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Variants search result for Homo sapiens
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97 records found for search term Pcdh18
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156124548CV2350112single nucleotide variantNM_019035.5(PCDH18):c.27C>A (p.His9Gln)not specified [RCV004200034]uncertain significance4137532062137532062Humanname
155940442CV2222142single nucleotide variantNM_019035.5(PCDH18):c.239A>C (p.Asn80Thr)not specified [RCV004104900]uncertain significance4137531850137531850Humanname
156191349CV2385211single nucleotide variantNM_019035.5(PCDH18):c.188C>T (p.Thr63Ile)not specified [RCV004228459]uncertain significance4137531901137531901Humanname
329390082CV2441275single nucleotide variantNM_019035.5(PCDH18):c.271A>G (p.Thr91Ala)not specified [RCV004264005]uncertain significance4137531818137531818Humanname
405787132CV3371466single nucleotide variantNM_019035.5(PCDH18):c.257T>C (p.Ile86Thr)not specified [RCV004505061]uncertain significance4137531832137531832Humanname
405787115CV3375019single nucleotide variantNM_019035.5(PCDH18):c.194G>A (p.Arg65Gln)not specified [RCV004505058]uncertain significance4137531895137531895Humanname
598246432CV3999271single nucleotide variantNM_019035.5(PCDH18):c.131T>C (p.Ile44Thr)not specified [RCV005384048]uncertain significance4137531958137531958Humanname
598246452CV3999274single nucleotide variantNM_019035.5(PCDH18):c.164T>C (p.Leu55Ser)not specified [RCV005384051]uncertain significance4137531925137531925Humanname
598246459CV3999275single nucleotide variantNM_019035.5(PCDH18):c.277G>A (p.Asp93Asn)not specified [RCV005384052]uncertain significance4137531812137531812Humanname
155925513CV2348408single nucleotide variantNM_019035.5(PCDH18):c.435G>T (p.Glu145Asp)not specified [RCV004193600]uncertain significance4137531654137531654Humanname
401773844CV2691427single nucleotide variantNM_019035.5(PCDH18):c.599T>C (p.Val200Ala)not specified [RCV004305285]uncertain significance4137531490137531490Humanname
401885404CV2759601single nucleotide variantNM_019035.5(PCDH18):c.536A>G (p.Asn179Ser)not specified [RCV004338574]uncertain significance4137531553137531553Humanname
401928525CV2820181single nucleotide variantNM_019035.5(PCDH18):c.3216A>G (p.Pro1072=)not provided [RCV003439499]likely benign4137521221137521221Humanname
405787160CV3371471single nucleotide variantNM_019035.5(PCDH18):c.379G>A (p.Val127Met)not specified [RCV004505066]uncertain significance4137531710137531710Humanname
405787166CV3371472single nucleotide variantNM_019035.5(PCDH18):c.463C>T (p.Arg155Cys)not specified [RCV004505067]uncertain significance4137531626137531626Humanname
405787176CV3371474single nucleotide variantNM_019035.5(PCDH18):c.560G>A (p.Arg187Gln)not specified [RCV004505069]uncertain significance4137531529137531529Humanname
405787181CV3371475single nucleotide variantNM_019035.5(PCDH18):c.605G>A (p.Arg202Lys)not specified [RCV004505070]uncertain significance4137531484137531484Humanname
407523178CV3462895single nucleotide variantNM_019035.5(PCDH18):c.398A>G (p.Asn133Ser)not specified [RCV004653062]uncertain significance4137531691137531691Humanname
407523182CV3462898single nucleotide variantNM_019035.5(PCDH18):c.781G>A (p.Val261Ile)not specified [RCV004653063]uncertain significance4137531308137531308Humanname
597672556CV3578592single nucleotide variantNM_019035.5(PCDH18):c.571G>C (p.Asp191His)not specified [RCV004836517]uncertain significance4137531518137531518Humanname
597672593CV3578597single nucleotide variantNM_019035.5(PCDH18):c.634T>C (p.Tyr212His)not specified [RCV004836522]uncertain significance4137531455137531455Humanname
598246423CV3999270single nucleotide variantNM_019035.5(PCDH18):c.694C>A (p.Leu232Ile)not specified [RCV005384047]uncertain significance4137531395137531395Humanname
598195159CV3999283single nucleotide variantNM_019035.5(PCDH18):c.965T>C (p.Ile322Thr)not specified [RCV005397494]uncertain significance4137531124137531124Humanname
