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38 records found for search term Cyth4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597675473CV3655002single nucleotide variantNM_013385.5(CYTH4):c.26C>A (p.Ala9Glu)not specified [RCV004913497]uncertain significance223729262737292627Humanname
597675461CV3655003single nucleotide variantNM_013385.5(CYTH4):c.16C>A (p.Pro6Thr)not specified [RCV004913498]uncertain significance223728258537282585Humanname
597675450CV3655004single nucleotide variantNM_013385.5(CYTH4):c.22C>G (p.Pro8Ala)not specified [RCV004913499]uncertain significance223729262337292623Humanname
15189015CV742892single nucleotide variantNM_013385.5(CYTH4):c.262C>T (p.Leu88=)not provided [RCV000909530]benign223729759137297591Humanname
401723585CV2724954single nucleotide variantNM_013385.5(CYTH4):c.38G>A (p.Ser13Asn)not specified [RCV004319718]uncertain significance223729263937292639Humanname
405867548CV2842272single nucleotide variantNM_013385.5(CYTH4):c.40G>A (p.Gly14Arg)EBV-positive nodal T- and NK-cell lymphoma [RCV004560221]|not specified [RCV004907850]likely benign|uncertain significance223729264137292641Humanname
407452738CV3420299single nucleotide variantNM_013385.5(CYTH4):c.277G>A (p.Val93Ile)not specified [RCV004608648]likely benign223729760637297606Humanname
15121321CV717438single nucleotide variantNM_013385.5(CYTH4):c.220A>G (p.Met74Val)not provided [RCV000962873]benign223729605137296051Humanname
156385661CV2227993single nucleotide variantNM_013385.5(CYTH4):c.908T>C (p.Ile303Thr)not specified [RCV004096237]uncertain significance223731147837311478Humanname
155987485CV2234108single nucleotide variantNM_013385.5(CYTH4):c.748G>A (p.Gly250Ser)not specified [RCV004106207]uncertain significance223730926337309263Humanname
156003764CV2357490single nucleotide variantNM_013385.5(CYTH4):c.995A>G (p.Gln332Arg)not specified [RCV004202775]uncertain significance223731205737312057Humanname
156201005CV2362994single nucleotide variantNM_013385.5(CYTH4):c.373G>A (p.Val125Ile)not specified [RCV004211135]uncertain significance223729924537299245Humanname
156019539CV2366962single nucleotide variantNM_013385.5(CYTH4):c.439T>C (p.Phe147Leu)not specified [RCV004213367]uncertain significance223730091137300911Humanname
156387362CV2372722single nucleotide variantNM_013385.5(CYTH4):c.652C>T (p.Arg218Cys)not specified [RCV004221914]uncertain significance223730335837303358Humanname
156349125CV2376464single nucleotide variantNM_013385.5(CYTH4):c.650A>G (p.Asn217Ser)not specified [RCV004220641]uncertain significance223730335637303356Humanname
329372446CV2443016single nucleotide variantNM_013385.5(CYTH4):c.366C>A (p.Asn122Lys)not specified [RCV004253607]uncertain significance223729923837299238Humanname
401721368CV2673692single nucleotide variantNM_013385.5(CYTH4):c.989G>A (p.Arg330Gln)not specified [RCV004282422]uncertain significance223731205137312051Humanname
401768474CV2675372single nucleotide variantNM_013385.5(CYTH4):c.496G>A (p.Ala166Thr)not specified [RCV004292179]likely benign223730096837300968Humanname
401777561CV2704152single nucleotide variantNM_013385.5(CYTH4):c.664A>G (p.Asn222Asp)not specified [RCV004311167]likely benign223730337037303370Humanname
401858591CV2774355single nucleotide variantNM_013385.5(CYTH4):c.653G>A (p.Arg218His)not specified [RCV004347704]uncertain significance223730335937303359Humanname
401893840CV2777757single nucleotide variantNM_013385.5(CYTH4):c.497C>T (p.Ala166Val)not specified [RCV004345589]uncertain significance223730096937300969Humanname
405678679CV3236515single nucleotide variantNM_013385.5(CYTH4):c.302A>G (p.Tyr101Cys)not specified [RCV004370666]uncertain significance223729763137297631Humanname
405678683CV3236516single nucleotide variantNM_013385.5(CYTH4):c.695G>A (p.Arg232Gln)not specified [RCV004370667]uncertain significance223730340137303401Humanname
405678688CV3236517single nucleotide variantNM_013385.5(CYTH4):c.962G>A (p.Cys321Tyr)not specified [RCV004370668]uncertain significance223731202437312024Humanname
407452740CV3420300single nucleotide variantNM_013385.5(CYTH4):c.437A>T (p.Gln146Leu)not specified [RCV004608649]uncertain significance223730090937300909Humanname
597675483CV3655001single nucleotide variantNM_013385.5(CYTH4):c.310G>A (p.Glu104Lys)not specified [RCV004913496]uncertain significance223729763937297639Humanname
598250495CV3952675single nucleotide variantNM_013385.5(CYTH4):c.532G>A (p.Val178Ile)not specified [RCV005322894]uncertain significance223730100437301004Humanname
598250502CV3952676single nucleotide variantNM_013385.5(CYTH4):c.634C>T (p.Arg212Cys)not specified [RCV005322895]uncertain significance223730334037303340Humanname
598250510CV3952677single nucleotide variantNM_013385.5(CYTH4):c.682G>A (p.Glu228Lys)not specified [RCV005322896]uncertain significance223730338837303388Humanname
598250517CV3952678single nucleotide variantNM_013385.5(CYTH4):c.910C>T (p.Pro304Ser)not specified [RCV005322897]uncertain significance223731148037311480Humanname
598250526CV3952679single nucleotide variantNM_013385.5(CYTH4):c.694C>T (p.Arg232Trp)not specified [RCV005322898]uncertain significance223730340037303400Humanname
598250533CV3952680single nucleotide variantNM_013385.5(CYTH4):c.791G>T (p.Gly264Val)not specified [RCV005322899]uncertain significance223730930637309306Humanname
15189018CV742893single nucleotide variantNM_013385.5(CYTH4):c.319A>C (p.Asn107His)not provided [RCV000909531]benign223729764837297648Humanname
155921042CV2340384single nucleotide variantNM_013385.5(CYTH4):c.1157G>A (p.Arg386Gln)not specified [RCV004197115]uncertain significance223731348337313483Humanname
156182058CV2353126single nucleotide variantNM_013385.5(CYTH4):c.1016C>T (p.Thr339Ile)not specified [RCV004203605]uncertain significance223731207837312078Humanname
156087703CV2366416single nucleotide variantNM_013385.5(CYTH4):c.1156C>T (p.Arg386Trp)not specified [RCV004212460]uncertain significance223731348237313482Humanname
401742770CV2673869single nucleotide variantNM_013385.5(CYTH4):c.1051G>A (p.Glu351Lys)not specified [RCV004293249]uncertain significance223731211337312113Humanname
405678676CV3236514single nucleotide variantNM_013385.5(CYTH4):c.1127G>A (p.Arg376His)not specified [RCV004370665]uncertain significance223731345337313453Humanname