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Variants search result for Homo sapiens
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58 records found for search term Dedd
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401748062CV2717480single nucleotide variantNM_032998.3(DEDD):c.19C>T (p.Arg7Trp)not specified [RCV004330259]uncertain significance1161124444161124444Humanname
405668498CV3240111single nucleotide variantNM_032998.3(DEDD):c.83G>A (p.Arg28His)not specified [RCV004368163]uncertain significance1161124380161124380Humanname
598223446CV3956488single nucleotide variantNM_032998.3(DEDD):c.74G>C (p.Ser25Thr)not specified [RCV005318079]uncertain significance1161124389161124389Humanname
156291046CV2296590single nucleotide variantNM_032998.3(DEDD):c.205T>G (p.Leu69Val)not specified [RCV004154654]uncertain significance1161124258161124258Humanname
401744683CV2694618single nucleotide variantNM_032998.3(DEDD):c.117C>G (p.His39Gln)not specified [RCV004298733]uncertain significance1161124346161124346Humanname
405668480CV3240107single nucleotide variantNM_032998.3(DEDD):c.247C>G (p.Arg83Gly)not specified [RCV004368159]uncertain significance1161124216161124216Humanname
407482473CV3426727single nucleotide variantNM_032998.3(DEDD):c.172C>T (p.Arg58Cys)not specified [RCV004613748]uncertain significance1161124291161124291Humanname
407482487CV3426729single nucleotide variantNM_032998.3(DEDD):c.115C>T (p.His39Tyr)not specified [RCV004613750]uncertain significance1161124348161124348Humanname
329349991CV2451108single nucleotide variantNM_032998.3(DEDD):c.682C>T (p.Arg228Cys)not specified [RCV004270047]uncertain significance1161122422161122422Humanname
405668483CV3240108single nucleotide variantNM_032998.3(DEDD):c.301G>A (p.Val101Ile)not specified [RCV004368160]uncertain significance1161124162161124162Humanname
405668489CV3240109single nucleotide variantNM_032998.3(DEDD):c.373T>C (p.Tyr125His)not specified [RCV004368161]uncertain significance1161123899161123899Humanname
405668493CV3240110single nucleotide variantNM_032998.3(DEDD):c.520G>C (p.Gly174Arg)not specified [RCV004368162]uncertain significance1161123135161123135Humanname
405668503CV3240112single nucleotide variantNM_032998.3(DEDD):c.938T>C (p.Met313Thr)not specified [RCV004368164]uncertain significance1161122166161122166Humanname
407482479CV3426728single nucleotide variantNM_032998.3(DEDD):c.371G>A (p.Arg124His)not specified [RCV004613749]uncertain significance1161123901161123901Humanname
597693095CV3658488single nucleotide variantNM_032998.3(DEDD):c.535C>T (p.Arg179Cys)not specified [RCV004908937]uncertain significance1161123120161123120Humanname
597693105CV3658489single nucleotide variantNM_032998.3(DEDD):c.599G>A (p.Arg200Gln)not specified [RCV004908938]uncertain significance1161122505161122505Humanname
598223455CV3956489single nucleotide variantNM_032998.3(DEDD):c.797G>A (p.Gly266Asp)not specified [RCV005318080]uncertain significance1161122307161122307Humanname
598223461CV3956490single nucleotide variantNM_032998.3(DEDD):c.337C>G (p.Leu113Val)not specified [RCV005318081]uncertain significance1161123935161123935Humanname
598223468CV3956491single nucleotide variantNM_032998.3(DEDD):c.394A>C (p.Ser132Arg)not specified [RCV005318082]uncertain significance1161123878161123878Humanname
598223475CV3956492single nucleotide variantNM_032998.3(DEDD):c.527A>C (p.Gln176Pro)not specified [RCV005318083]uncertain significance1161123128161123128Humanname
598223482CV3956493single nucleotide variantNM_032998.3(DEDD):c.829A>G (p.Ile277Val)not specified [RCV005318084]uncertain significance1161122275161122275Humanname
156280010CV2338356single nucleotide variantNM_133328.4(DEDD2):c.83G>A (p.Arg28His)not specified [RCV004186407]uncertain significance194221692542216925Humanname
401741501CV2680421single nucleotide variantNM_133328.4(DEDD2):c.53T>A (p.Leu18Gln)not specified [RCV004288661]uncertain significance194221695542216955Humanname
407465603CV3426730single nucleotide variantNM_133328.4(DEDD2):c.89T>A (p.Phe30Tyr)not specified [RCV004613751]uncertain significance194221691942216919Humanname
597887850CV3804376single nucleotide variantNM_133328.4(DEDD2):c.831C>T (p.Gly277=)not provided [RCV005150827]likely benign194219958842199588Humanname
616939442CV4013933single nucleotide variantNM_133328.4(DEDD2):c.621C>T (p.Cys207=)not provided [RCV005413425]benign194219979842199798Humanname
156326879CV2219711single nucleotide variantNM_133328.4(DEDD2):c.191G>A (p.Ser64Asn)not specified [RCV004095418]uncertain significance194221681742216817Humanname
405668508CV3240113single nucleotide variantNM_133328.4(DEDD2):c.125T>A (p.Leu42Gln)not specified [RCV004368165]uncertain significance194221688342216883Humanname
