Cwc22 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

96 records found for search term Cwc22

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
616939453	CV4013944	single nucleotide variant	NM_020943.3(CWC22):c.2141-5C>T	not provided [RCV005413436]	benign	2	179945720	179945720	Human		name
15158774	CV730089	duplication	NM_020943.3(CWC22):c.1147+2dup	not provided [RCV000881071]	benign	2	179970647	179970648	Human		name
8576811	CV111179	single nucleotide variant	NM_020943.2(CWC22):c.2140+1410C>G	Lung cancer [RCV000091702]	uncertain significance	2	179949102	179949102	Human		name
598236358	CV3956113	single nucleotide variant	NM_020943.3(CWC22):c.8G>A (p.Ser3Asn)	not specified [RCV005320416]	uncertain significance	2	179993334	179993334	Human		name
405701741	CV3243124	single nucleotide variant	NM_020943.3(CWC22):c.20A>C (p.Gln7Pro)	not specified [RCV004375372]	uncertain significance	2	179993322	179993322	Human		name
155945714	CV2301291	single nucleotide variant	NM_020943.3(CWC22):c.50G>C (p.Arg17Thr)	not specified [RCV004160466]	uncertain significance	2	179988622	179988622	Human		name
405665174	CV3243134	single nucleotide variant	NM_020943.3(CWC22):c.40C>G (p.His14Asp)	not specified [RCV004367487]	uncertain significance	2	179988632	179988632	Human		name
405665206	CV3243141	single nucleotide variant	NM_020943.3(CWC22):c.98A>G (p.Tyr33Cys)	not specified [RCV004367494]	uncertain significance	2	179986803	179986803	Human		name
598236336	CV3956108	single nucleotide variant	NM_020943.3(CWC22):c.43G>A (p.Asp15Asn)	not specified [RCV005320412]	uncertain significance	2	179988629	179988629	Human		name
15125099	CV733015	single nucleotide variant	NM_020943.3(CWC22):c.648A>G (p.Ala216=)	not provided [RCV000896701]	likely benign	2	179973736	179973736	Human		name
156400889	CV2217375	single nucleotide variant	NM_020943.3(CWC22):c.265C>T (p.Arg89Trp)	not specified [RCV004087808]	uncertain significance	2	179981939	179981939	Human		name
155975088	CV2221318	single nucleotide variant	NM_020943.3(CWC22):c.221A>G (p.Glu74Gly)	not specified [RCV004094742]	uncertain significance	2	179981983	179981983	Human		name
156312493	CV2256879	single nucleotide variant	NM_020943.3(CWC22):c.122G>A (p.Arg41Gln)	not specified [RCV004121086]	uncertain significance	2	179986779	179986779	Human		name
156053970	CV2344597	single nucleotide variant	NM_020943.3(CWC22):c.254G>A (p.Arg85Gln)	not specified [RCV004197370]	uncertain significance	2	179981950	179981950	Human		name
156306418	CV2359936	single nucleotide variant	NM_020943.3(CWC22):c.218G>A (p.Arg73Gln)	not specified [RCV004212780]	uncertain significance	2	179981986	179981986	Human		name
329367383	CV2427386	single nucleotide variant	NM_020943.3(CWC22):c.248C>T (p.Thr83Met)	not specified [RCV004248242]	likely benign	2	179981956	179981956	Human		name
401727236	CV2684526	single nucleotide variant	NM_020943.3(CWC22):c.179G>A (p.Arg60His)	not specified [RCV004291595]	likely benign	2	179986722	179986722	Human		name
405701703	CV3243119	single nucleotide variant	NM_020943.3(CWC22):c.119C>G (p.Pro40Arg)	not specified [RCV004375367]	uncertain significance	2	179986782	179986782	Human		name
405701713	CV3243120	single nucleotide variant	NM_020943.3(CWC22):c.119C>T (p.Pro40Leu)	not specified [RCV004375368]	uncertain significance	2	179986782	179986782	Human		name
405701776	CV3243129	single nucleotide variant	NM_020943.3(CWC22):c.253C>T (p.Arg85Trp)	not specified [RCV004375377]	uncertain significance	2	179981951	179981951	Human		name
