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Variants search result for Homo sapiens
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8 records found for search term Rcan3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329363498CV2471678single nucleotide variantNM_013441.4(RCAN3):c.262A>G (p.Arg88Gly)not specified [RCV004286963]uncertain significance12453128424531284Humanname
597764427CV3582846single nucleotide variantNM_013441.4(RCAN3):c.110A>G (p.Asp37Gly)not specified [RCV004849777]uncertain significance12451448224514482Humanname
155916430CV2282060single nucleotide variantNM_013441.4(RCAN3):c.572A>T (p.Glu191Val)not specified [RCV004138809]uncertain significance12453512324535123Humanname
156104739CV2352474single nucleotide variantNM_013441.4(RCAN3):c.461C>T (p.Pro154Leu)not specified [RCV004202982]uncertain significance12453317424533174Humanname
401894329CV2780697single nucleotide variantNM_013441.4(RCAN3):c.641C>T (p.Pro214Leu)not specified [RCV004352036]uncertain significance12453519224535192Humanname
405682412CV3319330single nucleotide variantNM_013441.4(RCAN3):c.566G>C (p.Gly189Ala)not specified [RCV004443598]uncertain significance12453511724535117Humanname
405682418CV3319331single nucleotide variantNM_013441.4(RCAN3):c.667C>T (p.Arg223Cys)not specified [RCV004443599]uncertain significance12453521824535218Humanname
597729221CV3582847single nucleotide variantNM_013441.4(RCAN3):c.488C>T (p.Ala163Val)not specified [RCV004862891]uncertain significance12453320124533201Humanname