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Variants search result for Homo sapiens
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64 records found for search term Pnn
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15105678CV779624single nucleotide variantNM_002687.4(PNN):c.185+10C>Tnot provided [RCV000959932]benign143917615939176159Humanname
329353895CV2439933single nucleotide variantNM_002687.4(PNN):c.8T>C (p.Val3Ala)not specified [RCV004257966]uncertain significance143917528739175287Humanname
405652460CV3376594single nucleotide variantNM_002687.4(PNN):c.11C>T (p.Ala4Val)not specified [RCV004509804]uncertain significance143917529039175290Humanname
597743795CV3590632single nucleotide variantNM_002687.4(PNN):c.85C>T (p.Leu29Phe)not specified [RCV004845132]uncertain significance143917536439175364Humanname
15163388CV714123single nucleotide variantNM_002687.4(PNN):c.553A>C (p.Arg185=)not provided [RCV000970474]benign|likely benign143917914539179145Humanname
597743813CV3590635single nucleotide variantNM_002687.4(PNN):c.217C>T (p.Pro73Ser)not specified [RCV004845135]uncertain significance143917655839176558Humanname
597743829CV3590638single nucleotide variantNM_002687.4(PNN):c.259G>A (p.Gly87Ser)not specified [RCV004845138]uncertain significance143917741639177416Humanname
598187624CV4003511single nucleotide variantNM_002687.4(PNN):c.200A>T (p.Asp67Val)not specified [RCV005395945]uncertain significance143917654139176541Humanname
598187644CV4003514single nucleotide variantNM_002687.4(PNN):c.164G>A (p.Gly55Glu)not specified [RCV005395948]uncertain significance143917612839176128Humanname
15160835CV702869single nucleotide variantNM_002687.4(PNN):c.1872C>T (p.Ser624=)not provided [RCV000947563]benign143918158139181581Humanname
156107374CV2214162single nucleotide variantNM_002687.4(PNN):c.748C>A (p.Pro250Thr)not specified [RCV004086160]uncertain significance143917941739179417Humanname
156269498CV2326385single nucleotide variantNM_002687.4(PNN):c.373C>T (p.Arg125Cys)not specified [RCV004182962]uncertain significance143917763839177638Humanname
155995520CV2375825single nucleotide variantNM_002687.4(PNN):c.948G>T (p.Glu316Asp)not specified [RCV004224405]uncertain significance143918065739180657Humanname
156391061CV2385057single nucleotide variantNM_002687.4(PNN):c.766A>G (p.Ile256Val)not specified [RCV004228322]uncertain significance143917943539179435Humanname
401745279CV2698505single nucleotide variantNM_002687.4(PNN):c.331G>A (p.Ala111Thr)not specified [RCV004299003]uncertain significance143917759639177596Humanname
407524110CV3463830single nucleotide variantNM_002687.4(PNN):c.896G>A (p.Arg299His)not specified [RCV004653563]uncertain significance143918060539180605Humanname
597743784CV3590630single nucleotide variantNM_002687.4(PNN):c.557A>G (p.Lys186Arg)not specified [RCV004845130]uncertain significance143917914939179149Humanname
597743807CV3590634single nucleotide variantNM_002687.4(PNN):c.496A>G (p.Arg166Gly)not specified [RCV004845134]uncertain significance143917791439177914Humanname
597743973CV3590642single nucleotide variantNM_002687.4(PNN):c.389A>G (p.Gln130Arg)not specified [RCV004845142]uncertain significance143917765439177654Humanname
597743977CV3590643single nucleotide variantNM_002687.4(PNN):c.636A>C (p.Lys212Asn)not specified [RCV004845143]uncertain significance143917922839179228Humanname
598187654CV4003516single nucleotide variantNM_002687.4(PNN):c.763C>G (p.Leu255Val)not specified [RCV005395950]uncertain significance143917943239179432Humanname
