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Variants search result for Homo sapiens
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51 records found for search term Krt39
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156074222CV2321649single nucleotide variantNM_213656.4(KRT39):c.13G>T (p.Gly5Cys)not specified [RCV004179661]uncertain significance174096684440966844Humanname
156279221CV2338294single nucleotide variantNM_213656.4(KRT39):c.170A>G (p.Gln57Arg)not specified [RCV004186349]uncertain significance174096668740966687Humanname
401780166CV2676851single nucleotide variantNM_213656.4(KRT39):c.197G>C (p.Cys66Ser)not specified [RCV004291017]uncertain significance174096666040966660Humanname
405817402CV3269308single nucleotide variantNM_213656.4(KRT39):c.235C>T (p.Arg79Cys)not specified [RCV004412388]likely benign174096662240966622Humanname
407500096CV3445567single nucleotide variantNM_213656.4(KRT39):c.148G>A (p.Val50Ile)not specified [RCV004644530]uncertain significance174096670940966709Humanname
597794958CV3698601single nucleotide variantNM_213656.4(KRT39):c.130T>C (p.Cys44Arg)not specified [RCV004934685]uncertain significance174096672740966727Humanname
598184340CV3980418single nucleotide variantNM_213656.4(KRT39):c.208A>T (p.Ile70Phe)not specified [RCV005353049]uncertain significance174096664940966649Humanname
156179157CV2201638single nucleotide variantNM_213656.4(KRT39):c.842A>G (p.Lys281Arg)not specified [RCV004082100]likely benign174096243040962430Humanname
155921291CV2207150single nucleotide variantNM_213656.4(KRT39):c.541T>A (p.Leu181Met)not specified [RCV004087889]uncertain significance174096445640964456Humanname
156388551CV2231884single nucleotide variantNM_213656.4(KRT39):c.758T>G (p.Val253Gly)not specified [RCV004098677]uncertain significance174096251440962514Humanname
155932422CV2232077single nucleotide variantNM_213656.4(KRT39):c.992G>A (p.Arg331Gln)not specified [RCV004093119]uncertain significance174096216640962166Humanname
156198992CV2255953single nucleotide variantNM_213656.4(KRT39):c.866C>T (p.Thr289Met)not specified [RCV004122404]uncertain significance174096240640962406Humanname
156313687CV2257045single nucleotide variantNM_213656.4(KRT39):c.950G>T (p.Arg317Leu)not specified [RCV004123015]uncertain significance174096220840962208Humanname
155940772CV2294134single nucleotide variantNM_213656.4(KRT39):c.847G>A (p.Val283Met)not specified [RCV004149504]uncertain significance174096242540962425Humanname
155917635CV2362369single nucleotide variantNM_213656.4(KRT39):c.449T>C (p.Ile150Thr)not specified [RCV004212999]uncertain significance174096640840966408Humanname
156090443CV2375237single nucleotide variantNM_213656.4(KRT39):c.877G>A (p.Glu293Lys)not specified [RCV004230269]uncertain significance174096228140962281Humanname
329390941CV2437458single nucleotide variantNM_213656.4(KRT39):c.949C>T (p.Arg317Cys)not specified [RCV004256323]uncertain significance174096220940962209Humanname
401877487CV2761149single nucleotide variantNM_213656.4(KRT39):c.751A>G (p.Ile251Val)not specified [RCV004341035]uncertain significance174096252140962521Humanname
405817404CV3269310single nucleotide variantNM_213656.4(KRT39):c.790G>A (p.Val264Ile)not specified [RCV004412390]uncertain significance174096248240962482Humanname
405817405CV3269311single nucleotide variantNM_213656.4(KRT39):c.938T>C (p.Ile313Thr)not specified [RCV004412391]uncertain significance174096222040962220Humanname
407500082CV3445563single nucleotide variantNM_213656.4(KRT39):c.499C>G (p.Leu167Val)not specified [RCV004644526]uncertain significance174096449840964498Humanname
407500279CV3445564single nucleotide variantNM_213656.4(KRT39):c.727T>C (p.Cys243Arg)not specified [RCV004644527]uncertain significance174096254540962545Humanname
407500089CV3445565single nucleotide variantNM_213656.4(KRT39):c.317G>A (p.Arg106His)not specified [RCV004644528]uncertain significance174096654040966540Humanname
597794955CV3698597single nucleotide variantNM_213656.4(KRT39):c.676G>A (p.Glu226Lys)not specified [RCV004934684]uncertain significance174096365940963659Humanname
597798368CV3698599single nucleotide variantNM_213656.4(KRT39):c.908A>C (p.Gln303Pro)not specified [RCV004936112]uncertain significance174096225040962250Humanname
