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Variants search result for Homo sapiens
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86 records found for search term Ppp1r15a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15166037CV779945single nucleotide variantNM_014330.5(PPP1R15A):c.1666-7C>Tnot provided [RCV000971083]benign194887560748875607Humanname
401868133CV2767154single nucleotide variantNM_014330.5(PPP1R15A):c.7C>T (p.Pro3Ser)not specified [RCV004347551]uncertain significance194887324048873240Humanname
597759015CV3587674single nucleotide variantNM_014330.5(PPP1R15A):c.10G>T (p.Gly4Cys)not specified [RCV004848655]uncertain significance194887324348873243Humanname
156095902CV2253078single nucleotide variantNM_014330.5(PPP1R15A):c.82C>T (p.Leu28Phe)not specified [RCV004120864]likely benign194887331548873315Humanname
407483173CV3471593single nucleotide variantNM_014330.5(PPP1R15A):c.51C>A (p.His17Gln)not specified [RCV004664903]uncertain significance194887328448873284Humanname
15103905CV705148single nucleotide variantNM_014330.5(PPP1R15A):c.552G>A (p.Arg184=)not provided [RCV000959575]benign194887378548873785Humanname
156107590CV2304007single nucleotide variantNM_014330.5(PPP1R15A):c.218C>T (p.Thr73Ile)not specified [RCV004170062]uncertain significance194887345148873451Humanname
329398923CV2471792single nucleotide variantNM_014330.5(PPP1R15A):c.121C>T (p.Pro41Ser)not specified [RCV004280833]uncertain significance194887335448873354Humanname
401732300CV2708766single nucleotide variantNM_014330.5(PPP1R15A):c.194G>T (p.Arg65Met)not specified [RCV004307730]uncertain significance194887342748873427Humanname
401880391CV2763024single nucleotide variantNM_014330.5(PPP1R15A):c.191C>T (p.Ala64Val)not specified [RCV004336085]uncertain significance194887342448873424Humanname
401896030CV2776356single nucleotide variantNM_014330.5(PPP1R15A):c.166G>A (p.Val56Ile)not specified [RCV004355490]uncertain significance194887339948873399Humanname
401929064CV2818548single nucleotide variantNM_014330.5(PPP1R15A):c.1605C>T (p.Leu535=)not provided [RCV003407064]benign194887483848874838Humanname
405795355CV3366639single nucleotide variantNM_014330.5(PPP1R15A):c.211C>T (p.Pro71Ser)not specified [RCV004507341]uncertain significance194887344448873444Humanname
597758978CV3587666single nucleotide variantNM_014330.5(PPP1R15A):c.206C>T (p.Ala69Val)not specified [RCV004848647]uncertain significance194887343948873439Humanname
597759006CV3587672single nucleotide variantNM_014330.5(PPP1R15A):c.232C>T (p.Arg78Cys)not specified [RCV004848653]likely benign194887346548873465Humanname
598222341CV3893867single nucleotide variantNM_014330.5(PPP1R15A):c.1002A>C (p.Pro334=)not provided [RCV005257110]likely benign194887423548874235Humanname
156249414CV2222115single nucleotide variantNM_014330.5(PPP1R15A):c.509A>T (p.Glu170Val)not specified [RCV004104876]uncertain significance194887374248873742Humanname
156240697CV2265585single nucleotide variantNM_014330.5(PPP1R15A):c.650C>T (p.Pro217Leu)not specified [RCV004124321]uncertain significance194887388348873883Humanname
156278757CV2297510single nucleotide variantNM_014330.5(PPP1R15A):c.896T>C (p.Leu299Pro)not specified [RCV004153436]uncertain significance194887412948874129Humanname
156195303CV2306630single nucleotide variantNM_014330.5(PPP1R15A):c.787C>T (p.Arg263Cys)not specified [RCV004157228]likely benign194887402048874020Humanname
155964147CV2330413single nucleotide variantNM_014330.5(PPP1R15A):c.415C>T (p.Arg139Cys)not specified [RCV004180987]uncertain significance194887364848873648Humanname