598187660CV4003517single nucleotide variantNM_002687.4(PNN):c.428G>A (p.Arg143Gln)not specified [RCV005395951]uncertain significance143917784639177846Humanname
156375835CV2210327single nucleotide variantNM_002687.4(PNN):c.1592C>T (p.Pro531Leu)not specified [RCV004089484]uncertain significance143918130139181301Humanname
156223303CV2232949single nucleotide variantNM_002687.4(PNN):c.1585G>A (p.Asp529Asn)not specified [RCV004103328]uncertain significance143918129439181294Humanname
156085749CV2244639single nucleotide variantNM_002687.4(PNN):c.1813A>G (p.Ser605Gly)not specified [RCV004102355]uncertain significance143918152239181522Humanname
155914707CV2264627single nucleotide variantNM_002687.4(PNN):c.2135G>A (p.Arg712Lys)not specified [RCV004132632]uncertain significance143918184439181844Humanname
156295820CV2297509single nucleotide variantNM_002687.4(PNN):c.1480C>G (p.Leu494Val)not specified [RCV004153435]uncertain significance143918118939181189Humanname
156050528CV2323282single nucleotide variantNM_002687.4(PNN):c.2096A>C (p.Lys699Thr)not specified [RCV004171698]uncertain significance143918180539181805Humanname
155913317CV2341753single nucleotide variantNM_002687.4(PNN):c.1360A>G (p.Met454Val)not specified [RCV004182667]uncertain significance143918106939181069Humanname
156385486CV2364478single nucleotide variantNM_002687.4(PNN):c.2056G>A (p.Asp686Asn)not specified [RCV004217348]uncertain significance143918176539181765Humanname
156096046CV2375275single nucleotide variantNM_002687.4(PNN):c.1262C>T (p.Ala421Val)not specified [RCV004232685]uncertain significance143918097139180971Humanname
156092812CV2381963single nucleotide variantNM_002687.4(PNN):c.2087G>A (p.Arg696Gln)not specified [RCV004225895]uncertain significance143918179639181796Humanname
329373475CV2434217single nucleotide variantNM_002687.4(PNN):c.1383A>C (p.Lys461Asn)not specified [RCV004250104]uncertain significance143918109239181092Humanname
329400887CV2449711single nucleotide variantNM_002687.4(PNN):c.1160T>C (p.Met387Thr)not specified [RCV004268611]uncertain significance143918086939180869Humanname
329391119CV2452049single nucleotide variantNM_002687.4(PNN):c.1553A>G (p.Gln518Arg)not specified [RCV004278779]uncertain significance143918126239181262Humanname
329361356CV2459420single nucleotide variantNM_002687.4(PNN):c.2009G>T (p.Gly670Val)not specified [RCV004275110]uncertain significance143918171839181718Humanname
329396217CV2459421single nucleotide variantNM_002687.4(PNN):c.2030G>A (p.Gly677Glu)not specified [RCV004275111]uncertain significance143918173939181739Humanname
329396851CV2468261single nucleotide variantNM_002687.4(PNN):c.1028C>T (p.Ala343Val)not specified [RCV004275823]uncertain significance143918073739180737Humanname
401731388CV2674356single nucleotide variantNM_002687.4(PNN):c.1610T>C (p.Leu537Pro)not specified [RCV004289229]uncertain significance143918131939181319Humanname
401772722CV2687791single nucleotide variantNM_002687.4(PNN):c.1261G>C (p.Ala421Pro)not specified [RCV004302773]uncertain significance143918097039180970Humanname
401731415CV2701354single nucleotide variantNM_002687.4(PNN):c.2079G>C (p.Glu693Asp)not specified [RCV004311727]uncertain significance143918178839181788Humanname
401768612CV2716672single nucleotide variantNM_002687.4(PNN):c.1162G>A (p.Asp388Asn)not specified [RCV004327728]uncertain significance143918087139180871Humanname
