Cpped1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

55 records found for search term Cpped1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156043826	CV2381579	single nucleotide variant	NM_018340.3(CPPED1):c.8C>T (p.Ala3Val)	not specified [RCV004232057]	uncertain significance	16	12803769	12803769	Human		name
156068514	CV2356871	single nucleotide variant	NM_018340.3(CPPED1):c.25G>C (p.Val9Leu)	not specified [RCV004204248]	uncertain significance	16	12803752	12803752	Human		name
156367727	CV2203571	single nucleotide variant	NM_018340.3(CPPED1):c.59C>G (p.Ala20Gly)	not specified [RCV004072768]	uncertain significance	16	12803718	12803718	Human		name
401877236	CV2764550	single nucleotide variant	NM_018340.3(CPPED1):c.67G>T (p.Ala23Ser)	not specified [RCV004339105]	likely benign	16	12803710	12803710	Human		name
401885829	CV2783402	single nucleotide variant	NM_018340.3(CPPED1):c.48G>C (p.Arg16Ser)	not specified [RCV004365753]	uncertain significance	16	12803729	12803729	Human		name
405697436	CV3245686	single nucleotide variant	NM_018340.3(CPPED1):c.82G>A (p.Glu28Lys)	not specified [RCV004374610]	uncertain significance	16	12781392	12781392	Human		name
405697456	CV3245689	single nucleotide variant	NM_018340.3(CPPED1):c.91G>A (p.Gly31Ser)	not specified [RCV004374613]	uncertain significance	16	12781383	12781383	Human		name
407457315	CV3419692	single nucleotide variant	NM_018340.3(CPPED1):c.53T>C (p.Leu18Pro)	not specified [RCV004611086]	uncertain significance	16	12803724	12803724	Human		name
597667181	CV3651228	single nucleotide variant	NM_018340.3(CPPED1):c.58G>A (p.Ala20Thr)	not specified [RCV004912677]	uncertain significance	16	12803719	12803719	Human		name
597667210	CV3651233	single nucleotide variant	NM_018340.3(CPPED1):c.29T>G (p.Phe10Cys)	not specified [RCV004912681]	uncertain significance	16	12803748	12803748	Human		name
597667219	CV3651234	single nucleotide variant	NM_018340.3(CPPED1):c.71A>G (p.Glu24Gly)	not specified [RCV004912682]	uncertain significance	16	12781403	12781403	Human		name
155973787	CV2224742	single nucleotide variant	NM_018340.3(CPPED1):c.163G>A (p.Asp55Asn)	not specified [RCV004092570]	uncertain significance	16	12781311	12781311	Human		name
156186255	CV2295008	single nucleotide variant	NM_018340.3(CPPED1):c.157G>C (p.Asp53His)	not specified [RCV004156142]	uncertain significance	16	12781317	12781317	Human		name
156005933	CV2357715	single nucleotide variant	NM_018340.3(CPPED1):c.131G>A (p.Gly44Glu)	not specified [RCV004205013]	uncertain significance	16	12781343	12781343	Human		name
156090313	CV2375205	single nucleotide variant	NM_018340.3(CPPED1):c.178G>A (p.Glu60Lys)	not specified [RCV004230243]	uncertain significance	16	12781296	12781296	Human		name
401773896	CV2727666	single nucleotide variant	NM_018340.3(CPPED1):c.227A>G (p.Asn76Ser)	not specified [RCV004329841]	uncertain significance	16	12781247	12781247	Human		name
401896424	CV2781319	single nucleotide variant	NM_018340.3(CPPED1):c.296C>T (p.Pro99Leu)	not specified [RCV004352336]	uncertain significance	16	12705043	12705043	Human		name
405697374	CV3245674	single nucleotide variant	NM_018340.3(CPPED1):c.215T>C (p.Val72Ala)	not specified [RCV004374598]	uncertain significance	16	12781259	12781259	Human		name
