Angptl6 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

62 records found for search term Angptl6

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15199871	CV756593	single nucleotide variant	NM_031917.3(ANGPTL6):c.15G>A (p.Trp5Ter)	not provided [RCV000912679]	likely benign	19	10096549	10096549	Human		name
405655069	CV3276836	single nucleotide variant	NM_031917.3(ANGPTL6):c.71C>A (p.Ala24Asp)	not specified [RCV004415181]	uncertain significance	19	10096493	10096493	Human		name
598236199	CV3973010	single nucleotide variant	NM_031917.3(ANGPTL6):c.29A>G (p.Gln10Arg)	not specified [RCV005363800]	uncertain significance	19	10096535	10096535	Human		name
15203419	CV756592	single nucleotide variant	NM_031917.3(ANGPTL6):c.426C>T (p.Arg142=)	not provided [RCV000913971]	likely benign	19	10096138	10096138	Human		name
15198042	CV772273	single nucleotide variant	NM_031917.3(ANGPTL6):c.369C>G (p.Gly123=)	not provided [RCV000934690]	likely benign	19	10096195	10096195	Human		name
329360271	CV2458662	single nucleotide variant	NM_031917.3(ANGPTL6):c.193C>A (p.Leu65Met)	not specified [RCV004268330]	uncertain significance	19	10096371	10096371	Human		name
401780105	CV2725875	single nucleotide variant	NM_031917.3(ANGPTL6):c.232G>C (p.Glu78Gln)	not specified [RCV004324259]	uncertain significance	19	10096332	10096332	Human		name
401884972	CV2771103	single nucleotide variant	NM_031917.3(ANGPTL6):c.205G>C (p.Val69Leu)	not specified [RCV004346107]	uncertain significance	19	10096359	10096359	Human		name
401908424	CV2811548	single nucleotide variant	NM_031917.3(ANGPTL6):c.287T>C (p.Leu96Pro)	not provided [RCV003423323]	benign	19	10096277	10096277	Human		name
405654952	CV3276793	single nucleotide variant	NM_031917.3(ANGPTL6):c.152G>A (p.Arg51Gln)	not specified [RCV004415138]	uncertain significance	19	10096412	10096412	Human		name
405654979	CV3276803	single nucleotide variant	NM_031917.3(ANGPTL6):c.230G>A (p.Arg77His)	not specified [RCV004415148]	uncertain significance	19	10096334	10096334	Human		name
407518126	CV3449897	single nucleotide variant	NM_031917.3(ANGPTL6):c.260G>A (p.Gly87Asp)	not specified [RCV004628761]	uncertain significance	19	10096304	10096304	Human		name
407518146	CV3449918	single nucleotide variant	NM_031917.3(ANGPTL6):c.196C>T (p.Arg66Cys)	not specified [RCV004628767]	uncertain significance	19	10096368	10096368	Human		name
596946560	CV3548352	single nucleotide variant	NM_031917.3(ANGPTL6):c.1383C>T (p.Ala461=)	not provided [RCV004810178]	likely benign	19	10092619	10092619	Human		name
597643184	CV3693062	single nucleotide variant	NM_031917.3(ANGPTL6):c.191C>T (p.Ala64Val)	not specified [RCV004942018]	uncertain significance	19	10096373	10096373	Human		name
597643478	CV3693115	single nucleotide variant	NM_031917.3(ANGPTL6):c.175G>A (p.Ala59Thr)	not specified [RCV004942041]	uncertain significance	19	10096389	10096389	Human		name
598236179	CV3973001	single nucleotide variant	NM_031917.3(ANGPTL6):c.115A>G (p.Thr39Ala)	not specified [RCV005363796]	uncertain significance	19	10096449	10096449	Human		name
598270456	CV3973023	single nucleotide variant	NM_031917.3(ANGPTL6):c.155C>T (p.Ala52Val)	not specified [RCV005350111]	uncertain significance	19	10096409	10096409	Human		name
15099407	CV704696	single nucleotide variant	NM_031917.3(ANGPTL6):c.1104C>T (p.Pro368=)	not provided [RCV000958757]	benign	19	10093467	10093467	Human		name
156193731	CV2146466	single nucleotide variant	NM_031917.3(ANGPTL6):c.404C>G (p.Ala135Gly)	not provided [RCV003006087]	uncertain significance	19	10096160	10096160	Human		name
155924479	CV2211558	single nucleotide variant	NM_031917.3(ANGPTL6):c.371C>T (p.Pro124Leu)	not specified [RCV004084463]	uncertain significance	19	10096193	10096193	Human		name
