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32 records found for search term Hdac11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156045909CV2268635single nucleotide variantNM_024827.4(HDAC11):c.50C>A (p.Pro17Gln)not specified [RCV004124042]uncertain significance31348129313481293Humanname
156048945CV2370697single nucleotide variantNM_024827.4(HDAC11):c.41C>T (p.Thr14Ile)not specified [RCV004209101]uncertain significance31348128413481284Humanname
329353422CV2469253single nucleotide variantNM_024827.4(HDAC11):c.128G>A (p.Gly43Asp)not specified [RCV004280594]uncertain significance31348137113481371Humanname
597711122CV3679076single nucleotide variantNM_024827.4(HDAC11):c.152A>T (p.Glu51Val)not specified [RCV004917452]uncertain significance31348346413483464Humanname
597710398CV3679077single nucleotide variantNM_024827.4(HDAC11):c.150A>C (p.Lys50Asn)not specified [RCV004917453]uncertain significance31348139313481393Humanname
598266268CV3971640single nucleotide variantNM_024827.4(HDAC11):c.292G>A (p.Val98Ile)not specified [RCV005349239]uncertain significance31349677513496775Humanname
156164166CV2246756single nucleotide variantNM_024827.4(HDAC11):c.598A>G (p.Ile200Val)not specified [RCV004112291]uncertain significance31350292913502929Humanname
156187487CV2332782single nucleotide variantNM_024827.4(HDAC11):c.907G>A (p.Gly303Arg)not specified [RCV004189451]uncertain significance31350454613504546Humanname
156213448CV2385850single nucleotide variantNM_024827.4(HDAC11):c.994G>A (p.Val332Ile)not specified [RCV004226896]likely benign31350463313504633Humanname
155933919CV2399413single nucleotide variantNM_024827.4(HDAC11):c.661C>T (p.Arg221Trp)not specified [RCV004242692]uncertain significance31350410513504105Humanname
401768176CV2675082single nucleotide variantNM_024827.4(HDAC11):c.974T>C (p.Ile325Thr)not specified [RCV004289863]uncertain significance31350461313504613Humanname
401725627CV2721863single nucleotide variantNM_024827.4(HDAC11):c.638G>T (p.Arg213Leu)not specified [RCV004326374]uncertain significance31350296913502969Humanname
401881003CV2763207single nucleotide variantNM_024827.4(HDAC11):c.502C>T (p.Arg168Cys)not specified [RCV004336243]uncertain significance31350188313501883Humanname
405795978CV3266433single nucleotide variantNM_024827.4(HDAC11):c.466G>T (p.Ala156Ser)not specified [RCV004401425]uncertain significance31350076613500766Humanname
405795981CV3266434single nucleotide variantNM_024827.4(HDAC11):c.662G>A (p.Arg221Gln)not specified [RCV004401426]uncertain significance31350410613504106Humanname
405795984CV3266435single nucleotide variantNM_024827.4(HDAC11):c.678G>T (p.Glu226Asp)not specified [RCV004401427]uncertain significance31350412213504122Humanname
405795987CV3266436single nucleotide variantNM_024827.4(HDAC11):c.877C>T (p.Arg293Trp)not specified [RCV004401428]uncertain significance31350451613504516Humanname
405795990CV3266437single nucleotide variantNM_024827.4(HDAC11):c.988C>G (p.Pro330Ala)not specified [RCV004401429]uncertain significance31350462713504627Humanname
407514424CV3440219single nucleotide variantNM_024827.4(HDAC11):c.301C>T (p.Leu101Phe)not specified [RCV004627604]uncertain significance31349678413496784Humanname
407514429CV3440221single nucleotide variantNM_024827.4(HDAC11):c.746A>G (p.His249Arg)not specified [RCV004627606]uncertain significance31350419013504190Humanname
407504804CV3440223single nucleotide variantNM_024827.4(HDAC11):c.878G>A (p.Arg293Gln)not specified [RCV004624154]likely benign31350451713504517Humanname
407514431CV3440224single nucleotide variantNM_024827.4(HDAC11):c.409G>A (p.Val137Met)not specified [RCV004627607]uncertain significance31349855213498552Humanname
597781586CV3679074single nucleotide variantNM_024827.4(HDAC11):c.638G>A (p.Arg213His)not specified [RCV004930934]uncertain significance31350296913502969Humanname
597781591CV3679075single nucleotide variantNM_024827.4(HDAC11):c.874C>T (p.Arg292Cys)not specified [RCV004930935]uncertain significance31350451313504513Humanname
598266247CV3971636single nucleotide variantNM_024827.4(HDAC11):c.646A>G (p.Lys216Glu)not specified [RCV005349235]uncertain significance31350297713502977Humanname
598266251CV3971637single nucleotide variantNM_024827.4(HDAC11):c.799C>T (p.Arg267Cys)not specified [RCV005349236]uncertain significance31350424313504243Humanname
598266257CV3971638single nucleotide variantNM_024827.4(HDAC11):c.505G>A (p.Val169Met)not specified [RCV005349237]uncertain significance31350188613501886Humanname
598266264CV3971639single nucleotide variantNM_024827.4(HDAC11):c.470A>G (p.Asp157Gly)not specified [RCV005349238]uncertain significance31350077013500770Humanname
598266274CV3971641single nucleotide variantNM_024827.4(HDAC11):c.532A>G (p.Ile178Val)not specified [RCV005349240]likely benign31350191313501913Humanname
155965916CV2330620single nucleotide variantNM_024827.4(HDAC11):c.1007A>G (p.Asn336Ser)not specified [RCV004183215]uncertain significance31350464613504646Humanname
407514427CV3440220single nucleotide variantNM_024827.4(HDAC11):c.1019C>T (p.Pro340Leu)not specified [RCV004627605]uncertain significance31350465813504658Humanname
15137776CV748028single nucleotide variantNM_024827.4(HDAC11):c.1028C>A (p.Pro343His)not provided [RCV000921226]likely benign31350466713504667Humanname