Fam83e Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

79 records found for search term Fam83e

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message