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15 records found for search term Ucn2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156252617CV2192895single nucleotide variantNM_033199.4(UCN2):c.91C>T (p.Arg31Cys)not specified [RCV004069459]uncertain significance34856303448563034Humanname
597685489CV3622807single nucleotide variantNM_033199.4(UCN2):c.92G>A (p.Arg31His)not specified [RCV004884050]uncertain significance34856303348563033Humanname
156327555CV2219875single nucleotide variantNM_033199.4(UCN2):c.196C>T (p.Arg66Cys)not specified [RCV004095508]uncertain significance34856292948562929Humanname
156359648CV2257862single nucleotide variantNM_033199.4(UCN2):c.214A>C (p.Ile72Leu)not specified [RCV004127904]uncertain significance34856291148562911Humanname
329385435CV2432147single nucleotide variantNM_033199.4(UCN2):c.212G>A (p.Arg71His)not specified [RCV004249293]uncertain significance34856291348562913Humanname
405800486CV3337908single nucleotide variantNM_033199.4(UCN2):c.194C>T (p.Thr65Ile)not specified [RCV004477295]uncertain significance34856293148562931Humanname
405800488CV3337909single nucleotide variantNM_033199.4(UCN2):c.209C>T (p.Ser70Leu)not specified [RCV004477296]uncertain significance34856291648562916Humanname
407523423CV3491253single nucleotide variantNM_033199.4(UCN2):c.241G>A (p.Gly81Ser)not specified [RCV004677970]uncertain significance34856288448562884Humanname
597685481CV3622806single nucleotide variantNM_033199.4(UCN2):c.116C>T (p.Thr39Ile)not specified [RCV004884049]uncertain significance34856300948563009Humanname
597685498CV3622808single nucleotide variantNM_033199.4(UCN2):c.211C>T (p.Arg71Cys)not specified [RCV004884051]uncertain significance34856291448562914Humanname
598190182CV3929158single nucleotide variantNM_033199.4(UCN2):c.278G>A (p.Arg93Lys)not specified [RCV005288174]uncertain significance34856284748562847Humanname
155963862CV2282781single nucleotide variantNM_033199.4(UCN2):c.311G>A (p.Arg104His)not specified [RCV004141635]uncertain significance34856281448562814Humanname
329375587CV2431574single nucleotide variantNM_033199.4(UCN2):c.306C>A (p.Asn102Lys)not specified [RCV004254725]uncertain significance34856281948562819Humanname
598190168CV3929156single nucleotide variantNM_033199.4(UCN2):c.307G>A (p.Ala103Thr)not specified [RCV005288172]uncertain significance34856281848562818Humanname
598190175CV3929157single nucleotide variantNM_033199.4(UCN2):c.302C>A (p.Thr101Asn)not specified [RCV005288173]uncertain significance34856282348562823Humanname