156074613	CV2230076	single nucleotide variant	NM_031917.3(ANGPTL6):c.439T>C (p.Ser147Pro)	not specified [RCV004099731]	uncertain significance	19	10096125	10096125	Human		name
156255377	CV2264726	single nucleotide variant	NM_031917.3(ANGPTL6):c.502G>A (p.Ala168Thr)	not specified [RCV004132712]	uncertain significance	19	10096062	10096062	Human		name
156093208	CV2300202	single nucleotide variant	NM_031917.3(ANGPTL6):c.502G>C (p.Ala168Pro)	not specified [RCV004151389]	uncertain significance	19	10096062	10096062	Human		name
156050091	CV2336571	single nucleotide variant	NM_031917.3(ANGPTL6):c.446A>C (p.Glu149Ala)	not specified [RCV004196819]	uncertain significance	19	10096118	10096118	Human		name
156033567	CV2376602	single nucleotide variant	NM_031917.3(ANGPTL6):c.790C>T (p.Arg264Cys)	not specified [RCV004222808]	uncertain significance	19	10093854	10093854	Human		name
156087632	CV2388191	single nucleotide variant	NM_031917.3(ANGPTL6):c.301C>G (p.Arg101Gly)	not specified [RCV004234653]	uncertain significance	19	10096263	10096263	Human		name
329376992	CV2435770	single nucleotide variant	NM_031917.3(ANGPTL6):c.299G>A (p.Ser100Asn)	not provided [RCV004696346]\|not specified [RCV004253398]	uncertain significance	19	10096265	10096265	Human		name
329366075	CV2438073	single nucleotide variant	NM_031917.3(ANGPTL6):c.965G>A (p.Arg322Gln)	not specified [RCV004256861]	likely benign	19	10093606	10093606	Human		name
329389526	CV2445200	single nucleotide variant	NM_031917.3(ANGPTL6):c.623G>A (p.Arg208His)	not specified [RCV004263835]	uncertain significance	19	10094898	10094898	Human		name
329386822	CV2452568	single nucleotide variant	NM_031917.3(ANGPTL6):c.493C>T (p.Arg165Cys)	not specified [RCV004273152]	uncertain significance	19	10096071	10096071	Human		name
401861083	CV2758741	single nucleotide variant	NM_031917.3(ANGPTL6):c.382C>G (p.Leu128Val)	not specified [RCV004337801]	uncertain significance	19	10096182	10096182	Human		name
405295372	CV3204520	single nucleotide variant	NM_031917.3(ANGPTL6):c.392A>T (p.Glu131Val)	ANGPTL6-related disorder [RCV003937318]	likely benign	19	10096172	10096172	Human		name , trait , alternate_id
405654997	CV3276810	single nucleotide variant	NM_031917.3(ANGPTL6):c.305G>A (p.Gly102Asp)	not specified [RCV004415155]	uncertain significance	19	10096259	10096259	Human		name
405655014	CV3276816	single nucleotide variant	NM_031917.3(ANGPTL6):c.404C>A (p.Ala135Glu)	not specified [RCV004415161]	uncertain significance	19	10096160	10096160	Human		name
405655077	CV3276839	single nucleotide variant	NM_031917.3(ANGPTL6):c.781G>A (p.Ala261Thr)	not specified [RCV004415184]	uncertain significance	19	10093863	10093863	Human		name
407502790	CV3449886	single nucleotide variant	NM_031917.3(ANGPTL6):c.307C>A (p.Leu103Met)	not specified [RCV004645265]	uncertain significance	19	10096257	10096257	Human		name
407518136	CV3449907	single nucleotide variant	NM_031917.3(ANGPTL6):c.714G>T (p.Met238Ile)	not specified [RCV004628764]	uncertain significance	19	10094807	10094807	Human		name
597643220	CV3693070	single nucleotide variant	NM_031917.3(ANGPTL6):c.743C>T (p.Ala248Val)	not specified [RCV004942024]	uncertain significance	19	10094778	10094778	Human		name
597643448	CV3693086	single nucleotide variant	NM_031917.3(ANGPTL6):c.300C>G (p.Ser100Arg)	not specified [RCV004942036]	uncertain significance	19	10096264	10096264	Human		name
598236146	CV3972987	single nucleotide variant	NM_031917.3(ANGPTL6):c.400G>T (p.Ala134Ser)	not specified [RCV005363789]	uncertain significance	19	10096164	10096164	Human		name
598235991	CV3976439	single nucleotide variant	NM_031917.3(ANGPTL6):c.472C>T (p.His158Tyr)	not specified [RCV005363761]	uncertain significance	19	10096092	10096092	Human		name
