Fam83e Variant Search Result - Rat Genome Database

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79 records found for search term Fam83e

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156343817	CV2232928	single nucleotide variant	NM_017708.4(FAM83E):c.23C>T (p.Ala8Val)	not specified [RCV004103309]	uncertain significance	19	48613350	48613350	Human		name
407509190	CV3431939	single nucleotide variant	NM_017708.4(FAM83E):c.20C>T (p.Ala7Val)	not specified [RCV004625637]	uncertain significance	19	48613353	48613353	Human		name
155968910	CV2312897	single nucleotide variant	NM_017708.4(FAM83E):c.85G>A (p.Glu29Lys)	not specified [RCV004171385]	uncertain significance	19	48613288	48613288	Human		name
401758690	CV2700701	single nucleotide variant	NM_017708.4(FAM83E):c.58G>T (p.Gly20Trp)	not specified [RCV004313414]	uncertain significance	19	48613315	48613315	Human		name
401929052	CV2818536	single nucleotide variant	NM_017708.4(FAM83E):c.363G>A (p.Ala121=)	not provided [RCV003407060]	likely benign	19	48613010	48613010	Human		name
401910638	CV2818537	single nucleotide variant	NM_017708.4(FAM83E):c.315G>A (p.Ser105=)	not provided [RCV003425307]	likely benign	19	48613058	48613058	Human	1	name
401910638	CV2818537	single nucleotide variant	NM_017708.4(FAM83E):c.315G>A (p.Ser105=)	not provided [RCV003425307]	likely benign	19	48613058	48613059	Human	1	name
407509183	CV3431937	single nucleotide variant	NM_017708.4(FAM83E):c.41C>T (p.Ser14Phe)	not specified [RCV004625635]	uncertain significance	19	48613332	48613332	Human		name
156232493	CV2346117	single nucleotide variant	NM_017708.4(FAM83E):c.148G>A (p.Val50Met)	not specified [RCV004201580]	uncertain significance	19	48613225	48613225	Human		name
156151660	CV2369189	single nucleotide variant	NM_017708.4(FAM83E):c.203C>G (p.Ala68Gly)	not specified [RCV004208110]	uncertain significance	19	48613170	48613170	Human		name
329393536	CV2467078	single nucleotide variant	NM_017708.4(FAM83E):c.266C>T (p.Thr89Ile)	not specified [RCV004282812]	uncertain significance	19	48613107	48613107	Human		name
329388072	CV2468657	single nucleotide variant	NM_017708.4(FAM83E):c.274G>A (p.Asp92Asn)	not specified [RCV004278206]	uncertain significance	19	48613099	48613099	Human		name
401742868	CV2697885	single nucleotide variant	NM_017708.4(FAM83E):c.247G>A (p.Gly83Arg)	not specified [RCV004300596]	likely benign	19	48613126	48613126	Human		name
401861797	CV2756701	single nucleotide variant	NM_017708.4(FAM83E):c.241C>T (p.Pro81Ser)	not specified [RCV004345208]	uncertain significance	19	48613132	48613132	Human		name
401889580	CV2758221	single nucleotide variant	NM_017708.4(FAM83E):c.154C>T (p.Arg52Cys)	not specified [RCV004341586]	uncertain significance	19	48613219	48613219	Human		name
405761254	CV3256631	single nucleotide variant	NM_017708.4(FAM83E):c.155G>A (p.Arg52His)	not specified [RCV004383513]	uncertain significance	19	48613218	48613218	Human		name
405761260	CV3256632	single nucleotide variant	NM_017708.4(FAM83E):c.186T>G (p.Asp62Glu)	not specified [RCV004383514]	uncertain significance	19	48613187	48613187	Human		name
597750454	CV3665786	single nucleotide variant	NM_017708.4(FAM83E):c.283G>A (p.Ala95Thr)	not specified [RCV004923537]	uncertain significance	19	48613090	48613090	Human		name
598238376	CV3962457	single nucleotide variant	NM_017708.4(FAM83E):c.178A>G (p.Ser60Gly)	not specified [RCV005343791]	uncertain significance	19	48613195	48613195	Human		name
