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Variants search result for Homo sapiens
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92 records found for search term Cdh24
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156142769CV2200037single nucleotide variantNM_144985.4(CDH24):c.1363+390G>Anot specified [RCV004074194]uncertain significance142305208323052083Humanname
405720607CV3296536single nucleotide variantNM_144985.4(CDH24):c.1363+461C>Tnot specified [RCV004428085]likely benign142305201223052012Humanname
597795444CV3641889single nucleotide variantNM_144985.4(CDH24):c.1363+476G>Tnot specified [RCV004903676]uncertain significance142305199723051997Humanname
598168968CV3947402single nucleotide variantNM_144985.4(CDH24):c.1363+486C>Tnot specified [RCV005308339]uncertain significance142305198723051987Humanname
156112058CV2217983single nucleotide variantNM_144985.4(CDH24):c.94C>T (p.Arg32Trp)not specified [RCV004086432]uncertain significance142305564023055640Humanname
156203725CV2300756single nucleotide variantNM_144985.4(CDH24):c.59G>A (p.Arg20His)not specified [RCV004155688]uncertain significance142305567523055675Humanname
401862693CV2762349single nucleotide variantNM_144985.4(CDH24):c.98A>G (p.Glu33Gly)not specified [RCV004335461]likely benign142305563623055636Humanname
405720706CV3296549single nucleotide variantNM_144985.4(CDH24):c.95G>A (p.Arg32Gln)not specified [RCV004428098]uncertain significance142305563923055639Humanname
407454980CV3422300single nucleotide variantNM_144985.4(CDH24):c.77G>A (p.Arg26Gln)not specified [RCV004610091]uncertain significance142305565723055657Humanname
597789133CV3641884single nucleotide variantNM_144985.4(CDH24):c.92C>T (p.Ser31Phe)not specified [RCV004901687]uncertain significance142305564223055642Humanname
155985903CV2368187single nucleotide variantNM_144985.4(CDH24):c.233G>A (p.Arg78His)not specified [RCV004216528]uncertain significance142305532223055322Humanname
155966669CV2396101single nucleotide variantNM_144985.4(CDH24):c.253G>A (p.Gly85Arg)not specified [RCV004237633]uncertain significance142305530223055302Humanname
401887557CV2772012single nucleotide variantNM_144985.4(CDH24):c.128G>A (p.Arg43Gln)not specified [RCV004344690]uncertain significance142305560623055606Humanname
405720650CV3296542single nucleotide variantNM_144985.4(CDH24):c.221G>A (p.Arg74Gln)not specified [RCV004428091]uncertain significance142305533423055334Humanname
407454968CV3422294single nucleotide variantNM_144985.4(CDH24):c.271G>A (p.Val91Ile)not specified [RCV004610085]uncertain significance142305528423055284Humanname
156271142CV2195217single nucleotide variantNM_144985.4(CDH24):c.796T>G (p.Phe266Val)not specified [RCV004080155]uncertain significance142305431723054317Humanname
156281799CV2348805single nucleotide variantNM_144985.4(CDH24):c.902G>A (p.Gly301Glu)not specified [RCV004203251]uncertain significance142305421123054211Humanname
156267136CV2371742single nucleotide variantNM_144985.4(CDH24):c.925A>T (p.Ile309Phe)not specified [RCV004219410]uncertain significance142305418823054188Humanname
155956572CV2387315single nucleotide variantNM_144985.4(CDH24):c.994C>T (p.Arg332Cys)not specified [RCV004238403]uncertain significance142305372823053728Humanname
329353886CV2439915single nucleotide variantNM_144985.4(CDH24):c.356C>T (p.Ala119Val)not specified [RCV004257950]uncertain significance142305519923055199Humanname
329357346CV2457504single nucleotide variantNM_144985.4(CDH24):c.494T>G (p.Val165Gly)not specified [RCV004267315]uncertain significance142305506123055061Humanname
401726955CV2691913single nucleotide variantNM_144985.4(CDH24):c.845G>A (p.Arg282Gln)not specified [RCV004299650]uncertain significance142305426823054268Humanname
