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13 records found for search term Magoh
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401862977CV2775432single nucleotide variantNM_002370.4(MAGOH):c.163A>G (p.Ser55Gly)not specified [RCV004348828]uncertain significance15323363753233637Humanname
155939104CV2376546single nucleotide variantNM_002370.4(MAGOH):c.332A>G (p.Asn111Ser)not specified [RCV004220715]uncertain significance15322888153228881Humanname
407484822CV3449698single nucleotide variantNM_002370.4(MAGOH):c.359G>T (p.Arg120Leu)not specified [RCV004640595]uncertain significance15322712753227127Humanname
15167388CV779490single nucleotide variantNM_018048.5(MAGOHB):c.347+10T>Anot provided [RCV000971390]benign121060784410607844Humanname
155965759CV2330605single nucleotide variantNM_018048.5(MAGOHB):c.26T>A (p.Leu9Gln)not specified [RCV004183201]uncertain significance121061350710613507Humanname
401749163CV2694577single nucleotide variantNM_018048.5(MAGOHB):c.14G>A (p.Ser5Asn)not specified [RCV004298698]uncertain significance121061351910613519Humanname
156121684CV2276033single nucleotide variantNM_018048.5(MAGOHB):c.214A>G (p.Thr72Ala)not specified [RCV004141710]uncertain significance121060988110609881Humanname
598165229CV3992473single nucleotide variantNM_018048.5(MAGOHB):c.171T>G (p.Ser57Arg)not specified [RCV005369135]uncertain significance121060992410609924Humanname
401767080CV2721471single nucleotide variantNM_018048.5(MAGOHB):c.346A>C (p.Lys116Gln)not specified [RCV004322202]uncertain significance121060785510607855Humanname
405651608CV3277727single nucleotide variantNM_018048.5(MAGOHB):c.416T>C (p.Ile139Thr)not specified [RCV004413705]uncertain significance121060630610606306Humanname
597623840CV3702529single nucleotide variantNM_018048.5(MAGOHB):c.367G>A (p.Val123Ile)not specified [RCV004936860]uncertain significance121060635510606355Humanname
597623841CV3702530single nucleotide variantNM_018048.5(MAGOHB):c.353C>T (p.Pro118Leu)not specified [RCV004936861]uncertain significance121060636910606369Humanname
597623842CV3702531single nucleotide variantNM_018048.5(MAGOHB):c.427T>G (p.Phe143Val)not specified [RCV004936862]uncertain significance121060629510606295Humanname