156271065CV2195212single nucleotide variantNM_019035.5(PCDH18):c.2176C>T (p.Arg726Cys)not specified [RCV004080150]uncertain significance4137529913137529913Humanname
156398329CV2200672single nucleotide variantNM_019035.5(PCDH18):c.2696A>C (p.Glu899Ala)not specified [RCV004081333]uncertain significance4137528522137528522Humanname
156235607CV2245447single nucleotide variantNM_019035.5(PCDH18):c.2599A>C (p.Lys867Gln)not specified [RCV004109227]uncertain significance4137528619137528619Humanname
156139533CV2246879single nucleotide variantNM_019035.5(PCDH18):c.2461C>T (p.Leu821Phe)not specified [RCV004112684]uncertain significance4137529628137529628Humanname
156248185CV2263959single nucleotide variantNM_019035.5(PCDH18):c.1954T>C (p.Trp652Arg)not specified [RCV004137991]uncertain significance4137530135137530135Humanname
155950629CV2267886single nucleotide variantNM_019035.5(PCDH18):c.2153T>C (p.Val718Ala)not specified [RCV004136180]uncertain significance4137529936137529936Humanname
156255931CV2277543single nucleotide variantNM_019035.5(PCDH18):c.2066C>G (p.Thr689Ser)not specified [RCV004145231]uncertain significance4137530023137530023Humanname
156263956CV2282619single nucleotide variantNM_019035.5(PCDH18):c.2851G>T (p.Gly951Trp)not specified [RCV004135178]uncertain significance4137521586137521586Humanname
156170252CV2296769single nucleotide variantNM_019035.5(PCDH18):c.2540C>T (p.Pro847Leu)not specified [RCV004148669]uncertain significance4137528768137528768Humanname
155904646CV2298838single nucleotide variantNM_019035.5(PCDH18):c.2141T>C (p.Leu714Pro)not specified [RCV004156387]uncertain significance4137529948137529948Humanname
156157432CV2314449single nucleotide variantNM_019035.5(PCDH18):c.1699A>G (p.Ile567Val)not specified [RCV004168558]uncertain significance4137530390137530390Humanname
156340215CV2347792single nucleotide variantNM_019035.5(PCDH18):c.2021G>A (p.Cys674Tyr)not specified [RCV004195450]uncertain significance4137530068137530068Humanname
156180585CV2356100single nucleotide variantNM_019035.5(PCDH18):c.1951G>A (p.Glu651Lys)not specified [RCV004203512]uncertain significance4137530138137530138Humanname
155929880CV2360987single nucleotide variantNM_019035.5(PCDH18):c.2254C>T (p.Arg752Trp)not specified [RCV004216185]uncertain significance4137529835137529835Humanname
155909151CV2397637single nucleotide variantNM_019035.5(PCDH18):c.2284G>T (p.Val762Leu)not specified [RCV004237089]uncertain significance4137529805137529805Humanname
156006229CV2401176single nucleotide variantNM_019035.5(PCDH18):c.1696A>G (p.Ile566Val)not specified [RCV004245733]uncertain significance4137530393137530393Humanname
329357573CV2427769single nucleotide variantNM_019035.5(PCDH18):c.2488C>A (p.Gln830Lys)not specified [RCV004252550]uncertain significance4137528820137528820Humanname
329399163CV2436301single nucleotide variantNM_019035.5(PCDH18):c.2866A>G (p.Thr956Ala)not specified [RCV004251706]likely benign4137521571137521571Humanname
329385946CV2458629single nucleotide variantNM_019035.5(PCDH18):c.2458G>C (p.Glu820Gln)not specified [RCV004268302]uncertain significance4137529631137529631Humanname
329396081CV2463239single nucleotide variantNM_019035.5(PCDH18):c.2435A>G (p.His812Arg)not specified [RCV004275010]uncertain significance4137529654137529654Humanname
329374445CV2463564single nucleotide variantNM_019035.5(PCDH18):c.1807A>T (p.Ile603Leu)not specified [RCV004277371]uncertain significance4137530282137530282Humanname
329393061CV2469261single nucleotide variantNM_019035.5(PCDH18):c.2308C>T (p.Pro770Ser)not specified [RCV004280601]uncertain significance4137529781137529781Humanname
401757272CV2675206single nucleotide variantNM_019035.5(PCDH18):c.1030G>A (p.Val344Ile)not specified [RCV004289977]uncertain significance4137531059137531059Humanname
401730171CV2680024single nucleotide variantNM_019035.5(PCDH18):c.2807T>C (p.Leu936Pro)not specified [RCV004286527]uncertain significance4137521630137521630Humanname
401754754CV2682293single nucleotide variantNM_019035.5(PCDH18):c.1717G>A (p.Val573Ile)not specified [RCV004290335]likely benign4137530372137530372Humanname
