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19 records found for search term Cenpq
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405762071CV3300302single nucleotide variantNM_018132.4(CENPQ):c.34G>A (p.Ala12Thr)not specified [RCV004433819]uncertain significance64947021049470210Humanname
405762086CV3300304single nucleotide variantNM_018132.4(CENPQ):c.65A>T (p.Lys22Ile)not specified [RCV004433821]uncertain significance64947024149470241Humanname
598208156CV3951468single nucleotide variantNM_018132.4(CENPQ):c.41A>G (p.Gln14Arg)not specified [RCV005315417]uncertain significance64947021749470217Humanname
156005984CV2401150single nucleotide variantNM_018132.4(CENPQ):c.192G>C (p.Lys64Asn)not specified [RCV004245711]uncertain significance64947209749472097Humanname
329388662CV2447743single nucleotide variantNM_018132.4(CENPQ):c.134A>G (p.His45Arg)not specified [RCV004258526]uncertain significance64947100549471005Humanname
407461918CV3419022single nucleotide variantNM_018132.4(CENPQ):c.283A>G (p.Ile95Val)not specified [RCV004612723]uncertain significance64947279449472794Humanname
156238260CV2235771single nucleotide variantNM_018132.4(CENPQ):c.617G>A (p.Ser206Asn)not specified [RCV004111900]uncertain significance64948862649488626Humanname
155954496CV2274330single nucleotide variantNM_018132.4(CENPQ):c.688G>A (p.Ala230Thr)not specified [RCV004136719]likely benign64949215649492156Humanname
155965419CV2286948single nucleotide variantNM_018132.4(CENPQ):c.602A>G (p.His201Arg)not specified [RCV004144550]uncertain significance64948861149488611Humanname
156160593CV2311680single nucleotide variantNM_018132.4(CENPQ):c.541A>G (p.Asn181Asp)not specified [RCV004170561]uncertain significance64948841549488415Humanname
405762065CV3300301single nucleotide variantNM_018132.4(CENPQ):c.343A>G (p.Lys115Glu)not specified [RCV004433818]uncertain significance64947285449472854Humanname
405762078CV3300303single nucleotide variantNM_018132.4(CENPQ):c.503C>G (p.Thr168Ser)not specified [RCV004433820]uncertain significance64948837749488377Humanname
405762092CV3300305single nucleotide variantNM_018132.4(CENPQ):c.723C>G (p.Asp241Glu)not specified [RCV004433822]uncertain significance64949219149492191Humanname
405762098CV3300306single nucleotide variantNM_018132.4(CENPQ):c.725T>G (p.Leu242Trp)not specified [RCV004433823]uncertain significance64949219349492193Humanname
407461920CV3419023single nucleotide variantNM_018132.4(CENPQ):c.585G>C (p.Glu195Asp)not specified [RCV004612724]uncertain significance64948845949488459Humanname
597779646CV3645544single nucleotide variantNM_018132.4(CENPQ):c.367A>G (p.Thr123Ala)not specified [RCV004899317]uncertain significance64948097049480970Humanname
597779650CV3645545single nucleotide variantNM_018132.4(CENPQ):c.599T>C (p.Met200Thr)not specified [RCV004899318]uncertain significance64948860849488608Humanname
598208150CV3951467single nucleotide variantNM_018132.4(CENPQ):c.647A>C (p.Gln216Pro)not specified [RCV005315416]uncertain significance64948865649488656Humanname
8632098CV87304single nucleotide variantNM_018132.3(CENPQ):c.547A>C (p.Ile183Leu)Malignant melanoma [RCV000067395]not provided64948842149488421Humanname