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Variants search result for All species
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127 records found for search term Zic4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155934511CV2225317single nucleotide variantNM_032153.6(ZIC4):c.-7T>Gnot specified [RCV004098954]uncertain significance3147402804147402804Humanname
156366082CV1908483single nucleotide variantNM_032153.6(ZIC4):c.689-5G>Anot provided [RCV002582074]likely benign3147391251147391251Humanname
156131529CV1918009single nucleotide variantNM_032153.6(ZIC4):c.71-10T>Cnot provided [RCV002623330]likely benign3147396479147396479Humanname
156391083CV2118657single nucleotide variantNM_032153.6(ZIC4):c.-15-6A>Gnot provided [RCV002943914]benign3147402818147402818Humanname
405120237CV2952280single nucleotide variantNM_032153.6(ZIC4):c.71-11T>Anot provided [RCV003671392]likely benign3147396480147396480Humanname
156130827CV2022732single nucleotide variantNM_032153.6(ZIC4):c.688+17G>Anot provided [RCV002740557]likely benign3147395835147395835Humanname
156144430CV2033090single nucleotide variantNM_032153.6(ZIC4):c.688+19C>Tnot provided [RCV002741014]likely benign3147395833147395833Humanname
156024047CV2145505single nucleotide variantNM_032153.6(ZIC4):c.689-14G>Anot provided [RCV003018368]likely benign3147391260147391260Humanname
405147948CV2960148single nucleotide variantNM_032153.6(ZIC4):c.688+10C>Anot provided [RCV003669841]likely benign3147395842147395842Humanname
405224757CV2979492deletionNM_032153.6(ZIC4):c.-15-20delnot provided [RCV003681234]likely benign3147402832147402832Humanname
597974048CV3821056single nucleotide variantNM_032153.6(ZIC4):c.1004+7G>Anot provided [RCV005168377]likely benign3147390924147390924Humanname
156133626CV2195967single nucleotide variantNM_032153.6(ZIC4):c.-16+901C>Tnot specified [RCV004072221]uncertain significance3147405462147405462Humanname
156054817CV2320489single nucleotide variantNM_032153.6(ZIC4):c.-16+952G>Anot specified [RCV004172123]likely benign3147405411147405411Humanname
156392747CV2386647single nucleotide variantNM_032153.6(ZIC4):c.-16+986C>Tnot specified [RCV004230988]uncertain significance3147405377147405377Humanname
405140722CV3029742single nucleotide variantNM_032153.6(ZIC4):c.1005-15A>Cnot provided [RCV003702397]benign3147388874147388874Humanname
407459794CV3490353single nucleotide variantNM_032153.6(ZIC4):c.-16+967A>Tnot specified [RCV004687226]uncertain significance3147405396147405396Humanname
597728716CV3625060single nucleotide variantNM_032153.6(ZIC4):c.-16+928G>Cnot specified [RCV004888576]uncertain significance3147405435147405435Humanname
598159412CV3934083single nucleotide variantNM_032153.6(ZIC4):c.-16+961G>Tnot specified [RCV005306567]uncertain significance3147405402147405402Humanname
156137556CV1902164single nucleotide variantNM_032153.6(ZIC4):c.-15-1282C>Tnot provided [RCV003082074]uncertain significance3147404094147404094Humanname
156442123CV1938026single nucleotide variantNM_032153.6(ZIC4):c.-15-1225G>Anot provided [RCV003112460]|not specified [RCV004686767]uncertain significance3147404037147404037Humanname
402500358CV2872789single nucleotide variantNM_032153.6(ZIC4):c.-15-1159G>Anot provided [RCV003545836]uncertain significance3147403971147403971Humanname
405238390CV2891386single nucleotide variantNM_032153.6(ZIC4):c.-15-1271A>Cnot provided [RCV003556855]likely benign3147404083147404083Humanname
