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Variants search result for Homo sapiens
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35 records found for search term Ifna4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15169135CV751647single nucleotide variantNM_021068.4(IFNA4):c.141C>T (p.Ile47=)not provided [RCV000927436]likely benign92118739121187391Humanname
8626698CV81842single nucleotide variantNM_021068.2(IFNA4):c.177C>T (p.Phe59=)Malignant melanoma [RCV000061920]not provided92118735521187355Humanname
150534787CV1311616single nucleotide variantNM_021068.4(IFNA4):c.60T>A (p.Cys20Ter)Multisystem inflammatory syndrome in children [RCV001779426]risk factor92118747221187472Human1name
156070047CV2354084single nucleotide variantNM_021068.4(IFNA4):c.41T>A (p.Leu14His)not specified [RCV004206523]uncertain significance92118749121187491Humanname
155909340CV2397725single nucleotide variantNM_021068.4(IFNA4):c.29C>T (p.Ala10Val)not specified [RCV004237159]uncertain significance92118750321187503Humanname
405867771CV2842370single nucleotide variantNM_021068.4(IFNA4):c.528G>T (p.Ser176=)EBV-positive nodal T- and NK-cell lymphoma [RCV004560319]likely benign92118700421187004Humanname
405792344CV3263692single nucleotide variantNM_021068.4(IFNA4):c.31G>A (p.Val11Met)not specified [RCV004400162]uncertain significance92118750121187501Humanname
597763498CV3683307single nucleotide variantNM_021068.4(IFNA4):c.86C>T (p.Thr29Ile)not specified [RCV004926349]uncertain significance92118744621187446Humanname
150480241CV1221931single nucleotide variantNM_021068.4(IFNA4):c.220G>A (p.Ala74Thr)not provided [RCV001616727]benign92118731221187312Humanname
156199911CV2256031single nucleotide variantNM_021068.4(IFNA4):c.266A>G (p.Asn89Ser)not specified [RCV004122464]uncertain significance92118726621187266Humanname
156286415CV2345666single nucleotide variantNM_021068.4(IFNA4):c.133G>C (p.Gly45Arg)not specified [RCV004205609]likely benign92118739921187399Humanname
156252830CV2390088single nucleotide variantNM_021068.4(IFNA4):c.202G>A (p.Gly68Ser)not specified [RCV004238690]uncertain significance92118733021187330Humanname
329375155CV2431395single nucleotide variantNM_021068.4(IFNA4):c.231C>G (p.Ile77Met)not specified [RCV004254561]uncertain significance92118730121187301Humanname
401861299CV2779605single nucleotide variantNM_021068.4(IFNA4):c.221C>T (p.Ala74Val)not specified [RCV004351313]uncertain significance92118731121187311Humanname
405792327CV3263687single nucleotide variantNM_021068.4(IFNA4):c.146A>T (p.His49Leu)not specified [RCV004400157]uncertain significance92118738621187386Humanname
405792331CV3263688single nucleotide variantNM_021068.4(IFNA4):c.164A>G (p.Asp55Gly)not specified [RCV004400158]uncertain significance92118736821187368Humanname
405792335CV3263689single nucleotide variantNM_021068.4(IFNA4):c.201T>A (p.Asp67Glu)not specified [RCV004400159]uncertain significance92118733121187331Humanname
405792338CV3263690single nucleotide variantNM_021068.4(IFNA4):c.219G>T (p.Lys73Asn)not specified [RCV004400160]uncertain significance92118731321187313Humanname
407511058CV3440588single nucleotide variantNM_021068.4(IFNA4):c.110C>T (p.Ala37Val)not specified [RCV004626339]uncertain significance92118742221187422Humanname
407466314CV3440590single nucleotide variantNM_021068.4(IFNA4):c.277A>C (p.Thr93Pro)not specified [RCV004635596]uncertain significance92118725521187255Humanname
597763494CV3683306single nucleotide variantNM_021068.4(IFNA4):c.134G>A (p.Gly45Glu)not specified [RCV004926348]uncertain significance92118739821187398Humanname
598206611CV3979245single nucleotide variantNM_021068.4(IFNA4):c.226G>A (p.Ala76Thr)not specified [RCV005337816]uncertain significance92118730621187306Humanname
598268205CV3979248single nucleotide variantNM_021068.4(IFNA4):c.179G>C (p.Gly60Ala)not specified [RCV005349655]uncertain significance92118735321187353Humanname
15134295CV711926single nucleotide variantNM_021068.4(IFNA4):c.103A>G (p.Arg35Gly)not provided [RCV000965102]benign92118742921187429Humanname
150508492CV1229657single nucleotide variantNM_021068.4(IFNA4):c.410A>T (p.Glu137Val)not provided [RCV001636235]benign92118712221187122Humanname
156172708CV2286956single nucleotide variantNM_021068.4(IFNA4):c.433A>G (p.Lys145Glu)not specified [RCV004144558]uncertain significance92118709921187099Humanname
155909226CV2369517single nucleotide variantNM_021068.4(IFNA4):c.496G>A (p.Val166Ile)not specified [RCV004210452]uncertain significance92118703621187036Humanname
156262522CV2376994single nucleotide variantNM_021068.4(IFNA4):c.334C>A (p.Leu112Ile)not specified [RCV004229675]uncertain significance92118719821187198Humanname
156008235CV2390089single nucleotide variantNM_021068.4(IFNA4):c.383G>A (p.Gly128Glu)not specified [RCV004238691]uncertain significance92118714921187149Humanname
329354802CV2449061single nucleotide variantNM_021068.4(IFNA4):c.428T>C (p.Val143Ala)not specified [RCV004264129]uncertain significance92118710421187104Humanname
401769456CV2735065single nucleotide variantNM_021068.4(IFNA4):c.354C>A (p.Asp118Glu)not specified [RCV004333762]uncertain significance92118717821187178Humanname
405792347CV3263693single nucleotide variantNM_021068.4(IFNA4):c.451A>C (p.Thr151Pro)not specified [RCV004400163]uncertain significance92118708121187081Humanname
405792350CV3263694single nucleotide variantNM_021068.4(IFNA4):c.506C>G (p.Ala169Gly)not specified [RCV004400164]uncertain significance92118702621187026Humanname
407466319CV3440591single nucleotide variantNM_021068.4(IFNA4):c.334C>G (p.Leu112Val)not specified [RCV004635597]uncertain significance92118719821187198Humanname
598268200CV3979247single nucleotide variantNM_021068.4(IFNA4):c.306G>C (p.Gln102His)not specified [RCV005349654]uncertain significance92118722621187226Humanname