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Pathways
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2 records found for search term Tp53i11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401904273CV2816577microsatelliteNM_006034.5(TP53I11):c.437-12TC[2]not provided [RCV003394822]likely benign114493502444935025Humanname
8634044CV89262single nucleotide variantNM_006034.3(TP53I11):c.477G>A (p.Leu159=)Malignant melanoma [RCV000069359]not provided114493497744934977Humanname