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37 records found for search term Fip1l1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401923295CV2822520single nucleotide variantNM_030917.4(FIP1L1):c.1500-8A>Cnot provided [RCV003435016]likely benign45345864553458645Humanname
15171841CV777475single nucleotide variantNM_030917.4(FIP1L1):c.1638-4C>Tnot provided [RCV000949905]likely benign45345929853459298Humanname
9689908CV173814single nucleotide variantNM_030917.4(FIP1L1):c.1285+11T>Gnot provided [RCV004715747]|not specified [RCV000155542]benign45344411453444114Humanname
597698757CV3669657single nucleotide variantNM_030917.4(FIP1L1):c.16G>T (p.Val6Phe)not specified [RCV004916164]uncertain significance45337785453377854Humanname
155989600CV2282804single nucleotide variantNM_030917.4(FIP1L1):c.55G>A (p.Gly19Arg)not specified [RCV004141652]uncertain significance45337789353377893Humanname
401928107CV2822519single nucleotide variantNM_030917.4(FIP1L1):c.810G>A (p.Pro270=)not provided [RCV003439309]likely benign45339983453399834Humanname
8687700CV138160single nucleotide variantNM_030917.4(FIP1L1):c.101A>G (p.His34Arg)not specified [RCV000121097]not provided45337908853379088Humanname
155920570CV2279618single nucleotide variantNM_030917.4(FIP1L1):c.260G>A (p.Ser87Asn)not specified [RCV004142118]uncertain significance45338380453383804Humanname
401728072CV2685810single nucleotide variantNM_030917.4(FIP1L1):c.1500C>T (p.Ser500=)not specified [RCV004294799]likely benign45345865353458653Humanname
598200512CV3955846single nucleotide variantNM_030917.4(FIP1L1):c.143T>C (p.Val48Ala)not specified [RCV005336665]uncertain significance45337923753379237Humanname
8631205CV86361single nucleotide variantNM_030917.3(FIP1L1):c.1071T>C (p.Pro357=)Malignant melanoma [RCV000066452]not provided45342808053428080Humanname
8687698CV138158single nucleotide variantNM_030917.4(FIP1L1):c.695A>G (p.Asn232Ser)not specified [RCV000121095]not provided45339148853391488Humanname
8687699CV138159single nucleotide variantNM_030917.4(FIP1L1):c.784T>C (p.Ser262Pro)not specified [RCV000121096]uncertain significance|not provided45339980853399808Humanname
156317738CV2204050single nucleotide variantNM_030917.4(FIP1L1):c.551C>A (p.Thr184Asn)not specified [RCV004076520]uncertain significance45339105453391054Humanname
156202322CV2256236single nucleotide variantNM_030917.4(FIP1L1):c.907G>A (p.Glu303Lys)not specified [RCV004116491]uncertain significance45341470653414706Humanname
156265061CV2275368single nucleotide variantNM_030917.4(FIP1L1):c.575A>T (p.Gln192Leu)not specified [RCV004135253]uncertain significance45339107853391078Humanname
156199502CV2365331single nucleotide variantNM_030917.4(FIP1L1):c.785C>G (p.Ser262Cys)not specified [RCV004209417]uncertain significance45339980953399809Humanname
329401283CV2442287single nucleotide variantNM_030917.4(FIP1L1):c.550A>G (p.Thr184Ala)not specified [RCV004264768]uncertain significance45339105353391053Humanname
329396948CV2468349single nucleotide variantNM_030917.4(FIP1L1):c.866A>G (p.Asn289Ser)not specified [RCV004275893]uncertain significance45341466553414665Humanname
401766973CV2680211single nucleotide variantNM_030917.4(FIP1L1):c.452C>T (p.Pro151Leu)not specified [RCV004286685]uncertain significance45339057553390575Humanname
405779794CV3260640single nucleotide variantNM_030917.4(FIP1L1):c.398G>T (p.Gly133Val)not specified [RCV004386575]uncertain significance45339052153390521Humanname
405779800CV3260641single nucleotide variantNM_030917.4(FIP1L1):c.601G>A (p.Val201Ile)not specified [RCV004386576]uncertain significance45339110453391104Humanname
405779808CV3260642single nucleotide variantNM_030917.4(FIP1L1):c.607C>G (p.Pro203Ala)not specified [RCV004386577]uncertain significance45339111053391110Humanname
407502707CV3435895single nucleotide variantNM_030917.4(FIP1L1):c.542A>T (p.Asn181Ile)not specified [RCV004623539]uncertain significance45339104553391045Humanname
407502718CV3435898single nucleotide variantNM_030917.4(FIP1L1):c.763G>A (p.Ala255Thr)not specified [RCV004623542]uncertain significance45339978753399787Humanname
597699612CV3669656single nucleotide variantNM_030917.4(FIP1L1):c.581G>A (p.Arg194Lys)not specified [RCV004916163]uncertain significance45339108453391084Humanname
598200518CV3955847single nucleotide variantNM_030917.4(FIP1L1):c.797C>T (p.Thr266Ile)not specified [RCV005336666]uncertain significance45339982153399821Humanname
155912408CV2245531single nucleotide variantNM_030917.4(FIP1L1):c.1380C>A (p.Asp460Glu)not specified [RCV004109623]uncertain significance45345301453453014Humanname
401856503CV2764829single nucleotide variantNM_030917.4(FIP1L1):c.1730C>T (p.Ala577Val)not provided [RCV003436022]|not specified [RCV004334929]uncertain significance45345939453459394Humanname
405867598CV2842327single nucleotide variantNM_030917.4(FIP1L1):c.1411C>T (p.Arg471Ter)EBV-positive nodal T- and NK-cell lymphoma [RCV004560276]likely benign45345304553453045Humanname
405867602CV2842328single nucleotide variantNM_030917.4(FIP1L1):c.1633C>T (p.Arg545Ter)EBV-positive nodal T- and NK-cell lymphoma [RCV004560277]likely benign45345878653458786Humanname
405779788CV3260639single nucleotide variantNM_030917.4(FIP1L1):c.1761C>G (p.Ser587Arg)not specified [RCV004386574]uncertain significance45345942553459425Humanname
407502703CV3435894single nucleotide variantNM_030917.4(FIP1L1):c.1470T>A (p.Asp490Glu)not specified [RCV004623538]uncertain significance45345310453453104Humanname
407502715CV3435897single nucleotide variantNM_030917.4(FIP1L1):c.1039A>G (p.Thr347Ala)not specified [RCV004623541]uncertain significance45342804853428048Humanname
597698741CV3669655single nucleotide variantNM_030917.4(FIP1L1):c.1073C>T (p.Pro358Leu)not specified [RCV004916162]uncertain significance45342808253428082Humanname
598200498CV3955844single nucleotide variantNM_030917.4(FIP1L1):c.1283A>G (p.Asn428Ser)not specified [RCV005336663]uncertain significance45344410153444101Humanname
598200504CV3955845single nucleotide variantNM_030917.4(FIP1L1):c.1147A>G (p.Thr383Ala)not specified [RCV005336664]uncertain significance45342815653428156Humanname