598238416	CV3962465	single nucleotide variant	NM_017708.4(FAM83E):c.185A>G (p.Asp62Gly)	not specified [RCV005343798]	uncertain significance	19	48613188	48613188	Human		name
598238432	CV3962468	single nucleotide variant	NM_017708.4(FAM83E):c.134C>T (p.Ala45Val)	not specified [RCV005343801]	uncertain significance	19	48613239	48613239	Human		name
156030765	CV2243280	single nucleotide variant	NM_017708.4(FAM83E):c.992C>G (p.Pro331Arg)	not specified [RCV004110159]	uncertain significance	19	48603678	48603678	Human		name
155976456	CV2245988	single nucleotide variant	NM_017708.4(FAM83E):c.686G>A (p.Arg229Gln)	not specified [RCV004113912]	uncertain significance	19	48609948	48609948	Human		name
156218637	CV2253971	single nucleotide variant	NM_017708.4(FAM83E):c.676C>T (p.Arg226Cys)	not specified [RCV004127643]	uncertain significance	19	48609958	48609958	Human		name
156175502	CV2254665	single nucleotide variant	NM_017708.4(FAM83E):c.380G>A (p.Arg127Gln)	not specified [RCV004115152]	uncertain significance	19	48612993	48612993	Human		name
156192666	CV2255402	single nucleotide variant	NM_017708.4(FAM83E):c.685C>T (p.Arg229Trp)	not specified [RCV004117764]	uncertain significance	19	48609949	48609949	Human		name
156161965	CV2272643	single nucleotide variant	NM_017708.4(FAM83E):c.524A>G (p.Asp175Gly)	not specified [RCV004133522]	uncertain significance	19	48610789	48610789	Human		name
156162235	CV2311804	single nucleotide variant	NM_017708.4(FAM83E):c.401C>T (p.Pro134Leu)	not specified [RCV004170653]	uncertain significance	19	48612972	48612972	Human		name
156050186	CV2336577	single nucleotide variant	NM_017708.4(FAM83E):c.883C>T (p.Pro295Ser)	not specified [RCV004196825]	uncertain significance	19	48603787	48603787	Human		name
156265193	CV2364466	single nucleotide variant	NM_017708.4(FAM83E):c.845G>A (p.Arg282Gln)	not specified [RCV004216944]	uncertain significance	19	48603825	48603825	Human		name
156348122	CV2383044	single nucleotide variant	NM_017708.4(FAM83E):c.947G>A (p.Arg316His)	not specified [RCV004217625]	likely benign	19	48603723	48603723	Human		name
156392726	CV2386636	single nucleotide variant	NM_017708.4(FAM83E):c.952C>T (p.Arg318Cys)	not specified [RCV004230978]	likely benign	19	48603718	48603718	Human		name
156000476	CV2391754	single nucleotide variant	NM_017708.4(FAM83E):c.977C>T (p.Pro326Leu)	not specified [RCV004242289]	uncertain significance	19	48603693	48603693	Human		name
156057955	CV2396407	single nucleotide variant	NM_017708.4(FAM83E):c.940G>A (p.Val314Met)	not specified [RCV004242126]	uncertain significance	19	48603730	48603730	Human		name
329368320	CV2442701	single nucleotide variant	NM_017708.4(FAM83E):c.421C>T (p.Pro141Ser)	not specified [RCV004265046]	likely benign	19	48612952	48612952	Human		name
329367850	CV2457134	single nucleotide variant	NM_017708.4(FAM83E):c.730G>C (p.Gly244Arg)	not specified [RCV004264909]	uncertain significance	19	48609904	48609904	Human		name
329393137	CV2469247	single nucleotide variant	NM_017708.4(FAM83E):c.974C>T (p.Pro325Leu)	not specified [RCV004280588]	uncertain significance	19	48603696	48603696	Human		name
401727356	CV2684599	single nucleotide variant	NM_017708.4(FAM83E):c.379C>T (p.Arg127Trp)	not specified [RCV004293703]	uncertain significance	19	48612994	48612994	Human		name
401735639	CV2692160	single nucleotide variant	NM_017708.4(FAM83E):c.581C>G (p.Pro194Arg)	not specified [RCV004301859]	uncertain significance	19	48610732	48610732	Human		name
