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Variants search result for Homo sapiens
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27 records found for search term Lcn8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156343797CV2349262single nucleotide variantNM_178469.4(LCN8):c.17G>A (p.Arg6Gln)not specified [RCV004199209]uncertain significance9136757914136757914Humanname
407460498CV3452536single nucleotide variantNM_178469.4(LCN8):c.17G>T (p.Arg6Leu)not specified [RCV004633907]likely benign9136757914136757914Humanname
597632267CV3698801single nucleotide variantNM_178469.4(LCN8):c.16C>G (p.Arg6Gly)not specified [RCV004939968]uncertain significance9136757915136757915Humanname
405817531CV3283859single nucleotide variantNM_178469.4(LCN8):c.86C>T (p.Pro29Leu)not specified [RCV004412517]uncertain significance9136757107136757107Humanname
407460494CV3452534single nucleotide variantNM_178469.4(LCN8):c.50G>A (p.Gly17Asp)not specified [RCV004633906]uncertain significance9136757143136757143Humanname
407491409CV3452537single nucleotide variantNM_178469.4(LCN8):c.35T>C (p.Phe12Ser)not specified [RCV004642210]uncertain significance9136757158136757158Humanname
598229737CV3987881single nucleotide variantNM_178469.4(LCN8):c.58T>G (p.Ser20Ala)not specified [RCV005362592]uncertain significance9136757135136757135Humanname
155926681CV2208265single nucleotide variantNM_178469.4(LCN8):c.161G>A (p.Gly54Glu)not specified [RCV004088711]uncertain significance9136756587136756587Humanname
156380075CV2211761single nucleotide variantNM_178469.4(LCN8):c.121G>A (p.Gly41Arg)not specified [RCV004086602]uncertain significance9136757072136757072Humanname
156368025CV2266923single nucleotide variantNM_178469.4(LCN8):c.237G>C (p.Glu79Asp)not specified [RCV004131584]uncertain significance9136755506136755506Humanname
156036959CV2283109single nucleotide variantNM_178469.4(LCN8):c.148T>A (p.Tyr50Asn)not specified [RCV004143713]uncertain significance9136757045136757045Humanname
155983222CV2347953single nucleotide variantNM_178469.4(LCN8):c.136G>A (p.Val46Met)not specified [RCV004197643]uncertain significance9136757057136757057Humanname
156097455CV2392700single nucleotide variantNM_178469.4(LCN8):c.283G>A (p.Val95Met)not specified [RCV004247075]uncertain significance9136755460136755460Humanname
329382956CV2424608single nucleotide variantNM_178469.4(LCN8):c.281G>A (p.Arg94Gln)not specified [RCV004254104]uncertain significance9136755462136755462Humanname
401777849CV2704394single nucleotide variantNM_178469.4(LCN8):c.171G>T (p.Glu57Asp)not specified [RCV004311362]uncertain significance9136756577136756577Humanname
405817527CV3283855single nucleotide variantNM_178469.4(LCN8):c.104T>C (p.Leu35Ser)not specified [RCV004412513]uncertain significance9136757089136757089Humanname
405817529CV3283857single nucleotide variantNM_178469.4(LCN8):c.165C>G (p.Ser55Arg)not specified [RCV004412515]uncertain significance9136756583136756583Humanname
405817530CV3283858single nucleotide variantNM_178469.4(LCN8):c.262G>C (p.Glu88Gln)not specified [RCV004412516]uncertain significance9136755481136755481Humanname
156128975CV2238500single nucleotide variantNM_178469.4(LCN8):c.356G>A (p.Arg119Gln)not specified [RCV004107124]likely benign9136755309136755309Humanname
329370395CV2435568single nucleotide variantNM_178469.4(LCN8):c.377G>A (p.Arg126Gln)not specified [RCV004254823]uncertain significance9136755288136755288Humanname
401718818CV2679318single nucleotide variantNM_178469.4(LCN8):c.299G>A (p.Arg100Gln)not specified [RCV004285858]likely benign9136755444136755444Humanname
401719525CV2679563single nucleotide variantNM_178469.4(LCN8):c.355C>T (p.Arg119Trp)not specified [RCV004287864]uncertain significance9136755310136755310Humanname
407491404CV3452535single nucleotide variantNM_178469.4(LCN8):c.398G>A (p.Gly133Asp)not specified [RCV004642209]uncertain significance9136755267136755267Humanname
597632271CV3698802single nucleotide variantNM_178469.4(LCN8):c.346G>A (p.Asp116Asn)not specified [RCV004939969]uncertain significance9136755319136755319Humanname
597632276CV3698803single nucleotide variantNM_178469.4(LCN8):c.376C>T (p.Arg126Trp)not specified [RCV004939970]uncertain significance9136755289136755289Humanname
598175228CV3987882single nucleotide variantNM_178469.4(LCN8):c.362G>C (p.Gly121Ala)not specified [RCV005371236]uncertain significance9136755303136755303Humanname
598175238CV3987883single nucleotide variantNM_178469.4(LCN8):c.313C>T (p.Arg105Cys)not specified [RCV005371237]uncertain significance9136755430136755430Humanname