Ruvbl2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

36 records found for search term Ruvbl2

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598233938	CV3910093	single nucleotide variant	NM_006666.3(RUVBL2):c.5C>T (p.Ala2Val)	not specified [RCV005274957]	uncertain significance	19	48993916	48993916	Human		name
597733747	CV3597642	single nucleotide variant	NM_006666.3(RUVBL2):c.22A>G (p.Thr8Ala)	not specified [RCV004863357]	uncertain significance	19	48999328	48999328	Human		name
401876465	CV2761067	single nucleotide variant	NM_006666.3(RUVBL2):c.32C>T (p.Pro11Leu)	not specified [RCV004338729]	uncertain significance	19	48999338	48999338	Human		name
401888936	CV2761577	single nucleotide variant	NM_006666.3(RUVBL2):c.41G>A (p.Arg14His)	not specified [RCV004337206]	uncertain significance	19	48999347	48999347	Human		name
401929067	CV2818554	single nucleotide variant	NM_006666.3(RUVBL2):c.645C>T (p.Tyr215=)	not provided [RCV003407065]	likely benign	19	49010048	49010048	Human		name
15120644	CV716589	single nucleotide variant	NM_006666.3(RUVBL2):c.639C>T (p.Arg213=)	not provided [RCV000962754]	benign	19	49010042	49010042	Human		name
15157960	CV728327	single nucleotide variant	NM_006666.3(RUVBL2):c.852C>T (p.Arg284=)	not provided [RCV000880917]	benign	19	49011063	49011063	Human		name
15197281	CV757167	single nucleotide variant	NM_006666.3(RUVBL2):c.567C>T (p.Ala189=)	not provided [RCV000911932]	benign	19	49009880	49009880	Human		name
156143184	CV2200073	single nucleotide variant	NM_006666.3(RUVBL2):c.106G>A (p.Ala36Thr)	not specified [RCV004069655]	uncertain significance	19	49003317	49003317	Human		name
405700912	CV3310009	single nucleotide variant	NM_006666.3(RUVBL2):c.172G>A (p.Val58Met)	not specified [RCV004447087]	uncertain significance	19	49004325	49004325	Human		name
597733771	CV3597646	single nucleotide variant	NM_006666.3(RUVBL2):c.161G>A (p.Arg54Gln)	not specified [RCV004863361]	uncertain significance	19	49004314	49004314	Human		name
15183521	CV728328	single nucleotide variant	NM_006666.3(RUVBL2):c.1203C>T (p.Tyr401=)	not provided [RCV000886243]	benign	19	49015102	49015102	Human		name
156253613	CV2193096	single nucleotide variant	NM_006666.3(RUVBL2):c.307A>G (p.Ile103Val)	not specified [RCV004071102]	uncertain significance	19	49007059	49007059	Human		name
156176829	CV2327134	single nucleotide variant	NM_006666.3(RUVBL2):c.452C>A (p.Ala151Glu)	not specified [RCV004178699]	uncertain significance	19	49007358	49007358	Human		name
156184463	CV2335596	single nucleotide variant	NM_006666.3(RUVBL2):c.389G>A (p.Arg130His)	not specified [RCV004193801]	uncertain significance	19	49007141	49007141	Human		name
156105269	CV2361180	single nucleotide variant	NM_006666.3(RUVBL2):c.704G>A (p.Arg235His)	not provided [RCV004695713]\|not specified [RCV004216365]	uncertain significance	19	49010528	49010528	Human		name
156169165	CV2373867	single nucleotide variant	NM_006666.3(RUVBL2):c.975C>G (p.Ile325Met)	not specified [RCV004224800]	uncertain significance	19	49011284	49011284	Human		name
329368929	CV2424699	single nucleotide variant	NM_006666.3(RUVBL2):c.758G>A (p.Arg253His)	not specified [RCV004248595]	uncertain significance	19	49010582	49010582	Human		name