401754744	CV2715983	single nucleotide variant	NM_017708.4(FAM83E):c.937C>T (p.Arg313Cys)	not specified [RCV004323244]	uncertain significance	19	48603733	48603733	Human		name
401877953	CV2757717	single nucleotide variant	NM_017708.4(FAM83E):c.385C>A (p.Gln129Lys)	not specified [RCV004336870]	uncertain significance	19	48612988	48612988	Human		name
401871541	CV2759855	single nucleotide variant	NM_017708.4(FAM83E):c.629C>T (p.Thr210Met)	not specified [RCV004345289]	uncertain significance	19	48610684	48610684	Human		name
401885964	CV2770980	single nucleotide variant	NM_017708.4(FAM83E):c.331G>A (p.Val111Ile)	not specified [RCV004344000]	likely benign	19	48613042	48613042	Human		name
405761266	CV3256633	single nucleotide variant	NM_017708.4(FAM83E):c.439C>T (p.Arg147Trp)	not specified [RCV004383515]	uncertain significance	19	48612934	48612934	Human		name
407509168	CV3431933	single nucleotide variant	NM_017708.4(FAM83E):c.637G>A (p.Val213Met)	not specified [RCV004625631]	likely benign	19	48609997	48609997	Human		name
407509172	CV3431934	single nucleotide variant	NM_017708.4(FAM83E):c.464A>G (p.Lys155Arg)	not specified [RCV004625632]	uncertain significance	19	48612909	48612909	Human		name
597750440	CV3665783	single nucleotide variant	NM_017708.4(FAM83E):c.971C>T (p.Ser324Leu)	not specified [RCV004923534]	uncertain significance	19	48603699	48603699	Human		name
597750444	CV3665784	single nucleotide variant	NM_017708.4(FAM83E):c.743T>C (p.Ile248Thr)	not specified [RCV004923535]	uncertain significance	19	48609891	48609891	Human		name
597750449	CV3665785	single nucleotide variant	NM_017708.4(FAM83E):c.949C>T (p.Arg317Cys)	not specified [RCV004923536]	uncertain significance	19	48603721	48603721	Human		name
598238439	CV3958521	single nucleotide variant	NM_017708.4(FAM83E):c.608T>A (p.Leu203Gln)	not specified [RCV005343802]	uncertain significance	19	48610705	48610705	Human		name
598238444	CV3958522	single nucleotide variant	NM_017708.4(FAM83E):c.950G>A (p.Arg317His)	not specified [RCV005343803]	uncertain significance	19	48603720	48603720	Human		name
598238449	CV3958523	single nucleotide variant	NM_017708.4(FAM83E):c.533C>A (p.Thr178Lys)	not specified [RCV005343804]	uncertain significance	19	48610780	48610780	Human		name
598238456	CV3958524	single nucleotide variant	NM_017708.4(FAM83E):c.887C>T (p.Pro296Leu)	not specified [RCV005343805]	uncertain significance	19	48603783	48603783	Human		name
598195297	CV3962461	single nucleotide variant	NM_017708.4(FAM83E):c.773A>G (p.Asp258Gly)	not specified [RCV005335547]	uncertain significance	19	48603897	48603897	Human		name
598238404	CV3962463	single nucleotide variant	NM_017708.4(FAM83E):c.644T>C (p.Val215Ala)	not specified [RCV005343796]	uncertain significance	19	48609990	48609990	Human		name
598238421	CV3962466	single nucleotide variant	NM_017708.4(FAM83E):c.538C>T (p.Arg180Cys)	not specified [RCV005343799]	uncertain significance	19	48610775	48610775	Human		name
598238427	CV3962467	single nucleotide variant	NM_017708.4(FAM83E):c.389T>G (p.Leu130Arg)	not specified [RCV005343800]	uncertain significance	19	48612984	48612984	Human		name
156185369	CV2195559	single nucleotide variant	NM_017708.4(FAM83E):c.1114C>T (p.Arg372Cys)	not specified [RCV004082773]	uncertain significance	19	48603556	48603556	Human		name
156110585	CV2387665	single nucleotide variant	NM_017708.4(FAM83E):c.1306G>A (p.Ala436Thr)	not specified [RCV004234210]	uncertain significance	19	48601240	48601240	Human		name