407457320	CV3419694	single nucleotide variant	NM_018340.3(CPPED1):c.284T>C (p.Met95Thr)	not specified [RCV004611088]	uncertain significance	16	12781190	12781190	Human		name
598246861	CV3945333	single nucleotide variant	NM_018340.3(CPPED1):c.280G>A (p.Ala94Thr)	not specified [RCV005322380]	uncertain significance	16	12781194	12781194	Human		name
156169746	CV2197819	single nucleotide variant	NM_018340.3(CPPED1):c.641A>T (p.Asp214Val)	not specified [RCV004077058]	uncertain significance	16	12704698	12704698	Human		name
156193655	CV2214142	single nucleotide variant	NM_018340.3(CPPED1):c.730T>G (p.Phe244Val)	not specified [RCV004086144]	uncertain significance	16	12665101	12665101	Human		name
156057637	CV2239111	single nucleotide variant	NM_018340.3(CPPED1):c.615C>A (p.His205Gln)	not specified [RCV004112110]	uncertain significance	16	12704724	12704724	Human		name
155901415	CV2242002	single nucleotide variant	NM_018340.3(CPPED1):c.712G>A (p.Ala238Thr)	not specified [RCV004108948]	uncertain significance	16	12704627	12704627	Human		name
155990522	CV2352480	single nucleotide variant	NM_018340.3(CPPED1):c.521G>A (p.Cys174Tyr)	not specified [RCV004202986]	uncertain significance	16	12704818	12704818	Human		name
156252807	CV2390084	single nucleotide variant	NM_018340.3(CPPED1):c.841G>A (p.Val281Met)	not specified [RCV004238686]	uncertain significance	16	12664990	12664990	Human		name
401762216	CV2723360	single nucleotide variant	NM_018340.3(CPPED1):c.706A>T (p.Ile236Phe)	not specified [RCV004329573]	uncertain significance	16	12704633	12704633	Human		name
401858369	CV2774066	single nucleotide variant	NM_018340.3(CPPED1):c.329G>A (p.Arg110Gln)	not specified [RCV004345668]	uncertain significance	16	12705010	12705010	Human	1	name
401858369	CV2774066	single nucleotide variant	NM_018340.3(CPPED1):c.329G>A (p.Arg110Gln)	not specified [RCV004345668]	uncertain significance	16	12705010	12705011	Human	1	name
405697379	CV3245675	single nucleotide variant	NM_018340.3(CPPED1):c.349A>G (p.Arg117Gly)	not specified [RCV004374599]	uncertain significance	16	12704990	12704990	Human		name
405697385	CV3245676	single nucleotide variant	NM_018340.3(CPPED1):c.352G>T (p.Ala118Ser)	not specified [RCV004374600]	uncertain significance	16	12704987	12704987	Human		name
405697387	CV3245677	single nucleotide variant	NM_018340.3(CPPED1):c.398C>A (p.Thr133Asn)	not specified [RCV004374601]	uncertain significance	16	12704941	12704941	Human		name
405697395	CV3245678	single nucleotide variant	NM_018340.3(CPPED1):c.410A>T (p.Glu137Val)	not specified [RCV004374602]	uncertain significance	16	12704929	12704929	Human		name
405697400	CV3245679	single nucleotide variant	NM_018340.3(CPPED1):c.511C>T (p.Pro171Ser)	not specified [RCV004374603]	uncertain significance	16	12704828	12704828	Human		name
405697404	CV3245680	single nucleotide variant	NM_018340.3(CPPED1):c.583C>T (p.Arg195Trp)	not specified [RCV004374604]	uncertain significance	16	12704756	12704756	Human		name
405697410	CV3245681	single nucleotide variant	NM_018340.3(CPPED1):c.637A>G (p.Ile213Val)	not specified [RCV004374605]	uncertain significance	16	12704702	12704702	Human		name
405697414	CV3245682	single nucleotide variant	NM_018340.3(CPPED1):c.642C>A (p.Asp214Glu)	not specified [RCV004374606]	uncertain significance	16	12704697	12704697	Human		name