401746803CV2731970single nucleotide variantNM_002687.4(PNN):c.1564C>T (p.His522Tyr)not specified [RCV004333206]uncertain significance143918127339181273Humanname
405652456CV3376592single nucleotide variantNM_002687.4(PNN):c.1040G>T (p.Ser347Ile)not specified [RCV004509802]uncertain significance143918074939180749Humanname
405652458CV3376593single nucleotide variantNM_002687.4(PNN):c.1102G>A (p.Glu368Lys)not specified [RCV004509803]uncertain significance143918081139180811Humanname
405652463CV3376595single nucleotide variantNM_002687.4(PNN):c.1421C>T (p.Ala474Val)not specified [RCV004509805]uncertain significance143918113039181130Humanname
405652465CV3376596single nucleotide variantNM_002687.4(PNN):c.1528T>G (p.Leu510Val)not specified [RCV004509806]uncertain significance143918123739181237Humanname
405652467CV3376597single nucleotide variantNM_002687.4(PNN):c.1763C>T (p.Thr588Ile)not specified [RCV004509807]uncertain significance143918147239181472Humanname
405652469CV3376598single nucleotide variantNM_002687.4(PNN):c.1874C>T (p.Thr625Ile)not specified [RCV004509808]uncertain significance143918158339181583Humanname
405652471CV3376599single nucleotide variantNM_002687.4(PNN):c.1888G>A (p.Glu630Lys)not specified [RCV004509809]uncertain significance143918159739181597Humanname
405652473CV3376600single nucleotide variantNM_002687.4(PNN):c.1955G>A (p.Arg652Gln)not specified [RCV004509810]uncertain significance143918166439181664Humanname
405652523CV3376601single nucleotide variantNM_002687.4(PNN):c.2073A>G (p.Ile691Met)not specified [RCV004509811]uncertain significance143918178239181782Humanname
407524107CV3463829single nucleotide variantNM_002687.4(PNN):c.2095A>C (p.Lys699Gln)not specified [RCV004653562]uncertain significance143918180439181804Humanname
407524113CV3463831single nucleotide variantNM_002687.4(PNN):c.1508A>G (p.Glu503Gly)not specified [RCV004653564]uncertain significance143918121739181217Humanname
407471916CV3463832single nucleotide variantNM_002687.4(PNN):c.1055A>T (p.Glu352Val)not specified [RCV004662396]uncertain significance143918076439180764Humanname
597743789CV3590631single nucleotide variantNM_002687.4(PNN):c.2050C>T (p.Arg684Trp)not specified [RCV004845131]uncertain significance143918175939181759Humanname
597743801CV3590633single nucleotide variantNM_002687.4(PNN):c.1139A>G (p.Asp380Gly)not specified [RCV004845133]uncertain significance143918084839180848Humanname
597743817CV3590636single nucleotide variantNM_002687.4(PNN):c.1924A>G (p.Arg642Gly)not specified [RCV004845136]uncertain significance143918163339181633Humanname
597743958CV3590639single nucleotide variantNM_002687.4(PNN):c.1663A>G (p.Lys555Glu)not specified [RCV004845139]uncertain significance143918137239181372Humanname
597743963CV3590640single nucleotide variantNM_002687.4(PNN):c.2057A>G (p.Asp686Gly)not specified [RCV004845140]uncertain significance143918176639181766Humanname
597743968CV3590641single nucleotide variantNM_002687.4(PNN):c.1752T>A (p.Ser584Arg)not specified [RCV004845141]uncertain significance143918146139181461Humanname
598187630CV4003512single nucleotide variantNM_002687.4(PNN):c.1325T>A (p.Leu442His)not specified [RCV005395946]uncertain significance143918103439181034Humanname
598187648CV4003515single nucleotide variantNM_002687.4(PNN):c.1948G>T (p.Val650Leu)not specified [RCV005395949]uncertain significance143918165739181657Humanname
15141004CV714124single nucleotide variantNM_002687.4(PNN):c.1576G>A (p.Glu526Lys)not provided [RCV000966236]benign143918128539181285Humanname