401893769CV2762061single nucleotide variantNM_019035.5(PCDH18):c.2434C>A (p.His812Asn)not specified [RCV004341878]uncertain significance4137529655137529655Humanname
401881253CV2784576single nucleotide variantNM_019035.5(PCDH18):c.1976A>G (p.Gln659Arg)not specified [RCV004358729]uncertain significance4137530113137530113Humanname
405787120CV3371464single nucleotide variantNM_019035.5(PCDH18):c.2227T>C (p.Tyr743His)not specified [RCV004505059]uncertain significance4137529862137529862Humanname
405787138CV3371467single nucleotide variantNM_019035.5(PCDH18):c.2709C>A (p.Asp903Glu)not specified [RCV004505062]uncertain significance4137528509137528509Humanname
405787090CV3375014single nucleotide variantNM_019035.5(PCDH18):c.1079C>A (p.Ser360Tyr)not specified [RCV004505053]uncertain significance4137531010137531010Humanname
405787095CV3375015single nucleotide variantNM_019035.5(PCDH18):c.1248A>C (p.Leu416Phe)not specified [RCV004505054]uncertain significance4137530841137530841Humanname
405787099CV3375016single nucleotide variantNM_019035.5(PCDH18):c.1288G>C (p.Glu430Gln)not specified [RCV004505055]uncertain significance4137530801137530801Humanname
405787105CV3375017single nucleotide variantNM_019035.5(PCDH18):c.1357G>C (p.Val453Leu)not specified [RCV004505056]uncertain significance4137530732137530732Humanname
405787110CV3375018single nucleotide variantNM_019035.5(PCDH18):c.1856C>T (p.Ala619Val)not specified [RCV004505057]uncertain significance4137530233137530233Humanname
407523168CV3462890single nucleotide variantNM_019035.5(PCDH18):c.1706A>G (p.Glu569Gly)not specified [RCV004653059]uncertain significance4137530383137530383Humanname
407480124CV3462893single nucleotide variantNM_019035.5(PCDH18):c.2566A>T (p.Arg856Trp)not specified [RCV004664295]uncertain significance4137528742137528742Humanname
407523174CV3462894single nucleotide variantNM_019035.5(PCDH18):c.1956G>C (p.Trp652Cys)not specified [RCV004653061]uncertain significance4137530133137530133Humanname
407480135CV3462897single nucleotide variantNM_019035.5(PCDH18):c.1717G>C (p.Val573Leu)not specified [RCV004664297]uncertain significance4137530372137530372Humanname
407480141CV3462899single nucleotide variantNM_019035.5(PCDH18):c.1939G>C (p.Val647Leu)not specified [RCV004664298]uncertain significance4137530150137530150Humanname
597672526CV3578587single nucleotide variantNM_019035.5(PCDH18):c.2666G>A (p.Arg889Gln)not specified [RCV004836513]uncertain significance4137528552137528552Humanname
597672534CV3578588single nucleotide variantNM_019035.5(PCDH18):c.2824G>A (p.Asp942Asn)not specified [RCV004836514]uncertain significance4137521613137521613Humanname
597672543CV3578589single nucleotide variantNM_019035.5(PCDH18):c.2098A>G (p.Met700Val)not specified [RCV004836515]uncertain significance4137529991137529991Humanname
597672550CV3578590single nucleotide variantNM_019035.5(PCDH18):c.1991C>T (p.Pro664Leu)not specified [RCV004836516]uncertain significance4137530098137530098Humanname
597672563CV3578593single nucleotide variantNM_019035.5(PCDH18):c.1144G>A (p.Val382Ile)not specified [RCV004836518]uncertain significance4137530945137530945Humanname
597672569CV3578594single nucleotide variantNM_019035.5(PCDH18):c.1600G>C (p.Asp534His)not specified [RCV004836519]uncertain significance4137530489137530489Humanname
597672576CV3578595single nucleotide variantNM_019035.5(PCDH18):c.2451C>G (p.Phe817Leu)not specified [RCV004836520]uncertain significance4137529638137529638Humanname
597672585CV3578596single nucleotide variantNM_019035.5(PCDH18):c.1274G>C (p.Arg425Thr)not specified [RCV004836521]uncertain significance4137530815137530815Humanname
597672602CV3578598single nucleotide variantNM_019035.5(PCDH18):c.2174A>T (p.Asn725Ile)not specified [RCV004836523]uncertain significance4137529915137529915Humanname
597672609CV3578599single nucleotide variantNM_019035.5(PCDH18):c.2332T>A (p.Ser778Thr)not specified [RCV004836524]uncertain significance4137529757137529757Humanname
