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Variants search result for Homo sapiens
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43 records found for search term Mrps5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156202077CV2334641single nucleotide variantNM_031902.5(MRPS5):c.25G>T (p.Gly9Cys)not specified [RCV004188626]uncertain significance29512176795121767Humanname
155999598CV2373437single nucleotide variantNM_031902.5(MRPS5):c.83C>T (p.Ser28Phe)not specified [RCV004220136]uncertain significance29511792195117921Humanname
405742859CV3367938single nucleotide variantNM_031902.5(MRPS5):c.55G>A (p.Ala19Thr)not specified [RCV004498005]uncertain significance29512173795121737Humanname
407474865CV3450463single nucleotide variantNM_031902.5(MRPS5):c.47G>T (p.Ser16Ile)not specified [RCV004638268]uncertain significance29512174595121745Humanname
597634676CV3557464single nucleotide variantNM_031902.5(MRPS5):c.74G>A (p.Arg25Lys)not specified [RCV004831017]uncertain significance29511793095117930Humanname
598213522CV3993580single nucleotide variantNM_031902.5(MRPS5):c.37G>A (p.Val13Met)not specified [RCV005378363]uncertain significance29512175595121755Humanname
156330949CV2224344single nucleotide variantNM_031902.5(MRPS5):c.202C>G (p.Gln68Glu)not specified [RCV004097690]uncertain significance29511514195115141Humanname
155985238CV2247844single nucleotide variantNM_031902.5(MRPS5):c.194G>A (p.Arg65His)not specified [RCV004121305]likely benign29511514995115149Humanname
329401732CV2457346single nucleotide variantNM_031902.5(MRPS5):c.181G>T (p.Ala61Ser)not specified [RCV004267185]uncertain significance29511516295115162Humanname
401912216CV2812083single nucleotide variantNM_031902.5(MRPS5):c.1119C>A (p.Ile373=)not provided [RCV003427109]likely benign29508753195087531Humanname
597634666CV3557462single nucleotide variantNM_031902.5(MRPS5):c.211T>C (p.Cys71Arg)not specified [RCV004831015]uncertain significance29511513295115132Humanname
597634671CV3557463single nucleotide variantNM_031902.5(MRPS5):c.115G>T (p.Ala39Ser)not specified [RCV004831016]uncertain significance29511788995117889Humanname
598213526CV3993581single nucleotide variantNM_031902.5(MRPS5):c.149C>T (p.Ser50Leu)not specified [RCV005378364]uncertain significance29511519495115194Humanname
155971225CV2262315single nucleotide variantNM_031902.5(MRPS5):c.559G>T (p.Val187Phe)not specified [RCV004128511]uncertain significance29510825395108253Humanname
155910313CV2303567single nucleotide variantNM_031902.5(MRPS5):c.797A>T (p.Asp266Val)not specified [RCV004161658]uncertain significance29510169095101690Humanname
156219385CV2344891single nucleotide variantNM_031902.5(MRPS5):c.944G>A (p.Arg315His)not specified [RCV004191029]uncertain significance29509051095090510Humanname
155921169CV2350623single nucleotide variantNM_031902.5(MRPS5):c.514A>G (p.Met172Val)not specified [RCV004204963]uncertain significance29510829895108298Humanname
329397706CV2456506single nucleotide variantNM_031902.5(MRPS5):c.533A>G (p.Glu178Gly)not specified [RCV004275649]uncertain significance29510827995108279Humanname
329378172CV2457176single nucleotide variantNM_031902.5(MRPS5):c.614C>T (p.Pro205Leu)not specified [RCV004265261]uncertain significance29510819895108198Humanname
329360504CV2458794single nucleotide variantNM_031902.5(MRPS5):c.566G>A (p.Arg189Gln)not specified [RCV004270222]uncertain significance29510824695108246Humanname
401884140CV2765058single nucleotide variantNM_031902.5(MRPS5):c.791G>A (p.Arg264Gln)not specified [RCV004337175]uncertain significance29510169695101696Humanname
