Arrdc4 Variant Search Result - Rat Genome Database

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47 records found for search term Arrdc4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15179234	CV731033	single nucleotide variant	NM_183376.3(ARRDC4):c.883-5A>T	not provided [RCV000885244]	likely benign	15	97969878	97969878	Human		name
150439947	CV1221382	single nucleotide variant	NM_183376.3(ARRDC4):c.231C>T (p.Ala77=)	not provided [RCV001610077]	benign	15	97961092	97961092	Human		name
405664331	CV3290436	single nucleotide variant	NM_183376.3(ARRDC4):c.95A>G (p.Tyr32Cys)	not specified [RCV004418209]	uncertain significance	15	97960956	97960956	Human		name
407461076	CV3483830	single nucleotide variant	NM_183376.3(ARRDC4):c.61G>C (p.Gly21Arg)	not specified [RCV004658619]	uncertain significance	15	97960922	97960922	Human		name
597765215	CV3593303	single nucleotide variant	NM_183376.3(ARRDC4):c.34G>T (p.Gly12Cys)	not specified [RCV004849977]	uncertain significance	15	97960895	97960895	Human		name
150507029	CV1258115	single nucleotide variant	NM_183376.3(ARRDC4):c.235A>G (p.Thr79Ala)	not provided [RCV001678332]	benign	15	97961096	97961096	Human		name
155988564	CV2234224	single nucleotide variant	NM_183376.3(ARRDC4):c.233G>A (p.Ser78Asn)	not specified [RCV004106304]	uncertain significance	15	97961094	97961094	Human		name
156042642	CV2261472	single nucleotide variant	NM_183376.3(ARRDC4):c.227C>T (p.Ser76Leu)	not specified [RCV004130093]	uncertain significance	15	97961088	97961088	Human		name
401738029	CV2714296	single nucleotide variant	NM_183376.3(ARRDC4):c.170T>A (p.Leu57Gln)	not specified [RCV004315980]	uncertain significance	15	97961031	97961031	Human		name
405664314	CV3290432	single nucleotide variant	NM_183376.3(ARRDC4):c.182G>A (p.Gly61Glu)	not specified [RCV004418205]	uncertain significance	15	97961043	97961043	Human		name
405664318	CV3290433	single nucleotide variant	NM_183376.3(ARRDC4):c.200G>C (p.Trp67Ser)	not specified [RCV004418206]	uncertain significance	15	97961061	97961061	Human		name
597765147	CV3593260	single nucleotide variant	NM_183376.3(ARRDC4):c.146C>T (p.Pro49Leu)	not specified [RCV004849959]	uncertain significance	15	97961007	97961007	Human		name
598185645	CV3902351	single nucleotide variant	NM_183376.3(ARRDC4):c.155T>G (p.Leu52Arg)	not specified [RCV005265950]	uncertain significance	15	97961016	97961016	Human		name
156182482	CV2222299	single nucleotide variant	NM_183376.3(ARRDC4):c.320T>G (p.Ile107Ser)	not specified [RCV004105316]	uncertain significance	15	97965612	97965612	Human		name
156186444	CV2236198	single nucleotide variant	NM_183376.3(ARRDC4):c.424G>A (p.Val142Met)	not specified [RCV004107908]	uncertain significance	15	97965944	97965944	Human		name
155975119	CV2342629	single nucleotide variant	NM_183376.3(ARRDC4):c.635T>C (p.Ile212Thr)	not specified [RCV004196716]	uncertain significance	15	97969132	97969132	Human		name
156062276	CV2353753	single nucleotide variant	NM_183376.3(ARRDC4):c.758A>G (p.Asn253Ser)	not specified [RCV004201762]	uncertain significance	15	97969255	97969255	Human		name
156382795	CV2362938	single nucleotide variant	NM_183376.3(ARRDC4):c.459T>A (p.Asp153Glu)	not specified [RCV004209041]	uncertain significance	15	97965979	97965979	Human		name
155984630	CV2367973	single nucleotide variant	NM_183376.3(ARRDC4):c.953A>G (p.Tyr318Cys)	not specified [RCV004223064]	uncertain significance	15	97969953	97969953	Human		name
329371848	CV2442921	single nucleotide variant	NM_183376.3(ARRDC4):c.754G>A (p.Ala252Thr)	not specified [RCV004253523]	uncertain significance	15	97969251	97969251	Human		name
401760369	CV2695018	single nucleotide variant	NM_183376.3(ARRDC4):c.793G>C (p.Asp265His)	not specified [RCV004301391]	uncertain significance	15	97969290	97969290	Human		name
401879527	CV2769641	single nucleotide variant	NM_183376.3(ARRDC4):c.853T>C (p.Cys285Arg)	not specified [RCV004351571]	uncertain significance	15	97969350	97969350	Human		name
401870298	CV2772697	single nucleotide variant	NM_183376.3(ARRDC4):c.785G>A (p.Gly262Glu)	not specified [RCV004357217]	uncertain significance	15	97969282	97969282	Human		name