405145097CV3027254single nucleotide variantNM_032153.6(ZIC4):c.-15-1133C>Gnot provided [RCV003702763]likely benign3147403945147403945Humanname
405144572CV3027344single nucleotide variantNM_032153.6(ZIC4):c.-15-1138C>Tnot provided [RCV003702807]likely benign3147403950147403950Humanname
405133019CV3051366single nucleotide variantNM_032153.6(ZIC4):c.-15-1142C>Gnot provided [RCV003724998]likely benign3147403954147403954Humanname
405154804CV3068809single nucleotide variantNM_032153.6(ZIC4):c.-15-1245T>Cnot provided [RCV003726669]likely benign3147404057147404057Humanname
405246199CV3162254single nucleotide variantNM_032153.6(ZIC4):c.-15-1272T>Cnot provided [RCV003868773]likely benign3147404084147404084Humanname
597976386CV3829634single nucleotide variantNM_032153.6(ZIC4):c.-15-1253C>Tnot provided [RCV005169901]uncertain significance3147404065147404065Humanname
12896529CV389565single nucleotide variantNM_032153.6(ZIC4):c.-15-1152G>Anot provided [RCV002522753]|not specified [RCV000455473]benign3147403964147403964Human5name
12896529CV389565single nucleotide variantNM_032153.6(ZIC4):c.-15-1152G>Anot provided [RCV002522753]|not specified [RCV000455473]benign3147403964147403965Human5name
15178034CV733860single nucleotide variantNM_032153.6(ZIC4):c.-15-1281G>Anot provided [RCV000906782]|not specified [RCV004887661]likely benign3147404093147404093Humanname
402506904CV3039217single nucleotide variantNM_032153.6(ZIC4):c.37T>C (p.Leu13=)not provided [RCV003715289]likely benign3147402761147402761Humanname
156245062CV1894097single nucleotide variantNM_032153.6(ZIC4):c.273T>C (p.Ala91=)not provided [RCV003085891]likely benign3147396267147396267Humanname
156361611CV1900576single nucleotide variantNM_032153.6(ZIC4):c.105C>T (p.Thr35=)not provided [RCV002581764]likely benign3147396435147396435Humanname
156131303CV1917975single nucleotide variantNM_032153.6(ZIC4):c.132G>A (p.Pro44=)not provided [RCV002623321]likely benign3147396408147396408Humanname
156417883CV1920640single nucleotide variantNM_032153.6(ZIC4):c.198G>C (p.Gly66=)not provided [RCV002611051]likely benign3147396342147396342Humanname
597936615CV3764877single nucleotide variantNM_032153.6(ZIC4):c.276C>T (p.Ala92=)not provided [RCV005117576]likely benign3147396264147396264Humanname
597913451CV3833797single nucleotide variantNM_032153.6(ZIC4):c.258C>T (p.Ser86=)not provided [RCV005183156]likely benign3147396282147396282Humanname
8661114CV136234single nucleotide variantNM_032153.6(ZIC4):c.966G>C (p.Ser322=)not provided [RCV002515803]|not specified [RCV000118906]benign|likely benign|conflicting interpretations of pathogenicity3147390969147390969Humanname
156408104CV1911465single nucleotide variantNM_032153.6(ZIC4):c.765G>A (p.Ser255=)not provided [RCV002607119]likely benign3147391170147391170Humanname
156269171CV1915185single nucleotide variantNM_032153.6(ZIC4):c.849G>A (p.Lys283=)not provided [RCV002628030]likely benign3147391086147391086Humanname
156314229CV1931479single nucleotide variantNM_032153.6(ZIC4):c.49C>T (p.Arg17Ter)not provided [RCV002629957]uncertain significance3147402749147402749Humanname
155916486CV1941566single nucleotide variantNM_032153.6(ZIC4):c.74G>A (p.Ser25Asn)not provided [RCV003111729]|not specified [RCV004189749]uncertain significance3147396466147396466Humanname