401875066CV2791058single nucleotide variantNM_031902.5(MRPS5):c.925C>G (p.Pro309Ala)not specified [RCV004356450]uncertain significance29510048095100480Humanname
405742711CV3367915single nucleotide variantNM_031902.5(MRPS5):c.313G>C (p.Glu105Gln)not specified [RCV004497982]uncertain significance29511000695110006Humanname
405742725CV3367917single nucleotide variantNM_031902.5(MRPS5):c.445A>G (p.Met149Val)not specified [RCV004497984]uncertain significance29510836795108367Humanname
405742755CV3367922single nucleotide variantNM_031902.5(MRPS5):c.502G>A (p.Val168Met)not specified [RCV004497989]uncertain significance29510831095108310Humanname
405742900CV3367944single nucleotide variantNM_031902.5(MRPS5):c.565C>T (p.Arg189Trp)not specified [RCV004498011]uncertain significance29510824795108247Humanname
405744608CV3367952single nucleotide variantNM_031902.5(MRPS5):c.570G>T (p.Glu190Asp)not specified [RCV004498019]uncertain significance29510824295108242Humanname
407474853CV3450460single nucleotide variantNM_031902.5(MRPS5):c.613C>T (p.Pro205Ser)not specified [RCV004638265]uncertain significance29510819995108199Humanname
407474861CV3450462single nucleotide variantNM_031902.5(MRPS5):c.989A>C (p.Lys330Thr)not specified [RCV004638267]uncertain significance29509046595090465Humanname
597634686CV3557466single nucleotide variantNM_031902.5(MRPS5):c.332A>T (p.Lys111Ile)not specified [RCV004831019]uncertain significance29510998795109987Humanname
597638151CV3557467single nucleotide variantNM_031902.5(MRPS5):c.526A>G (p.Arg176Gly)not specified [RCV004824870]uncertain significance29510828695108286Humanname
598179365CV3993579single nucleotide variantNM_031902.5(MRPS5):c.691A>G (p.Met231Val)not specified [RCV005371918]uncertain significance29510471295104712Humanname
329380382CV2444359single nucleotide variantNM_031902.5(MRPS5):c.1026G>T (p.Met342Ile)not specified [RCV004263110]uncertain significance29509042895090428Humanname
329380601CV2464241single nucleotide variantNM_031902.5(MRPS5):c.1221C>G (p.Asp407Glu)not specified [RCV004276209]uncertain significance29508742995087429Humanname
401769685CV2689889single nucleotide variantNM_031902.5(MRPS5):c.1217T>G (p.Leu406Arg)not specified [RCV004297784]uncertain significance29508743395087433Humanname
401725587CV2721843single nucleotide variantNM_031902.5(MRPS5):c.1129T>A (p.Cys377Ser)not specified [RCV004326356]uncertain significance29508752195087521Humanname
405742634CV3367905single nucleotide variantNM_031902.5(MRPS5):c.1255C>T (p.Arg419Cys)not specified [RCV004497972]uncertain significance29508739595087395Humanname
405742282CV3371875single nucleotide variantNM_031902.5(MRPS5):c.1022A>G (p.Asn341Ser)not specified [RCV004497948]uncertain significance29509043295090432Humanname
405742517CV3371882single nucleotide variantNM_031902.5(MRPS5):c.1084C>G (p.Leu362Val)not specified [RCV004497955]uncertain significance29508756695087566Humanname
405742551CV3371887single nucleotide variantNM_031902.5(MRPS5):c.1210G>A (p.Val404Ile)not specified [RCV004497960]likely benign29508744095087440Humanname
407525228CV3450459single nucleotide variantNM_031902.5(MRPS5):c.1157C>T (p.Ser386Phe)not specified [RCV004631679]uncertain significance29508749395087493Humanname
407474857CV3450461single nucleotide variantNM_031902.5(MRPS5):c.1040A>G (p.Gln347Arg)not specified [RCV004638266]likely benign29509041495090414Humanname
597634681CV3557465single nucleotide variantNM_031902.5(MRPS5):c.1003A>G (p.Lys335Glu)not specified [RCV004831018]uncertain significance29509045195090451Humanname