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Variants search result for Homo sapiens
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10 records found for search term Efna5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401757269CV2675205single nucleotide variantNM_001962.3(EFNA5):c.76A>G (p.Lys26Glu)not specified [RCV004289976]uncertain significance5107670538107670538Humanname
597736520CV3664336single nucleotide variantNM_001962.3(EFNA5):c.40C>T (p.Leu14Phe)not specified [RCV004920651]uncertain significance5107670574107670574Humanname
597645968CV3664335single nucleotide variantNM_001962.3(EFNA5):c.208C>A (p.Pro70Thr)not specified [RCV004909896]uncertain significance5107427427107427427Humanname
156379389CV2207954single nucleotide variantNM_001962.3(EFNA5):c.488G>A (p.Ser163Asn)not specified [RCV004084369]uncertain significance5107387312107387312Humanname
329395324CV2458271single nucleotide variantNM_001962.3(EFNA5):c.574G>A (p.Val192Ile)not specified [RCV004265922]uncertain significance5107381368107381368Humanname
401881241CV2789486single nucleotide variantNM_001962.3(EFNA5):c.316C>T (p.His106Tyr)not specified [RCV004360104]uncertain significance5107427319107427319Humanname
405715999CV3241668single nucleotide variantNM_001962.3(EFNA5):c.433G>C (p.Asp145His)not specified [RCV004377405]uncertain significance5107387757107387757Humanname
405716005CV3241669single nucleotide variantNM_001962.3(EFNA5):c.512A>G (p.His171Arg)not specified [RCV004377406]uncertain significance5107387288107387288Humanname
597645961CV3664334single nucleotide variantNM_001962.3(EFNA5):c.599G>A (p.Arg200His)not specified [RCV004909895]uncertain significance5107381343107381343Humanname
597645973CV3664337single nucleotide variantNM_001962.3(EFNA5):c.572C>A (p.Thr191Asn)not specified [RCV004909897]uncertain significance5107381370107381370Humanname