Asb11 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 Asb11

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401931068	CV2823916	single nucleotide variant	NM_080873.3(ASB11):c.847+6C>A	not provided [RCV003441034]	likely benign	X	15287875	15287875	Human		name
405675183	CV3286696	single nucleotide variant	NM_080873.3(ASB11):c.14C>T (p.Pro5Leu)	not specified [RCV004420504]	uncertain significance	X	15315592	15315592	Human		name
156021778	CV2264494	single nucleotide variant	NM_080873.3(ASB11):c.59C>T (p.Thr20Met)	not specified [RCV004138386]	uncertain significance	X	15315547	15315547	Human		name
329388142	CV2437122	single nucleotide variant	NM_080873.3(ASB11):c.42T>G (p.Phe14Leu)	not specified [RCV004262929]	uncertain significance	X	15315564	15315564	Human		name
401931070	CV2823917	single nucleotide variant	NM_080873.3(ASB11):c.684G>A (p.Leu228=)	not provided [RCV003441035]	likely benign	X	15288044	15288044	Human		name
405675187	CV3286697	single nucleotide variant	NM_080873.3(ASB11):c.40T>C (p.Phe14Leu)	not specified [RCV004420505]	uncertain significance	X	15315566	15315566	Human		name
41407376	CV982285	single nucleotide variant	NM_080873.3(ASB11):c.306C>G (p.Leu102=)	not provided [RCV001810676]	uncertain significance	X	15297637	15297637	Human		name
156001276	CV2296394	single nucleotide variant	NM_080873.3(ASB11):c.116A>G (p.Tyr39Cys)	not specified [RCV004148142]	uncertain significance	X	15315490	15315490	Human		name
405675179	CV3286695	single nucleotide variant	NM_080873.3(ASB11):c.121G>A (p.Val41Ile)	not specified [RCV004420503]	uncertain significance	X	15315485	15315485	Human		name
598215563	CV3905548	single nucleotide variant	NM_080873.3(ASB11):c.202C>T (p.Pro68Ser)	not specified [RCV005271721]	uncertain significance	X	15302787	15302787	Human		name
155959679	CV2193981	single nucleotide variant	NM_080873.3(ASB11):c.874C>T (p.Arg292Cys)	not specified [RCV004074706]	uncertain significance	X	15283603	15283603	Human		name
155919923	CV2209785	single nucleotide variant	NM_080873.3(ASB11):c.886C>T (p.Arg296Trp)	not specified [RCV004076257]	uncertain significance	X	15283591	15283591	Human		name
155940019	CV2221920	single nucleotide variant	NM_080873.3(ASB11):c.341C>G (p.Ala114Gly)	not specified [RCV004102932]	uncertain significance	X	15297602	15297602	Human		name
156153826	CV2242177	single nucleotide variant	NM_080873.3(ASB11):c.379G>A (p.Val127Met)	not specified [RCV004109390]	uncertain significance	X	15293311	15293311	Human		name
156210203	CV2259790	single nucleotide variant	NM_080873.3(ASB11):c.460G>A (p.Gly154Arg)	not specified [RCV004117066]	uncertain significance	X	15293230	15293230	Human		name
156243393	CV2306768	single nucleotide variant	NM_080873.3(ASB11):c.803C>T (p.Ala268Val)	not specified [RCV004159347]	uncertain significance	X	15287925	15287925	Human		name
156290897	CV2324949	single nucleotide variant	NM_080873.3(ASB11):c.688A>T (p.Thr230Ser)	not specified [RCV004175205]	uncertain significance	X	15288040	15288040	Human		name
156120414	CV2354164	single nucleotide variant	NM_080873.3(ASB11):c.767G>A (p.Arg256His)	not provided [RCV004695659]\|not specified [RCV004206598]	uncertain significance	X	15287961	15287961	Human		name
329374496	CV2443754	single nucleotide variant	NM_080873.3(ASB11):c.965A>G (p.Tyr322Cys)	not specified [RCV004256053]	uncertain significance	X	15283512	15283512	Human		name
329401933	CV2457999	single nucleotide variant	NM_080873.3(ASB11):c.841C>T (p.Arg281Cys)	not specified [RCV004271573]	uncertain significance	X	15287887	15287887	Human		name
401931071	CV2823918	single nucleotide variant	NM_080873.3(ASB11):c.494C>T (p.Ser165Leu)	not provided [RCV003441036]	likely benign	X	15293196	15293196	Human		name
405675461	CV3286698	single nucleotide variant	NM_080873.3(ASB11):c.589G>A (p.Gly197Arg)	not specified [RCV004420506]	uncertain significance	X	15289570	15289570	Human		name
405675194	CV3286699	single nucleotide variant	NM_080873.3(ASB11):c.767G>T (p.Arg256Leu)	not specified [RCV004420507]	likely benign	X	15287961	15287961	Human		name
405675199	CV3286700	single nucleotide variant	NM_080873.3(ASB11):c.820G>A (p.Val274Met)	not specified [RCV004420508]	uncertain significance	X	15287908	15287908	Human		name
407492193	CV3476803	single nucleotide variant	NM_080873.3(ASB11):c.488T>C (p.Leu163Pro)	not specified [RCV004667050]	uncertain significance	X	15293202	15293202	Human		name
597686405	CV3593998	single nucleotide variant	NM_080873.3(ASB11):c.433G>A (p.Ala145Thr)	not specified [RCV004858380]	uncertain significance	X	15293257	15293257	Human		name
597686495	CV3594022	single nucleotide variant	NM_080873.3(ASB11):c.875G>T (p.Arg292Leu)	not specified [RCV004858390]	uncertain significance	X	15283602	15283602	Human		name
597686545	CV3594032	single nucleotide variant	NM_080873.3(ASB11):c.868C>T (p.Leu290Phe)	not specified [RCV004858395]	uncertain significance	X	15283609	15283609	Human		name
598215546	CV3905544	single nucleotide variant	NM_080873.3(ASB11):c.529G>A (p.Glu177Lys)	not specified [RCV005271717]	uncertain significance	X	15289630	15289630	Human		name
598215573	CV3905550	single nucleotide variant	NM_080873.3(ASB11):c.958C>T (p.Leu320Phe)	not specified [RCV005271723]	uncertain significance	X	15283519	15283519	Human		name
598215580	CV3905551	single nucleotide variant	NM_080873.3(ASB11):c.443A>T (p.Asn148Ile)	not specified [RCV005271724]	uncertain significance	X	15293247	15293247	Human		name
598215601	CV3905555	single nucleotide variant	NM_080873.3(ASB11):c.776C>G (p.Ala259Gly)	not specified [RCV005271728]	uncertain significance	X	15287952	15287952	Human		name
15181205	CV717693	single nucleotide variant	NM_080873.3(ASB11):c.745G>A (p.Asp249Asn)	not provided [RCV000974335]	benign	X	15287983	15287983	Human		name
15130471	CV717694	single nucleotide variant	NM_080873.3(ASB11):c.622A>T (p.Arg208Trp)	not provided [RCV000964441]	benign	X	15289537	15289537	Human		name
39457121	CV965871	single nucleotide variant	NM_080873.3(ASB11):c.871T>C (p.Cys291Arg)	not specified [RCV001255481]	uncertain significance	X	15283606	15283606	Human		name
150411055	CV1196331	deletion	NM_080873.3(ASB11):c.287_290del (p.Ile96fs)	not provided [RCV001573458]	uncertain significance	X	15297653	15297656	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