156133071CV2022824single nucleotide variantNM_032153.6(ZIC4):c.35G>A (p.Arg12Gln)not provided [RCV002740636]uncertain significance3147402763147402763Humanname
155938630CV2041482single nucleotide variantNM_032153.6(ZIC4):c.28A>G (p.Arg10Gly)not provided [RCV002775046]uncertain significance3147402770147402770Humanname
156017119CV2046925single nucleotide variantNM_032153.6(ZIC4):c.744C>T (p.Ser248=)not provided [RCV002756994]likely benign3147391191147391191Humanname
155906507CV2080378single nucleotide variantNM_032153.6(ZIC4):c.459G>A (p.Glu153=)not provided [RCV002858187]likely benign3147396081147396081Humanname
156103086CV2113451single nucleotide variantNM_032153.6(ZIC4):c.468G>A (p.Thr156=)not provided [RCV002952811]likely benign3147396072147396072Humanname
156018477CV2114678single nucleotide variantNM_032153.6(ZIC4):c.831C>T (p.His277=)not provided [RCV002909495]likely benign3147391104147391104Humanname
156306764CV2115642single nucleotide variantNM_032153.6(ZIC4):c.699C>T (p.Pro233=)not provided [RCV002922857]likely benign3147391236147391236Humanname
156070696CV2168857single nucleotide variantNM_032153.6(ZIC4):c.307C>T (p.Leu103=)not provided [RCV003037558]likely benign3147396233147396233Humanname
155959090CV2193736single nucleotide variantNM_032153.6(ZIC4):c.40C>T (p.Arg14Trp)not specified [RCV004074499]uncertain significance3147402758147402758Humanname
156347238CV2375404single nucleotide variantNM_032153.6(ZIC4):c.50G>A (p.Arg17Gln)not provided [RCV003548965]|not specified [RCV004232799]uncertain significance3147402748147402748Humanname
404996820CV2851494single nucleotide variantNM_032153.6(ZIC4):c.34C>T (p.Arg12Ter)not provided [RCV003491856]uncertain significance3147402764147402764Humanname
405223677CV2887580single nucleotide variantNM_032153.6(ZIC4):c.963C>T (p.Ser321=)not provided [RCV003554306]likely benign3147390972147390972Humanname
405128459CV2954907single nucleotide variantNM_032153.6(ZIC4):c.900G>C (p.Ser300=)not provided [RCV003668158]likely benign3147391035147391035Humanname
405222176CV3056911single nucleotide variantNM_032153.6(ZIC4):c.966G>T (p.Ser322=)not provided [RCV003733480]likely benign3147390969147390969Humanname
405211162CV3146306single nucleotide variantNM_032153.6(ZIC4):c.354C>T (p.Arg118=)not provided [RCV003845837]likely benign3147396186147396186Humanname
597728708CV3625061single nucleotide variantNM_032153.6(ZIC4):c.41G>A (p.Arg14Gln)not specified [RCV004888577]uncertain significance3147402757147402757Humanname
597860909CV3826072single nucleotide variantNM_032153.6(ZIC4):c.957G>A (p.Val319=)not provided [RCV005174971]likely benign3147390978147390978Humanname
15163035CV733859single nucleotide variantNM_032153.6(ZIC4):c.840G>T (p.Ser280=)not provided [RCV000903684]benign3147391095147391095Humanname
156181176CV1901757single nucleotide variantNM_032153.6(ZIC4):c.209A>G (p.Asp70Gly)not provided [RCV002595067]uncertain significance3147396331147396331Humanname
156400715CV1907881single nucleotide variantNM_032153.6(ZIC4):c.277G>T (p.Ala93Ser)not provided [RCV002584845]|not specified [RCV004073379]uncertain significance3147396263147396263Humanname
155990585CV2026935single nucleotide variantNM_032153.6(ZIC4):c.152C>T (p.Pro51Leu)not provided [RCV002755732]uncertain significance3147396388147396388Humanname
155935262CV2063767single nucleotide variantNM_032153.6(ZIC4):c.161C>G (p.Ser54Cys)not provided [RCV002839031]uncertain significance3147396379147396379Humanname
