Dcun1d2 Variant Search Result - Rat Genome Database

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31 records found for search term Dcun1d2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156160830	CV2236388	single nucleotide variant	NM_001014283.2(DCUN1D2):c.95A>C (p.Gln32Pro)	not specified [RCV004108067]	uncertain significance	13	113483965	113483965	Human		name
407458285	CV3430410	single nucleotide variant	NM_001014283.2(DCUN1D2):c.92C>T (p.Thr31Met)	not specified [RCV004611511]	uncertain significance	13	113483968	113483968	Human		name
26902937	CV858320	single nucleotide variant	NM_001014283.2(DCUN1D2):c.38G>A (p.Arg13His)	Epidermolysis bullosa simplex with nail dystrophy [RCV001089668]	uncertain significance	13	113484022	113484022	Human	1	name
156189173	CV2356591	single nucleotide variant	NM_001014283.2(DCUN1D2):c.263A>C (p.Gln88Pro)	not specified [RCV004201957]	uncertain significance	13	113480701	113480701	Human		name
329372864	CV2451697	single nucleotide variant	NM_001014283.2(DCUN1D2):c.184A>G (p.Lys62Glu)	not specified [RCV004274610]	uncertain significance	13	113483876	113483876	Human		name
405703137	CV3243414	single nucleotide variant	NM_001014283.2(DCUN1D2):c.109C>A (p.Leu37Ile)	not specified [RCV004375470]	uncertain significance	13	113483951	113483951	Human		name
405702894	CV3243415	single nucleotide variant	NM_001014283.2(DCUN1D2):c.128G>A (p.Ser43Asn)	not specified [RCV004375471]	likely benign	13	113483932	113483932	Human		name
405702721	CV3243416	single nucleotide variant	NM_001014283.2(DCUN1D2):c.146A>T (p.Asp49Val)	not specified [RCV004375472]	uncertain significance	13	113483914	113483914	Human		name
407458287	CV3430411	single nucleotide variant	NM_001014283.2(DCUN1D2):c.101A>G (p.Glu34Gly)	not specified [RCV004611512]	uncertain significance	13	113483959	113483959	Human		name
597801185	CV3661830	single nucleotide variant	NM_001014283.2(DCUN1D2):c.188A>G (p.Lys63Arg)	not specified [RCV004906076]	uncertain significance	13	113483872	113483872	Human		name
598262815	CV3959878	single nucleotide variant	NM_001014283.2(DCUN1D2):c.272A>G (p.Asp91Gly)	not specified [RCV005325485]	uncertain significance	13	113480692	113480692	Human		name
156073012	CV2263697	single nucleotide variant	NM_001014283.2(DCUN1D2):c.691G>A (p.Asp231Asn)	not specified [RCV004135992]	uncertain significance	13	113459321	113459321	Human		name
156063506	CV2321082	single nucleotide variant	NM_001014283.2(DCUN1D2):c.583C>G (p.Leu195Val)	not specified [RCV004174908]	uncertain significance	13	113461074	113461074	Human		name
156182072	CV2353127	single nucleotide variant	NM_001014283.2(DCUN1D2):c.712G>A (p.Val238Ile)	not specified [RCV004203606]	uncertain significance	13	113458097	113458097	Human		name
329365191	CV2440124	single nucleotide variant	NM_001014283.2(DCUN1D2):c.679A>G (p.Met227Val)	not specified [RCV004260588]	uncertain significance	13	113459333	113459333	Human		name
329398903	CV2471781	single nucleotide variant	NM_001014283.2(DCUN1D2):c.385C>T (p.Leu129Phe)	not specified [RCV004280823]	uncertain significance	13	113480579	113480579	Human		name
401726125	CV2699105	single nucleotide variant	NM_001014283.2(DCUN1D2):c.665T>C (p.Met222Thr)	not specified [RCV004303615]	uncertain significance	13	113459347	113459347	Human		name
401759771	CV2701711	single nucleotide variant	NM_001014283.2(DCUN1D2):c.439G>A (p.Glu147Lys)	not specified [RCV004314118]	uncertain significance	13	113474205	113474205	Human		name
401773638	CV2705462	single nucleotide variant	NM_001014283.2(DCUN1D2):c.487A>G (p.Thr163Ala)	not specified [RCV004316553]	uncertain significance	13	113474157	113474157	Human		name
401865587	CV2778827	single nucleotide variant	NM_001014283.2(DCUN1D2):c.635C>T (p.Thr212Ile)	not specified [RCV004346721]	uncertain significance	13	113459377	113459377	Human		name
401891871	CV2780869	single nucleotide variant	NM_001014283.2(DCUN1D2):c.299T>C (p.Ile100Thr)	not specified [RCV004352180]	uncertain significance	13	113480665	113480665	Human		name
405702450	CV3243418	single nucleotide variant	NM_001014283.2(DCUN1D2):c.662A>G (p.Asn221Ser)	not specified [RCV004375474]	uncertain significance	13	113459350	113459350	Human		name
405702457	CV3243419	single nucleotide variant	NM_001014283.2(DCUN1D2):c.680T>C (p.Met227Thr)	not specified [RCV004375475]	uncertain significance	13	113459332	113459332	Human		name
405702462	CV3243420	single nucleotide variant	NM_001014283.2(DCUN1D2):c.767G>A (p.Arg256His)	not specified [RCV004375476]	uncertain significance	13	113458042	113458042	Human		name
407458283	CV3430409	single nucleotide variant	NM_001014283.2(DCUN1D2):c.454G>C (p.Ala152Pro)	not specified [RCV004611510]	uncertain significance	13	113474190	113474190	Human		name
597801187	CV3661831	single nucleotide variant	NM_001014283.2(DCUN1D2):c.493G>A (p.Ala165Thr)	not specified [RCV004906077]	uncertain significance	13	113474151	113474151	Human		name
597801189	CV3661832	single nucleotide variant	NM_001014283.2(DCUN1D2):c.637T>C (p.Trp213Arg)	not specified [RCV004906078]	uncertain significance	13	113459375	113459375	Human		name
598262797	CV3959874	single nucleotide variant	NM_001014283.2(DCUN1D2):c.298A>G (p.Ile100Val)	not specified [RCV005325481]	uncertain significance	13	113480666	113480666	Human		name
598262802	CV3959875	single nucleotide variant	NM_001014283.2(DCUN1D2):c.689A>G (p.Tyr230Cys)	not specified [RCV005325482]	uncertain significance	13	113459323	113459323	Human		name
598262811	CV3959877	single nucleotide variant	NM_001014283.2(DCUN1D2):c.406A>C (p.Lys136Gln)	not specified [RCV005325484]	uncertain significance	13	113474238	113474238	Human		name
598262820	CV3959879	single nucleotide variant	NM_001014283.2(DCUN1D2):c.410T>C (p.Leu137Pro)	not specified [RCV005325486]	uncertain significance	13	113474234	113474234	Human		name

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