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Variants search result for Homo sapiens
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44 records found for search term Arid3c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156137290CV2280575single nucleotide variantNM_001017363.4(ARID3C):c.38C>T (p.Ala13Val)not specified [RCV004143058]uncertain significance93462797734627977Humanname
401869332CV2772361single nucleotide variantNM_001017363.4(ARID3C):c.31C>G (p.Arg11Gly)not specified [RCV004353372]uncertain significance93462798434627984Humanname
407476010CV3479519single nucleotide variantNM_001017363.4(ARID3C):c.80C>G (p.Pro27Arg)not specified [RCV004663373]uncertain significance93462793534627935Humanname
407508571CV3479528single nucleotide variantNM_001017363.4(ARID3C):c.49G>A (p.Gly17Arg)not specified [RCV004672087]uncertain significance93462796634627966Humanname
597683157CV3585480single nucleotide variantNM_001017363.4(ARID3C):c.71C>T (p.Pro24Leu)not specified [RCV004858044]uncertain significance93462794434627944Humanname
156317581CV2251065single nucleotide variantNM_001017363.4(ARID3C):c.289G>A (p.Glu97Lys)not specified [RCV004123614]uncertain significance93462772634627726Humanname
156166492CV2315241single nucleotide variantNM_001017363.4(ARID3C):c.188G>A (p.Arg63Gln)not specified [RCV004167231]uncertain significance93462782734627827Humanname
156363227CV2330624single nucleotide variantNM_001017363.4(ARID3C):c.254C>T (p.Ser85Leu)not specified [RCV004183219]uncertain significance93462776134627761Humanname
156242181CV2346980single nucleotide variantNM_001017363.4(ARID3C):c.232C>T (p.Pro78Ser)not specified [RCV004202424]uncertain significance93462778334627783Humanname
156038108CV2374130single nucleotide variantNM_001017363.4(ARID3C):c.143T>G (p.Val48Gly)not specified [RCV004229286]uncertain significance93462787234627872Humanname
401731910CV2690201single nucleotide variantNM_001017363.4(ARID3C):c.110C>G (p.Thr37Ser)not specified [RCV004302210]uncertain significance93462790534627905Humanname
597752841CV3585490single nucleotide variantNM_001017363.4(ARID3C):c.122C>A (p.Pro41His)not specified [RCV004846911]uncertain significance93462789334627893Humanname
597683215CV3585519single nucleotide variantNM_001017363.4(ARID3C):c.296C>A (p.Thr99Asn)not specified [RCV004858050]uncertain significance93462771934627719Humanname
598171973CV3908426single nucleotide variantNM_001017363.4(ARID3C):c.143T>C (p.Val48Ala)not specified [RCV005263457]uncertain significance93462787234627872Humanname
155922796CV2219151single nucleotide variantNM_001017363.4(ARID3C):c.683C>T (p.Ala228Val)not specified [RCV004087306]uncertain significance93462360734623607Humanname
156300577CV2244941single nucleotide variantNM_001017363.4(ARID3C):c.551C>G (p.Ser184Trp)not specified [RCV004104684]uncertain significance93462388834623888Humanname
156341566CV2268281single nucleotide variantNM_001017363.4(ARID3C):c.598T>C (p.Tyr200His)not specified [RCV004138577]uncertain significance93462369234623692Humanname
156173757CV2326788single nucleotide variantNM_001017363.4(ARID3C):c.409G>C (p.Val137Leu)not specified [RCV004176628]uncertain significance93462403034624030Humanname
329386302CV2455840single nucleotide variantNM_001017363.4(ARID3C):c.526C>T (p.Leu176Phe)not specified [RCV004279125]uncertain significance93462391334623913Humanname
329381122CV2464517single nucleotide variantNM_001017363.4(ARID3C):c.301G>A (p.Glu101Lys)not specified [RCV004276432]uncertain significance93462771434627714Humanname
405866919CV2842436single nucleotide variantNM_001017363.4(ARID3C):c.766C>T (p.Pro256Ser)EBV-positive nodal T- and NK-cell lymphoma [RCV004557793]likely benign93462352434623524Humanname