156211395CV2103318single nucleotide variantNM_032153.6(ZIC4):c.248C>T (p.Ala83Val)not provided [RCV002918176]likely benign3147396292147396292Humanname
155934190CV2113997single nucleotide variantNM_032153.6(ZIC4):c.295G>C (p.Gly99Arg)not provided [RCV002904011]benign|likely benign3147396245147396245Humanname
156236310CV2118436single nucleotide variantNM_032153.6(ZIC4):c.274G>C (p.Ala92Pro)not provided [RCV002958704]uncertain significance3147396266147396266Humanname
156368737CV2193774single nucleotide variantNM_032153.6(ZIC4):c.236C>T (p.Pro79Leu)not specified [RCV004074533]uncertain significance3147396304147396304Humanname
156084782CV2249284single nucleotide variantNM_032153.6(ZIC4):c.182G>C (p.Gly61Ala)not specified [RCV004118310]uncertain significance3147396358147396358Humanname
156346915CV2353802single nucleotide variantNM_032153.6(ZIC4):c.127T>G (p.Phe43Val)not provided [RCV005098996]|not specified [RCV004201807]uncertain significance3147396413147396413Humanname
156006541CV2401207single nucleotide variantNM_032153.6(ZIC4):c.149C>G (p.Pro50Arg)not provided [RCV005099222]|not specified [RCV004245761]uncertain significance3147396391147396391Humanname
401863561CV2776980single nucleotide variantNM_032153.6(ZIC4):c.140A>G (p.His47Arg)not specified [RCV004351790]uncertain significance3147396400147396400Humanname
402519628CV2946239single nucleotide variantNM_032153.6(ZIC4):c.169C>T (p.Arg57Cys)not provided [RCV003663204]uncertain significance3147396371147396371Humanname
405245281CV2969068single nucleotide variantNM_032153.6(ZIC4):c.202C>G (p.Pro68Ala)not provided [RCV003685111]uncertain significance3147396338147396338Humanname
405210267CV2970554single nucleotide variantNM_032153.6(ZIC4):c.224C>T (p.Pro75Leu)not provided [RCV003679297]uncertain significance3147396316147396316Humanname
404982801CV2979531single nucleotide variantNM_032153.6(ZIC4):c.210C>G (p.Asp70Glu)not provided [RCV003691481]uncertain significance3147396330147396330Humanname
405226491CV3039323single nucleotide variantNM_032153.6(ZIC4):c.295G>A (p.Gly99Arg)not provided [RCV003710739]uncertain significance3147396245147396245Humanname
405208607CV3065458single nucleotide variantNM_032153.6(ZIC4):c.281C>A (p.Ala94Asp)not provided [RCV003731669]uncertain significance3147396259147396259Humanname
405020634CV3139167single nucleotide variantNM_032153.6(ZIC4):c.199C>T (p.Leu67Phe)not provided [RCV003829809]uncertain significance3147396341147396341Humanname
405681911CV3357139single nucleotide variantNM_032153.6(ZIC4):c.235C>A (p.Pro79Thr)not specified [RCV004488865]uncertain significance3147396305147396305Humanname
407459786CV3490351single nucleotide variantNM_032153.6(ZIC4):c.136C>A (p.Leu46Ile)not specified [RCV004687224]uncertain significance3147396404147396404Humanname
407459790CV3490352single nucleotide variantNM_032153.6(ZIC4):c.188T>A (p.Leu63Gln)not specified [RCV004687225]uncertain significance3147396352147396352Humanname
597728679CV3625066single nucleotide variantNM_032153.6(ZIC4):c.168C>A (p.Ser56Arg)not specified [RCV004888581]uncertain significance3147396372147396372Humanname
597875789CV3775877single nucleotide variantNM_032153.6(ZIC4):c.166A>C (p.Ser56Arg)not provided [RCV005123404]uncertain significance3147396374147396374Humanname
