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Variants search result for Homo sapiens
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52 records found for search term Cpne2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401757622CV2675421single nucleotide variantNM_152727.6(CPNE2):c.23G>T (p.Gly8Val)not specified [RCV004292221]uncertain significance165711076557110765Humanname
155974313CV2341418single nucleotide variantNM_152727.6(CPNE2):c.71G>A (p.Cys24Tyr)not specified [RCV004188816]uncertain significance165711081357110813Humanname
155928771CV2369560single nucleotide variantNM_152727.6(CPNE2):c.41C>A (p.Ala14Glu)not specified [RCV004214979]uncertain significance165711078357110783Humanname
401752406CV2682808single nucleotide variantNM_152727.6(CPNE2):c.35C>T (p.Ala12Val)not specified [RCV004281779]uncertain significance165711077757110777Humanname
401733210CV2713012single nucleotide variantNM_152727.6(CPNE2):c.65G>A (p.Cys22Tyr)not specified [RCV004314715]uncertain significance165711080757110807Humanname
401866860CV2769647single nucleotide variantNM_152727.6(CPNE2):c.47C>T (p.Pro16Leu)not specified [RCV004351576]uncertain significance165711078957110789Humanname
156397950CV2194009single nucleotide variantNM_152727.6(CPNE2):c.280G>A (p.Ala94Thr)not specified [RCV004076775]uncertain significance165711338757113387Humanname
405697214CV3245605single nucleotide variantNM_152727.6(CPNE2):c.119T>C (p.Val40Ala)not specified [RCV004374529]uncertain significance165711086157110861Humanname
405697201CV3245607single nucleotide variantNM_152727.6(CPNE2):c.184G>A (p.Asp62Asn)not specified [RCV004374531]uncertain significance165711329157113291Humanname
407457151CV3419651single nucleotide variantNM_152727.6(CPNE2):c.246C>G (p.Asp82Glu)not specified [RCV004611045]uncertain significance165711335357113353Humanname
597651553CV3651140single nucleotide variantNM_152727.6(CPNE2):c.202A>G (p.Ile68Val)not specified [RCV004910608]likely benign165711330957113309Humanname
156278674CV2210065single nucleotide variantNM_152727.6(CPNE2):c.439G>A (p.Ala147Thr)not specified [RCV004076494]uncertain significance165711749957117499Humanname
155980948CV2212097single nucleotide variantNM_152727.6(CPNE2):c.884C>T (p.Ser295Phe)not specified [RCV004089005]uncertain significance165712343057123430Humanname
156059383CV2239330single nucleotide variantNM_152727.6(CPNE2):c.575T>A (p.Leu192Gln)not specified [RCV004114070]uncertain significance165711926257119262Humanname
156283231CV2249739single nucleotide variantNM_152727.6(CPNE2):c.730G>A (p.Glu244Lys)not specified [RCV004122509]uncertain significance165712114157121141Humanname
156355512CV2324499single nucleotide variantNM_152727.6(CPNE2):c.766C>G (p.Arg256Gly)not specified [RCV004178980]uncertain significance165712117757121177Humanname
156388340CV2380317single nucleotide variantNM_152727.6(CPNE2):c.767G>A (p.Arg256Gln)not specified [RCV004224664]uncertain significance165712117857121178Humanname
155908231CV2387254single nucleotide variantNM_152727.6(CPNE2):c.698A>G (p.Tyr233Cys)not specified [RCV004238349]uncertain significance165712110957121109Humanname
329376061CV2437952single nucleotide variantNM_152727.6(CPNE2):c.466G>A (p.Val156Ile)not specified [RCV004263671]uncertain significance165711752657117526Humanname
329372242CV2443072single nucleotide variantNM_152727.6(CPNE2):c.967G>A (p.Asp323Asn)not specified [RCV004253659]uncertain significance165712589957125899Humanname
401863799CV2770835single nucleotide variantNM_152727.6(CPNE2):c.408C>G (p.Asp136Glu)not specified [RCV004349867]uncertain significance165711552357115523Humanname
401873011CV2776401single nucleotide variantNM_152727.6(CPNE2):c.461A>G (p.Asn154Ser)not specified [RCV004355527]uncertain significance165711752157117521Humanname
401880881CV2789414single nucleotide variantNM_152727.6(CPNE2):c.347G>A (p.Cys116Tyr)not specified [RCV004360054]uncertain significance165711345457113454Humanname
405697193CV3245608single nucleotide variantNM_152727.6(CPNE2):c.434C>T (p.Thr145Met)not specified [RCV004374532]uncertain significance165711554957115549Humanname
405697187CV3245609single nucleotide variantNM_152727.6(CPNE2):c.704A>G (p.Asn235Ser)not specified [RCV004374533]uncertain significance165712111557121115Humanname
