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Variants search result for Homo sapiens
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27 records found for search term Etnk1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156156847CV2238577single nucleotide variantNM_018638.5(ETNK1):c.-161C>Tnot specified [RCV004107189]uncertain significance122262527022625270Humanname
156202631CV2334733single nucleotide variantNM_018638.5(ETNK1):c.-180C>Tnot specified [RCV004188712]uncertain significance122262525122625251Humanname
401781128CV2681898single nucleotide variantNM_018638.5(ETNK1):c.-243A>Gnot specified [RCV004296890]uncertain significance122262518822625188Humanname
407499184CV3438398single nucleotide variantNM_018638.5(ETNK1):c.-198T>Gnot specified [RCV004622718]uncertain significance122262523322625233Humanname
598193598CV3958368single nucleotide variantNM_018638.5(ETNK1):c.-254G>Anot specified [RCV005335218]uncertain significance122262517722625177Humanname
598193603CV3958369single nucleotide variantNM_018638.5(ETNK1):c.-209C>Tnot specified [RCV005335219]uncertain significance122262522222625222Humanname
329354938CV2473333single nucleotide variantNM_018638.5(ETNK1):c.416+197C>TTeratoma [RCV003221376]uncertain significance122264421922644219Human2name
156065115CV2272473single nucleotide variantNM_018638.4(ETNK1):c.4C>G (p.Leu2Val)not specified [RCV004133390]uncertain significance122262516722625167Humanname
407499171CV3438395single nucleotide variantNM_018638.5(ETNK1):c.25C>G (p.Pro9Ala)not specified [RCV004622715]uncertain significance122262545522625455Humanname
401784053CV2720994single nucleotide variantNM_018638.5(ETNK1):c.70C>G (p.Gln24Glu)not specified [RCV004328287]uncertain significance122262550022625500Humanname
405758831CV3256043single nucleotide variantNM_018638.5(ETNK1):c.80A>T (p.His27Leu)not specified [RCV004383108]uncertain significance122262551022625510Humanname
405758838CV3256044single nucleotide variantNM_018638.5(ETNK1):c.93G>C (p.Glu31Asp)not specified [RCV004383109]uncertain significance122262552322625523Humanname
407499179CV3438397single nucleotide variantNM_018638.5(ETNK1):c.52A>T (p.Asn18Tyr)not specified [RCV004622717]uncertain significance122262548222625482Humanname
156112372CV2218047single nucleotide variantNM_018638.5(ETNK1):c.149C>A (p.Thr50Asn)not specified [RCV004086487]uncertain significance122262557922625579Humanname
407499175CV3438396single nucleotide variantNM_018638.5(ETNK1):c.244A>C (p.Asn82His)not specified [RCV004622716]uncertain significance122264385022643850Humanname
598193593CV3958367single nucleotide variantNM_018638.5(ETNK1):c.293G>A (p.Arg98Gln)not specified [RCV005335217]uncertain significance122264389922643899Humanname
329389146CV2467181single nucleotide variantNM_018638.5(ETNK1):c.322C>G (p.Gln108Glu)not specified [RCV004285001]uncertain significance122264392822643928Humanname
329382155CV2467530single nucleotide variantNM_018638.5(ETNK1):c.907G>A (p.Val303Ile)not specified [RCV004287130]uncertain significance122267362222673622Humanname
401868646CV2767297single nucleotide variantNM_018638.5(ETNK1):c.594G>T (p.Gln198His)not specified [RCV004349465]uncertain significance122266109922661099Humanname
405758824CV3256042single nucleotide variantNM_018638.5(ETNK1):c.819T>G (p.Asp273Glu)not specified [RCV004383107]uncertain significance122267353422673534Humanname
405758844CV3256045single nucleotide variantNM_018638.5(ETNK1):c.571A>G (p.Ile191Val)not specified [RCV004383110]uncertain significance122266107622661076Humanname
407499168CV3438394single nucleotide variantNM_018638.5(ETNK1):c.896C>T (p.Thr299Ile)not specified [RCV004622714]uncertain significance122267361122673611Humanname
597692011CV3665201single nucleotide variantNM_018638.5(ETNK1):c.693G>C (p.Glu231Asp)not specified [RCV004915434]uncertain significance122266119822661198Humanname
597692020CV3665202single nucleotide variantNM_018638.5(ETNK1):c.574C>G (p.Pro192Ala)not specified [RCV004915435]uncertain significance122266107922661079Humanname
598193588CV3958366single nucleotide variantNM_018638.5(ETNK1):c.845G>A (p.Arg282His)not specified [RCV005335216]uncertain significance122267356022673560Humanname
597692032CV3665203single nucleotide variantNM_018638.5(ETNK1):c.1039A>G (p.Asn347Asp)not specified [RCV004915436]uncertain significance122268490122684901Humanname
597692042CV3665204single nucleotide variantNM_018638.5(ETNK1):c.1084C>G (p.Pro362Ala)not specified [RCV004915437]uncertain significance122268494622684946Humanname