598260375CV3934082single nucleotide variantNM_032153.6(ZIC4):c.185T>A (p.Leu62His)not specified [RCV005300412]uncertain significance3147396355147396355Humanname
598260380CV3934084single nucleotide variantNM_032153.6(ZIC4):c.107C>T (p.Ala36Val)not specified [RCV005300413]uncertain significance3147396433147396433Humanname
156169651CV1874057single nucleotide variantNM_032153.6(ZIC4):c.487G>T (p.Val163Phe)not provided [RCV003083189]uncertain significance3147396053147396053Humanname
156447070CV1944705single nucleotide variantNM_032153.6(ZIC4):c.334G>A (p.Gly112Ser)not provided [RCV003118597]uncertain significance3147396206147396206Humanname
155951056CV2026221single nucleotide variantNM_032153.6(ZIC4):c.455A>G (p.His152Arg)not provided [RCV002730683]uncertain significance3147396085147396085Humanname
156111955CV2038844single nucleotide variantNM_032153.6(ZIC4):c.899C>G (p.Ser300Trp)not provided [RCV002785434]uncertain significance3147391036147391036Humanname
156149870CV2091028single nucleotide variantNM_032153.6(ZIC4):c.506C>G (p.Ala169Gly)not provided [RCV002890616]benign3147396034147396034Humanname
155922046CV2102462single nucleotide variantNM_032153.6(ZIC4):c.493G>A (p.Gly165Ser)not provided [RCV002903400]benign3147396047147396047Humanname
156018625CV2114690single nucleotide variantNM_032153.6(ZIC4):c.794C>T (p.Thr265Met)not provided [RCV002909501]|not specified [RCV004066241]uncertain significance3147391141147391141Humanname
156236837CV2193511single nucleotide variantNM_032153.6(ZIC4):c.971C>A (p.Ala324Glu)not specified [RCV004072992]uncertain significance3147390964147390964Humanname
155951823CV2238851single nucleotide variantNM_032153.6(ZIC4):c.326C>A (p.Ala109Glu)not specified [RCV004109765]uncertain significance3147396214147396214Humanname
155932492CV2290684single nucleotide variantNM_032153.6(ZIC4):c.968C>G (p.Ala323Gly)not specified [RCV004149209]uncertain significance3147390967147390967Humanname
156356651CV2320829single nucleotide variantNM_032153.6(ZIC4):c.550C>G (p.Pro184Ala)not specified [RCV004172659]uncertain significance3147395990147395990Humanname
401724756CV2693408single nucleotide variantNM_032153.6(ZIC4):c.815A>G (p.Asp272Gly)not specified [RCV004295362]uncertain significance3147391120147391120Humanname
401759835CV2707163single nucleotide variantNM_032153.6(ZIC4):c.783C>G (p.Asp261Glu)not specified [RCV004315527]uncertain significance3147391152147391152Humanname
401770824CV2726272single nucleotide variantNM_032153.6(ZIC4):c.351C>A (p.Phe117Leu)not specified [RCV004326721]uncertain significance3147396189147396189Humanname
401891609CV2780574single nucleotide variantNM_032153.6(ZIC4):c.529G>A (p.Glu177Lys)not specified [RCV004351946]uncertain significance3147396011147396011Humanname
401888471CV2785011single nucleotide variantNM_032153.6(ZIC4):c.793A>C (p.Thr265Pro)not specified [RCV004355033]uncertain significance3147391142147391142Humanname
401877607CV2790229single nucleotide variantNM_032153.6(ZIC4):c.790T>C (p.Tyr264His)not specified [RCV004364141]uncertain significance3147391145147391145Humanname
402479204CV2853899single nucleotide variantNM_032153.6(ZIC4):c.865G>T (p.Gly289Trp)not provided [RCV003543835]uncertain significance3147391070147391070Humanname
405236105CV2887850single nucleotide variantNM_032153.6(ZIC4):c.547A>G (p.Lys183Glu)not provided [RCV003556419]uncertain significance3147395993147395993Humanname
