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Variants search result for Homo sapiens
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101 records found for search term Pcdhga4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401917937CV2825337single nucleotide variantNM_018917.4(PCDHGA4):c.409C>T (p.Leu137=)not provided [RCV003429841]likely benign5141355516141355516Humanname
156382006CV2212520single nucleotide variantNM_018917.4(PCDHGA4):c.277C>G (p.Arg93Gly)not specified [RCV004091404]uncertain significance5141355384141355384Humanname
329361943CV2456572single nucleotide variantNM_018917.4(PCDHGA4):c.296C>T (p.Ser99Phe)not specified [RCV004277772]uncertain significance5141355403141355403Humanname
401741732CV2676513single nucleotide variantNM_018917.4(PCDHGA4):c.100G>A (p.Ala34Thr)not specified [RCV004288708]uncertain significance5141355207141355207Humanname
401742395CV2715147single nucleotide variantNM_018917.4(PCDHGA4):c.293T>C (p.Val98Ala)not specified [RCV004322717]uncertain significance5141355400141355400Humanname
405744864CV3368213single nucleotide variantNM_018917.4(PCDHGA4):c.292G>C (p.Val98Leu)not specified [RCV004498280]uncertain significance5141355399141355399Humanname
597738162CV3575331single nucleotide variantNM_018917.4(PCDHGA4):c.133C>T (p.Leu45Phe)not specified [RCV004844056]uncertain significance5141355240141355240Humanname
597738172CV3575333single nucleotide variantNM_018917.4(PCDHGA4):c.295T>A (p.Ser99Thr)not specified [RCV004844058]uncertain significance5141355402141355402Humanname
597738210CV3575343single nucleotide variantNM_018917.4(PCDHGA4):c.127C>G (p.Arg43Gly)not specified [RCV004844065]uncertain significance5141355234141355234Humanname
597738228CV3575347single nucleotide variantNM_018917.4(PCDHGA4):c.194C>T (p.Ser65Leu)not specified [RCV004844068]uncertain significance5141355301141355301Humanname
598270587CV3996289single nucleotide variantNM_018917.4(PCDHGA4):c.262C>T (p.Arg88Trp)not specified [RCV005389006]uncertain significance5141355369141355369Humanname
598270580CV3996290single nucleotide variantNM_018917.4(PCDHGA4):c.143G>A (p.Cys48Tyr)not specified [RCV005389007]uncertain significance5141355250141355250Humanname
8657780CV86646single nucleotide variantNM_018917.3(PCDHGA4):c.2340C>T (p.Phe780=)Malignant melanoma [RCV000066737]not provided5141357447141357447Humanname
155920697CV2211924single nucleotide variantNM_018917.4(PCDHGA4):c.466G>T (p.Asp156Tyr)not specified [RCV004087054]uncertain significance5141355573141355573Humanname
156295804CV2233769single nucleotide variantNM_018917.4(PCDHGA4):c.731C>A (p.Thr244Lys)not specified [RCV004100206]uncertain significance5141355838141355838Humanname
156365104CV2272054single nucleotide variantNM_018917.4(PCDHGA4):c.914A>G (p.Asn305Ser)not specified [RCV004124851]uncertain significance5141356021141356021Humanname
156257106CV2277632single nucleotide variantNM_018917.4(PCDHGA4):c.461T>C (p.Ile154Thr)not specified [RCV004147097]uncertain significance5141355568141355568Humanname
156295154CV2297444single nucleotide variantNM_018917.4(PCDHGA4):c.901G>A (p.Asp301Asn)not specified [RCV004153381]uncertain significance5141356008141356008Humanname
156038036CV2313601single nucleotide variantNM_018917.4(PCDHGA4):c.347T>C (p.Val116Ala)not specified [RCV004157538]uncertain significance5141355454141355454Humanname
