg468Gln)not specified [RCV004339120]uncertain significance1738659503865950Humanname
401885584CV2778155single nucleotide variantNM_032294.3(CAMKK1):c.1240G>A (p.Glu414Lys)not specified [RCV004349883]uncertain significance1738695883869588Humanname
405767203CV3302637single nucleotide variantNM_032294.3(CAMKK1):c.1021G>A (p.Val341Ile)not specified [RCV004434651]uncertain significance1738734383873438Humanname
405767206CV3302638single nucleotide variantNM_032294.3(CAMKK1):c.1141G>A (p.Glu381Lys)not specified [RCV004434652]uncertain significance1738698723869872Humanname
405767212CV3302639single nucleotide variantNM_032294.3(CAMKK1):c.1186A>G (p.Thr396Ala)not specified [RCV004434653]uncertain significance1738698273869827Humanname
405767218CV3302640single nucleotide variantNM_032294.3(CAMKK1):c.1370G>A (p.Arg457His)not specified [RCV004434654]uncertain significance1738659833865983Humanname
407474516CV3424476single nucleotide variantNM_032294.3(CAMKK1):c.1456T>C (p.Phe486Leu)not specified [RCV004600638]uncertain significance1738622733862273Humanname
407474531CV3424479single nucleotide variantNM_032294.3(CAMKK1):c.1136G>T (p.Ser379Ile)not specified [RCV004600641]uncertain significance1738698773869877Humanname
597763959CV3647432single nucleotide variantNM_032294.3(CAMKK1):c.1040T>C (p.Val347Ala)not specified [RCV004895502]uncertain significance1738734193873419Humanname
597763971CV3647436single nucleotide variantNM_032294.3(CAMKK1):c.1237G>A (p.Gly413Arg)not specified [RCV004895505]uncertain significance1738695913869591Humanname
597763979CV3647438single nucleotide variantNM_032294.3(CAMKK1):c.1447A>C (p.Lys483Gln)not specified [RCV004895507]uncertain significance1738622823862282Humanname
597750768CV3647439single nucleotide variantNM_032294.3(CAMKK1):c.1459G>C (p.Gly487Arg)not specified [RCV004892628]uncertain significance1738622703862270Humanname
598212640CV3942975single nucleotide variantNM_032294.3(CAMKK1):c.1332G>C (p.Trp444Cys)not specified [RCV005316195]uncertain significance1738694963869496Humanname
598204029CV3942976single nucleotide variantNM_032294.3(CAMKK1):c.1454G>A (p.Gly485Glu)not specified [RCV005314721]uncertain significance1738622753862275Humanname
8636162CV91386single nucleotide variantNM_032294.2(CAMKK1):c.1252C>T (p.Pro418Ser)Malignant melanoma [RCV000071484]not provided1738695763869576Humanname