401860495CV2758502single nucleotide variantNM_144985.4(CDH24):c.800C>G (p.Ser267Cys)not specified [RCV004335554]uncertain significance142305431323054313Humanname
401898100CV2780974single nucleotide variantNM_144985.4(CDH24):c.650G>A (p.Arg217Gln)not specified [RCV004354506]uncertain significance142305464023054640Humanname
401866711CV2782922single nucleotide variantNM_144985.4(CDH24):c.734T>A (p.Val245Glu)not specified [RCV004361721]uncertain significance142305455623054556Humanname
405720685CV3296546single nucleotide variantNM_144985.4(CDH24):c.658C>A (p.Gln220Lys)not specified [RCV004428095]uncertain significance142305463223054632Humanname
405720691CV3296547single nucleotide variantNM_144985.4(CDH24):c.743C>T (p.Thr248Met)not specified [RCV004428096]uncertain significance142305454723054547Humanname
405720698CV3296548single nucleotide variantNM_144985.4(CDH24):c.890G>A (p.Ser297Asn)not specified [RCV004428097]uncertain significance142305422323054223Humanname
407454970CV3422295single nucleotide variantNM_144985.4(CDH24):c.947G>A (p.Arg316Gln)not specified [RCV004610086]uncertain significance142305416623054166Humanname
597789122CV3641881single nucleotide variantNM_144985.4(CDH24):c.386C>T (p.Pro129Leu)not specified [RCV004901684]uncertain significance142305516923055169Humanname
597795438CV3641887single nucleotide variantNM_144985.4(CDH24):c.307G>C (p.Val103Leu)not specified [RCV004903674]uncertain significance142305524823055248Humanname
597795441CV3641888single nucleotide variantNM_144985.4(CDH24):c.920T>G (p.Phe307Cys)not specified [RCV004903675]uncertain significance142305419323054193Humanname
598229650CV3947394single nucleotide variantNM_144985.4(CDH24):c.364G>A (p.Val122Met)not specified [RCV005319263]uncertain significance142305519123055191Humanname
598168938CV3947396single nucleotide variantNM_144985.4(CDH24):c.943G>A (p.Gly315Ser)not specified [RCV005308334]uncertain significance142305417023054170Humanname
598168945CV3947397single nucleotide variantNM_144985.4(CDH24):c.317G>A (p.Ser106Asn)not specified [RCV005308335]uncertain significance142305523823055238Humanname
598168974CV3947403single nucleotide variantNM_144985.4(CDH24):c.760G>A (p.Asp254Asn)not specified [RCV005308340]uncertain significance142305453023054530Humanname
598168988CV3947406single nucleotide variantNM_144985.4(CDH24):c.509T>A (p.Ile170Asn)not specified [RCV005308342]uncertain significance142305485423054854Humanname
8635174CV90396single nucleotide variantNM_022478.3(CDH24):c.473C>T (p.Thr158Ile)Malignant melanoma [RCV000070494]not provided142305508223055082Humanname
155919747CV2202771single nucleotide variantNM_144985.4(CDH24):c.2059C>T (p.Arg687Trp)not specified [RCV004083010]uncertain significance142304826723048267Humanname
156107651CV2214246single nucleotide variantNM_144985.4(CDH24):c.1274A>T (p.Gln425Leu)not specified [RCV004086239]uncertain significance142305256223052562Humanname
156133633CV2216854single nucleotide variantNM_144985.4(CDH24):c.2098G>A (p.Ala700Thr)not specified [RCV004083280]uncertain significance142304822823048228Humanname
156223599CV2229561single nucleotide variantNM_144985.4(CDH24):c.1847C>G (p.Ala616Gly)not specified [RCV004103383]uncertain significance142304847923048479Humanname
156368465CV2267010single nucleotide variantNM_144985.4(CDH24):c.2077C>G (p.Gln693Glu)not specified [RCV004131650]uncertain significance142304824923048249Humanname
155991538CV2276602single nucleotide variantNM_144985.4(CDH24):c.1643G>A (p.Arg548His)not specified [RCV004146089]uncertain significance142304923023049230Humanname
155903610CV2282261single nucleotide variantNM_144985.4(CDH24):c.1022C>T (p.Thr341Ile)not specified [RCV004133101]uncertain significance142305370023053700Humanname
156191987CV2289385single nucleotide variantNM_144985.4(CDH24):c.1874G>A (p.Arg625Gln)not specified [RCV004152348]uncertain significance142304845223048452Humanname
