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Variants search result for Homo sapiens
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22 records found for search term Hhex
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
151740974CV1245532single nucleotide variantNM_002729.5(HHEX):c.17C>G (p.Pro6Arg)Autosomal dominant polycystic liver disease [RCV001844930]uncertain significance109269000392690003Human1name
156332273CV2218292single nucleotide variantNM_002729.5(HHEX):c.136A>C (p.Thr46Pro)not specified [RCV004088479]uncertain significance109269012292690122Humanname
156246352CV2228294single nucleotide variantNM_002729.5(HHEX):c.200C>T (p.Thr67Ile)not specified [RCV004098298]uncertain significance109269018692690186Humanname
156262467CV2319790single nucleotide variantNM_002729.5(HHEX):c.131C>T (p.Ala44Val)not specified [RCV004187318]uncertain significance109269011792690117Humanname
156061287CV2320125single nucleotide variantNM_002729.5(HHEX):c.106G>A (p.Asp36Asn)not specified [RCV004167969]uncertain significance109269009292690092Humanname
329371826CV2454909single nucleotide variantNM_002729.5(HHEX):c.125C>T (p.Pro42Leu)not specified [RCV004270402]uncertain significance109269011192690111Humanname
401882063CV2774684single nucleotide variantNM_002729.5(HHEX):c.218C>T (p.Thr73Met)not specified [RCV004343792]uncertain significance109269020492690204Humanname
405777478CV3270100single nucleotide variantNM_002729.5(HHEX):c.230C>T (p.Pro77Leu)not specified [RCV004397017]uncertain significance109269021692690216Humanname
407521982CV3437268single nucleotide variantNM_002729.5(HHEX):c.155C>A (p.Pro52Gln)not specified [RCV004630576]uncertain significance109269014192690141Humanname
597761679CV3685776single nucleotide variantNM_002729.5(HHEX):c.269C>T (p.Ala90Val)not specified [RCV004925960]uncertain significance109269025592690255Humanname
597761686CV3685778single nucleotide variantNM_002729.5(HHEX):c.269C>G (p.Ala90Gly)not specified [RCV004925962]uncertain significance109269025592690255Humanname
155982773CV2347786single nucleotide variantNM_002729.5(HHEX):c.441C>A (p.Asp147Glu)not specified [RCV004195444]uncertain significance109269244792692447Humanname
329368322CV2442702single nucleotide variantNM_002729.5(HHEX):c.476A>G (p.Gln159Arg)not specified [RCV004265047]uncertain significance109269248292692482Humanname
329356486CV2460357single nucleotide variantNM_002729.5(HHEX):c.638G>T (p.Ser213Ile)not specified [RCV004268675]uncertain significance109269459392694593Humanname
401743442CV2687953single nucleotide variantNM_002729.5(HHEX):c.682G>C (p.Gly228Arg)not specified [RCV004305038]uncertain significance109269463792694637Humanname
401876648CV2783017single nucleotide variantNM_002729.5(HHEX):c.787G>A (p.Asp263Asn)not specified [RCV004361805]uncertain significance109269474292694742Humanname
405777489CV3270102single nucleotide variantNM_002729.5(HHEX):c.704A>C (p.Gln235Pro)not specified [RCV004397019]uncertain significance109269465992694659Humanname
405777496CV3270103single nucleotide variantNM_002729.5(HHEX):c.718C>T (p.Pro240Ser)not specified [RCV004397020]uncertain significance109269467392694673Humanname
407521976CV3437266single nucleotide variantNM_002729.5(HHEX):c.700T>C (p.Ser234Pro)not specified [RCV004630574]uncertain significance109269465592694655Humanname
407521979CV3437267single nucleotide variantNM_002729.5(HHEX):c.730G>A (p.Glu244Lys)not specified [RCV004630575]uncertain significance109269468592694685Humanname
597761684CV3685777single nucleotide variantNM_002729.5(HHEX):c.367C>T (p.Pro123Ser)not specified [RCV004925961]uncertain significance109269237392692373Humanname
15176118CV701475single nucleotide variantNM_002729.5(HHEX):c.701C>G (p.Ser234Cys)not provided [RCV000950750]benign109269465692694656Humanname