155973409CV2334434single nucleotide variantNM_014330.5(PPP1R15A):c.982T>C (p.Cys328Arg)not specified [RCV004188408]uncertain significance194887421548874215Humanname
156170261CV2400555single nucleotide variantNM_014330.5(PPP1R15A):c.665C>G (p.Ser222Cys)not specified [RCV004246745]likely benign194887389848873898Humanname
329365907CV2441223single nucleotide variantNM_014330.5(PPP1R15A):c.502G>T (p.Val168Phe)not specified [RCV004263613]uncertain significance194887373548873735Humanname
401728243CV2676027single nucleotide variantNM_014330.5(PPP1R15A):c.881C>T (p.Ala294Val)not specified [RCV004282013]uncertain significance194887411448874114Humanname
401742918CV2697899single nucleotide variantNM_014330.5(PPP1R15A):c.742G>A (p.Val248Met)not specified [RCV004300609]uncertain significance194887397548873975Humanname
401736126CV2703050single nucleotide variantNM_014330.5(PPP1R15A):c.430C>G (p.Pro144Ala)not specified [RCV004321354]uncertain significance194887366348873663Humanname
401780899CV2716968single nucleotide variantNM_014330.5(PPP1R15A):c.385G>A (p.Gly129Arg)not specified [RCV004330042]uncertain significance194887361848873618Humanname
401888626CV2757916single nucleotide variantNM_014330.5(PPP1R15A):c.952G>A (p.Gly318Arg)not specified [RCV004337052]uncertain significance194887418548874185Humanname
401866110CV2762528single nucleotide variantNM_014330.5(PPP1R15A):c.568G>A (p.Val190Met)not specified [RCV004338062]uncertain significance194887380148873801Humanname
405795361CV3366641single nucleotide variantNM_014330.5(PPP1R15A):c.407A>G (p.Asp136Gly)not specified [RCV004507343]uncertain significance194887364048873640Humanname
405795364CV3376775single nucleotide variantNM_014330.5(PPP1R15A):c.553G>C (p.Glu185Gln)not specified [RCV004507344]uncertain significance194887378648873786Humanname
405795367CV3376776single nucleotide variantNM_014330.5(PPP1R15A):c.766G>A (p.Asp256Asn)not specified [RCV004507345]likely benign194887399948873999Humanname
405795372CV3376777single nucleotide variantNM_014330.5(PPP1R15A):c.788G>A (p.Arg263His)not specified [RCV004507346]uncertain significance194887402148874021Humanname
407483179CV3471594single nucleotide variantNM_014330.5(PPP1R15A):c.620C>T (p.Ser207Phe)not specified [RCV004664904]uncertain significance194887385348873853Humanname
407529796CV3471595single nucleotide variantNM_014330.5(PPP1R15A):c.828C>G (p.His276Gln)not specified [RCV004656222]uncertain significance194887406148874061Humanname
597758952CV3587661single nucleotide variantNM_014330.5(PPP1R15A):c.791C>T (p.Ser264Leu)not specified [RCV004848642]uncertain significance194887402448874024Humanname
597758963CV3587663single nucleotide variantNM_014330.5(PPP1R15A):c.487G>A (p.Ala163Thr)not specified [RCV004848644]uncertain significance194887372048873720Humanname
597759020CV3587675single nucleotide variantNM_014330.5(PPP1R15A):c.863C>T (p.Pro288Leu)not specified [RCV004848656]uncertain significance194887409648874096Humanname
597759025CV3587676single nucleotide variantNM_014330.5(PPP1R15A):c.817G>A (p.Glu273Lys)not specified [RCV004848657]uncertain significance194887405048874050Humanname
597759030CV3587677single nucleotide variantNM_014330.5(PPP1R15A):c.611A>C (p.His204Pro)not specified [RCV004848658]likely benign194887384448873844Humanname
597759033CV3587678single nucleotide variantNM_014330.5(PPP1R15A):c.737C>A (p.Thr246Asn)not specified [RCV004848659]uncertain significance194887397048873970Humanname
156257343CV2204572single nucleotide variantNM_014330.5(PPP1R15A):c.1610G>A (p.Arg537His)not specified [RCV004081683]likely benign194887484348874843Humanname
