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38 records found for search term Pnmt
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407524104CV3463827single nucleotide variantNM_002686.4(PNMT):c.10G>A (p.Ala4Thr)not specified [RCV004653561]uncertain significance173966848539668485Humanname
15110694CV727129single nucleotide variantNM_002686.4(PNMT):c.123G>A (p.Ala41=)not provided [RCV000894120]benign173966859839668598Humanname
405652454CV3376591single nucleotide variantNM_002686.4(PNMT):c.70G>T (p.Ala24Ser)not specified [RCV004509801]uncertain significance173966854539668545Humanname
407471912CV3463828single nucleotide variantNM_002686.4(PNMT):c.62C>A (p.Ala21Glu)not specified [RCV004662395]uncertain significance173966853739668537Humanname
598187583CV4003505single nucleotide variantNM_002686.4(PNMT):c.53C>T (p.Pro18Leu)not specified [RCV005395939]uncertain significance173966852839668528Humanname
155975529CV2231372single nucleotide variantNM_002686.4(PNMT):c.122C>T (p.Ala41Val)not specified [RCV004096460]uncertain significance173966859739668597Humanname
156282754CV2252431single nucleotide variantNM_002686.4(PNMT):c.109C>T (p.Arg37Cys)not specified [RCV004116269]uncertain significance173966858439668584Humanname
156279588CV2325302single nucleotide variantNM_002686.4(PNMT):c.134G>C (p.Gly45Ala)not specified [RCV004177693]uncertain significance173966860939668609Humanname
156290462CV2342620single nucleotide variantNM_002686.4(PNMT):c.142T>C (p.Cys48Arg)not specified [RCV004196708]uncertain significance173966861739668617Humanname
156137373CV2357420single nucleotide variantNM_002686.4(PNMT):c.217C>T (p.Arg73Cys)not specified [RCV004200298]uncertain significance173966964339669643Humanname
156265332CV2389051single nucleotide variantNM_002686.4(PNMT):c.250G>A (p.Val84Met)not specified [RCV004235389]uncertain significance173966967639669676Humanname
155958456CV2395183single nucleotide variantNM_002686.4(PNMT):c.251T>C (p.Val84Ala)not specified [RCV004236852]uncertain significance173966967739669677Humanname
401780365CV2726021single nucleotide variantNM_002686.4(PNMT):c.211T>G (p.Ser71Ala)not specified [RCV004324382]uncertain significance173966963739669637Humanname
405652442CV3376585single nucleotide variantNM_002686.4(PNMT):c.176G>A (p.Arg59His)not specified [RCV004509795]uncertain significance173966865139668651Humanname
405652444CV3376586single nucleotide variantNM_002686.4(PNMT):c.221C>T (p.Thr74Ile)not specified [RCV004509796]uncertain significance173966964739669647Humanname
597743756CV3590625single nucleotide variantNM_002686.4(PNMT):c.110G>T (p.Arg37Leu)not specified [RCV004845125]uncertain significance173966858539668585Humanname
597743779CV3590629single nucleotide variantNM_002686.4(PNMT):c.224T>C (p.Leu75Pro)not specified [RCV004845129]uncertain significance173966965039669650Humanname
598187602CV4003508single nucleotide variantNM_002686.4(PNMT):c.154G>A (p.Gly52Ser)not specified [RCV005395942]uncertain significance173966862939668629Humanname
155973670CV2224713single nucleotide variantNM_002686.4(PNMT):c.478C>T (p.His160Tyr)not specified [RCV004092547]uncertain significance173967001839670018Humanname
156134863CV2347148single nucleotide variantNM_002686.4(PNMT):c.734G>A (p.Arg245His)not specified [RCV004204624]likely benign173967027439670274Humanname
329373651CV2447309single nucleotide variantNM_002686.4(PNMT):c.838G>C (p.Val280Leu)not specified [RCV004262595]uncertain significance173967037839670378Humanname
401745939CV2678736single nucleotide variantNM_002686.4(PNMT):c.369G>C (p.Trp123Cys)not specified [RCV004292732]uncertain significance173966979539669795Humanname
401872991CV2793178single nucleotide variantNM_002686.4(PNMT):c.619C>T (p.Pro207Ser)not specified [RCV004360485]uncertain significance173967015939670159Humanname
405652446CV3376587single nucleotide variantNM_002686.4(PNMT):c.298A>G (p.Thr100Ala)not specified [RCV004509797]uncertain significance173966972439669724Humanname
405652448CV3376588single nucleotide variantNM_002686.4(PNMT):c.355G>C (p.Gly119Arg)not specified [RCV004509798]uncertain significance173966978139669781Humanname
405652450CV3376589single nucleotide variantNM_002686.4(PNMT):c.386A>G (p.His129Arg)not specified [RCV004509799]uncertain significance173966981239669812Humanname
405652452CV3376590single nucleotide variantNM_002686.4(PNMT):c.673G>T (p.Gly225Trp)not specified [RCV004509800]uncertain significance173967021339670213Humanname
407471908CV3463826single nucleotide variantNM_002686.4(PNMT):c.676G>A (p.Glu226Lys)not specified [RCV004662394]uncertain significance173967021639670216Humanname
597743762CV3590626single nucleotide variantNM_002686.4(PNMT):c.472G>A (p.Asp158Asn)not specified [RCV004845126]uncertain significance173967001239670012Humanname
597743773CV3590628single nucleotide variantNM_002686.4(PNMT):c.776C>T (p.Pro259Leu)not specified [RCV004845128]uncertain significance173967031639670316Humanname
598187565CV4003502single nucleotide variantNM_002686.4(PNMT):c.719G>C (p.Arg240Thr)not specified [RCV005395936]uncertain significance173967025939670259Humanname
598187579CV4003504single nucleotide variantNM_002686.4(PNMT):c.814G>A (p.Val272Ile)not specified [RCV005395938]likely benign173967035439670354Humanname
598187591CV4003506single nucleotide variantNM_002686.4(PNMT):c.320G>A (p.Arg107His)not specified [RCV005395940]uncertain significance173966974639669746Humanname
598187597CV4003507single nucleotide variantNM_002686.4(PNMT):c.641T>C (p.Ile214Thr)not specified [RCV005395941]uncertain significance173967018139670181Humanname
598187609CV4003509single nucleotide variantNM_002686.4(PNMT):c.416G>A (p.Cys139Tyr)not specified [RCV005395943]uncertain significance173966995639669956Humanname
598187617CV4003510single nucleotide variantNM_002686.4(PNMT):c.554A>T (p.Glu185Val)not specified [RCV005395944]uncertain significance173967009439670094Humanname
617152613CV4020834single nucleotide variantNM_002686.4(PNMT):c.334C>T (p.Arg112Cys)not provided [RCV005428587]likely benign173966976039669760Humanname
15170169CV704109single nucleotide variantNM_002686.4(PNMT):c.523G>A (p.Ala175Thr)not provided [RCV000949599]benign173967006339670063Humanname