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68 records found for search term Krt76
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155915311CV2200209single nucleotide variantNM_015848.4(KRT76):c.59G>A (p.Arg20His)not specified [RCV004076560]uncertain significance125277723352777233Humanname
156108273CV2355388single nucleotide variantNM_015848.4(KRT76):c.58C>T (p.Arg20Cys)not specified [RCV004205247]uncertain significance125277723452777234Humanname
401736245CV2689294single nucleotide variantNM_015848.4(KRT76):c.82A>G (p.Ser28Gly)not specified [RCV004306127]uncertain significance125277721052777210Humanname
8627310CV82454single nucleotide variantNM_015848.4(KRT76):c.852G>A (p.Glu284=)Malignant melanoma [RCV000062533]not provided125277360652773606Humanname
405653268CV3269452single nucleotide variantNM_015848.4(KRT76):c.230G>A (p.Arg77Gln)not specified [RCV004414516]uncertain significance125277706252777062Humanname
407460029CV3445632single nucleotide variantNM_015848.4(KRT76):c.266G>C (p.Gly89Ala)not specified [RCV004633738]uncertain significance125277702652777026Humanname
597624633CV3695663single nucleotide variantNM_015848.4(KRT76):c.253C>T (p.Arg85Trp)not specified [RCV004937655]uncertain significance125277703952777039Humanname
597624640CV3695669single nucleotide variantNM_015848.4(KRT76):c.156C>A (p.Ser52Arg)not specified [RCV004937661]uncertain significance125277713652777136Humanname
598195850CV3980537single nucleotide variantNM_015848.4(KRT76):c.245G>A (p.Gly82Glu)not specified [RCV005355074]uncertain significance125277704752777047Humanname
598163379CV3980540single nucleotide variantNM_015848.4(KRT76):c.173T>C (p.Leu58Pro)not specified [RCV005368817]uncertain significance125277711952777119Humanname
598163391CV3980544single nucleotide variantNM_015848.4(KRT76):c.101C>T (p.Ala34Val)not specified [RCV005368819]uncertain significance125277719152777191Humanname
156399470CV2205138single nucleotide variantNM_015848.4(KRT76):c.337G>C (p.Gly113Arg)not specified [RCV004077736]uncertain significance125277695552776955Humanname
155926897CV2208314single nucleotide variantNM_015848.4(KRT76):c.319G>A (p.Gly107Ser)not specified [RCV004088751]uncertain significance125277697352776973Humanname
156278866CV2252117single nucleotide variantNM_015848.4(KRT76):c.311G>A (p.Gly104Asp)not specified [RCV004122141]uncertain significance125277698152776981Humanname
156160044CV2322795single nucleotide variantNM_015848.4(KRT76):c.380G>T (p.Gly127Val)not specified [RCV004182897]uncertain significance125277691252776912Humanname
156072604CV2325342single nucleotide variantNM_015848.4(KRT76):c.762C>G (p.Asn254Lys)not specified [RCV004177723]uncertain significance125277544152775441Humanname
156395873CV2325975single nucleotide variantNM_015848.4(KRT76):c.986T>G (p.Met329Arg)not specified [RCV004176188]uncertain significance125277224552772245Humanname
156383078CV2361399single nucleotide variantNM_015848.4(KRT76):c.838C>T (p.Arg280Cys)not specified [RCV004221048]uncertain significance125277362052773620Humanname
401780056CV2676798single nucleotide variantNM_015848.4(KRT76):c.346T>G (p.Phe116Val)not specified [RCV004290968]uncertain significance125277694652776946Humanname
405653270CV3269453single nucleotide variantNM_015848.4(KRT76):c.385G>T (p.Gly129Cys)not specified [RCV004414517]uncertain significance125277690752776907Humanname
405653272CV3269454single nucleotide variantNM_015848.4(KRT76):c.397G>A (p.Val133Ile)not specified [RCV004414518]uncertain significance125277689552776895Humanname
405653274CV3269455single nucleotide variantNM_015848.4(KRT76):c.551G>A (p.Arg184Gln)not specified [RCV004414519]uncertain significance125277674152776741Humanname