156380082CV2211763single nucleotide variantNM_014330.5(PPP1R15A):c.1609C>T (p.Arg537Cys)not specified [RCV004086604]uncertain significance194887484248874842Humanname
155969917CV2213405single nucleotide variantNM_014330.5(PPP1R15A):c.1622C>T (p.Pro541Leu)not specified [RCV004087385]uncertain significance194887485548874855Humanname
156057660CV2262825single nucleotide variantNM_014330.5(PPP1R15A):c.1258G>C (p.Ala420Pro)not specified [RCV004131242]uncertain significance194887449148874491Humanname
156051896CV2269390single nucleotide variantNM_014330.5(PPP1R15A):c.1793A>G (p.Gln598Arg)not specified [RCV004124521]likely benign194887574148875741Humanname
156108300CV2304206single nucleotide variantNM_014330.5(PPP1R15A):c.1014C>G (p.Phe338Leu)not specified [RCV004170228]uncertain significance194887424748874247Humanname
155969508CV2309080single nucleotide variantNM_014330.5(PPP1R15A):c.1922C>G (p.Ser641Trp)not specified [RCV004171442]uncertain significance194887587048875870Humanname
155991234CV2384177single nucleotide variantNM_014330.5(PPP1R15A):c.1705G>A (p.Val569Ile)not specified [RCV004227575]uncertain significance194887565348875653Humanname
156189273CV2395643single nucleotide variantNM_014330.5(PPP1R15A):c.1760G>C (p.Arg587Pro)not specified [RCV004241484]uncertain significance194887570848875708Humanname
329385370CV2451317single nucleotide variantNM_014330.5(PPP1R15A):c.1763A>T (p.Asp588Val)not specified [RCV004272011]uncertain significance194887571148875711Humanname
329376901CV2460647single nucleotide variantNM_014330.5(PPP1R15A):c.1807C>A (p.Leu603Met)not specified [RCV004270698]uncertain significance194887575548875755Humanname
401745566CV2693282single nucleotide variantNM_014330.5(PPP1R15A):c.1256C>A (p.Ser419Tyr)not specified [RCV004295250]uncertain significance194887448948874489Humanname
401737302CV2699721single nucleotide variantNM_014330.5(PPP1R15A):c.1163C>T (p.Ser388Phe)not specified [RCV004308063]uncertain significance194887439648874396Humanname
401898709CV2782615single nucleotide variantNM_014330.5(PPP1R15A):c.1772G>A (p.Arg591His)not specified [RCV004359640]uncertain significance194887572048875720Humanname
405795327CV3366630single nucleotide variantNM_014330.5(PPP1R15A):c.1006A>G (p.Ser336Gly)not specified [RCV004507332]uncertain significance194887423948874239Humanname
405795330CV3366631single nucleotide variantNM_014330.5(PPP1R15A):c.1291G>T (p.Ala431Ser)not specified [RCV004507333]likely benign194887452448874524Humanname
405795333CV3366632single nucleotide variantNM_014330.5(PPP1R15A):c.1303C>T (p.Arg435Trp)not specified [RCV004507334]uncertain significance194887453648874536Humanname
405795336CV3366633single nucleotide variantNM_014330.5(PPP1R15A):c.1326G>C (p.Glu442Asp)not specified [RCV004507335]uncertain significance194887455948874559Humanname
405795340CV3366634single nucleotide variantNM_014330.5(PPP1R15A):c.1759C>T (p.Arg587Trp)not specified [RCV004507336]uncertain significance194887570748875707Humanname
405795343CV3366635single nucleotide variantNM_014330.5(PPP1R15A):c.1783C>T (p.Arg595Cys)not specified [RCV004507337]uncertain significance194887573148875731Humanname
405795349CV3366637single nucleotide variantNM_014330.5(PPP1R15A):c.1795G>A (p.Ala599Thr)not specified [RCV004507339]uncertain significance194887574348875743Humanname
405795352CV3366638single nucleotide variantNM_014330.5(PPP1R15A):c.1874C>A (p.Ala625Asp)not specified [RCV004507340]uncertain significance194887582248875822Humanname
