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32 records found for search term Mknk1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401757024CV2678190single nucleotide variantNM_001135553.4(MKNK1):c.-9C>Anot specified [RCV004296697]uncertain significance14659411946594119Humanname
401927693CV2812786single nucleotide variantNM_001135553.4(MKNK1):c.199-7C>Tnot provided [RCV003406478]likely benign14657666146576661Humanname
405744450CV3368187single nucleotide variantNM_001135553.4(MKNK1):c.13G>A (p.Glu5Lys)not specified [RCV004498254]uncertain significance14658331546583315Humanname
156387216CV2372678single nucleotide variantNM_001135553.4(MKNK1):c.68G>A (p.Arg23Gln)not specified [RCV004221875]uncertain significance14658326046583260Humanname
401927690CV2812785single nucleotide variantNM_001135553.4(MKNK1):c.705C>T (p.Gly235=)not provided [RCV003406477]likely benign14656274846562748Humanname
8629566CV84713single nucleotide variantNM_003684.5(MKNK1):c.1310C>T (p.Ser437Phe)Malignant melanoma [RCV000064795]not provided14655866346558663Humanname
155953967CV2274270single nucleotide variantNM_001135553.4(MKNK1):c.163G>A (p.Val55Met)not specified [RCV004136669]uncertain significance14658056546580565Humanname
401739582CV2683109single nucleotide variantNM_001135553.4(MKNK1):c.1044C>T (p.Phe348=)not specified [RCV004286114]likely benign14655877046558770Humanname
405773153CV3364453single nucleotide variantNM_001135553.4(MKNK1):c.134A>C (p.Glu45Ala)not specified [RCV004502638]uncertain significance14658059446580594Humanname
405786437CV3374867single nucleotide variantNM_001135553.4(MKNK1):c.143A>G (p.Tyr48Cys)not specified [RCV004504906]uncertain significance14658058546580585Humanname
597640638CV3560700single nucleotide variantNM_001135553.4(MKNK1):c.276C>G (p.Asn92Lys)not specified [RCV004825319]uncertain significance14657657746576577Humanname
156029593CV2278637single nucleotide variantNM_001135553.4(MKNK1):c.757G>A (p.Gly253Arg)not specified [RCV004134844]uncertain significance14656269646562696Humanname
156067641CV2284831single nucleotide variantNM_001135553.4(MKNK1):c.962T>C (p.Val321Ala)not specified [RCV004143004]uncertain significance14656148546561485Humanname
156282412CV2348854single nucleotide variantNM_001135553.4(MKNK1):c.980A>C (p.Glu327Ala)not specified [RCV004203295]uncertain significance14656026746560267Humanname
329367432CV2456850single nucleotide variantNM_001135553.4(MKNK1):c.986G>C (p.Gly329Ala)not specified [RCV004270813]uncertain significance14656026146560261Humanname
329364144CV2460359single nucleotide variantNM_001135553.4(MKNK1):c.778C>T (p.Arg260Trp)not specified [RCV004268677]uncertain significance14656267546562675Humanname
329359732CV2462249single nucleotide variantNM_001135553.4(MKNK1):c.917C>G (p.Ala306Gly)not specified [RCV004266247]uncertain significance14656153046561530Humanname
401773267CV2709217single nucleotide variantNM_001135553.4(MKNK1):c.749G>T (p.Gly250Val)not specified [RCV004316388]uncertain significance14656270446562704Humanname
401877969CV2786912single nucleotide variantNM_001135553.4(MKNK1):c.706G>A (p.Val236Met)not specified [RCV004366057]uncertain significance14656274746562747Humanname
405761072CV3364602single nucleotide variantNM_001135553.4(MKNK1):c.578C>T (p.Thr193Ile)not specified [RCV004500617]uncertain significance14656507246565072Humanname
405763587CV3365188single nucleotide variantNM_001135553.4(MKNK1):c.784G>A (p.Glu262Lys)not specified [RCV004501034]uncertain significance14656266946562669Humanname
405777558CV3371942single nucleotide variantNM_001135553.4(MKNK1):c.734A>G (p.Tyr245Cys)not specified [RCV004503381]uncertain significance14656271946562719Humanname
405775999CV3375238single nucleotide variantNM_001135553.4(MKNK1):c.722T>C (p.Met241Thr)not specified [RCV004503114]uncertain significance14656273146562731Humanname
407486305CV3457240single nucleotide variantNM_001135553.4(MKNK1):c.493T>G (p.Leu165Val)not specified [RCV004640868]uncertain significance14656846346568463Humanname
597640642CV3560701single nucleotide variantNM_001135553.4(MKNK1):c.923A>G (p.Gln308Arg)not specified [RCV004825320]uncertain significance14656152446561524Humanname
598187378CV3989252single nucleotide variantNM_001135553.4(MKNK1):c.554G>A (p.Gly185Glu)not specified [RCV005373553]uncertain significance14656509646565096Humanname
598255323CV3989253single nucleotide variantNM_001135553.4(MKNK1):c.578C>G (p.Thr193Ser)not specified [RCV005367337]uncertain significance14656507246565072Humanname
598187387CV3989254single nucleotide variantNM_001135553.4(MKNK1):c.905T>C (p.Leu302Pro)not specified [RCV005373554]uncertain significance14656154246561542Humanname
155917131CV2202218single nucleotide variantNM_001135553.4(MKNK1):c.1169G>A (p.Arg390His)not specified [RCV004078164]uncertain significance14655864546558645Humanname
329393557CV2453429single nucleotide variantNM_001135553.4(MKNK1):c.1184G>C (p.Arg395Pro)not specified [RCV004267038]uncertain significance14655863046558630Humanname
407486296CV3457238single nucleotide variantNM_001135553.4(MKNK1):c.1202G>A (p.Gly401Asp)not specified [RCV004640866]uncertain significance14655861246558612Humanname
597640631CV3560699single nucleotide variantNM_001135553.4(MKNK1):c.1081C>G (p.Gln361Glu)not specified [RCV004825318]uncertain significance14655873346558733Humanname