405653276CV3269456single nucleotide variantNM_015848.4(KRT76):c.764T>A (p.Leu255Gln)not specified [RCV004414520]uncertain significance125277543952775439Humanname
405653278CV3269457single nucleotide variantNM_015848.4(KRT76):c.947G>A (p.Ser316Asn)not specified [RCV004414521]likely benign125277280852772808Humanname
407460025CV3445631single nucleotide variantNM_015848.4(KRT76):c.583G>T (p.Ala195Ser)not specified [RCV004633737]uncertain significance125277670952776709Humanname
598222087CV3980538single nucleotide variantNM_015848.4(KRT76):c.691G>A (p.Glu231Lys)not specified [RCV005360928]uncertain significance125277551252775512Humanname
598195870CV3980545single nucleotide variantNM_015848.4(KRT76):c.445G>A (p.Gly149Arg)not specified [RCV005355078]uncertain significance125277684752776847Humanname
156096764CV2210536single nucleotide variantNM_015848.4(KRT76):c.1375G>A (p.Asp459Asn)not specified [RCV004089663]uncertain significance125277110852771108Humanname
156329761CV2216486single nucleotide variantNM_015848.4(KRT76):c.1041C>G (p.Cys347Trp)not specified [RCV004097288]uncertain significance125277219052772190Humanname
156240377CV2221332single nucleotide variantNM_015848.4(KRT76):c.1771A>G (p.Ile591Val)not specified [RCV004094754]uncertain significance125276885952768859Humanname
156191343CV2223089single nucleotide variantNM_015848.4(KRT76):c.1331A>G (p.Asn444Ser)not specified [RCV004103942]uncertain significance125277115252771152Humanname
156113489CV2263818single nucleotide variantNM_015848.4(KRT76):c.1232T>C (p.Leu411Pro)not specified [RCV004136095]uncertain significance125277190252771902Humanname
155984037CV2273140single nucleotide variantNM_015848.4(KRT76):c.1327G>A (p.Ala443Thr)not specified [RCV004137776]uncertain significance125277115652771156Humanname
155901534CV2274532single nucleotide variantNM_015848.4(KRT76):c.1350G>T (p.Leu450Phe)not specified [RCV004138940]uncertain significance125277113352771133Humanname
156042779CV2305719single nucleotide variantNM_015848.4(KRT76):c.1498T>A (p.Cys500Ser)not specified [RCV004167537]uncertain significance125276957052769570Humanname
155918407CV2332995single nucleotide variantNM_015848.4(KRT76):c.1235G>A (p.Arg412Gln)not specified [RCV004194295]uncertain significance125277189952771899Humanname
156184643CV2335653single nucleotide variantNM_015848.4(KRT76):c.1618G>A (p.Gly540Ser)not specified [RCV004193855]likely benign125276901252769012Humanname
156201263CV2338389single nucleotide variantNM_015848.4(KRT76):c.1280C>T (p.Thr427Met)not specified [RCV004186437]uncertain significance125277120352771203Humanname
329390924CV2437434single nucleotide variantNM_015848.4(KRT76):c.1510G>A (p.Val504Met)not specified [RCV004256300]uncertain significance125276955852769558Humanname
329357628CV2453689single nucleotide variantNM_015848.4(KRT76):c.1498T>C (p.Cys500Arg)not specified [RCV004269338]uncertain significance125276957052769570Humanname
401866472CV2472766single nucleotide variantNM_015848.4(KRT76):c.1096C>T (p.Gln366Ter)not provided [RCV003331463]uncertain significance125277213552772135Humanname
401768891CV2686418single nucleotide variantNM_015848.4(KRT76):c.1001G>C (p.Ser334Thr)not specified [RCV004297488]uncertain significance125277223052772230Humanname
401733256CV2691248single nucleotide variantNM_015848.4(KRT76):c.1805C>G (p.Ser602Cys)not specified [RCV004303014]uncertain significance125276882552768825Humanname
401779370CV2718520single nucleotide variantNM_015848.4(KRT76):c.1711G>C (p.Gly571Arg)not specified [RCV004318327]uncertain significance125276891952768919Humanname
401755549CV2730927single nucleotide variantNM_015848.4(KRT76):c.1820C>T (p.Thr607Ile)not specified [RCV004332631]uncertain significance125276881052768810Humanname
