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Variants search result for Homo sapiens
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8 records found for search term Ncbp2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8630757CV85912single nucleotide variantNM_001042540.1(NCBP2):c.-271G>AMalignant melanoma [RCV000065996]not provided3196942774196942774Humanname
598216967CV3983745single nucleotide variantNM_007362.5(NCBP2):c.13C>G (p.Leu5Val)not specified [RCV005378989]uncertain significance3196942491196942491Humanname
597648506CV3562364single nucleotide variantNM_007362.5(NCBP2):c.46G>A (p.Glu16Lys)not specified [RCV004826545]uncertain significance3196942458196942458Humanname
156061040CV2263094single nucleotide variantNM_007362.5(NCBP2):c.131T>C (p.Val44Ala)not specified [RCV004131342]uncertain significance3196939380196939380Humanname
405776011CV3344082single nucleotide variantNM_007362.5(NCBP2):c.290C>T (p.Ala97Val)not specified [RCV004471118]uncertain significance3196937619196937619Humanname
401740105CV2709817single nucleotide variantNM_007362.5(NCBP2):c.326G>A (p.Arg109Gln)not specified [RCV004320792]uncertain significance3196937583196937583Humanname
405776046CV3344088single nucleotide variantNM_007362.5(NCBP2):c.363G>C (p.Glu121Asp)not specified [RCV004471124]uncertain significance3196937546196937546Humanname
598216982CV3983747single nucleotide variantNM_007362.5(NCBP2):c.439G>A (p.Gly147Arg)not specified [RCV005378991]uncertain significance3196937043196937043Humanname