156063471CV2321079single nucleotide variantNM_018917.4(PCDHGA4):c.724G>A (p.Val242Ile)not specified [RCV004174905]uncertain significance5141355831141355831Humanname
156156813CV2368114single nucleotide variantNM_018917.4(PCDHGA4):c.538G>A (p.Gly180Arg)not specified [RCV004216463]uncertain significance5141355645141355645Humanname
329390408CV2459192single nucleotide variantNM_018917.4(PCDHGA4):c.343T>G (p.Leu115Val)not specified [RCV004272635]uncertain significance5141355450141355450Humanname
401865882CV2755675single nucleotide variantNM_018917.4(PCDHGA4):c.364G>C (p.Asp122His)not specified [RCV004342060]uncertain significance5141355471141355471Humanname
401870951CV2759353single nucleotide variantNM_018917.4(PCDHGA4):c.745G>C (p.Gly249Arg)not specified [RCV004335935]uncertain significance5141355852141355852Humanname
401892742CV2791752single nucleotide variantNM_018917.4(PCDHGA4):c.572C>A (p.Pro191Gln)not specified [RCV004353073]uncertain significance5141355679141355679Humanname
405744904CV3368217single nucleotide variantNM_018917.4(PCDHGA4):c.597G>C (p.Gln199His)not specified [RCV004498284]uncertain significance5141355704141355704Humanname
405744914CV3368218single nucleotide variantNM_018917.4(PCDHGA4):c.847C>T (p.Arg283Cys)not specified [RCV004498285]uncertain significance5141355954141355954Humanname
405744921CV3368219single nucleotide variantNM_018917.4(PCDHGA4):c.903T>A (p.Asp301Glu)not specified [RCV004498286]uncertain significance5141356010141356010Humanname
405744931CV3368220single nucleotide variantNM_018917.4(PCDHGA4):c.938G>A (p.Arg313Gln)not specified [RCV004498287]uncertain significance5141356045141356045Humanname
407484512CV3463244single nucleotide variantNM_018917.4(PCDHGA4):c.855C>G (p.Asn285Lys)not specified [RCV004659478]uncertain significance5141355962141355962Humanname
407484517CV3463251single nucleotide variantNM_018917.4(PCDHGA4):c.367A>T (p.Arg123Trp)not specified [RCV004659479]uncertain significance5141355474141355474Humanname
597756435CV3575335single nucleotide variantNM_018917.4(PCDHGA4):c.488G>A (p.Ser163Asn)not specified [RCV004848122]likely benign5141355595141355595Humanname
597738205CV3575342single nucleotide variantNM_018917.4(PCDHGA4):c.865G>A (p.Gly289Ser)not specified [RCV004844064]uncertain significance5141355972141355972Humanname
597738217CV3575344single nucleotide variantNM_018917.4(PCDHGA4):c.610A>G (p.Asn204Asp)not specified [RCV004844066]uncertain significance5141355717141355717Humanname
597738238CV3575350single nucleotide variantNM_018917.4(PCDHGA4):c.799A>G (p.Asn267Asp)not specified [RCV004844070]uncertain significance5141355906141355906Humanname
597738244CV3575352single nucleotide variantNM_018917.4(PCDHGA4):c.400G>A (p.Val134Met)not specified [RCV004844071]uncertain significance5141355507141355507Humanname
598270614CV3996284single nucleotide variantNM_018917.4(PCDHGA4):c.535C>T (p.Pro179Ser)not specified [RCV005389002]uncertain significance5141355642141355642Humanname
598270255CV3996294single nucleotide variantNM_018917.4(PCDHGA4):c.758G>A (p.Arg253His)not specified [RCV005389011]likely benign5141355865141355865Humanname
156369550CV2194014single nucleotide variantNM_018917.4(PCDHGA4):c.1203C>A (p.Asn401Lys)not specified [RCV004076780]uncertain significance5141356310141356310Humanname
155960257CV2204137single nucleotide variantNM_018917.4(PCDHGA4):c.1658A>C (p.Tyr553Ser)not specified [RCV004076944]uncertain significance5141356765141356765Humanname