405664323	CV3290434	single nucleotide variant	NM_183376.3(ARRDC4):c.439G>A (p.Glu147Lys)	not specified [RCV004418207]	uncertain significance	15	97965959	97965959	Human		name
405664326	CV3290435	single nucleotide variant	NM_183376.3(ARRDC4):c.748A>G (p.Met250Val)	not specified [RCV004418208]	uncertain significance	15	97969245	97969245	Human		name
407461043	CV3483819	single nucleotide variant	NM_183376.3(ARRDC4):c.320T>C (p.Ile107Thr)	not specified [RCV004658611]	uncertain significance	15	97965612	97965612	Human		name
407461119	CV3483841	single nucleotide variant	NM_183376.3(ARRDC4):c.880G>T (p.Ala294Ser)	not specified [RCV004658629]	uncertain significance	15	97969377	97969377	Human		name
407461185	CV3483863	single nucleotide variant	NM_183376.3(ARRDC4):c.500A>T (p.Asp167Val)	not specified [RCV004658646]	uncertain significance	15	97966020	97966020	Human		name
408385140	CV3505603	single nucleotide variant	NM_183376.3(ARRDC4):c.544G>C (p.Glu182Gln)	ARRDC4-related condition [RCV004732367]	uncertain significance	15	97968035	97968035	Human		name , trait
597765139	CV3593243	single nucleotide variant	NM_183376.3(ARRDC4):c.802A>G (p.Asn268Asp)	not specified [RCV004849957]	uncertain significance	15	97969299	97969299	Human		name
597765143	CV3593251	single nucleotide variant	NM_183376.3(ARRDC4):c.473G>A (p.Arg158Gln)	not specified [RCV004849958]	uncertain significance	15	97965993	97965993	Human		name
597765161	CV3593269	single nucleotide variant	NM_183376.3(ARRDC4):c.355C>T (p.Arg119Cys)	not specified [RCV004849963]	uncertain significance	15	97965647	97965647	Human		name
597730958	CV3593276	single nucleotide variant	NM_183376.3(ARRDC4):c.743G>A (p.Arg248Gln)	not specified [RCV004863083]	uncertain significance	15	97969240	97969240	Human		name
597731022	CV3593285	single nucleotide variant	NM_183376.3(ARRDC4):c.457G>T (p.Asp153Tyr)	not specified [RCV004863089]	uncertain significance	15	97965977	97965977	Human		name
598185561	CV3902336	single nucleotide variant	NM_183376.3(ARRDC4):c.671G>A (p.Arg224His)	not specified [RCV005265936]	uncertain significance	15	97969168	97969168	Human		name
598185588	CV3902341	single nucleotide variant	NM_183376.3(ARRDC4):c.526C>G (p.Pro176Ala)	not specified [RCV005265941]	uncertain significance	15	97968017	97968017	Human		name
598185607	CV3902344	single nucleotide variant	NM_183376.3(ARRDC4):c.998G>C (p.Ser333Thr)	not specified [RCV005265944]	uncertain significance	15	97969998	97969998	Human		name
598185618	CV3902346	single nucleotide variant	NM_183376.3(ARRDC4):c.631G>A (p.Ala211Thr)	not specified [RCV005265946]	uncertain significance	15	97969128	97969128	Human		name
598185639	CV3902349	single nucleotide variant	NM_183376.3(ARRDC4):c.805G>C (p.Gly269Arg)	not specified [RCV005265949]	uncertain significance	15	97969302	97969302	Human		name
15188141	CV726368	single nucleotide variant	NM_183376.3(ARRDC4):c.417G>C (p.Gln139His)	not provided [RCV000887448]	benign	15	97965937	97965937	Human		name
156186480	CV2377976	single nucleotide variant	NM_183376.3(ARRDC4):c.1237C>T (p.Pro413Ser)	not specified [RCV004230539]	uncertain significance	15	97971167	97971167	Human		name
329367511	CV2427298	single nucleotide variant	NM_183376.3(ARRDC4):c.1165G>A (p.Glu389Lys)	not specified [RCV004248160]	uncertain significance	15	97970708	97970708	Human		name
329381070	CV2464482	single nucleotide variant	NM_183376.3(ARRDC4):c.1115C>T (p.Pro372Leu)	not specified [RCV004276403]	uncertain significance	15	97970658	97970658	Human		name
407461149	CV3483852	single nucleotide variant	NM_183376.3(ARRDC4):c.1019C>T (p.Thr340Ile)	not specified [RCV004658637]	uncertain significance	15	97970019	97970019	Human		name
597765189	CV3593294	single nucleotide variant	NM_183376.3(ARRDC4):c.1109C>T (p.Pro370Leu)	not specified [RCV004849970]	uncertain significance	15	97970652	97970652	Human		name
597731158	CV3593314	single nucleotide variant	NM_183376.3(ARRDC4):c.1171C>G (p.Arg391Gly)	not specified [RCV004863103]	uncertain significance	15	97970714	97970714	Human		name
598185625	CV3902347	single nucleotide variant	NM_183376.3(ARRDC4):c.1141T>C (p.Cys381Arg)	not specified [RCV005265947]	uncertain significance	15	97970684	97970684	Human		name

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