598246466CV3999276single nucleotide variantNM_019035.5(PCDH18):c.2509A>G (p.Met837Val)not specified [RCV005384053]uncertain significance4137528799137528799Humanname
598246473CV3999277single nucleotide variantNM_019035.5(PCDH18):c.1204C>T (p.His402Tyr)not specified [RCV005384054]uncertain significance4137530885137530885Humanname
598246481CV3999278single nucleotide variantNM_019035.5(PCDH18):c.1508C>T (p.Thr503Ile)not specified [RCV005384055]uncertain significance4137530581137530581Humanname
598246488CV3999279single nucleotide variantNM_019035.5(PCDH18):c.2611A>C (p.Lys871Gln)not specified [RCV005384056]uncertain significance4137528607137528607Humanname
598246496CV3999280single nucleotide variantNM_019035.5(PCDH18):c.1312G>A (p.Glu438Lys)not specified [RCV005384057]uncertain significance4137530777137530777Humanname
598246505CV3999281single nucleotide variantNM_019035.5(PCDH18):c.2194A>G (p.Arg732Gly)not specified [RCV005384058]uncertain significance4137529895137529895Humanname
8625712CV80836single nucleotide variantNM_019035.4(PCDH18):c.1573G>A (p.Gly525Arg)Malignant melanoma [RCV000060913]not provided4137530516137530516Humanname
8625713CV80837single nucleotide variantNM_019035.4(PCDH18):c.1270G>A (p.Asp424Asn)Malignant melanoma [RCV000060914]not provided4137530819137530819Humanname
156293366CV2233538single nucleotide variantNM_019035.5(PCDH18):c.3154G>C (p.Gly1052Arg)not specified [RCV004100017]uncertain significance4137521283137521283Humanname
156273701CV2254637single nucleotide variantNM_019035.5(PCDH18):c.3217C>T (p.Leu1073Phe)not specified [RCV004115125]uncertain significance4137521220137521220Humanname
156063830CV2272386single nucleotide variantNM_019035.5(PCDH18):c.3143G>A (p.Gly1048Asp)not specified [RCV004133310]uncertain significance4137521294137521294Humanname
156289210CV2299318single nucleotide variantNM_019035.5(PCDH18):c.3024G>A (p.Met1008Ile)not specified [RCV004152636]uncertain significance4137521413137521413Humanname
156134604CV2347073single nucleotide variantNM_019035.5(PCDH18):c.3214C>T (p.Pro1072Ser)not specified [RCV004204556]uncertain significance4137521223137521223Humanname
156214404CV2385917single nucleotide variantNM_019035.5(PCDH18):c.3161C>T (p.Ala1054Val)not specified [RCV004226955]uncertain significance4137521276137521276Humanname
156185855CV2397508single nucleotide variantNM_019035.5(PCDH18):c.3336A>T (p.Lys1112Asn)not specified [RCV004236977]uncertain significance4137521101137521101Humanname
401740875CV2679824single nucleotide variantNM_019035.5(PCDH18):c.3361C>G (p.Leu1121Val)not specified [RCV004282282]uncertain significance4137521076137521076Humanname
401728123CV2685875single nucleotide variantNM_019035.5(PCDH18):c.3359A>G (p.Glu1120Gly)not specified [RCV004294857]uncertain significance4137521078137521078Humanname
401729615CV2690378single nucleotide variantNM_019035.5(PCDH18):c.3329A>G (p.Asp1110Gly)not specified [RCV004302369]uncertain significance4137521108137521108Humanname
401856245CV2761343single nucleotide variantNM_019035.5(PCDH18):c.3143G>C (p.Gly1048Ala)not specified [RCV004341209]uncertain significance4137521294137521294Humanname
405787144CV3371468single nucleotide variantNM_019035.5(PCDH18):c.3098A>G (p.Asn1033Ser)not specified [RCV004505063]uncertain significance4137521339137521339Humanname
405787149CV3371469single nucleotide variantNM_019035.5(PCDH18):c.3134A>G (p.Lys1045Arg)not specified [RCV004505064]uncertain significance4137521303137521303Humanname
405787155CV3371470single nucleotide variantNM_019035.5(PCDH18):c.3142G>T (p.Gly1048Cys)not specified [RCV004505065]uncertain significance4137521295137521295Humanname
407480118CV3462891single nucleotide variantNM_019035.5(PCDH18):c.3101C>A (p.Ser1034Tyr)not specified [RCV004664294]uncertain significance4137521336137521336Humanname
407523171CV3462892single nucleotide variantNM_019035.5(PCDH18):c.3163G>T (p.Ala1055Ser)not specified [RCV004653060]uncertain significance4137521274137521274Humanname
598246445CV3999273single nucleotide variantNM_019035.5(PCDH18):c.3326A>G (p.Asn1109Ser)not specified [RCV005384050]uncertain significance4137521111137521111Humanname