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44 records found for search term Psmd5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8651096CV127671single nucleotide variantNR_024408.1(PSMD5-AS1):n.868C>ALung cancer [RCV000108158]uncertain significance9120851443120851443Humanname
156087356CV2258981single nucleotide variantNM_005047.4(PSMD5):c.5C>T (p.Ala2Val)not specified [RCV004120254]uncertain significance9120842905120842905Humanname
156136878CV2210328single nucleotide variantNM_005047.4(PSMD5):c.20C>G (p.Ala7Gly)not specified [RCV004089485]uncertain significance9120842890120842890Humanname
155911394CV2303808single nucleotide variantNM_005047.4(PSMD5):c.19G>C (p.Ala7Pro)not specified [RCV004163647]uncertain significance9120842891120842891Humanname
329359077CV2450830single nucleotide variantNM_005047.4(PSMD5):c.20C>A (p.Ala7Glu)not specified [RCV004267745]uncertain significance9120842890120842890Humanname
156075083CV2198067single nucleotide variantNM_005047.4(PSMD5):c.92C>G (p.Ala31Gly)not provided [RCV004695345]|not specified [RCV004599438]uncertain significance9120842818120842818Humanname
405662224CV3378589single nucleotide variantNM_005047.4(PSMD5):c.121G>A (p.Ala41Thr)not specified [RCV004513363]uncertain significance9120842789120842789Humanname
405662227CV3378590single nucleotide variantNM_005047.4(PSMD5):c.244C>T (p.Arg82Trp)not specified [RCV004513364]uncertain significance9120833386120833386Humanname
405662230CV3378591single nucleotide variantNM_005047.4(PSMD5):c.255G>C (p.Arg85Ser)not specified [RCV004513365]uncertain significance9120833375120833375Humanname
407531734CV3471913single nucleotide variantNM_005047.4(PSMD5):c.245G>T (p.Arg82Leu)not specified [RCV004657757]uncertain significance9120833385120833385Humanname
597750147CV3592093single nucleotide variantNM_005047.4(PSMD5):c.245G>A (p.Arg82Gln)not specified [RCV004846376]uncertain significance9120833385120833385Humanname
597750158CV3592095single nucleotide variantNM_005047.4(PSMD5):c.286G>C (p.Asp96His)not specified [RCV004846378]uncertain significance9120833344120833344Humanname
155928598CV2224406single nucleotide variantNM_005047.4(PSMD5):c.569T>G (p.Ile190Arg)not specified [RCV004098015]uncertain significance9120829201120829201Humanname
156335160CV2228353single nucleotide variantNM_005047.4(PSMD5):c.770T>C (p.Ile257Thr)not specified [RCV004098338]uncertain significance9120826809120826809Humanname
156141150CV2260445single nucleotide variantNM_005047.4(PSMD5):c.583G>A (p.Val195Met)not specified [RCV004123240]uncertain significance9120829187120829187Humanname
156061620CV2320213single nucleotide variantNM_005047.4(PSMD5):c.553G>T (p.Val185Leu)not specified [RCV004169833]uncertain significance9120831339120831339Humanname
156332906CV2339857single nucleotide variantNM_005047.4(PSMD5):c.875G>A (p.Arg292His)not specified [RCV004196540]uncertain significance9120824625120824625Humanname
401734461CV2688514single nucleotide variantNM_005047.4(PSMD5):c.413A>C (p.Asn138Thr)not specified [RCV004301484]uncertain significance9120831851120831851Humanname
405662232CV3378592single nucleotide variantNM_005047.4(PSMD5):c.778G>T (p.Ala260Ser)not specified [RCV004513366]uncertain significance9120826801120826801Humanname
407491042CV3471910single nucleotide variantNM_005047.4(PSMD5):c.758T>G (p.Ile253Ser)not specified [RCV004666772]uncertain significance9120826821120826821Humanname
407491045CV3471911single nucleotide variantNM_005047.4(PSMD5):c.667G>A (p.Val223Ile)not specified [RCV004666773]uncertain significance9120829103120829103Humanname
407531732CV3471912single nucleotide variantNM_005047.4(PSMD5):c.433G>C (p.Ala145Pro)not specified [RCV004657756]uncertain significance9120831459120831459Humanname
