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Pathways
Variants search result for All species
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12 records found for search term Kcnmb4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329378507CV2459827single nucleotide variantNM_014505.6(KCNMB4):c.23A>C (p.Tyr8Ser)not specified [RCV004279328]uncertain significance127036675770366757Humanname
329378097CV2460678single nucleotide variantNM_014505.6(KCNMB4):c.16G>T (p.Val6Leu)not specified [RCV004271026]uncertain significance127036675070366750Humanname
156280325CV2348438single nucleotide variantNM_014505.6(KCNMB4):c.76A>G (p.Ile26Val)not specified [RCV004193628]uncertain significance127036681070366810Humanname
597767249CV3694723single nucleotide variantNM_014505.6(KCNMB4):c.128C>T (p.Ala43Val)not specified [RCV004927244]uncertain significance127036686270366862Humanname
155962693CV2197629single nucleotide variantNM_014505.6(KCNMB4):c.440C>T (p.Thr147Ile)not specified [RCV004074845]uncertain significance127040031270400312Humanname
156241557CV2265776single nucleotide variantNM_014505.6(KCNMB4):c.620G>A (p.Arg207His)not specified [RCV004126397]uncertain significance127043064070430640Humanname
156001521CV2378822single nucleotide variantNM_014505.6(KCNMB4):c.553G>T (p.Val185Phe)not specified [RCV004231266]uncertain significance127043057370430573Humanname
401867867CV2767100single nucleotide variantNM_014505.6(KCNMB4):c.574A>G (p.Ile192Val)not specified [RCV004347501]uncertain significance127043059470430594Humanname
401871013CV2788985single nucleotide variantNM_014505.6(KCNMB4):c.585G>T (p.Lys195Asn)not specified [RCV004363299]uncertain significance127043060570430605Humanname
405806996CV3264984single nucleotide variantNM_014505.6(KCNMB4):c.619C>T (p.Arg207Cys)not specified [RCV004406332]uncertain significance127043063970430639Humanname
597796378CV3694722single nucleotide variantNM_014505.6(KCNMB4):c.307G>A (p.Asp103Asn)not specified [RCV004935451]uncertain significance127036704170367041Humanname
597796379CV3694724single nucleotide variantNM_014505.6(KCNMB4):c.314A>G (p.His105Arg)not specified [RCV004935452]uncertain significance127036704870367048Humanname