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Variants search result for Homo sapiens
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24 records found for search term Map2k4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
151662523CV1330413single nucleotide variantNM_003010.4(MAP2K4):c.1087-1G>Cnot provided [RCV001823950]not provided171214114612141146Humanname
156388285CV2231764single nucleotide variantNM_003010.4(MAP2K4):c.14G>T (p.Ser5Ile)not specified [RCV004098578]uncertain significance171202090012020900Humanname
156307385CV2331963single nucleotide variantNM_003010.4(MAP2K4):c.16C>G (p.Pro6Ala)not specified [RCV004189023]uncertain significance171202090212020902Humanname
155968533CV2337853single nucleotide variantNM_003010.4(MAP2K4):c.25G>A (p.Gly9Ser)not specified [RCV004183863]uncertain significance171202091112020911Humanname
156090337CV2344653single nucleotide variantNM_003010.4(MAP2K4):c.25G>C (p.Gly9Arg)not specified [RCV004197420]uncertain significance171202091112020911Humanname
597626690CV3699994single nucleotide variantNM_003010.4(MAP2K4):c.26G>A (p.Gly9Asp)not specified [RCV004938731]uncertain significance171202091212020912Humanname
156056008CV2326628single nucleotide variantNM_003010.4(MAP2K4):c.70G>A (p.Val24Ile)not specified [RCV004183166]uncertain significance171202095612020956Humanname
156049000CV2336488single nucleotide variantNM_003010.4(MAP2K4):c.59C>T (p.Thr20Ile)not specified [RCV004194699]uncertain significance171202094512020945Humanname
401731859CV2674501single nucleotide variantNM_003010.4(MAP2K4):c.43G>A (p.Gly15Ser)not specified [RCV004291384]uncertain significance171202092912020929Humanname
405657610CV3288574single nucleotide variantNM_003010.4(MAP2K4):c.67C>A (p.Pro23Thr)not specified [RCV004416170]uncertain significance171202095312020953Humanname
597626700CV3699997single nucleotide variantNM_003010.4(MAP2K4):c.80C>A (p.Pro27Gln)not specified [RCV004938734]uncertain significance171202096612020966Humanname
401894518CV2788308single nucleotide variantNM_003010.4(MAP2K4):c.265A>C (p.Ile89Leu)not specified [RCV004352893]uncertain significance171208140212081402Humanname
405657605CV3288573single nucleotide variantNM_003010.4(MAP2K4):c.188C>A (p.Pro63His)not specified [RCV004416169]uncertain significance171205496112054961Humanname
156115687CV2221529single nucleotide variantNM_003010.4(MAP2K4):c.357G>T (p.Met119Ile)not specified [RCV004096797]uncertain significance171208149412081494Humanname
156290718CV2226220single nucleotide variantNM_003010.4(MAP2K4):c.868G>A (p.Val290Ile)not specified [RCV004099478]uncertain significance171212534812125348Humanname
401732510CV2675105single nucleotide variantNM_003010.4(MAP2K4):c.572A>G (p.Tyr191Cys)not specified [RCV004289885]uncertain significance171210784812107848Humanname
407424921CV3410863single nucleotide variantNM_003010.4(MAP2K4):c.947A>T (p.Gln316Leu)Neurodevelopmental disorder [RCV004586507]uncertain significance171212919412129194Human1name
597626693CV3699995single nucleotide variantNM_003010.4(MAP2K4):c.598A>G (p.Ile200Val)not specified [RCV004938732]uncertain significance171210787412107874Humanname
598196854CV3988652single nucleotide variantNM_003010.4(MAP2K4):c.706C>A (p.Leu236Ile)not specified [RCV005375337]uncertain significance171211325312113253Humanname
598166184CV3988653single nucleotide variantNM_003010.4(MAP2K4):c.784A>G (p.Arg262Gly)not specified [RCV005369302]uncertain significance171211333112113331Humanname
13435619CV432406single nucleotide variantNM_003010.4(MAP2K4):c.538C>G (p.Leu180Val)Neuroblastoma [RCV000505661]other171210781412107814Human2name
155978698CV2266542single nucleotide variantNM_003010.4(MAP2K4):c.1141G>A (p.Val381Ile)not specified [RCV004131099]uncertain significance171214120112141201Humanname
598166189CV3988654single nucleotide variantNM_003010.4(MAP2K4):c.1132G>C (p.Ala378Pro)not specified [RCV005369303]uncertain significance171214119212141192Humanname
8636011CV91234single nucleotide variantNM_001281435.1(MAP2K4):c.1010C>T (p.Pro337Leu)Malignant melanoma [RCV000071332]not provided171212922412129224Humanname