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Variants search result for Homo sapiens
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7 records found for search term Cbln4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597785720CV3641259single nucleotide variantNM_080617.6(CBLN4):c.26C>T (p.Ser9Phe)not specified [RCV004900798]uncertain significance205600414656004146Humanname
156053508CV2312467single nucleotide variantNM_080617.6(CBLN4):c.193C>T (p.Arg65Trp)not specified [RCV004167143]uncertain significance205600397956003979Humanname
329377550CV2453480single nucleotide variantNM_080617.6(CBLN4):c.281A>G (p.Tyr94Cys)not specified [RCV004267079]uncertain significance205600389156003891Humanname
405738500CV3292067single nucleotide variantNM_080617.6(CBLN4):c.269C>G (p.Thr90Arg)not specified [RCV004430331]uncertain significance205600390356003903Humanname
401887101CV2775608single nucleotide variantNM_080617.6(CBLN4):c.406C>A (p.Gln136Lys)not specified [RCV004350763]uncertain significance205600073356000733Humanname
405738507CV3292068single nucleotide variantNM_080617.6(CBLN4):c.316T>C (p.Phe106Leu)not specified [RCV004430332]uncertain significance205600082356000823Humanname
405738512CV3292069single nucleotide variantNM_080617.6(CBLN4):c.473G>A (p.Arg158His)not specified [RCV004430333]uncertain significance205599869055998690Humanname