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26 records found for search term Chmp6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15194025CV778559deletionNM_024591.5(CHMP6):c.495+14delnot provided [RCV000955533]benign178099734980997349Humanname
156088873CV2359300single nucleotide variantNM_024591.5(CHMP6):c.92G>A (p.Arg31Lys)not specified [RCV004212585]likely benign178099460980994609Humanname
401782113CV2719181single nucleotide variantNM_024591.5(CHMP6):c.35G>C (p.Arg12Pro)not specified [RCV004324844]uncertain significance178099195380991953Humanname
15201680CV704454single nucleotide variantNM_024591.5(CHMP6):c.555C>T (p.Asn185=)not provided [RCV000957693]benign178099910280999102Humanname
156399538CV2205180single nucleotide variantNM_024591.5(CHMP6):c.175C>T (p.Arg59Trp)not specified [RCV004077774]uncertain significance178099502080995020Humanname
155943441CV2298577single nucleotide variantNM_024591.5(CHMP6):c.133C>T (p.Arg45Cys)not specified [RCV004162227]uncertain significance178099465080994650Humanname
156268094CV2329731single nucleotide variantNM_024591.5(CHMP6):c.236A>C (p.Asn79Thr)not specified [RCV004180831]uncertain significance178099508180995081Humanname
155928567CV2388900single nucleotide variantNM_024591.5(CHMP6):c.145C>T (p.Arg49Trp)not specified [RCV004241905]uncertain significance178099466280994662Humanname
329393030CV2469189single nucleotide variantNM_024591.5(CHMP6):c.124G>C (p.Glu42Gln)not specified [RCV004280542]uncertain significance178099464180994641Humanname
405661933CV3297141single nucleotide variantNM_024591.5(CHMP6):c.134G>A (p.Arg45His)not specified [RCV004439338]uncertain significance178099465180994651Humanname
405661936CV3297142single nucleotide variantNM_024591.5(CHMP6):c.136G>A (p.Ala46Thr)not specified [RCV004439339]uncertain significance178099465380994653Humanname
407455727CV3422762single nucleotide variantNM_024591.5(CHMP6):c.262G>A (p.Val88Ile)not specified [RCV004610390]uncertain significance178099567280995672Humanname
597769837CV3653203single nucleotide variantNM_024591.5(CHMP6):c.158G>A (p.Arg53Gln)not specified [RCV004896811]uncertain significance178099467580994675Humanname
597769843CV3653204single nucleotide variantNM_024591.5(CHMP6):c.181A>G (p.Lys61Glu)not specified [RCV004896812]uncertain significance178099502680995026Humanname
15201752CV704453single nucleotide variantNM_024591.5(CHMP6):c.163G>A (p.Gly55Ser)not provided [RCV000957714]benign178099468080994680Humanname
156004073CV2254251single nucleotide variantNM_024591.5(CHMP6):c.413G>A (p.Arg138Gln)not specified [RCV004129927]uncertain significance178099707180997071Humanname
156046975CV2304310single nucleotide variantNM_024591.5(CHMP6):c.352A>G (p.Met118Val)not specified [RCV004164430]uncertain significance178099701080997010Humanname
156101309CV2347793single nucleotide variantNM_024591.5(CHMP6):c.569C>A (p.Ala190Asp)not specified [RCV004195451]uncertain significance178099911680999116Humanname
405661938CV3297143single nucleotide variantNM_024591.5(CHMP6):c.317T>C (p.Phe106Ser)not specified [RCV004439340]uncertain significance178099572780995727Humanname
405661941CV3297144single nucleotide variantNM_024591.5(CHMP6):c.389C>T (p.Thr130Met)not specified [RCV004439341]uncertain significance178099704780997047Humanname
405661943CV3297145single nucleotide variantNM_024591.5(CHMP6):c.418A>G (p.Ile140Val)not specified [RCV004439342]uncertain significance178099726480997264Humanname
407455723CV3422763single nucleotide variantNM_024591.5(CHMP6):c.301A>T (p.Met101Leu)not specified [RCV004610391]uncertain significance178099571180995711Humanname
597769827CV3653201single nucleotide variantNM_024591.5(CHMP6):c.400G>A (p.Val134Met)not specified [RCV004896809]uncertain significance178099705880997058Humanname
597769832CV3653202single nucleotide variantNM_024591.5(CHMP6):c.452A>T (p.Glu151Val)not specified [RCV004896810]uncertain significance178099729880997298Humanname
597769849CV3653205single nucleotide variantNM_024591.5(CHMP6):c.347A>G (p.Gln116Arg)not specified [RCV004896813]uncertain significance178099575780995757Humanname
598214824CV3951652single nucleotide variantNM_024591.5(CHMP6):c.358A>T (p.Ile120Phe)not specified [RCV005316639]uncertain significance178099701680997016Humanname