156260062CV2204788single nucleotide variantNM_018917.4(PCDHGA4):c.1346A>G (p.Tyr449Cys)not specified [RCV004075046]uncertain significance5141356453141356453Humanname
155966837CV2216759single nucleotide variantNM_018917.4(PCDHGA4):c.1363G>A (p.Ala455Thr)not specified [RCV004083204]uncertain significance5141356470141356470Humanname
156315033CV2253344single nucleotide variantNM_018917.4(PCDHGA4):c.1309A>T (p.Thr437Ser)not specified [RCV004123173]uncertain significance5141356416141356416Humanname
156017533CV2262892single nucleotide variantNM_018917.4(PCDHGA4):c.1348A>G (p.Asn450Asp)not specified [RCV004125036]uncertain significance5141356455141356455Humanname
156172029CV2267814single nucleotide variantNM_018917.4(PCDHGA4):c.1865T>C (p.Val622Ala)not specified [RCV004136122]uncertain significance5141356972141356972Humanname
155915452CV2274186single nucleotide variantNM_018917.4(PCDHGA4):c.2458G>A (p.Glu820Lys)not specified [RCV004134818]uncertain significance5141357565141357565Humanname
155912155CV2308663single nucleotide variantNM_018917.4(PCDHGA4):c.1820A>G (p.Glu607Gly)not specified [RCV004167213]uncertain significance5141356927141356927Humanname
156351265CV2323731single nucleotide variantNM_018917.4(PCDHGA4):c.1499C>T (p.Ala500Val)not specified [RCV004176287]uncertain significance5141356606141356606Humanname
155979432CV2340048single nucleotide variantNM_018917.4(PCDHGA4):c.2765G>A (p.Arg922His)not specified [RCV004192294]uncertain significance5141511049141511049Humanname
156243792CV2347098single nucleotide variantNM_018917.4(PCDHGA4):c.2345A>T (p.Gln782Leu)not specified [RCV004204580]uncertain significance5141357452141357452Humanname
156338934CV2370830single nucleotide variantNM_018917.4(PCDHGA4):c.1469C>T (p.Ala490Val)not specified [RCV004209223]uncertain significance5141356576141356576Humanname
155995634CV2375841single nucleotide variantNM_018917.4(PCDHGA4):c.2188G>A (p.Ala730Thr)not specified [RCV004224419]uncertain significance5141357295141357295Humanname
329380218CV2444262single nucleotide variantNM_018917.4(PCDHGA4):c.2462C>T (p.Pro821Leu)not specified [RCV004263030]uncertain significance5141357569141357569Humanname
329388601CV2447690single nucleotide variantNM_018917.4(PCDHGA4):c.1076G>A (p.Arg359Gln)not specified [RCV004258481]uncertain significance5141356183141356183Humanname
329394426CV2469866single nucleotide variantNM_018917.4(PCDHGA4):c.1183A>G (p.Thr395Ala)not specified [RCV004285342]uncertain significance5141356290141356290Humanname
401731568CV2674418single nucleotide variantNM_018917.4(PCDHGA4):c.1028C>T (p.Ser343Phe)not specified [RCV004289284]uncertain significance5141356135141356135Humanname
401722216CV2680866single nucleotide variantNM_018917.4(PCDHGA4):c.2436C>G (p.Ser812Arg)not specified [RCV004293512]uncertain significance5141357543141357543Humanname
401752854CV2703328single nucleotide variantNM_018917.4(PCDHGA4):c.1249A>G (p.Ile417Val)not specified [RCV004315680]uncertain significance5141356356141356356Humanname
401739221CV2708378single nucleotide variantNM_018917.4(PCDHGA4):c.1142C>T (p.Thr381Ile)not specified [RCV004313494]uncertain significance5141356249141356249Humanname
401764806CV2728087single nucleotide variantNM_018917.4(PCDHGA4):c.2471T>G (p.Ile824Arg)not specified [RCV004324189]uncertain significance5141357578141357578Humanname
