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Pathways
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2 records found for search term Mettl11b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8629079CV84223single nucleotide variantNM_001136107.1(METTL11B):c.51C>T (p.Thr17=)Malignant melanoma [RCV000064305]not provided1170146158170146158Humanname
8629078CV84222single nucleotide variantNM_001136107.1(METTL11B):c.50C>T (p.Thr17Ile)Malignant melanoma [RCV000064304]not provided1170146157170146157Humanname