156225186	CV2399588	single nucleotide variant	NM_017708.4(FAM83E):c.1090A>C (p.Ser364Arg)	not specified [RCV004244108]	uncertain significance	19	48603580	48603580	Human		name
329366296	CV2438332	single nucleotide variant	NM_017708.4(FAM83E):c.1166G>C (p.Gly389Ala)	not specified [RCV004257082]	uncertain significance	19	48603504	48603504	Human		name
401748774	CV2709563	single nucleotide variant	NM_017708.4(FAM83E):c.1337G>C (p.Arg446Pro)	not specified [RCV004318795]	uncertain significance	19	48601209	48601209	Human		name
405761210	CV3256624	single nucleotide variant	NM_017708.4(FAM83E):c.1003C>T (p.Arg335Cys)	not specified [RCV004383506]	uncertain significance	19	48603667	48603667	Human		name
405761216	CV3256625	single nucleotide variant	NM_017708.4(FAM83E):c.1012G>C (p.Ala338Pro)	not specified [RCV004383507]	uncertain significance	19	48603658	48603658	Human		name
405761222	CV3256626	single nucleotide variant	NM_017708.4(FAM83E):c.1093G>A (p.Gly365Ser)	not specified [RCV004383508]	uncertain significance	19	48603577	48603577	Human		name
405761230	CV3256627	single nucleotide variant	NM_017708.4(FAM83E):c.1115G>A (p.Arg372His)	not specified [RCV004383509]	uncertain significance	19	48603555	48603555	Human		name
405761236	CV3256628	single nucleotide variant	NM_017708.4(FAM83E):c.1294C>A (p.Pro432Thr)	not specified [RCV004383510]	uncertain significance	19	48601252	48601252	Human		name
405761241	CV3256629	single nucleotide variant	NM_017708.4(FAM83E):c.1318C>T (p.Arg440Cys)	not specified [RCV004383511]	uncertain significance	19	48601228	48601228	Human		name
405761247	CV3256630	single nucleotide variant	NM_017708.4(FAM83E):c.1342C>T (p.Arg448Trp)	not specified [RCV004383512]	uncertain significance	19	48601204	48601204	Human		name
407509180	CV3431936	single nucleotide variant	NM_017708.4(FAM83E):c.1043C>G (p.Pro348Arg)	not specified [RCV004625634]	uncertain significance	19	48603627	48603627	Human		name
407509187	CV3431938	single nucleotide variant	NM_017708.4(FAM83E):c.1232G>A (p.Arg411Gln)	not specified [RCV004625636]	uncertain significance	19	48601314	48601314	Human		name
407509194	CV3431940	single nucleotide variant	NM_017708.4(FAM83E):c.1078G>A (p.Ala360Thr)	not specified [RCV004625638]	uncertain significance	19	48603592	48603592	Human		name
597750458	CV3665787	single nucleotide variant	NM_017708.4(FAM83E):c.1268C>A (p.Ser423Tyr)	not specified [RCV004923538]	uncertain significance	19	48601278	48601278	Human		name
597750466	CV3665789	single nucleotide variant	NM_017708.4(FAM83E):c.1424G>T (p.Gly475Val)	not specified [RCV004923540]	uncertain significance	19	48601122	48601122	Human		name
598238382	CV3962458	single nucleotide variant	NM_017708.4(FAM83E):c.1273C>T (p.Pro425Ser)	not specified [RCV005343792]	uncertain significance	19	48601273	48601273	Human		name
598238387	CV3962459	single nucleotide variant	NM_017708.4(FAM83E):c.1231C>T (p.Arg411Trp)	not specified [RCV005343793]	uncertain significance	19	48601315	48601315	Human		name
598238393	CV3962460	single nucleotide variant	NM_017708.4(FAM83E):c.1270C>G (p.Arg424Gly)	not specified [RCV005343794]	uncertain significance	19	48601276	48601276	Human		name
598238399	CV3962462	single nucleotide variant	NM_017708.4(FAM83E):c.1199A>G (p.Lys400Arg)	not specified [RCV005343795]	uncertain significance	19	48601347	48601347	Human		name
8636914	CV92139	single nucleotide variant	NM_017708.3(FAM83E):c.1174G>A (p.Glu392Lys)	Malignant melanoma [RCV000072237]	not provided	19	48603496	48603496	Human		name

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