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Variants search result for Homo sapiens
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9 records found for search term Med30
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407518025CV3453676single nucleotide variantNM_080651.4(MED30):c.13C>T (p.Pro5Ser)not specified [RCV004628725]uncertain significance8117520889117520889Humanname
156180798CV2324551single nucleotide variantNM_080651.4(MED30):c.31A>G (p.Met11Val)not specified [RCV004179024]uncertain significance8117520907117520907Humanname
407518021CV3453673single nucleotide variantNM_080651.4(MED30):c.55C>A (p.Pro19Thr)not specified [RCV004628724]uncertain significance8117520931117520931Humanname
15198149CV700361single nucleotide variantNM_080651.4(MED30):c.73G>T (p.Ala25Ser)not provided [RCV000956666]benign8117520949117520949Humanname
597676672CV3560251single nucleotide variantNM_080651.4(MED30):c.212A>G (p.Tyr71Cys)not specified [RCV004830380]uncertain significance8117528685117528685Humanname
329359988CV2446509single nucleotide variantNM_080651.4(MED30):c.419G>A (p.Arg140Gln)not specified [RCV004251410]uncertain significance8117530805117530805Humanname
405692462CV3281765single nucleotide variantNM_080651.4(MED30):c.446T>G (p.Leu149Arg)not specified [RCV004423916]uncertain significance8117539887117539887Humanname
407502395CV3453675single nucleotide variantNM_080651.4(MED30):c.334G>A (p.Glu112Lys)not specified [RCV004645138]uncertain significance8117528807117528807Humanname
598241046CV3985641single nucleotide variantNM_080651.4(MED30):c.377A>G (p.Asp126Gly)not specified [RCV005364748]uncertain significance8117530763117530763Humanname