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Variants search result for Homo sapiens
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78 records found for search term Dcst1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8628964CV84107single nucleotide variantNM_152494.3(DCST1):c.75C>T (p.Leu25=)Malignant melanoma [RCV000064188]not provided1155034448155034448Humanname
401736991CV2689539single nucleotide variantNM_152494.4(DCST1):c.88C>G (p.Leu30Val)not specified [RCV004308373]uncertain significance1155034461155034461Humanname
401773386CV2716549single nucleotide variantNM_152494.4(DCST1):c.34G>A (p.Gly12Arg)not specified [RCV004327625]likely benign1155034070155034070Humanname
407458533CV3430372single nucleotide variantNM_152494.4(DCST1):c.37C>G (p.Gln13Glu)not specified [RCV004611473]uncertain significance1155034073155034073Humanname
401775759CV2710703single nucleotide variantNM_152494.4(DCST1):c.173G>T (p.Gly58Val)not specified [RCV004319601]uncertain significance1155034546155034546Humanname
401868651CV2788434single nucleotide variantNM_152494.4(DCST1):c.125C>A (p.Pro42Gln)not specified [RCV004354960]uncertain significance1155034498155034498Humanname
405702073CV3243339single nucleotide variantNM_152494.4(DCST1):c.119G>A (p.Arg40His)not specified [RCV004375395]uncertain significance1155034492155034492Humanname
407458548CV3430367single nucleotide variantNM_152494.4(DCST1):c.210C>A (p.Asn70Lys)not specified [RCV004611468]uncertain significance1155034675155034675Humanname
598262530CV3963750single nucleotide variantNM_152494.4(DCST1):c.226G>A (p.Glu76Lys)not specified [RCV005325409]uncertain significance1155034691155034691Humanname
15168966CV706711single nucleotide variantNM_152494.4(DCST1):c.1086C>T (p.Tyr362=)not provided [RCV000971719]benign|likely benign1155043423155043423Humanname
156142887CV2200045single nucleotide variantNM_152494.4(DCST1):c.839C>T (p.Thr280Ile)not specified [RCV004074201]uncertain significance1155041804155041804Humanname
156198747CV2255929single nucleotide variantNM_152494.4(DCST1):c.793C>T (p.Arg265Cys)not specified [RCV004122384]uncertain significance1155041758155041758Humanname
156058668CV2262913single nucleotide variantNM_152494.4(DCST1):c.437C>T (p.Ser146Leu)not specified [RCV004125055]uncertain significance1155040530155040530Humanname
156116305CV2273560single nucleotide variantNM_152494.4(DCST1):c.525C>A (p.Asp175Glu)not specified [RCV004134090]uncertain significance1155040618155040618Humanname
156308764CV2341683single nucleotide variantNM_152494.4(DCST1):c.966G>C (p.Gln322His)not specified [RCV004599572]uncertain significance1155042808155042808Humanname
155903433CV2353579single nucleotide variantNM_152494.4(DCST1):c.487C>T (p.Arg163Cys)not specified [RCV004199559]uncertain significance1155040580155040580Humanname
156147446CV2358011single nucleotide variantNM_152494.4(DCST1):c.779G>A (p.Arg260His)not specified [RCV004209786]uncertain significance1155041744155041744Humanname
155933988CV2372374single nucleotide variantNM_152494.4(DCST1):c.476G>A (p.Arg159His)not specified [RCV004217141]uncertain significance1155040569155040569Humanname
329353272CV2469072single nucleotide variantNM_152494.4(DCST1):c.656C>T (p.Ala219Val)not specified [RCV004274316]uncertain significance1155041521155041521Humanname
401723722CV2684845single nucleotide variantNM_152494.4(DCST1):c.674G>A (p.Arg225His)not specified [RCV004296351]likely benign1155041539155041539Humanname
401736323CV2688759single nucleotide variantNM_152494.4(DCST1):c.862A>C (p.Lys288Gln)not specified [RCV004303785]uncertain significance1155041827155041827Humanname
401762809CV2720084single nucleotide variantNM_152494.4(DCST1):c.370G>A (p.Ala124Thr)not specified [RCV004323654]uncertain significance1155039510155039510Humanname
401889829CV2763434single nucleotide variantNM_152494.4(DCST1):c.475C>T (p.Arg159Cys)not specified [RCV004349323]uncertain significance1155040568155040568Humanname
405702109CV3243344single nucleotide variantNM_152494.4(DCST1):c.364G>C (p.Gly122Arg)not specified [RCV004375400]uncertain significance1155039504155039504Humanname
405702118CV3243345single nucleotide variantNM_152494.4(DCST1):c.562C>T (p.Arg188Trp)not specified [RCV004375401]uncertain significance1155041427155041427Humanname