401877710CV2779918single nucleotide variantNM_015848.4(KRT76):c.1388G>A (p.Arg463Gln)not specified [RCV004353529]uncertain significance125277109552771095Humanname
405653261CV3269448single nucleotide variantNM_015848.4(KRT76):c.1007C>T (p.Thr336Met)not specified [RCV004414512]uncertain significance125277222452772224Humanname
405653263CV3269449single nucleotide variantNM_015848.4(KRT76):c.1072C>T (p.Arg358Cys)not specified [RCV004414513]uncertain significance125277215952772159Humanname
405653265CV3269450single nucleotide variantNM_015848.4(KRT76):c.1752G>T (p.Arg584Ser)not specified [RCV004414514]uncertain significance125276887852768878Humanname
405653266CV3269451single nucleotide variantNM_015848.4(KRT76):c.1789G>A (p.Gly597Arg)not specified [RCV004414515]uncertain significance125276884152768841Humanname
407500338CV3445623single nucleotide variantNM_015848.4(KRT76):c.1382T>C (p.Leu461Pro)not specified [RCV004644573]uncertain significance125277110152771101Humanname
407460014CV3445624single nucleotide variantNM_015848.4(KRT76):c.1862C>A (p.Thr621Asn)not specified [RCV004633734]uncertain significance125276876852768768Humanname
407460018CV3445625single nucleotide variantNM_015848.4(KRT76):c.1718G>A (p.Ser573Asn)not specified [RCV004633735]uncertain significance125276891252768912Humanname
407500342CV3445626single nucleotide variantNM_015848.4(KRT76):c.1241A>C (p.Glu414Ala)not specified [RCV004644574]uncertain significance125277189352771893Humanname
407460021CV3445627single nucleotide variantNM_015848.4(KRT76):c.1734C>A (p.Ser578Arg)not specified [RCV004633736]uncertain significance125276889652768896Humanname
407500346CV3445628single nucleotide variantNM_015848.4(KRT76):c.1733G>A (p.Ser578Asn)not specified [RCV004644575]uncertain significance125276889752768897Humanname
407500350CV3445629single nucleotide variantNM_015848.4(KRT76):c.1702G>A (p.Gly568Arg)not specified [RCV004644576]uncertain significance125276892852768928Humanname
407500354CV3445630single nucleotide variantNM_015848.4(KRT76):c.1714A>G (p.Ser572Gly)not specified [RCV004644577]uncertain significance125276891652768916Humanname
407500358CV3445633single nucleotide variantNM_015848.4(KRT76):c.1282G>A (p.Ala428Thr)not specified [RCV004644578]uncertain significance125277120152771201Humanname
597624634CV3695664single nucleotide variantNM_015848.4(KRT76):c.1205T>C (p.Met402Thr)not specified [RCV004937656]uncertain significance125277192952771929Humanname
597624636CV3695666single nucleotide variantNM_015848.4(KRT76):c.1870C>T (p.Arg624Cys)not specified [RCV004937658]uncertain significance125276876052768760Humanname
597624637CV3695667single nucleotide variantNM_015848.4(KRT76):c.1106A>C (p.Lys369Thr)not specified [RCV004937659]uncertain significance125277212552772125Humanname
597624638CV3695668single nucleotide variantNM_015848.4(KRT76):c.1387C>T (p.Arg463Trp)not specified [RCV004937660]uncertain significance125277109652771096Humanname
597795012CV3695670single nucleotide variantNM_015848.4(KRT76):c.1621A>G (p.Ser541Gly)not specified [RCV004934704]likely benign125276900952769009Humanname
598163373CV3980536single nucleotide variantNM_015848.4(KRT76):c.1802G>A (p.Ser601Asn)not specified [RCV005368816]uncertain significance125276882852768828Humanname
598195859CV3980541single nucleotide variantNM_015848.4(KRT76):c.1862C>T (p.Thr621Ile)not specified [RCV005355076]uncertain significance125276876852768768Humanname
598195863CV3980542single nucleotide variantNM_015848.4(KRT76):c.1244T>C (p.Ile415Thr)not specified [RCV005355077]uncertain significance125277189052771890Humanname
598163385CV3980543single nucleotide variantNM_015848.4(KRT76):c.1288G>A (p.Ala430Thr)not specified [RCV005368818]uncertain significance125277119552771195Humanname