401885770CV2783381single nucleotide variantNM_018917.4(PCDHGA4):c.2290G>T (p.Ala764Ser)not specified [RCV004365735]uncertain significance5141357397141357397Humanname
401888218CV2788148single nucleotide variantNM_018917.4(PCDHGA4):c.2368C>G (p.Leu790Val)not specified [RCV004352767]uncertain significance5141357475141357475Humanname
405744805CV3368206single nucleotide variantNM_018917.4(PCDHGA4):c.1223G>A (p.Gly408Glu)not specified [RCV004498273]uncertain significance5141356330141356330Humanname
405744812CV3368207single nucleotide variantNM_018917.4(PCDHGA4):c.1268T>G (p.Phe423Cys)not specified [RCV004498274]uncertain significance5141356375141356375Humanname
405744821CV3368208single nucleotide variantNM_018917.4(PCDHGA4):c.1316G>C (p.Arg439Thr)not specified [RCV004498275]uncertain significance5141356423141356423Humanname
405744835CV3368209single nucleotide variantNM_018917.4(PCDHGA4):c.1724G>T (p.Ser575Ile)not specified [RCV004498276]uncertain significance5141356831141356831Humanname
405744845CV3368210single nucleotide variantNM_018917.4(PCDHGA4):c.1777A>C (p.Ile593Leu)not specified [RCV004498277]uncertain significance5141356884141356884Humanname
405744852CV3368211single nucleotide variantNM_018917.4(PCDHGA4):c.2002G>A (p.Ala668Thr)not specified [RCV004498278]uncertain significance5141357109141357109Humanname
405744857CV3368212single nucleotide variantNM_018917.4(PCDHGA4):c.2051C>T (p.Pro684Leu)not specified [RCV004498279]uncertain significance5141357158141357158Humanname
405744874CV3368214single nucleotide variantNM_018917.4(PCDHGA4):c.2114A>G (p.Asp705Gly)not specified [RCV004498281]uncertain significance5141357221141357221Humanname
405744885CV3368215single nucleotide variantNM_018917.4(PCDHGA4):c.2342T>C (p.Leu781Pro)not specified [RCV004498282]uncertain significance5141357449141357449Humanname
405744896CV3368216single nucleotide variantNM_018917.4(PCDHGA4):c.2375C>G (p.Ala792Gly)not specified [RCV004498283]uncertain significance5141357482141357482Humanname
405744939CV3368221single nucleotide variantNM_018917.4(PCDHGA4):c.1040A>G (p.Asp347Gly)not specified [RCV004498288]uncertain significance5141356147141356147Humanname
405744948CV3368222single nucleotide variantNM_018917.4(PCDHGA4):c.1049T>C (p.Val350Ala)not specified [RCV004498289]uncertain significance5141356156141356156Humanname
407483211CV3463245single nucleotide variantNM_018917.4(PCDHGA4):c.1984G>A (p.Ala662Thr)not specified [RCV004653253]uncertain significance5141357091141357091Humanname
407483219CV3463246single nucleotide variantNM_018917.4(PCDHGA4):c.1208A>G (p.His403Arg)not specified [RCV004653254]uncertain significance5141356315141356315Humanname
407483225CV3463248single nucleotide variantNM_018917.4(PCDHGA4):c.2414G>A (p.Ser805Asn)not specified [RCV004653256]likely benign5141357521141357521Humanname
407483233CV3463249single nucleotide variantNM_018917.4(PCDHGA4):c.2230G>A (p.Ala744Thr)not specified [RCV004653257]uncertain significance5141357337141357337Humanname
407483239CV3463250single nucleotide variantNM_018917.4(PCDHGA4):c.1006G>A (p.Gly336Arg)not specified [RCV004653258]uncertain significance5141356113141356113Humanname
597738150CV3575329single nucleotide variantNM_018917.4(PCDHGA4):c.1430A>G (p.Asn477Ser)not specified [RCV004844054]uncertain significance5141356537141356537Humanname
597738155CV3575330single nucleotide variantNM_018917.4(PCDHGA4):c.2426C>T (p.Thr809Met)not specified [RCV004844055]uncertain significance5141357533141357533Humanname
