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22 records found for search term Calu
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
11087756CV227760single nucleotide variantNM_001219.5(CALU):c.582+133A>Gwarfarin response - Dosage [RCV000211348]drug response7128759170128759170Humanname
329380711CV2440418single nucleotide variantNM_001219.5(CALU):c.-11-208C>Gnot specified [RCV004256355]uncertain significance7128748365128748365Humanname
597763864CV3647396single nucleotide variantNM_001219.5(CALU):c.6C>A (p.Asp2Glu)not specified [RCV004895473]uncertain significance7128748589128748589Humanname
405766933CV3302594single nucleotide variantNM_001219.5(CALU):c.80G>A (p.Arg27His)not specified [RCV004434608]uncertain significance7128748663128748663Humanname
598203800CV3942931single nucleotide variantNM_001219.5(CALU):c.37T>G (p.Cys13Gly)not specified [RCV005314686]uncertain significance7128748620128748620Humanname
156179904CV2201695single nucleotide variantNM_001219.5(CALU):c.227T>C (p.Ile76Thr)not specified [RCV004082146]uncertain significance7128754267128754267Humanname
155991856CV2253398single nucleotide variantNM_001219.5(CALU):c.268G>A (p.Val90Met)not specified [RCV004125130]uncertain significance7128754308128754308Humanname
401860715CV2776158single nucleotide variantNM_001219.5(CALU):c.262G>C (p.Val88Leu)not specified [RCV004353247]uncertain significance7128754302128754302Humanname
407474458CV3424455single nucleotide variantNM_001219.5(CALU):c.179C>A (p.Thr60Asn)not specified [RCV004600621]uncertain significance7128748762128748762Humanname
597763857CV3647394single nucleotide variantNM_001219.5(CALU):c.247G>A (p.Asp83Asn)not specified [RCV004895471]uncertain significance7128754287128754287Humanname
156242646CV2231449single nucleotide variantNM_001219.5(CALU):c.848G>A (p.Gly283Asp)not specified [RCV004096525]uncertain significance7128769067128769067Humanname
156286659CV2232977single nucleotide variantNM_001219.5(CALU):c.492C>G (p.Asp164Glu)not specified [RCV004103350]uncertain significance7128758947128758947Humanname
156278701CV2330941single nucleotide variantNM_001219.5(CALU):c.661G>C (p.Asp221His)not specified [RCV004185987]uncertain significance7128767473128767473Humanname
155969954CV2400823single nucleotide variantNM_001219.5(CALU):c.364G>A (p.Gly122Ser)not specified [RCV004242480]uncertain significance7128754404128754404Humanname
156435504CV2403609single nucleotide variantNM_001219.5(CALU):c.700C>T (p.Arg234Ter)Developmental disorder [RCV003128071]likely pathogenic7128767512128767512Human1name
329359434CV2446261single nucleotide variantNM_001219.5(CALU):c.932G>A (p.Arg311Gln)not specified [RCV004249400]uncertain significance7128769151128769151Humanname
401869988CV2755858single nucleotide variantNM_001219.5(CALU):c.734G>A (p.Arg245His)not specified [RCV004342226]uncertain significance7128767546128767546Humanname
405766940CV3302595single nucleotide variantNM_001219.5(CALU):c.554A>G (p.Tyr185Cys)not specified [RCV004434609]uncertain significance7128759009128759009Humanname
597763860CV3647395single nucleotide variantNM_001219.5(CALU):c.788A>G (p.Tyr263Cys)not specified [RCV004895472]uncertain significance7128767600128767600Humanname
598203775CV3942927single nucleotide variantNM_001219.5(CALU):c.871G>A (p.Val291Ile)not specified [RCV005314682]uncertain significance7128769090128769090Humanname
598203781CV3942928single nucleotide variantNM_001219.5(CALU):c.903G>T (p.Gln301His)not specified [RCV005314683]uncertain significance7128769122128769122Humanname
598203794CV3942930single nucleotide variantNM_001219.5(CALU):c.881A>G (p.Tyr294Cys)not specified [RCV005314685]uncertain significance7128769100128769100Humanname