598236311	CV3956104	single nucleotide variant	NM_020943.3(CWC22):c.134A>G (p.Tyr45Cys)	not specified [RCV005320408]	uncertain significance	2	179986767	179986767	Human		name
15107146	CV719462	single nucleotide variant	NM_020943.3(CWC22):c.1095A>G (p.Gln365=)	not provided [RCV000893418]	benign	2	179970702	179970702	Human		name
156107762	CV2214263	single nucleotide variant	NM_020943.3(CWC22):c.832C>T (p.Leu278Phe)	not specified [RCV004086255]	uncertain significance	2	179971049	179971049	Human		name
155994899	CV2278022	single nucleotide variant	NM_020943.3(CWC22):c.368A>C (p.Asp123Ala)	not specified [RCV004141252]	uncertain significance	2	179981836	179981836	Human		name
156271180	CV2290274	single nucleotide variant	NM_020943.3(CWC22):c.736C>G (p.Arg246Gly)	not specified [RCV004152921]	uncertain significance	2	179973648	179973648	Human		name
156087166	CV2295399	single nucleotide variant	NM_020943.3(CWC22):c.343A>G (p.Thr115Ala)	not specified [RCV004158742]	likely benign	2	179981861	179981861	Human		name
156099672	CV2306563	single nucleotide variant	NM_020943.3(CWC22):c.989A>G (p.Lys330Arg)	not specified [RCV004157170]	uncertain significance	2	179970808	179970808	Human		name
401765786	CV2683424	single nucleotide variant	NM_020943.3(CWC22):c.380C>T (p.Thr127Ile)	not specified [RCV004288191]	uncertain significance	2	179981824	179981824	Human		name
401733902	CV2713259	single nucleotide variant	NM_020943.3(CWC22):c.831G>A (p.Met277Ile)	not specified [RCV004316789]	uncertain significance	2	179971050	179971050	Human		name
405665160	CV3243131	single nucleotide variant	NM_020943.3(CWC22):c.319T>A (p.Ser107Thr)	not specified [RCV004367484]	uncertain significance	2	179981885	179981885	Human		name
405665164	CV3243132	single nucleotide variant	NM_020943.3(CWC22):c.329A>T (p.Gln110Leu)	not specified [RCV004367485]	uncertain significance	2	179981875	179981875	Human		name
405665168	CV3243133	single nucleotide variant	NM_020943.3(CWC22):c.353A>G (p.Lys118Arg)	not specified [RCV004367486]	uncertain significance	2	179981851	179981851	Human		name
405665179	CV3243135	single nucleotide variant	NM_020943.3(CWC22):c.475T>C (p.Trp159Arg)	not specified [RCV004367488]	uncertain significance	2	179978296	179978296	Human		name
405665182	CV3243136	single nucleotide variant	NM_020943.3(CWC22):c.704A>G (p.Lys235Arg)	not specified [RCV004367489]	uncertain significance	2	179973680	179973680	Human		name
405665187	CV3243137	single nucleotide variant	NM_020943.3(CWC22):c.737G>A (p.Arg246Gln)	not specified [RCV004367490]	uncertain significance	2	179973647	179973647	Human		name
405665191	CV3243138	single nucleotide variant	NM_020943.3(CWC22):c.791T>C (p.Ile264Thr)	not specified [RCV004367491]	uncertain significance	2	179973206	179973206	Human		name
405665196	CV3243139	single nucleotide variant	NM_020943.3(CWC22):c.953G>A (p.Arg318His)	not specified [RCV004367492]	uncertain significance	2	179970844	179970844	Human		name
405665201	CV3243140	single nucleotide variant	NM_020943.3(CWC22):c.965T>C (p.Ile322Thr)	not specified [RCV004367493]	uncertain significance	2	179970832	179970832	Human		name
407473160	CV3426540	single nucleotide variant	NM_020943.3(CWC22):c.383G>C (p.Arg128Pro)	not specified [RCV004616148]	uncertain significance	2	179981821	179981821	Human		name
597654660	CV3661712	single nucleotide variant	NM_020943.3(CWC22):c.467G>A (p.Arg156Lys)	not specified [RCV004910961]	uncertain significance	2	179978304	179978304	Human		name
597654668	CV3661713	single nucleotide variant	NM_020943.3(CWC22):c.959G>A (p.Arg320Gln)	not specified [RCV004910962]	uncertain significance	2	179970838	179970838	Human		name