156267827CV2305126single nucleotide variantNM_144985.4(CDH24):c.1411G>A (p.Asp471Asn)not specified [RCV004169000]uncertain significance142304989623049896Humanname
156159090CV2314585single nucleotide variantNM_144985.4(CDH24):c.1177G>A (p.Val393Ile)not specified [RCV004168668]uncertain significance142305354523053545Humanname
155977264CV2324981single nucleotide variantNM_144985.4(CDH24):c.1667T>C (p.Ile556Thr)not specified [RCV004175229]uncertain significance142304920623049206Humanname
156064227CV2340739single nucleotide variantNM_144985.4(CDH24):c.2015C>T (p.Ala672Val)not specified [RCV004188104]uncertain significance142304831123048311Humanname
156147428CV2358010single nucleotide variantNM_144985.4(CDH24):c.2261G>A (p.Gly754Asp)not specified [RCV004209785]uncertain significance142304806523048065Humanname
156383865CV2361712single nucleotide variantNM_144985.4(CDH24):c.1085G>A (p.Arg362His)not specified [RCV004223192]uncertain significance142305363723053637Humanname
156154537CV2374941single nucleotide variantNM_144985.4(CDH24):c.1279G>A (p.Glu427Lys)not specified [RCV004227962]uncertain significance142305255723052557Humanname
155905930CV2393832single nucleotide variantNM_144985.4(CDH24):c.1501C>T (p.Arg501Trp)not specified [RCV004233660]uncertain significance142304972323049723Humanname
329398813CV2471728single nucleotide variantNM_144985.4(CDH24):c.1691C>T (p.Pro564Leu)not specified [RCV004287005]uncertain significance142304918223049182Humanname
401720867CV2673518single nucleotide variantNM_144985.4(CDH24):c.1694C>T (p.Ala565Val)not specified [RCV004288485]uncertain significance142304917923049179Humanname
401780426CV2726069single nucleotide variantNM_144985.4(CDH24):c.2152G>A (p.Gly718Ser)not specified [RCV004324424]likely benign142304817423048174Humanname
401867244CV2759138single nucleotide variantNM_144985.4(CDH24):c.1877G>T (p.Arg626Leu)not specified [RCV004342436]uncertain significance142304844923048449Humanname
401892431CV2781939single nucleotide variantNM_144985.4(CDH24):c.1277C>T (p.Pro426Leu)not specified [RCV004357176]uncertain significance142305255923052559Humanname
405720579CV3296532single nucleotide variantNM_144985.4(CDH24):c.1046A>G (p.Tyr349Cys)not specified [RCV004428081]uncertain significance142305367623053676Humanname
405720585CV3296533single nucleotide variantNM_144985.4(CDH24):c.1073T>A (p.Val358Glu)not specified [RCV004428082]uncertain significance142305364923053649Humanname
405720596CV3296534single nucleotide variantNM_144985.4(CDH24):c.1084C>T (p.Arg362Cys)not specified [RCV004428083]uncertain significance142305363823053638Humanname
405720602CV3296535single nucleotide variantNM_144985.4(CDH24):c.1324C>T (p.Arg442Cys)not specified [RCV004428084]uncertain significance142305251223052512Humanname
405720614CV3296537single nucleotide variantNM_144985.4(CDH24):c.1411G>C (p.Asp471His)not specified [RCV004428086]uncertain significance142304989623049896Humanname
405720620CV3296538single nucleotide variantNM_144985.4(CDH24):c.1628G>A (p.Arg543His)not specified [RCV004428087]uncertain significance142304924523049245Humanname
405720628CV3296539single nucleotide variantNM_144985.4(CDH24):c.1789G>A (p.Ala597Thr)not specified [RCV004428088]likely benign142304908423049084Humanname
405720635CV3296540single nucleotide variantNM_144985.4(CDH24):c.1807G>A (p.Ala603Thr)not specified [RCV004428089]uncertain significance142304906623049066Humanname
405720642CV3296541single nucleotide variantNM_144985.4(CDH24):c.2056C>T (p.Pro686Ser)not specified [RCV004428090]uncertain significance142304827023048270Humanname
405720659CV3296543single nucleotide variantNM_144985.4(CDH24):c.2272C>T (p.Pro758Ser)not specified [RCV004428092]uncertain significance142304805423048054Humanname