597798371CV3698600single nucleotide variantNM_213656.4(KRT39):c.995T>C (p.Met332Thr)not specified [RCV004936113]uncertain significance174096216340962163Humanname
598184347CV3980419single nucleotide variantNM_213656.4(KRT39):c.299T>C (p.Met100Thr)not specified [RCV005353050]uncertain significance174096655840966558Humanname
598184352CV3980420single nucleotide variantNM_213656.4(KRT39):c.301C>A (p.Gln101Lys)not specified [RCV005353051]uncertain significance174096655640966556Humanname
598163102CV3980422single nucleotide variantNM_213656.4(KRT39):c.850G>C (p.Glu284Gln)not specified [RCV005368765]uncertain significance174096242240962422Humanname
8647123CV106759single nucleotide variantNM_213656.4(KRT39):c.1461A>C (p.Arg487Ser)not provided [RCV000087261]uncertain significance174095861640958616Humanname
156276634CV2209793single nucleotide variantNM_213656.4(KRT39):c.1234C>T (p.Arg412Cys)not specified [RCV004076264]likely benign174095884340958843Humanname
155949348CV2242687single nucleotide variantNM_213656.4(KRT39):c.1127A>G (p.Asn376Ser)not specified [RCV004113731]uncertain significance174096037140960371Humanname
156041857CV2310924single nucleotide variantNM_213656.4(KRT39):c.1036C>T (p.Arg346Cys)not specified [RCV004163960]uncertain significance174096046240960462Humanname
156362741CV2330350single nucleotide variantNM_213656.4(KRT39):c.1163G>A (p.Arg388Gln)not specified [RCV004180926]uncertain significance174096033540960335Humanname
156167728CV2345337single nucleotide variantNM_213656.4(KRT39):c.1414A>G (p.Lys472Glu)not specified [RCV004198117]uncertain significance174095866340958663Humanname
156284063CV2348988single nucleotide variantNM_213656.4(KRT39):c.1438G>T (p.Val480Leu)not specified [RCV004203418]uncertain significance174095863940958639Humanname
156284083CV2348989single nucleotide variantNM_213656.4(KRT39):c.1442A>T (p.Gln481Leu)not specified [RCV004203419]uncertain significance174095863540958635Humanname
156284856CV2349050single nucleotide variantNM_213656.4(KRT39):c.1193G>A (p.Ser398Asn)not specified [RCV004205491]uncertain significance174096030540960305Humanname
156344901CV2372837single nucleotide variantNM_213656.4(KRT39):c.1295C>T (p.Thr432Met)not provided [RCV004695733]|not specified [RCV004222019]uncertain significance174095878240958782Humanname
329364707CV2443776single nucleotide variantNM_213656.4(KRT39):c.1247G>A (p.Cys416Tyr)not specified [RCV004256072]uncertain significance174095883040958830Humanname
401764834CV2705435single nucleotide variantNM_213656.4(KRT39):c.1112C>T (p.Ala371Val)not specified [RCV004312095]uncertain significance174096038640960386Humanname
405817399CV3269305single nucleotide variantNM_213656.4(KRT39):c.1138G>A (p.Glu380Lys)not specified [RCV004412385]uncertain significance174096036040960360Humanname
405817400CV3269306single nucleotide variantNM_213656.4(KRT39):c.1201G>C (p.Glu401Gln)not specified [RCV004412386]uncertain significance174096029740960297Humanname
405817401CV3269307single nucleotide variantNM_213656.4(KRT39):c.1370T>C (p.Ile457Thr)not specified [RCV004412387]uncertain significance174095870740958707Humanname
407500074CV3445561single nucleotide variantNM_213656.4(KRT39):c.1349C>A (p.Ala450Asp)not specified [RCV004644524]uncertain significance174095872840958728Humanname
407500078CV3445562single nucleotide variantNM_213656.4(KRT39):c.1153G>A (p.Val385Ile)not specified [RCV004644525]uncertain significance174096034540960345Humanname
407500092CV3445566single nucleotide variantNM_213656.4(KRT39):c.1243A>G (p.Lys415Glu)not specified [RCV004644529]uncertain significance174095883440958834Humanname
597798365CV3698598single nucleotide variantNM_213656.4(KRT39):c.1397A>G (p.Lys466Arg)not specified [RCV004936111]uncertain significance174095868040958680Humanname
598221999CV3980421single nucleotide variantNM_213656.4(KRT39):c.1400A>G (p.Glu467Gly)not specified [RCV005360910]uncertain significance174095867740958677Humanname
598184359CV3980423single nucleotide variantNM_213656.4(KRT39):c.1316C>T (p.Ser439Leu)not specified [RCV005353052]uncertain significance174095876140958761Humanname
598163108CV3980424single nucleotide variantNM_213656.4(KRT39):c.1061T>G (p.Ile354Ser)not specified [RCV005368766]uncertain significance174096043740960437Humanname