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Pathways
Variants search result for All species
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3 records found for search term Pcnxl2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8575722CV110073single nucleotide variantNM_014801.3(PCNXL2):c.3518-6078A>GLung cancer [RCV000090596]uncertain significance1233145933233145933Humanname
8629349CV84494single nucleotide variantNM_014801.3(PCNXL2):c.3963C>T (p.Phe1321=)Malignant melanoma [RCV000064576]not provided1233090174233090174Humanname
8629350CV84495single nucleotide variantNM_014801.3(PCNXL2):c.1553C>T (p.Ser518Phe)Malignant melanoma [RCV000064577]not provided1233258309233258309Humanname