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59 records found for search term Pan3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582739CV117295single nucleotide variantNM_175854.7(PAN3):c.852+11141G>ALung cancer [RCV000097816]uncertain significance132820848728208487Humanname
150557195CV1310559deletionNM_175854.8(PAN3):c.85del (p.Ala29fs)not specified [RCV001775486]uncertain significance132813874128138741Humanname
597716929CV3571168single nucleotide variantNM_175854.8(PAN3):c.23C>T (p.Pro8Leu)not specified [RCV004841481]uncertain significance132813868028138680Humanname
329358580CV2454355single nucleotide variantNM_175854.8(PAN3):c.41C>T (p.Ala14Val)not specified [RCV004265808]uncertain significance132813869828138698Humanname
405758625CV3364031single nucleotide variantNM_175854.8(PAN3):c.50C>A (p.Ser17Tyr)not specified [RCV004500232]uncertain significance132813870728138707Humanname
405758632CV3364032single nucleotide variantNM_175854.8(PAN3):c.70G>A (p.Ala24Thr)not specified [RCV004500233]uncertain significance132813872728138727Humanname
405758648CV3364035single nucleotide variantNM_175854.8(PAN3):c.98T>G (p.Val33Gly)not specified [RCV004500236]uncertain significance132813875528138755Humanname
597716845CV3571159single nucleotide variantNM_175854.8(PAN3):c.83T>G (p.Val28Gly)not specified [RCV004841474]uncertain significance132813874028138740Humanname
155915870CV2200558single nucleotide variantNM_175854.8(PAN3):c.278C>G (p.Ala93Gly)not specified [RCV004078905]uncertain significance132813893528138935Humanname
405758579CV3364024single nucleotide variantNM_175854.8(PAN3):c.124G>T (p.Val42Leu)not specified [RCV004500225]uncertain significance132813878128138781Humanname
405758585CV3364025single nucleotide variantNM_175854.8(PAN3):c.127G>A (p.Gly43Arg)not specified [RCV004500226]uncertain significance132813878428138784Humanname
597657756CV3571160single nucleotide variantNM_175854.8(PAN3):c.229C>T (p.Pro77Ser)not specified [RCV004827671]uncertain significance132813888628138886Humanname
598259065CV4005767single nucleotide variantNM_175854.8(PAN3):c.121G>T (p.Ala41Ser)not specified [RCV005386408]uncertain significance132813877828138778Humanname
598259070CV4005768single nucleotide variantNM_175854.8(PAN3):c.122C>T (p.Ala41Val)not specified [RCV005386409]uncertain significance132813877928138779Humanname
598259074CV4005769single nucleotide variantNM_175854.8(PAN3):c.262C>G (p.Leu88Val)not specified [RCV005386410]uncertain significance132813891928138919Humanname
156330980CV2224350single nucleotide variantNM_175854.8(PAN3):c.490A>G (p.Thr164Ala)not specified [RCV004097695]uncertain significance132817433128174331Humanname
156177695CV2230423single nucleotide variantNM_175854.8(PAN3):c.308T>G (p.Val103Gly)not specified [RCV004095876]uncertain significance132813896528138965Humanname
156135610CV2256922single nucleotide variantNM_175854.8(PAN3):c.829A>G (p.Arg277Gly)not specified [RCV004121121]uncertain significance132819732328197323Humanname
155984854CV2270628single nucleotide variantNM_175854.8(PAN3):c.839A>G (p.Glu280Gly)not specified [RCV004137842]uncertain significance132819733328197333Humanname
156089986CV2392141single nucleotide variantNM_175854.8(PAN3):c.521G>A (p.Ser174Asn)not specified [RCV004238034]uncertain significance132817436228174362Humanname
329402645CV2451128single nucleotide variantNM_175854.8(PAN3):c.788G>C (p.Arg263Thr)not specified [RCV004270064]uncertain significance132819728228197282Humanname
401734956CV2688664single nucleotide variantNM_175854.8(PAN3):c.385G>A (p.Gly129Ser)not specified [RCV004301605]uncertain significance132813904228139042Humanname
401891351CV2779386single nucleotide variantNM_175854.8(PAN3):c.575C>T (p.Ser192Phe)not specified [RCV004351036]uncertain significance132817651528176515Humanname
405758620CV3364030single nucleotide variantNM_175854.8(PAN3):c.463A>G (p.Thr155Ala)not specified [RCV004500231]uncertain significance132817430428174304Humanname
405758636CV3364033single nucleotide variantNM_175854.8(PAN3):c.712A>T (p.Met238Leu)not specified [RCV004500234]uncertain significance132819720628197206Humanname
405758641CV3364034single nucleotide variantNM_175854.8(PAN3):c.836C>G (p.Thr279Arg)not specified [RCV004500235]uncertain significance132819733028197330Humanname
407479416CV3466410single nucleotide variantNM_175854.8(PAN3):c.898A>G (p.Thr300Ala)not specified [RCV004664128]uncertain significance132822027628220276Humanname
597716833CV3571158single nucleotide variantNM_175854.8(PAN3):c.482A>C (p.Tyr161Ser)not specified [RCV004841473]uncertain significance132817432328174323Humanname
597716869CV3571162single nucleotide variantNM_175854.8(PAN3):c.359G>C (p.Gly120Ala)not specified [RCV004841476]uncertain significance132813901628139016Humanname