405697419	CV3245683	single nucleotide variant	NM_018340.3(CPPED1):c.757G>A (p.Gly253Arg)	not specified [RCV004374607]	uncertain significance	16	12665074	12665074	Human		name
405697425	CV3245684	single nucleotide variant	NM_018340.3(CPPED1):c.784G>T (p.Val262Leu)	not specified [RCV004374608]	uncertain significance	16	12665047	12665047	Human		name
405697430	CV3245685	single nucleotide variant	NM_018340.3(CPPED1):c.807C>G (p.Cys269Trp)	not specified [RCV004374609]	uncertain significance	16	12665024	12665024	Human		name
405697443	CV3245687	single nucleotide variant	NM_018340.3(CPPED1):c.872G>A (p.Arg291Gln)	not specified [RCV004374611]	uncertain significance	16	12664959	12664959	Human		name
407457309	CV3419690	single nucleotide variant	NM_018340.3(CPPED1):c.856G>A (p.Glu286Lys)	not specified [RCV004611084]	uncertain significance	16	12664975	12664975	Human		name
407457313	CV3419691	single nucleotide variant	NM_018340.3(CPPED1):c.415G>A (p.Val139Ile)	not specified [RCV004611085]	likely benign	16	12704924	12704924	Human		name
407457317	CV3419693	single nucleotide variant	NM_018340.3(CPPED1):c.763A>G (p.Thr255Ala)	not specified [RCV004611087]	uncertain significance	16	12665068	12665068	Human		name
597667172	CV3651227	single nucleotide variant	NM_018340.3(CPPED1):c.878A>G (p.Tyr293Cys)	not specified [RCV004912676]	uncertain significance	16	12664953	12664953	Human		name
597667188	CV3651229	single nucleotide variant	NM_018340.3(CPPED1):c.431G>A (p.Arg144Gln)	not specified [RCV004912678]	likely benign	16	12704908	12704908	Human		name
597773977	CV3651230	single nucleotide variant	NM_018340.3(CPPED1):c.883C>G (p.Leu295Val)	not specified [RCV004897630]	uncertain significance	16	12664948	12664948	Human		name
597667195	CV3651231	single nucleotide variant	NM_018340.3(CPPED1):c.608T>G (p.Phe203Cys)	not specified [RCV004912679]	uncertain significance	16	12704731	12704731	Human		name
597667202	CV3651232	single nucleotide variant	NM_018340.3(CPPED1):c.332T>C (p.Val111Ala)	not specified [RCV004912680]	uncertain significance	16	12705007	12705007	Human		name
597667232	CV3651236	single nucleotide variant	NM_018340.3(CPPED1):c.397A>T (p.Thr133Ser)	not specified [RCV004912684]	uncertain significance	16	12704942	12704942	Human		name
598246853	CV3945332	single nucleotide variant	NM_018340.3(CPPED1):c.396C>G (p.Asn132Lys)	not specified [RCV005322379]	uncertain significance	16	12704943	12704943	Human		name
598160088	CV3945334	single nucleotide variant	NM_018340.3(CPPED1):c.586C>G (p.His196Asp)	not specified [RCV005328697]	uncertain significance	16	12704753	12704753	Human		name
598246868	CV3945335	single nucleotide variant	NM_018340.3(CPPED1):c.541C>G (p.Gln181Glu)	not specified [RCV005322381]	uncertain significance	16	12704798	12704798	Human		name
598246875	CV3945336	single nucleotide variant	NM_018340.3(CPPED1):c.870C>G (p.His290Gln)	not specified [RCV005322382]	uncertain significance	16	12664961	12664961	Human		name
8635670	CV90892	single nucleotide variant	NM_018340.2(CPPED1):c.494C>T (p.Ser165Phe)	Malignant melanoma [RCV000070990]	not provided	16	12704845	12704845	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