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24 records found for search term Aurkb
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405269720CV3201771single nucleotide variantNM_004217.4(AURKB):c.939G>A (p.Ser313=)AURKB-related disorder [RCV003899677]likely benign1782049678204967Humanname , trait , alternate_id
15137667CV771975single nucleotide variantNM_004217.4(AURKB):c.837C>T (p.Asn279=)not provided [RCV000943276]likely benign1782052408205240Humanname
8636405CV91630single nucleotide variantNM_004217.3(AURKB):c.342G>A (p.Glu114=)Malignant melanoma [RCV000071728]not provided1782072328207232Humanname
38461356CV919785single nucleotide variantNM_004217.4(AURKB):c.74C>T (p.Pro25Leu)not provided [RCV001197552]uncertain significance1782078158207815Humanname
156096071CV2253092single nucleotide variantNM_004217.4(AURKB):c.283C>G (p.Arg95Gly)not specified [RCV004120877]uncertain significance1782072918207291Humanname
156167057CV2279731single nucleotide variantNM_004217.4(AURKB):c.130C>T (p.Arg44Cys)not specified [RCV004144346]uncertain significance1782077598207759Humanname
401877568CV2769575single nucleotide variantNM_004217.4(AURKB):c.126G>A (p.Met42Ile)not specified [RCV004351223]uncertain significance1782077638207763Humanname
405679144CV3294233single nucleotide variantNM_004217.4(AURKB):c.169G>C (p.Val57Leu)not specified [RCV004421275]uncertain significance1782076088207608Humanname
405679149CV3294234single nucleotide variantNM_004217.4(AURKB):c.198C>A (p.Asp66Glu)not specified [RCV004421276]uncertain significance1782075798207579Humanname
407456263CV3493739single nucleotide variantNM_004217.4(AURKB):c.293A>G (p.Lys98Arg)not specified [RCV004685885]uncertain significance1782072818207281Humanname
598254788CV3936078single nucleotide variantNM_004217.4(AURKB):c.188G>A (p.Gly63Glu)not specified [RCV005299305]uncertain significance1782075898207589Humanname
598254856CV3936089single nucleotide variantNM_004217.4(AURKB):c.136A>G (p.Asn46Asp)not specified [RCV005299314]uncertain significance1782077538207753Humanname
156189097CV2205897single nucleotide variantNM_004217.4(AURKB):c.314T>C (p.Leu105Pro)not specified [RCV004078332]uncertain significance1782072608207260Humanname
155959606CV2285295single nucleotide variantNM_004217.4(AURKB):c.475C>T (p.Arg159Cys)not specified [RCV004139178]uncertain significance1782068128206812Humanname
401782431CV2719812single nucleotide variantNM_004217.4(AURKB):c.886G>A (p.Val296Met)not specified [RCV004329233]uncertain significance1782050208205020Humanname
405679154CV3294235single nucleotide variantNM_004217.4(AURKB):c.553G>T (p.Ala185Ser)not specified [RCV004421277]uncertain significance1782066248206624Humanname
405679159CV3294236single nucleotide variantNM_004217.4(AURKB):c.581A>G (p.Lys194Arg)not specified [RCV004421278]uncertain significance1782065968206596Humanname
405679164CV3294237single nucleotide variantNM_004217.4(AURKB):c.742C>T (p.Arg248Cys)not specified [RCV004421279]uncertain significance1782053358205335Humanname
405679169CV3294238single nucleotide variantNM_004217.4(AURKB):c.927G>C (p.Arg309Ser)not specified [RCV004421280]uncertain significance1782049798204979Humanname
405679175CV3294239single nucleotide variantNM_004217.4(AURKB):c.961G>T (p.Val321Phe)not specified [RCV004421281]uncertain significance1782049458204945Humanname
407456245CV3493732single nucleotide variantNM_004217.4(AURKB):c.836A>G (p.Asn279Ser)not specified [RCV004685878]uncertain significance1782052418205241Humanname
14702927CV626402single nucleotide variantNM_004217.4(AURKB):c.847C>T (p.Arg283Cys)NK-cell enteropathy [RCV000791307]likely pathogenic1782052308205230Human1name
38461354CV919784single nucleotide variantNM_004217.4(AURKB):c.634G>C (p.Gly212Arg)not provided [RCV001197551]benign|likely benign1782065438206543Humanname
8636404CV91629single nucleotide variantNM_004217.3(AURKB):c.1021C>T (p.Gln341Ter)Malignant melanoma [RCV000071727]not provided1782048858204885Humanname