405702127CV3243346single nucleotide variantNM_152494.4(DCST1):c.790G>C (p.Asp264His)not specified [RCV004375402]uncertain significance1155041755155041755Humanname
405702133CV3243347single nucleotide variantNM_152494.4(DCST1):c.794G>A (p.Arg265His)not specified [RCV004375403]likely benign1155041759155041759Humanname
407458561CV3430363single nucleotide variantNM_152494.4(DCST1):c.497C>T (p.Thr166Ile)not specified [RCV004611464]uncertain significance1155040590155040590Humanname
407458545CV3430368single nucleotide variantNM_152494.4(DCST1):c.768A>G (p.Ile256Met)not specified [RCV004611469]uncertain significance1155041733155041733Humanname
407458536CV3430371single nucleotide variantNM_152494.4(DCST1):c.632A>G (p.Asp211Gly)not specified [RCV004611472]uncertain significance1155041497155041497Humanname
597801107CV3652195single nucleotide variantNM_152494.4(DCST1):c.914A>G (p.Asn305Ser)not specified [RCV004906036]likely benign1155042756155042756Humanname
597801116CV3652199single nucleotide variantNM_152494.4(DCST1):c.414C>G (p.His138Gln)not specified [RCV004906040]uncertain significance1155040507155040507Humanname
597801118CV3652200single nucleotide variantNM_152494.4(DCST1):c.704C>T (p.Ser235Leu)not specified [RCV004906041]uncertain significance1155041569155041569Humanname
597801121CV3652202single nucleotide variantNM_152494.4(DCST1):c.952G>T (p.Asp318Tyr)not specified [RCV004906043]uncertain significance1155042794155042794Humanname
598262538CV3963752single nucleotide variantNM_152494.4(DCST1):c.973C>T (p.Arg325Cys)not specified [RCV005325411]uncertain significance1155042815155042815Humanname
598262549CV3963755single nucleotide variantNM_152494.4(DCST1):c.623C>G (p.Thr208Arg)not specified [RCV005325414]uncertain significance1155041488155041488Humanname
598262557CV3963757single nucleotide variantNM_152494.4(DCST1):c.307G>A (p.Ala103Thr)not specified [RCV005325416]uncertain significance1155039447155039447Humanname
15173799CV706710single nucleotide variantNM_152494.4(DCST1):c.596C>T (p.Ala199Val)not provided [RCV000972652]benign1155041461155041461Humanname
15173037CV718254single nucleotide variantNM_152494.4(DCST1):c.473C>T (p.Thr158Ile)not provided [RCV000883959]benign1155040566155040566Humanname
156271657CV2195253single nucleotide variantNM_152494.4(DCST1):c.1094G>A (p.Arg365His)not specified [RCV004080187]likely benign1155043431155043431Humanname
156325288CV2195279single nucleotide variantNM_152494.4(DCST1):c.1348G>T (p.Ala450Ser)not specified [RCV004080209]uncertain significance1155046200155046200Humanname
156247275CV2215317single nucleotide variantNM_152494.4(DCST1):c.1900G>A (p.Gly634Ser)not specified [RCV004087346]uncertain significance1155050647155050647Humanname
155922256CV2218796single nucleotide variantNM_152494.4(DCST1):c.1081G>C (p.Asp361His)not specified [RCV004085042]uncertain significance1155043418155043418Humanname
156337335CV2228675single nucleotide variantNM_152494.4(DCST1):c.1764G>T (p.Lys588Asn)not specified [RCV004092894]uncertain significance1155048065155048065Humanname
156050203CV2242045single nucleotide variantNM_152494.4(DCST1):c.1453G>C (p.Asp485His)not specified [RCV004108980]uncertain significance1155046444155046444Humanname
156109244CV2254529single nucleotide variantNM_152494.4(DCST1):c.1937G>A (p.Cys646Tyr)not specified [RCV004123887]uncertain significance1155050684155050684Humanname
156032966CV2259717single nucleotide variantNM_152494.4(DCST1):c.1369G>A (p.Val457Met)not specified [RCV004116731]uncertain significance1155046360155046360Humanname
156095562CV2377970single nucleotide variantNM_152494.4(DCST1):c.1613C>T (p.Pro538Leu)not specified [RCV004230535]uncertain significance1155047787155047787Humanname
156269410CV2379280single nucleotide variantNM_152494.4(DCST1):c.1318G>A (p.Val440Ile)not specified [RCV004223749]uncertain significance1155046170155046170Humanname
156156271CV2388849single nucleotide variantNM_152494.4(DCST1):c.1135G>T (p.Val379Leu)not specified [RCV004239695]uncertain significance1155043472155043472Humanname
329368201CV2424219single nucleotide variantNM_152494.4(DCST1):c.1061G>C (p.Arg354Pro)not specified [RCV004250344]uncertain significance1155043398155043398Humanname
329372443CV2443017single nucleotide variantNM_152494.4(DCST1):c.1114T>C (p.Trp372Arg)not specified [RCV004253608]uncertain significance1155043451155043451Humanname