405700917	CV3310010	single nucleotide variant	NM_006666.3(RUVBL2):c.451G>A (p.Ala151Thr)	not specified [RCV004447088]	uncertain significance	19	49007357	49007357	Human		name
405700923	CV3310011	single nucleotide variant	NM_006666.3(RUVBL2):c.814G>A (p.Val272Ile)	not specified [RCV004447089]	uncertain significance	19	49011025	49011025	Human		name
407514134	CV3473224	single nucleotide variant	NM_006666.3(RUVBL2):c.745G>A (p.Val249Ile)	not specified [RCV004674386]	uncertain significance	19	49010569	49010569	Human		name
597733731	CV3597639	single nucleotide variant	NM_006666.3(RUVBL2):c.620G>A (p.Arg207His)	not specified [RCV004863354]	uncertain significance	19	49010023	49010023	Human		name
597733737	CV3597640	single nucleotide variant	NM_006666.3(RUVBL2):c.673G>A (p.Val225Met)	not specified [RCV004863355]	uncertain significance	19	49010497	49010497	Human		name
597733760	CV3597644	single nucleotide variant	NM_006666.3(RUVBL2):c.496A>G (p.Thr166Ala)	not specified [RCV004863359]	uncertain significance	19	49009809	49009809	Human		name
597733766	CV3597645	single nucleotide variant	NM_006666.3(RUVBL2):c.776C>T (p.Ala259Val)	not specified [RCV004863360]	uncertain significance	19	49010600	49010600	Human		name
597733777	CV3597647	single nucleotide variant	NM_006666.3(RUVBL2):c.411C>G (p.Ile137Met)	not specified [RCV004863362]	uncertain significance	19	49007317	49007317	Human		name
597733782	CV3597648	single nucleotide variant	NM_006666.3(RUVBL2):c.602A>G (p.Lys201Arg)	not specified [RCV004863363]	uncertain significance	19	49010005	49010005	Human		name
598233958	CV3910096	single nucleotide variant	NM_006666.3(RUVBL2):c.446G>A (p.Arg149Gln)	not specified [RCV005274960]	uncertain significance	19	49007352	49007352	Human		name
155934912	CV2225447	single nucleotide variant	NM_006666.3(RUVBL2):c.1372G>A (p.Glu458Lys)	not specified [RCV004100846]	uncertain significance	19	49015822	49015822	Human		name
156242552	CV2347007	single nucleotide variant	NM_006666.3(RUVBL2):c.1240C>T (p.Arg414Trp)	not specified [RCV004204495]	uncertain significance	19	49015139	49015139	Human		name
156105231	CV2387006	single nucleotide variant	NM_006666.3(RUVBL2):c.1198C>T (p.Arg400Cys)	not specified [RCV004226758]	uncertain significance	19	49015097	49015097	Human		name
329369335	CV2424792	single nucleotide variant	NM_006666.3(RUVBL2):c.1114C>T (p.Arg372Cys)	not specified [RCV004248682]	uncertain significance	19	49014596	49014596	Human		name
329356811	CV2431157	single nucleotide variant	NM_006666.3(RUVBL2):c.1087A>T (p.Ser363Cys)	not specified [RCV004250508]	uncertain significance	19	49014569	49014569	Human		name
597733754	CV3597643	single nucleotide variant	NM_006666.3(RUVBL2):c.1007G>A (p.Arg336Gln)	not specified [RCV004863358]	uncertain significance	19	49014489	49014489	Human		name
598233944	CV3910094	single nucleotide variant	NM_006666.3(RUVBL2):c.1100C>T (p.Thr367Met)	not specified [RCV005274958]	uncertain significance	19	49014582	49014582	Human		name
598233951	CV3910095	single nucleotide variant	NM_006666.3(RUVBL2):c.1358A>G (p.Asn453Ser)	not specified [RCV005274959]	uncertain significance	19	49015678	49015678	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