598236017	CV3976448	single nucleotide variant	NM_031917.3(ANGPTL6):c.617C>T (p.Pro206Leu)	not specified [RCV005363766]	uncertain significance	19	10094904	10094904	Human		name
598236048	CV3976459	single nucleotide variant	NM_031917.3(ANGPTL6):c.539G>A (p.Arg180His)	not specified [RCV005363772]	uncertain significance	19	10096025	10096025	Human		name
598236123	CV3976478	single nucleotide variant	NM_031917.3(ANGPTL6):c.536C>A (p.Ala179Asp)	not specified [RCV005363784]	uncertain significance	19	10096028	10096028	Human		name
156163002	CV2246582	single nucleotide variant	NM_031917.3(ANGPTL6):c.1111G>A (p.Asp371Asn)	not specified [RCV004110329]	uncertain significance	19	10093460	10093460	Human		name
156078775	CV2300854	single nucleotide variant	NM_031917.3(ANGPTL6):c.1291G>A (p.Val431Met)	not specified [RCV004158059]	uncertain significance	19	10092711	10092711	Human		name
155961279	CV2311887	single nucleotide variant	NM_031917.3(ANGPTL6):c.1179C>G (p.Asp393Glu)	not specified [RCV004170721]	uncertain significance	19	10093392	10093392	Human		name
155905678	CV2357161	single nucleotide variant	NM_031917.3(ANGPTL6):c.1316G>A (p.Arg439Gln)	not specified [RCV004206949]	uncertain significance	19	10092686	10092686	Human		name
329370840	CV2435703	single nucleotide variant	NM_031917.3(ANGPTL6):c.1063C>T (p.Arg355Cys)	not specified [RCV004254936]	uncertain significance	19	10093508	10093508	Human		name
401749680	CV2710894	single nucleotide variant	NM_031917.3(ANGPTL6):c.1363G>A (p.Ala455Thr)	not specified [RCV004308803]	uncertain significance	19	10092639	10092639	Human		name
401770229	CV2715089	single nucleotide variant	NM_031917.3(ANGPTL6):c.1076C>G (p.Ala359Gly)	not specified [RCV004322674]	uncertain significance	19	10093495	10093495	Human		name
401775053	CV2723965	single nucleotide variant	NM_031917.3(ANGPTL6):c.1019G>A (p.Arg340His)	not specified [RCV004326125]	uncertain significance	19	10093552	10093552	Human		name
401902707	CV2799525	single nucleotide variant	NM_031917.3(ANGPTL6):c.1115A>C (p.His372Pro)	ANGPTL6-related disorder [RCV003419015]\|not specified [RCV004935327]	uncertain significance	19	10093456	10093456	Human		name , trait , alternate_id
401928478	CV2811547	single nucleotide variant	NM_031917.3(ANGPTL6):c.1072C>T (p.Arg358Cys)	not provided [RCV003406840]	benign	19	10093499	10093499	Human		name
405654931	CV3276786	single nucleotide variant	NM_031917.3(ANGPTL6):c.1120C>T (p.Arg374Cys)	not specified [RCV004415131]	uncertain significance	19	10093451	10093451	Human		name
407502770	CV3449878	single nucleotide variant	NM_031917.3(ANGPTL6):c.1208G>A (p.Arg403Gln)	not specified [RCV004645259]	uncertain significance	19	10093363	10093363	Human		name
597643430	CV3693081	single nucleotide variant	NM_031917.3(ANGPTL6):c.1045C>A (p.Leu349Met)	not specified [RCV004942033]	uncertain significance	19	10093526	10093526	Human		name
597796173	CV3693096	single nucleotide variant	NM_031917.3(ANGPTL6):c.1364C>T (p.Ala455Val)	not specified [RCV004935013]	uncertain significance	19	10092638	10092638	Human		name
597643491	CV3693127	single nucleotide variant	NM_031917.3(ANGPTL6):c.1258T>C (p.Tyr420His)	not specified [RCV004942043]	uncertain significance	19	10092744	10092744	Human		name
598270425	CV3972993	single nucleotide variant	NM_031917.3(ANGPTL6):c.1088G>T (p.Gly363Val)	not specified [RCV005350102]	uncertain significance	19	10093483	10093483	Human		name
598236226	CV3973016	single nucleotide variant	NM_031917.3(ANGPTL6):c.1055G>C (p.Trp352Ser)	not specified [RCV005363805]	uncertain significance	19	10093516	10093516	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