407465624CV3426735single nucleotide variantNM_133328.4(DEDD2):c.196C>G (p.Leu66Val)not specified [RCV004613756]uncertain significance194221681242216812Humanname
597640214CV3658492single nucleotide variantNM_133328.4(DEDD2):c.292C>A (p.Leu98Met)not specified [RCV004908941]uncertain significance194221671642216716Humanname
597640234CV3658495single nucleotide variantNM_133328.4(DEDD2):c.271C>G (p.Arg91Gly)not specified [RCV004908944]uncertain significance194221673742216737Humanname
598223526CV3956499single nucleotide variantNM_133328.4(DEDD2):c.193G>A (p.Gly65Ser)not specified [RCV005318090]uncertain significance194221681542216815Humanname
156227559CV2222839single nucleotide variantNM_133328.4(DEDD2):c.926G>A (p.Arg309His)not specified [RCV004101666]uncertain significance194219949342199493Humanname
156242833CV2262177single nucleotide variantNM_133328.4(DEDD2):c.511C>T (p.Arg171Trp)not specified [RCV004126611]uncertain significance194220977842209778Humanname
155922949CV2280183single nucleotide variantNM_133328.4(DEDD2):c.947A>T (p.Glu316Val)not specified [RCV004140407]uncertain significance194219947242199472Humanname
155994544CV2286424single nucleotide variantNM_133328.4(DEDD2):c.961C>T (p.Arg321Cys)not specified [RCV004139944]uncertain significance194219945842199458Humanname
156277565CV2300218single nucleotide variantNM_133328.4(DEDD2):c.340C>T (p.Arg114Cys)not specified [RCV004151403]uncertain significance194221524142215241Humanname
156038715CV2390229single nucleotide variantNM_133328.4(DEDD2):c.481C>T (p.Arg161Trp)not specified [RCV004240607]uncertain significance194220980842209808Humanname
156094376CV2398822single nucleotide variantNM_133328.4(DEDD2):c.958C>T (p.Arg320Trp)not specified [RCV004245146]uncertain significance194219946142199461Humanname
329368435CV2428018single nucleotide variantNM_133328.4(DEDD2):c.391C>T (p.Arg131Cys)not specified [RCV004254397]uncertain significance194221519042215190Humanname
329380977CV2440451single nucleotide variantNM_133328.4(DEDD2):c.601C>T (p.Arg201Trp)not specified [RCV004256383]uncertain significance194219981842199818Humanname
401856882CV2755149single nucleotide variantNM_133328.4(DEDD2):c.350A>G (p.Tyr117Cys)not specified [RCV004335298]uncertain significance194221523142215231Humanname
401885538CV2768234single nucleotide variantNM_133328.4(DEDD2):c.409A>C (p.Ser137Arg)not specified [RCV004350230]uncertain significance194221517242215172Humanname
405668513CV3240114single nucleotide variantNM_133328.4(DEDD2):c.562C>A (p.Pro188Thr)not specified [RCV004368166]uncertain significance194220972742209727Humanname
405668518CV3240115single nucleotide variantNM_133328.4(DEDD2):c.680G>A (p.Arg227Gln)not specified [RCV004368167]uncertain significance194219973942199739Humanname
405668523CV3240116single nucleotide variantNM_133328.4(DEDD2):c.965C>T (p.Pro322Leu)not specified [RCV004368168]uncertain significance194219945442199454Humanname
407465607CV3426731single nucleotide variantNM_133328.4(DEDD2):c.662G>A (p.Arg221Gln)not specified [RCV004613752]uncertain significance194219975742199757Humanname
407465611CV3426732single nucleotide variantNM_133328.4(DEDD2):c.394C>T (p.Arg132Cys)not specified [RCV004613753]uncertain significance194221518742215187Humanname
407465615CV3426733single nucleotide variantNM_133328.4(DEDD2):c.370A>G (p.Lys124Glu)not specified [RCV004613754]uncertain significance194221521142215211Humanname
597640202CV3658490single nucleotide variantNM_133328.4(DEDD2):c.514C>T (p.Arg172Trp)not specified [RCV004908939]uncertain significance194220977542209775Humanname
597640208CV3658491single nucleotide variantNM_133328.4(DEDD2):c.308C>A (p.Ala103Glu)not specified [RCV004908940]uncertain significance194221670042216700Humanname
597640221CV3658493single nucleotide variantNM_133328.4(DEDD2):c.868C>T (p.Arg290Trp)not specified [RCV004908942]uncertain significance194219955142199551Humanname
597640227CV3658494single nucleotide variantNM_133328.4(DEDD2):c.460A>G (p.Thr154Ala)not specified [RCV004908943]uncertain significance194220982942209829Humanname
598223497CV3956495single nucleotide variantNM_133328.4(DEDD2):c.458C>G (p.Pro153Arg)not specified [RCV005318086]uncertain significance194220983142209831Humanname
598223504CV3956496single nucleotide variantNM_133328.4(DEDD2):c.362G>T (p.Ser121Ile)not specified [RCV005318087]uncertain significance194221521942215219Humanname
598223512CV3956497single nucleotide variantNM_133328.4(DEDD2):c.691G>T (p.Val231Leu)not specified [RCV005318088]uncertain significance194219972842199728Humanname
598223519CV3956498single nucleotide variantNM_133328.4(DEDD2):c.602G>A (p.Arg201Gln)not specified [RCV005318089]uncertain significance194219981742199817Humanname
598223533CV3956500single nucleotide variantNM_133328.4(DEDD2):c.952G>A (p.Gly318Arg)not specified [RCV005318091]uncertain significance194219946742199467Humanname