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


3 records found for search term Aim1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8626068CV81212single nucleotide variantNM_001624.3(AIM1):c.1368C>T (p.Ser456=)Malignant melanoma [RCV000061290]not provided6106519800106519800Humanname
8631762CV86968single nucleotide variantNM_001624.3(AIM1):c.2767G>A (p.Glu923Lys)Malignant melanoma [RCV000067059]not provided6106521199106521199Humanname
8631763CV86969single nucleotide variantNM_001624.3(AIM1):c.3700G>A (p.Glu1234Lys)Malignant melanoma [RCV000067060]not provided6106543482106543482Humanname