405151478CV2888539single nucleotide variantNM_032153.6(ZIC4):c.626C>T (p.Pro209Leu)not provided [RCV003561763]uncertain significance3147395914147395914Humanname
402522485CV2940268single nucleotide variantNM_032153.6(ZIC4):c.503A>T (p.Gln168Leu)not provided [RCV003663413]uncertain significance3147396037147396037Humanname
405136564CV2963133single nucleotide variantNM_032153.6(ZIC4):c.913G>C (p.Ala305Pro)not provided [RCV003668839]uncertain significance3147391022147391022Humanname
405246608CV2966365single nucleotide variantNM_032153.6(ZIC4):c.311C>G (p.Thr104Arg)not provided [RCV003685464]uncertain significance3147396229147396229Humanname
402507735CV2979103single nucleotide variantNM_032153.6(ZIC4):c.454C>A (p.His152Asn)not provided [RCV003689229]uncertain significance3147396086147396086Humanname
405233475CV2985376single nucleotide variantNM_032153.6(ZIC4):c.731G>T (p.Arg244Leu)not provided [RCV003711766]uncertain significance3147391204147391204Humanname
405143503CV3056160single nucleotide variantNM_032153.6(ZIC4):c.482A>G (p.Glu161Gly)not provided [RCV003725855]uncertain significance3147396058147396058Humanname
405188637CV3069162single nucleotide variantNM_032153.6(ZIC4):c.875C>T (p.Pro292Leu)not provided [RCV003729510]uncertain significance3147391060147391060Humanname
405255199CV3175726single nucleotide variantNM_032153.6(ZIC4):c.988G>A (p.Ala330Thr)not provided [RCV003871994]uncertain significance3147390947147390947Humanname
402515161CV3178867single nucleotide variantNM_032153.6(ZIC4):c.965C>G (p.Ser322Trp)not provided [RCV003879300]uncertain significance3147390970147390970Humanname
405681915CV3357140single nucleotide variantNM_032153.6(ZIC4):c.427C>T (p.Leu143Phe)not provided [RCV005104786]|not specified [RCV004488866]uncertain significance3147396113147396113Humanname
405681921CV3357141single nucleotide variantNM_032153.6(ZIC4):c.776C>G (p.Thr259Ser)not specified [RCV004488867]uncertain significance3147391159147391159Humanname
597728702CV3625063single nucleotide variantNM_032153.6(ZIC4):c.422C>G (p.Pro141Arg)not specified [RCV004888578]uncertain significance3147396118147396118Humanname
597728695CV3625064single nucleotide variantNM_032153.6(ZIC4):c.881C>T (p.Pro294Leu)not specified [RCV004888579]uncertain significance3147391054147391054Humanname
597728687CV3625065single nucleotide variantNM_032153.6(ZIC4):c.907C>A (p.Pro303Thr)not specified [RCV004888580]uncertain significance3147391028147391028Humanname
597728672CV3625067single nucleotide variantNM_032153.6(ZIC4):c.440C>G (p.Thr147Ser)not specified [RCV004888582]uncertain significance3147396100147396100Humanname
597728420CV3625068single nucleotide variantNM_032153.6(ZIC4):c.908C>G (p.Pro303Arg)not specified [RCV004888583]uncertain significance3147391027147391027Humanname
597728171CV3625069single nucleotide variantNM_032153.6(ZIC4):c.869G>C (p.Arg290Pro)not specified [RCV004888584]uncertain significance3147391066147391066Humanname
597942924CV3816353single nucleotide variantNM_032153.6(ZIC4):c.996G>T (p.Leu332Phe)not provided [RCV005159414]uncertain significance3147390939147390939Humanname
598260385CV3934085single nucleotide variantNM_032153.6(ZIC4):c.471C>A (p.His157Gln)not specified [RCV005300414]uncertain significance3147396069147396069Humanname
15100394CV697872single nucleotide variantNM_032153.6(ZIC4):c.965C>T (p.Ser322Leu)not provided [RCV000958908]benign3147390970147390970Humanname