407483143CV3471585single nucleotide variantNM_014330.5(PPP1R15A):c.1291G>C (p.Ala431Pro)not specified [RCV004664898]uncertain significance194887452448874524Humanname
407483148CV3471586single nucleotide variantNM_014330.5(PPP1R15A):c.1706T>G (p.Val569Gly)not specified [RCV004664899]uncertain significance194887565448875654Humanname
407529790CV3471587single nucleotide variantNM_014330.5(PPP1R15A):c.1303C>G (p.Arg435Gly)not specified [RCV004656219]uncertain significance194887453648874536Humanname
407483154CV3471588single nucleotide variantNM_014330.5(PPP1R15A):c.1600C>T (p.Arg534Trp)not specified [RCV004664900]uncertain significance194887483348874833Humanname
407529792CV3471589single nucleotide variantNM_014330.5(PPP1R15A):c.1771C>G (p.Arg591Gly)not specified [RCV004656220]uncertain significance194887571948875719Humanname
407529794CV3471590single nucleotide variantNM_014330.5(PPP1R15A):c.1624A>G (p.Thr542Ala)not specified [RCV004656221]uncertain significance194887485748874857Humanname
407483165CV3471592single nucleotide variantNM_014330.5(PPP1R15A):c.1579C>G (p.Leu527Val)not specified [RCV004664902]uncertain significance194887481248874812Humanname
407529798CV3471596single nucleotide variantNM_014330.5(PPP1R15A):c.1700T>C (p.Leu567Pro)not specified [RCV004656223]uncertain significance194887564848875648Humanname
597758941CV3587659single nucleotide variantNM_014330.5(PPP1R15A):c.1922C>T (p.Ser641Leu)not specified [RCV004848640]likely benign194887587048875870Humanname
597758958CV3587662single nucleotide variantNM_014330.5(PPP1R15A):c.1733G>A (p.Arg578His)not specified [RCV004848643]uncertain significance194887568148875681Humanname
597758967CV3587664single nucleotide variantNM_014330.5(PPP1R15A):c.1919C>G (p.Pro640Arg)not specified [RCV004848645]uncertain significance194887586748875867Humanname
597758972CV3587665single nucleotide variantNM_014330.5(PPP1R15A):c.1627C>G (p.His543Asp)not specified [RCV004848646]uncertain significance194887486048874860Humanname
597758984CV3587667single nucleotide variantNM_014330.5(PPP1R15A):c.1235A>T (p.Asp412Val)not specified [RCV004848648]uncertain significance194887446848874468Humanname
597758988CV3587668single nucleotide variantNM_014330.5(PPP1R15A):c.1715G>A (p.Gly572Glu)not specified [RCV004848649]uncertain significance194887566348875663Humanname
597758992CV3587669single nucleotide variantNM_014330.5(PPP1R15A):c.1801G>A (p.Glu601Lys)not specified [RCV004848650]uncertain significance194887574948875749Humanname
597758997CV3587670single nucleotide variantNM_014330.5(PPP1R15A):c.1777G>C (p.Ala593Pro)not specified [RCV004848651]uncertain significance194887572548875725Humanname
597759011CV3587673single nucleotide variantNM_014330.5(PPP1R15A):c.1676C>T (p.Ser559Phe)not specified [RCV004848654]uncertain significance194887562448875624Humanname
598169460CV3897591single nucleotide variantNM_014330.5(PPP1R15A):c.1822A>T (p.Thr608Ser)not specified [RCV005262801]uncertain significance194887577048875770Humanname
598169464CV3897592single nucleotide variantNM_014330.5(PPP1R15A):c.1192G>A (p.Glu398Lys)not specified [RCV005262802]uncertain significance194887442548874425Humanname
598169468CV3897593single nucleotide variantNM_014330.5(PPP1R15A):c.1172A>G (p.Tyr391Cys)not specified [RCV005262803]uncertain significance194887440548874405Humanname
598169472CV3897594single nucleotide variantNM_014330.5(PPP1R15A):c.1360G>A (p.Glu454Lys)not specified [RCV005262804]uncertain significance194887459348874593Humanname
598169477CV3897595single nucleotide variantNM_014330.5(PPP1R15A):c.1991C>G (p.Ala664Gly)not specified [RCV005262805]uncertain significance194887593948875939Humanname