Csnk1g3 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

26 records found for search term Csnk1g3

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405272655	CV3210154	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1186-6A>G	CSNK1G3-related disorder [RCV003914399]	benign	5	123604718	123604718	Human		name , trait , alternate_id
405287339	CV3220693	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1186-4A>G	CSNK1G3-related disorder [RCV003959840]	likely benign	5	123604720	123604720	Human		name , trait , alternate_id
405687309	CV3236278	single nucleotide variant	NM_001364140.2(CSNK1G3):c.17A>G (p.Lys6Arg)	not specified [RCV004372602]	uncertain significance	5	123545680	123545680	Human		name
597805077	CV3654706	single nucleotide variant	NM_001364140.2(CSNK1G3):c.65C>T (p.Ser22Leu)	not specified [RCV004908278]	uncertain significance	5	123545728	123545728	Human		name
598218990	CV3959414	single nucleotide variant	NM_001364140.2(CSNK1G3):c.98C>T (p.Ser33Leu)	not specified [RCV005317325]	uncertain significance	5	123545761	123545761	Human		name
401866092	CV2786156	single nucleotide variant	NM_001364140.2(CSNK1G3):c.193A>T (p.Thr65Ser)	not specified [RCV004359962]	uncertain significance	5	123553121	123553121	Human		name
405281986	CV3216210	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1353C>T (p.Thr451=)	CSNK1G3-related disorder [RCV003956733]	likely benign	5	123614378	123614378	Human		name , trait , alternate_id
405278682	CV3216737	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1179G>A (p.Ser393=)	CSNK1G3-related disorder [RCV003954616]	likely benign	5	123595128	123595128	Human		name , trait , alternate_id
407465413	CV3430010	single nucleotide variant	NM_001364140.2(CSNK1G3):c.134T>C (p.Val45Ala)	not specified [RCV004613697]	uncertain significance	5	123545797	123545797	Human		name
155978087	CV2246985	single nucleotide variant	NM_001364140.2(CSNK1G3):c.584C>T (p.Pro195Leu)	not specified [RCV004112769]	uncertain significance	5	123575874	123575874	Human		name
155918686	CV2279270	single nucleotide variant	NM_001364140.2(CSNK1G3):c.335A>G (p.Asn112Ser)	not specified [RCV004139791]	uncertain significance	5	123573438	123573438	Human		name
155968963	CV2337898	single nucleotide variant	NM_001364140.2(CSNK1G3):c.805C>T (p.Arg269Trp)	not specified [RCV004183906]	uncertain significance	5	123588472	123588472	Human		name
156031726	CV2376398	single nucleotide variant	NM_001364140.2(CSNK1G3):c.940G>A (p.Asp314Asn)	not specified [RCV004220586]	uncertain significance	5	123590505	123590505	Human		name
156042915	CV2387901	single nucleotide variant	NM_001364140.2(CSNK1G3):c.398C>T (p.Thr133Ile)	not specified [RCV004236450]	uncertain significance	5	123573501	123573501	Human		name
405687315	CV3236279	single nucleotide variant	NM_001364140.2(CSNK1G3):c.305T>C (p.Val102Ala)	not specified [RCV004372603]	uncertain significance	5	123573408	123573408	Human		name
407465409	CV3430009	single nucleotide variant	NM_001364140.2(CSNK1G3):c.446G>A (p.Arg149His)	not specified [RCV004613696]	uncertain significance	5	123575736	123575736	Human		name
407465417	CV3430011	single nucleotide variant	NM_001364140.2(CSNK1G3):c.582T>A (p.Asp194Glu)	not specified [RCV004613698]	uncertain significance	5	123575872	123575872	Human		name
407465421	CV3430012	single nucleotide variant	NM_001364140.2(CSNK1G3):c.907G>C (p.Asp303His)	not specified [RCV004613699]	uncertain significance	5	123590472	123590472	Human		name
598218999	CV3959415	single nucleotide variant	NM_001364140.2(CSNK1G3):c.953A>G (p.Tyr318Cys)	not specified [RCV005317326]	uncertain significance	5	123590518	123590518	Human		name
156397512	CV2200627	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1010C>G (p.Ala337Gly)	not specified [RCV004078964]	uncertain significance	5	123591335	123591335	Human		name
156140724	CV2247123	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1196C>T (p.Ser399Phe)	not specified [RCV004114657]	uncertain significance	5	123604734	123604734	Human		name
156301103	CV2322663	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1049C>G (p.Ala350Gly)	not specified [RCV004182792]	uncertain significance	5	123591374	123591374	Human		name
329353664	CV2467025	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1186G>T (p.Val396Phe)	not specified [RCV004282768]	uncertain significance	5	123604724	123604724	Human		name
597805079	CV3654707	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1360C>T (p.Arg454Cys)	not specified [RCV004908279]	uncertain significance	5	123614385	123614385	Human		name
597805081	CV3654708	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1354A>G (p.Ile452Val)	not specified [RCV004908280]	uncertain significance	5	123614379	123614379	Human		name
597805083	CV3654709	single nucleotide variant	NM_001364140.2(CSNK1G3):c.1324T>C (p.Cys442Arg)	not specified [RCV004908281]	uncertain significance	5	123614349	123614349	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