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


2 records found for search term Prim2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582021CV116473single nucleotide variantNM_000947.4(PRIM2):c.694-6011T>CLung cancer [RCV000096996]uncertain significance65750137657501376Humanname
8582022CV116474single nucleotide variantNM_000947.4(PRIM2):c.761+1220A>TLung cancer [RCV000096997]uncertain significance65750867457508674Humanname