405720667CV3296544single nucleotide variantNM_144985.4(CDH24):c.2332C>T (p.Pro778Ser)not specified [RCV004428093]uncertain significance142304799423047994Humanname
405720679CV3296545single nucleotide variantNM_144985.4(CDH24):c.2341C>A (p.Pro781Thr)not specified [RCV004428094]uncertain significance142304798523047985Humanname
407454972CV3422296single nucleotide variantNM_144985.4(CDH24):c.1682G>T (p.Trp561Leu)not specified [RCV004610087]uncertain significance142304919123049191Humanname
407454974CV3422297single nucleotide variantNM_144985.4(CDH24):c.1747G>A (p.Gly583Ser)not specified [RCV004610088]uncertain significance142304912623049126Humanname
407454975CV3422298single nucleotide variantNM_144985.4(CDH24):c.1193C>T (p.Ala398Val)not specified [RCV004610089]uncertain significance142305352923053529Humanname
407454977CV3422299single nucleotide variantNM_144985.4(CDH24):c.1900G>A (p.Val634Ile)not specified [RCV004610090]uncertain significance142304842623048426Humanname
407454982CV3422301single nucleotide variantNM_144985.4(CDH24):c.2233T>G (p.Ser745Ala)not specified [RCV004610092]uncertain significance142304809323048093Humanname
407454984CV3422302single nucleotide variantNM_144985.4(CDH24):c.1382C>T (p.Ser461Leu)not specified [RCV004610093]uncertain significance142304992523049925Humanname
407454986CV3422303single nucleotide variantNM_144985.4(CDH24):c.1975G>A (p.Ala659Thr)not specified [RCV004610094]uncertain significance142304835123048351Humanname
597789100CV3641875single nucleotide variantNM_144985.4(CDH24):c.1592A>G (p.Asn531Ser)not specified [RCV004901678]uncertain significance142304963223049632Humanname
597789106CV3641877single nucleotide variantNM_144985.4(CDH24):c.1738C>G (p.Gln580Glu)not specified [RCV004901680]uncertain significance142304913523049135Humanname
597789110CV3641878single nucleotide variantNM_144985.4(CDH24):c.2194G>C (p.Gly732Arg)not specified [RCV004901681]uncertain significance142304813223048132Humanname
597789114CV3641879single nucleotide variantNM_144985.4(CDH24):c.1259G>A (p.Arg420His)not specified [RCV004901682]uncertain significance142305257723052577Humanname
597789118CV3641880single nucleotide variantNM_144985.4(CDH24):c.2291C>T (p.Pro764Leu)not specified [RCV004901683]uncertain significance142304803523048035Humanname
597789124CV3641882single nucleotide variantNM_144985.4(CDH24):c.1897A>T (p.Met633Leu)not specified [RCV004901685]uncertain significance142304842923048429Humanname
597789615CV3641883single nucleotide variantNM_144985.4(CDH24):c.1513A>G (p.Arg505Gly)not specified [RCV004901686]uncertain significance142304971123049711Humanname
597789137CV3641885single nucleotide variantNM_144985.4(CDH24):c.2017C>T (p.Pro673Ser)not specified [RCV004901688]uncertain significance142304830923048309Humanname
598168933CV3947395single nucleotide variantNM_144985.4(CDH24):c.1384C>T (p.Arg462Cys)not specified [RCV005308333]uncertain significance142304992323049923Humanname
598168951CV3947398single nucleotide variantNM_144985.4(CDH24):c.2211C>G (p.Cys737Trp)not specified [RCV005308336]uncertain significance142304811523048115Humanname
598168957CV3947400single nucleotide variantNM_144985.4(CDH24):c.2248G>C (p.Gly750Arg)not specified [RCV005308337]uncertain significance142304807823048078Humanname
598168961CV3947401single nucleotide variantNM_144985.4(CDH24):c.2112G>C (p.Gln704His)not specified [RCV005308338]uncertain significance142304821423048214Humanname
598168980CV3947404single nucleotide variantNM_144985.4(CDH24):c.1945G>C (p.Asp649His)not specified [RCV005308341]uncertain significance142304838123048381Humanname
598229662CV3947405single nucleotide variantNM_144985.4(CDH24):c.1093G>A (p.Val365Met)not specified [RCV005319265]uncertain significance142305362923053629Humanname