329362264CV2444525single nucleotide variantNM_152494.4(DCST1):c.1123G>A (p.Gly375Arg)not specified [RCV004256753]uncertain significance1155043460155043460Humanname
329398648CV2471629single nucleotide variantNM_152494.4(DCST1):c.1972T>C (p.Tyr658His)not specified [RCV004286922]uncertain significance1155050719155050719Humanname
401751996CV2672646single nucleotide variantNM_152494.4(DCST1):c.1877C>T (p.Pro626Leu)not specified [RCV004287668]uncertain significance1155050624155050624Humanname
401739565CV2683104single nucleotide variantNM_152494.4(DCST1):c.1431C>G (p.Asp477Glu)not specified [RCV004286111]uncertain significance1155046422155046422Humanname
401730739CV2686687single nucleotide variantNM_152494.4(DCST1):c.2002G>A (p.Val668Met)not specified [RCV004300097]uncertain significance1155050749155050749Humanname
401780299CV2725981single nucleotide variantNM_152494.4(DCST1):c.1856A>G (p.Gln619Arg)not specified [RCV004324347]uncertain significance1155048157155048157Humanname
401896472CV2781422single nucleotide variantNM_152494.4(DCST1):c.1408C>G (p.Leu470Val)not specified [RCV004352424]uncertain significance1155046399155046399Humanname
405702055CV3243337single nucleotide variantNM_152494.4(DCST1):c.1175C>T (p.Ser392Phe)not specified [RCV004375393]uncertain significance1155045895155045895Humanname
405702063CV3243338single nucleotide variantNM_152494.4(DCST1):c.1192A>G (p.Ser398Gly)not specified [RCV004375394]uncertain significance1155045912155045912Humanname
405702081CV3243340single nucleotide variantNM_152494.4(DCST1):c.1459A>G (p.Ile487Val)not specified [RCV004375396]uncertain significance1155046450155046450Humanname
405702089CV3243341single nucleotide variantNM_152494.4(DCST1):c.1553G>A (p.Arg518Gln)not specified [RCV004375397]uncertain significance1155047253155047253Humanname
405702102CV3243343single nucleotide variantNM_152494.4(DCST1):c.1894C>A (p.His632Asn)not specified [RCV004375399]uncertain significance1155050641155050641Humanname
407458550CV3430366single nucleotide variantNM_152494.4(DCST1):c.2033G>C (p.Arg678Pro)not specified [RCV004611467]uncertain significance1155050780155050780Humanname
407458541CV3430369single nucleotide variantNM_152494.4(DCST1):c.1847G>A (p.Arg616Gln)not specified [RCV004611470]uncertain significance1155048148155048148Humanname
407458539CV3430370single nucleotide variantNM_152494.4(DCST1):c.1327C>T (p.Pro443Ser)not specified [RCV004611471]uncertain significance1155046179155046179Humanname
597801105CV3652194single nucleotide variantNM_152494.4(DCST1):c.1501C>A (p.His501Asn)not specified [RCV004906035]uncertain significance1155047201155047201Humanname
597801109CV3652196single nucleotide variantNM_152494.4(DCST1):c.1060C>T (p.Arg354Cys)not specified [RCV004906037]uncertain significance1155043397155043397Humanname
597801112CV3652197single nucleotide variantNM_152494.4(DCST1):c.1135G>C (p.Val379Leu)not specified [RCV004906038]uncertain significance1155043472155043472Humanname
597801114CV3652198single nucleotide variantNM_152494.4(DCST1):c.2009G>A (p.Cys670Tyr)not specified [RCV004906039]uncertain significance1155050756155050756Humanname
597801119CV3652201single nucleotide variantNM_152494.4(DCST1):c.1921T>C (p.Trp641Arg)not specified [RCV004906042]uncertain significance1155050668155050668Humanname
598262534CV3963751single nucleotide variantNM_152494.4(DCST1):c.1562T>C (p.Ile521Thr)not specified [RCV005325410]uncertain significance1155047262155047262Humanname
598262543CV3963753single nucleotide variantNM_152494.4(DCST1):c.1220A>T (p.Asn407Ile)not specified [RCV005325412]uncertain significance1155045940155045940Humanname
598262546CV3963754single nucleotide variantNM_152494.4(DCST1):c.1283C>G (p.Thr428Ser)not specified [RCV005325413]uncertain significance1155046135155046135Humanname
598262553CV3963756single nucleotide variantNM_152494.4(DCST1):c.1739C>T (p.Ala580Val)not specified [RCV005325415]uncertain significance1155047913155047913Humanname
598262565CV3963759single nucleotide variantNM_152494.4(DCST1):c.1792C>G (p.Leu598Val)not specified [RCV005325418]uncertain significance1155048093155048093Humanname
8624716CV79830single nucleotide variantNM_152494.4(DCST1):c.1252G>A (p.Asp418Asn)not specified [RCV004232834]uncertain significance|not provided1155045972155045972Humanname