405697183CV3245610single nucleotide variantNM_152727.6(CPNE2):c.779C>T (p.Pro260Leu)not specified [RCV004374534]uncertain significance165712119057121190Humanname
405697177CV3245611single nucleotide variantNM_152727.6(CPNE2):c.878A>C (p.Asp293Ala)not specified [RCV004374535]uncertain significance165712342457123424Humanname
405697171CV3245612single nucleotide variantNM_152727.6(CPNE2):c.962C>T (p.Pro321Leu)not specified [RCV004374536]uncertain significance165712589457125894Humanname
405697163CV3245613single nucleotide variantNM_152727.6(CPNE2):c.995C>G (p.Pro332Arg)not specified [RCV004374537]uncertain significance165712592757125927Humanname
407457158CV3419654single nucleotide variantNM_152727.6(CPNE2):c.568T>G (p.Trp190Gly)not specified [RCV004611048]uncertain significance165711925557119255Humanname
597651507CV3651135single nucleotide variantNM_152727.6(CPNE2):c.577G>A (p.Val193Ile)not specified [RCV004910603]uncertain significance165711926457119264Humanname
597651536CV3651138single nucleotide variantNM_152727.6(CPNE2):c.875G>A (p.Arg292Gln)not specified [RCV004910606]uncertain significance165712342157123421Humanname
597651545CV3651139single nucleotide variantNM_152727.6(CPNE2):c.457G>A (p.Asp153Asn)not specified [RCV004910607]uncertain significance165711751757117517Humanname
597651578CV3651143single nucleotide variantNM_152727.6(CPNE2):c.475C>A (p.Leu159Ile)not specified [RCV004910611]uncertain significance165711753557117535Humanname
597651587CV3651144single nucleotide variantNM_152727.6(CPNE2):c.658G>A (p.Gly220Arg)not specified [RCV004910612]uncertain significance165711962757119627Humanname
597651596CV3651145single nucleotide variantNM_152727.6(CPNE2):c.370A>G (p.Ser124Gly)not specified [RCV004910613]uncertain significance165711548557115485Humanname
597651614CV3651147single nucleotide variantNM_152727.6(CPNE2):c.319G>A (p.Glu107Lys)not specified [RCV004910615]uncertain significance165711342657113426Humanname
598246517CV3945279single nucleotide variantNM_152727.6(CPNE2):c.581A>G (p.His194Arg)not specified [RCV005322330]uncertain significance165711926857119268Humanname
598246526CV3945280single nucleotide variantNM_152727.6(CPNE2):c.494G>A (p.Arg165Lys)not specified [RCV005322331]likely benign165711755457117554Humanname
598246540CV3945282single nucleotide variantNM_152727.6(CPNE2):c.760G>A (p.Glu254Lys)not specified [RCV005322333]uncertain significance165712117157121171Humanname
8627842CV82986single nucleotide variantNM_152727.5(CPNE2):c.905G>A (p.Gly302Glu)Malignant melanoma [RCV000063066]not provided165712345157123451Humanname
156301088CV2322662single nucleotide variantNM_152727.6(CPNE2):c.1424C>T (p.Ala475Val)not specified [RCV004182791]uncertain significance165714620657146206Humanname
156142738CV2383794single nucleotide variantNM_152727.6(CPNE2):c.1249G>A (p.Val417Ile)not specified [RCV004231666]uncertain significance165713722957137229Humanname
401869766CV2772513single nucleotide variantNM_152727.6(CPNE2):c.1561A>G (p.Lys521Glu)not specified [RCV004355285]uncertain significance165714757257147572Humanname
405697208CV3245606single nucleotide variantNM_152727.6(CPNE2):c.1385A>G (p.Lys462Arg)not specified [RCV004374530]uncertain significance165714616757146167Humanname
407457154CV3419652single nucleotide variantNM_152727.6(CPNE2):c.1432G>A (p.Ala478Thr)not specified [RCV004611046]uncertain significance165714621457146214Humanname
407457155CV3419653single nucleotide variantNM_152727.6(CPNE2):c.1277A>G (p.Gln426Arg)not specified [RCV004611047]uncertain significance165713725757137257Humanname
597651516CV3651136single nucleotide variantNM_152727.6(CPNE2):c.1642G>A (p.Ala548Thr)not specified [RCV004910604]uncertain significance165714765357147653Humanname
597651526CV3651137single nucleotide variantNM_152727.6(CPNE2):c.1412G>A (p.Gly471Asp)not specified [RCV004910605]uncertain significance165714619457146194Humanname
597651561CV3651141single nucleotide variantNM_152727.6(CPNE2):c.1126G>A (p.Glu376Lys)not specified [RCV004910609]uncertain significance165713478457134784Humanname
597651606CV3651146single nucleotide variantNM_152727.6(CPNE2):c.1384A>C (p.Lys462Gln)not specified [RCV004910614]uncertain significance165714616657146166Humanname
598246533CV3945281single nucleotide variantNM_152727.6(CPNE2):c.1526G>A (p.Arg509Gln)not specified [RCV005322332]uncertain significance165714630857146308Humanname