597716884CV3571163single nucleotide variantNM_175854.8(PAN3):c.808A>G (p.Ile270Val)not specified [RCV004841477]uncertain significance132819730228197302Humanname
597716908CV3571166single nucleotide variantNM_175854.8(PAN3):c.331C>T (p.Pro111Ser)not specified [RCV004841479]uncertain significance132813898828138988Humanname
597716939CV3571169single nucleotide variantNM_175854.8(PAN3):c.616C>T (p.His206Tyr)not specified [RCV004841482]uncertain significance132817655628176556Humanname
598259061CV4005766single nucleotide variantNM_175854.8(PAN3):c.304G>C (p.Ala102Pro)not specified [RCV005386407]uncertain significance132813896128138961Humanname
155978288CV2222661single nucleotide variantNM_175854.8(PAN3):c.2297T>C (p.Val766Ala)not specified [RCV004101527]uncertain significance132828051928280519Humanname
156181630CV2255118single nucleotide variantNM_175854.8(PAN3):c.2272G>A (p.Asp758Asn)not specified [RCV004115747]uncertain significance132828049428280494Humanname
156032388CV2275014single nucleotide variantNM_175854.8(PAN3):c.1187A>G (p.Glu396Gly)not specified [RCV004135055]uncertain significance132825647828256478Humanname
156288536CV2299207single nucleotide variantNM_175854.8(PAN3):c.1258A>G (p.Asn420Asp)not specified [RCV004152542]uncertain significance132826045628260456Humanname
155962817CV2308197single nucleotide variantNM_175854.8(PAN3):c.1788G>C (p.Lys596Asn)not specified [RCV004164701]uncertain significance132826739728267397Humanname
156057992CV2316851single nucleotide variantNM_175854.8(PAN3):c.1144C>G (p.Pro382Ala)not specified [RCV004174379]uncertain significance132825643528256435Humanname
156229171CV2352966single nucleotide variantNM_175854.8(PAN3):c.1793G>C (p.Gly598Ala)not specified [RCV004201003]uncertain significance132827070128270701Humanname
155985638CV2368141single nucleotide variantNM_175854.8(PAN3):c.2217G>A (p.Met739Ile)not specified [RCV004216487]uncertain significance132828043928280439Humanname
329388053CV2437082single nucleotide variantNM_175854.8(PAN3):c.1942A>G (p.Ile648Val)not specified [RCV004262890]uncertain significance132827085028270850Humanname
329379628CV2456364single nucleotide variantNM_175854.8(PAN3):c.1121G>C (p.Ser374Thr)not specified [RCV004275527]uncertain significance132825641228256412Humanname
329396015CV2463170single nucleotide variantNM_175854.8(PAN3):c.1760A>C (p.Asn587Thr)not specified [RCV004274952]uncertain significance132826736928267369Humanname
401745802CV2678709single nucleotide variantNM_175854.8(PAN3):c.2608C>T (p.Arg870Cys)not specified [RCV004292709]uncertain significance132829246628292466Humanname
401772035CV2687393single nucleotide variantNM_175854.8(PAN3):c.1788G>T (p.Lys596Asn)not specified [RCV004300643]uncertain significance132826739728267397Humanname
401749520CV2710790single nucleotide variantNM_175854.8(PAN3):c.1460C>T (p.Pro487Leu)not specified [RCV004308719]uncertain significance132826676328266763Humanname
401733038CV2712950single nucleotide variantNM_175854.8(PAN3):c.1510A>G (p.Thr504Ala)not specified [RCV004314660]uncertain significance132826681328266813Humanname
401774662CV2728230single nucleotide variantNM_175854.8(PAN3):c.1478G>A (p.Arg493Gln)not specified [RCV004326053]uncertain significance132826678128266781Humanname
401779248CV2733263single nucleotide variantNM_175854.8(PAN3):c.1807C>G (p.Pro603Ala)not specified [RCV004332175]uncertain significance132827071528270715Humanname
405758601CV3364027single nucleotide variantNM_175854.8(PAN3):c.1531A>G (p.Asn511Asp)not specified [RCV004500228]uncertain significance132826683428266834Humanname
405758607CV3364028single nucleotide variantNM_175854.8(PAN3):c.1907T>C (p.Leu636Ser)not specified [RCV004500229]uncertain significance132827081528270815Humanname
407517931CV3466407single nucleotide variantNM_175854.8(PAN3):c.1288C>A (p.His430Asn)not specified [RCV004650830]uncertain significance132826048628260486Humanname
407517937CV3466408single nucleotide variantNM_175854.8(PAN3):c.1080A>T (p.Arg360Ser)not specified [RCV004650831]uncertain significance132825637128256371Humanname
407517945CV3466411single nucleotide variantNM_175854.8(PAN3):c.1267A>G (p.Ile423Val)not specified [RCV004650833]uncertain significance132826046528260465Humanname
597716856CV3571161single nucleotide variantNM_175854.8(PAN3):c.1280C>A (p.Thr427Asn)not specified [RCV004841475]uncertain significance132826047828260478Humanname
597657763CV3571165single nucleotide variantNM_175854.8(PAN3):c.1163C>T (p.Ser388Phe)not specified [RCV004827672]uncertain significance132825645428256454Humanname
597716918CV3571167single nucleotide variantNM_175854.8(PAN3):c.1377A>G (p.Ile459Met)not specified [RCV004841480]uncertain significance132826142428261424Humanname
598259079CV4005770single nucleotide variantNM_175854.8(PAN3):c.2497A>G (p.Ser833Gly)not specified [RCV005386411]uncertain significance132828809628288096Humanname