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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


2 records found for search term Pabpc3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401929700CV2813786single nucleotide variantNM_030979.3(PABPC3):c.1836C>T (p.His612=)not provided [RCV003390346]likely benign132509803425098034Humanname
8635007CV90229single nucleotide variantNM_030979.2(PABPC3):c.700G>A (p.Gly234Arg)Malignant melanoma [RCV000070327]not provided132509689825096898Humanname