597738167CV3575332single nucleotide variantNM_018917.4(PCDHGA4):c.1837G>T (p.Ala613Ser)not specified [RCV004844057]uncertain significance5141356944141356944Humanname
597756430CV3575334single nucleotide variantNM_018917.4(PCDHGA4):c.1622A>G (p.Asn541Ser)not specified [RCV004848121]uncertain significance5141356729141356729Humanname
597738177CV3575336single nucleotide variantNM_018917.4(PCDHGA4):c.1694C>G (p.Ala565Gly)not specified [RCV004844059]uncertain significance5141356801141356801Humanname
597756440CV3575337single nucleotide variantNM_018917.4(PCDHGA4):c.1225G>A (p.Gly409Arg)not specified [RCV004848123]uncertain significance5141356332141356332Humanname
597738182CV3575338single nucleotide variantNM_018917.4(PCDHGA4):c.1982G>T (p.Arg661Leu)not specified [RCV004844060]uncertain significance5141357089141357089Humanname
597738189CV3575339single nucleotide variantNM_018917.4(PCDHGA4):c.1033T>C (p.Phe345Leu)not specified [RCV004844061]uncertain significance5141356140141356140Humanname
597738194CV3575340single nucleotide variantNM_018917.4(PCDHGA4):c.1192G>T (p.Ala398Ser)not specified [RCV004844062]uncertain significance5141356299141356299Humanname
597738199CV3575341single nucleotide variantNM_018917.4(PCDHGA4):c.1985C>T (p.Ala662Val)not specified [RCV004844063]uncertain significance5141357092141357092Humanname
597756445CV3575345single nucleotide variantNM_018917.4(PCDHGA4):c.1585G>C (p.Gly529Arg)not specified [RCV004848124]uncertain significance5141356692141356692Humanname
597738222CV3575346single nucleotide variantNM_018917.4(PCDHGA4):c.2477A>C (p.Gln826Pro)not specified [RCV004844067]uncertain significance5141357584141357584Humanname
597756450CV3575348single nucleotide variantNM_018917.4(PCDHGA4):c.2023G>T (p.Val675Leu)not specified [RCV004848125]uncertain significance5141357130141357130Humanname
597738233CV3575349single nucleotide variantNM_018917.4(PCDHGA4):c.1681C>A (p.Leu561Met)not specified [RCV004844069]uncertain significance5141356788141356788Humanname
598270626CV3996282single nucleotide variantNM_018917.4(PCDHGA4):c.2366C>T (p.Ser789Phe)not specified [RCV005389000]uncertain significance5141357473141357473Humanname
598270619CV3996283single nucleotide variantNM_018917.4(PCDHGA4):c.1094T>C (p.Leu365Pro)not specified [RCV005389001]uncertain significance5141356201141356201Humanname
598195649CV3996285single nucleotide variantNM_018917.4(PCDHGA4):c.2313T>G (p.Phe771Leu)not specified [RCV005397567]uncertain significance5141357420141357420Humanname
598270607CV3996286single nucleotide variantNM_018917.4(PCDHGA4):c.2300C>T (p.Pro767Leu)not specified [RCV005389003]uncertain significance5141357407141357407Humanname
598270599CV3996287single nucleotide variantNM_018917.4(PCDHGA4):c.1687A>C (p.Met563Leu)not specified [RCV005389004]uncertain significance5141356794141356794Humanname
598270593CV3996288single nucleotide variantNM_018917.4(PCDHGA4):c.1282A>G (p.Thr428Ala)not specified [RCV005389005]uncertain significance5141356389141356389Humanname
598270567CV3996292single nucleotide variantNM_018917.4(PCDHGA4):c.1951G>A (p.Gly651Arg)not specified [RCV005389009]uncertain significance5141357058141357058Humanname
598270250CV3996293single nucleotide variantNM_018917.4(PCDHGA4):c.1832G>A (p.Arg611His)not specified [RCV005389010]uncertain significance5141356939141356939Humanname