405700493CV3290023single nucleotide variantNM_001017363.4(ARID3C):c.419T>C (p.Met140Thr)not specified [RCV004425317]uncertain significance93462402034624020Humanname
405700500CV3290024single nucleotide variantNM_001017363.4(ARID3C):c.580A>G (p.Met194Val)not specified [RCV004425318]uncertain significance93462371034623710Humanname
407508549CV3483437single nucleotide variantNM_001017363.4(ARID3C):c.628C>G (p.Pro210Ala)not specified [RCV004672078]uncertain significance93462366234623662Humanname
597683147CV3585478single nucleotide variantNM_001017363.4(ARID3C):c.780G>T (p.Gln260His)not specified [RCV004858043]uncertain significance93462351034623510Humanname
597752846CV3585479single nucleotide variantNM_001017363.4(ARID3C):c.685T>C (p.Tyr229His)not specified [RCV004846910]uncertain significance93462360534623605Humanname
597683174CV3585483single nucleotide variantNM_001017363.4(ARID3C):c.885C>A (p.Asn295Lys)not specified [RCV004858046]uncertain significance93462251034622510Humanname
597683184CV3585485single nucleotide variantNM_001017363.4(ARID3C):c.652G>A (p.Asp218Asn)not specified [RCV004858047]uncertain significance93462363834623638Humanname
597752835CV3585497single nucleotide variantNM_001017363.4(ARID3C):c.701T>A (p.Leu234His)not specified [RCV004846912]uncertain significance93462358934623589Humanname
597683196CV3585500single nucleotide variantNM_001017363.4(ARID3C):c.746C>T (p.Ala249Val)not specified [RCV004858048]uncertain significance93462354434623544Humanname
597683206CV3585511single nucleotide variantNM_001017363.4(ARID3C):c.403A>G (p.Asn135Asp)not specified [RCV004858049]uncertain significance93462403634624036Humanname
597752832CV3585525single nucleotide variantNM_001017363.4(ARID3C):c.376T>C (p.Phe126Leu)not specified [RCV004846913]uncertain significance93462575734625757Humanname
597752659CV3585532single nucleotide variantNM_001017363.4(ARID3C):c.809C>T (p.Thr270Ile)not specified [RCV004846914]uncertain significance93462348134623481Humanname
598171985CV3908428single nucleotide variantNM_001017363.4(ARID3C):c.832T>G (p.Cys278Gly)not specified [RCV005263459]uncertain significance93462345834623458Humanname
156093585CV2213145single nucleotide variantNM_001017363.4(ARID3C):c.1156C>T (p.Arg386Cys)not specified [RCV004085379]uncertain significance93462154134621541Humanname
156030833CV2243309single nucleotide variantNM_001017363.4(ARID3C):c.1192C>T (p.Pro398Ser)not specified [RCV004112009]uncertain significance93462150534621505Humanname
156086174CV2340606single nucleotide variantNM_001017363.4(ARID3C):c.1234C>T (p.Pro412Ser)not specified [RCV004197314]uncertain significance93462146334621463Humanname
156069651CV2354013single nucleotide variantNM_001017363.4(ARID3C):c.1093A>T (p.Ser365Cys)not specified [RCV004204444]uncertain significance93462206534622065Humanname
401757356CV2675251single nucleotide variantNM_001017363.4(ARID3C):c.1216C>G (p.Pro406Ala)not specified [RCV004290018]uncertain significance93462148134621481Humanname
401767841CV2677834single nucleotide variantNM_001017363.4(ARID3C):c.1198C>T (p.Pro400Ser)not specified [RCV004294331]uncertain significance93462149934621499Humanname
401778766CV2735492single nucleotide variantNM_001017363.4(ARID3C):c.1153C>T (p.Arg385Cys)not specified [RCV004331051]uncertain significance93462154434621544Humanname
405700489CV3290022single nucleotide variantNM_001017363.4(ARID3C):c.1180G>A (p.Gly394Ser)not specified [RCV004425316]uncertain significance93462151734621517Humanname
407475956CV3483442single nucleotide variantNM_001017363.4(ARID3C):c.1086T>G (p.Ser362Arg)not specified [RCV004663357]uncertain significance93462207234622072Humanname
407475991CV3483451single nucleotide variantNM_001017363.4(ARID3C):c.1133A>G (p.Tyr378Cys)not specified [RCV004663364]uncertain significance93462202534622025Humanname