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26 records found for search term Erp29
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155997208CV2277493single nucleotide variantNM_006817.4(ERP29):c.7G>A (p.Ala3Thr)not specified [RCV004144886]uncertain significance12112013472112013472Humanname
155957465CV2304159single nucleotide variantNM_006817.4(ERP29):c.13G>A (p.Val5Met)not specified [RCV004170191]uncertain significance12112013478112013478Humanname
598181875CV3958148single nucleotide variantNM_006817.4(ERP29):c.16C>A (p.Pro6Thr)not specified [RCV005333024]uncertain significance12112013481112013481Humanname
156205640CV2249891single nucleotide variantNM_006817.4(ERP29):c.47C>G (p.Pro16Arg)not specified [RCV004122867]uncertain significance12112013512112013512Humanname
156277116CV2255877single nucleotide variantNM_006817.4(ERP29):c.58G>A (p.Gly20Ser)not specified [RCV004122033]uncertain significance12112013523112013523Humanname
155952488CV2264228single nucleotide variantNM_006817.4(ERP29):c.50T>C (p.Leu17Pro)not specified [RCV004138158]uncertain significance12112013515112013515Humanname
156263882CV2388905single nucleotide variantNM_006817.4(ERP29):c.70C>T (p.Leu24Phe)not specified [RCV004241910]uncertain significance12112013535112013535Humanname
405742579CV3259641single nucleotide variantNM_006817.4(ERP29):c.37C>T (p.Pro13Ser)not specified [RCV004380779]uncertain significance12112013502112013502Humanname
156400500CV2199224single nucleotide variantNM_006817.4(ERP29):c.239C>T (p.Ser80Leu)not provided [RCV004695354]|not specified [RCV004082586]uncertain significance12112019850112019850Humanname
156395685CV2325865single nucleotide variantNM_006817.4(ERP29):c.263T>C (p.Val88Ala)not specified [RCV004174050]uncertain significance12112019874112019874Humanname
401761443CV2702340single nucleotide variantNM_006817.4(ERP29):c.100C>T (p.His34Tyr)not specified [RCV004316870]uncertain significance12112013565112013565Humanname
405742553CV3259637single nucleotide variantNM_006817.4(ERP29):c.167T>C (p.Val56Ala)not specified [RCV004380775]uncertain significance12112019778112019778Humanname
405742561CV3259638single nucleotide variantNM_006817.4(ERP29):c.247A>G (p.Ser83Gly)not specified [RCV004380776]uncertain significance12112019858112019858Humanname
597689525CV3664939single nucleotide variantNM_006817.4(ERP29):c.250G>A (p.Asp84Asn)not specified [RCV004915197]uncertain significance12112019861112019861Humanname
598181879CV3958149single nucleotide variantNM_006817.4(ERP29):c.181G>A (p.Asp61Asn)not specified [RCV005333025]uncertain significance12112019792112019792Humanname
156068200CV2317972single nucleotide variantNM_006817.4(ERP29):c.401G>A (p.Gly134Glu)not specified [RCV004177092]uncertain significance12112022267112022267Humanname
155907710CV2354479single nucleotide variantNM_006817.4(ERP29):c.769G>A (p.Glu257Lys)not specified [RCV004202466]uncertain significance12112022635112022635Humanname
156180181CV2356072single nucleotide variantNM_006817.4(ERP29):c.640G>A (p.Glu214Lys)not specified [RCV004203488]uncertain significance12112022506112022506Humanname
156308691CV2369969single nucleotide variantNM_006817.4(ERP29):c.652G>A (p.Ala218Thr)not specified [RCV004208432]uncertain significance12112022518112022518Humanname
156226939CV2401284single nucleotide variantNM_006817.4(ERP29):c.358C>T (p.Leu120Phe)not specified [RCV004245830]uncertain significance12112022224112022224Humanname
329355597CV2445468single nucleotide variantNM_006817.4(ERP29):c.752T>A (p.Phe251Tyr)not specified [RCV004257528]uncertain significance12112022618112022618Humanname
405742567CV3259639single nucleotide variantNM_006817.4(ERP29):c.310C>A (p.Leu104Met)not specified [RCV004380777]uncertain significance12112022176112022176Humanname
405742586CV3259642single nucleotide variantNM_006817.4(ERP29):c.690G>T (p.Lys230Asn)not specified [RCV004380780]uncertain significance12112022556112022556Humanname
407480632CV3442176single nucleotide variantNM_006817.4(ERP29):c.629T>C (p.Leu210Ser)not specified [RCV004618052]uncertain significance12112022495112022495Humanname
407480637CV3442177single nucleotide variantNM_006817.4(ERP29):c.446G>C (p.Gly149Ala)not specified [RCV004618053]uncertain significance12112022312112022312Humanname
598181887CV3958151single nucleotide variantNM_006817.4(ERP29):c.550G>C (p.Gly184Arg)not specified [RCV005333027]uncertain significance12112022416112022416Humanname