597750142CV3592092single nucleotide variantNM_005047.4(PSMD5):c.650C>A (p.Thr217Asn)not specified [RCV004846375]uncertain significance9120829120120829120Humanname
597750153CV3592094single nucleotide variantNM_005047.4(PSMD5):c.795C>A (p.Phe265Leu)not specified [RCV004846377]uncertain significance9120826784120826784Humanname
597750175CV3592099single nucleotide variantNM_005047.4(PSMD5):c.998A>G (p.Gln333Arg)not specified [RCV004846382]uncertain significance9120824502120824502Humanname
598170917CV3908187single nucleotide variantNM_005047.4(PSMD5):c.401T>C (p.Ile134Thr)not specified [RCV005263225]uncertain significance9120831863120831863Humanname
598170921CV3908188single nucleotide variantNM_005047.4(PSMD5):c.806A>G (p.Tyr269Cys)not specified [RCV005263226]uncertain significance9120826773120826773Humanname
598170934CV3908191single nucleotide variantNM_005047.4(PSMD5):c.841G>T (p.Ala281Ser)not specified [RCV005263229]uncertain significance9120824659120824659Humanname
598170943CV3908193single nucleotide variantNM_005047.4(PSMD5):c.842C>T (p.Ala281Val)not specified [RCV005263231]uncertain significance9120824658120824658Humanname
156094013CV2252909single nucleotide variantNM_005047.4(PSMD5):c.1032G>A (p.Met344Ile)not specified [RCV004120735]uncertain significance9120821439120821439Humanname
155990910CV2255591single nucleotide variantNM_005047.4(PSMD5):c.1232A>T (p.His411Leu)not specified [RCV004120008]uncertain significance9120820864120820864Humanname
156000109CV2287344single nucleotide variantNM_005047.4(PSMD5):c.1439G>A (p.Arg480Lys)not specified [RCV004146964]uncertain significance9120817982120817982Humanname
155916332CV2366640single nucleotide variantNM_005047.4(PSMD5):c.1060C>T (p.Pro354Ser)not specified [RCV004210652]likely benign9120821411120821411Humanname
156097219CV2399178single nucleotide variantNM_005047.4(PSMD5):c.1100C>T (p.Ser367Phe)not specified [RCV004246609]uncertain significance9120821371120821371Humanname
329374393CV2443880single nucleotide variantNM_005047.4(PSMD5):c.1021C>T (p.Arg341Cys)not specified [RCV004258216]uncertain significance9120821450120821450Humanname
401770023CV2718999single nucleotide variantNM_005047.4(PSMD5):c.1375C>A (p.Leu459Ile)not specified [RCV004322587]uncertain significance9120818046120818046Humanname
405662221CV3378588single nucleotide variantNM_005047.4(PSMD5):c.1102C>A (p.Leu368Ile)not specified [RCV004513362]uncertain significance9120821369120821369Humanname
407491039CV3471909single nucleotide variantNM_005047.4(PSMD5):c.1367A>G (p.Lys456Arg)not specified [RCV004666771]uncertain significance9120818054120818054Humanname
407531736CV3471914single nucleotide variantNM_005047.4(PSMD5):c.1322T>C (p.Val441Ala)not specified [RCV004657758]uncertain significance9120818099120818099Humanname
597750170CV3592098single nucleotide variantNM_005047.4(PSMD5):c.1208G>A (p.Ser403Asn)not specified [RCV004846381]uncertain significance9120820888120820888Humanname
598170913CV3908185single nucleotide variantNM_005047.4(PSMD5):c.1054A>C (p.Asn352His)not specified [RCV005263224]uncertain significance9120821417120821417Humanname
598203146CV3908186single nucleotide variantNM_005047.4(PSMD5):c.1471T>G (p.Tyr491Asp)not specified [RCV005269327]uncertain significance9120817950120817950Humanname
598170926CV3908189single nucleotide variantNM_005047.4(PSMD5):c.1349A>G (p.Lys450Arg)not specified [RCV005263227]uncertain significance9120818072120818072Humanname
598170930CV3908190single nucleotide variantNM_005047.4(PSMD5):c.1367A>T (p.Lys456Ile)not specified [RCV005263228]uncertain significance9120818054120818054Humanname