597654676	CV3661714	single nucleotide variant	NM_020943.3(CWC22):c.919G>T (p.Val307Leu)	not specified [RCV004910963]	uncertain significance	2	179970962	179970962	Human		name
598236325	CV3956106	single nucleotide variant	NM_020943.3(CWC22):c.307G>A (p.Val103Ile)	not specified [RCV005320410]	uncertain significance	2	179981897	179981897	Human		name
598236331	CV3956107	single nucleotide variant	NM_020943.3(CWC22):c.707G>C (p.Arg236Thr)	not specified [RCV005320411]	uncertain significance	2	179973677	179973677	Human		name
598236353	CV3956112	single nucleotide variant	NM_020943.3(CWC22):c.653T>C (p.Leu218Ser)	not specified [RCV005320415]	uncertain significance	2	179973731	179973731	Human		name
598236362	CV3956114	single nucleotide variant	NM_020943.3(CWC22):c.751C>A (p.Gln251Lys)	not specified [RCV005320417]	uncertain significance	2	179973246	179973246	Human		name
156386301	CV2228173	single nucleotide variant	NM_020943.3(CWC22):c.2185G>A (p.Glu729Lys)	not specified [RCV004096383]	uncertain significance	2	179945671	179945671	Human		name
156059706	CV2239361	single nucleotide variant	NM_020943.3(CWC22):c.1370G>A (p.Arg457His)	not specified [RCV004114096]	uncertain significance	2	179964574	179964574	Human		name
156158586	CV2262498	single nucleotide variant	NM_020943.3(CWC22):c.2507A>G (p.His836Arg)	not specified [RCV004128928]	uncertain significance	2	179945349	179945349	Human		name
156060388	CV2263050	single nucleotide variant	NM_020943.3(CWC22):c.1295A>C (p.Glu432Ala)	not specified [RCV004131307]	uncertain significance	2	179965898	179965898	Human		name
156280398	CV2281752	single nucleotide variant	NM_020943.3(CWC22):c.2469A>T (p.Arg823Ser)	not specified [RCV004147891]	uncertain significance	2	179945387	179945387	Human		name
156078919	CV2300863	single nucleotide variant	NM_020943.3(CWC22):c.1678C>T (p.Leu560Phe)	not specified [RCV004158068]	uncertain significance	2	179954216	179954216	Human		name
156047059	CV2315658	single nucleotide variant	NM_020943.3(CWC22):c.1511A>C (p.Glu504Ala)	not specified [RCV004169689]	uncertain significance	2	179954982	179954982	Human		name
155974743	CV2318032	single nucleotide variant	NM_020943.3(CWC22):c.1702A>G (p.Ile568Val)	not specified [RCV004177139]	uncertain significance	2	179952586	179952586	Human		name
156362638	CV2330286	single nucleotide variant	NM_020943.3(CWC22):c.1027C>T (p.Arg343Trp)	not specified [RCV004187732]	uncertain significance	2	179970770	179970770	Human		name
156308472	CV2332346	single nucleotide variant	NM_020943.3(CWC22):c.2393G>A (p.Ser798Asn)	not specified [RCV004182510]	likely benign	2	179945463	179945463	Human		name
155971501	CV2335692	single nucleotide variant	NM_020943.3(CWC22):c.2587G>C (p.Gly863Arg)	not specified [RCV004193893]	uncertain significance	2	179945269	179945269	Human		name
156077565	CV2375116	single nucleotide variant	NM_020943.3(CWC22):c.1780A>G (p.Met594Val)	not specified [RCV004230161]	uncertain significance	2	179952508	179952508	Human		name
156225067	CV2390470	single nucleotide variant	NM_020943.3(CWC22):c.2054C>G (p.Ser685Cys)	not specified [RCV004239012]	uncertain significance	2	179950598	179950598	Human		name
156270620	CV2398700	single nucleotide variant	NM_020943.3(CWC22):c.1367G>A (p.Arg456His)	not specified [RCV004240044]	uncertain significance	2	179964577	179964577	Human		name
156003217	CV2399638	single nucleotide variant	NM_020943.3(CWC22):c.1961T>C (p.Ile654Thr)	not specified [RCV004244154]	uncertain significance	2	179950691	179950691	Human		name
329372649	CV2424165	single nucleotide variant	NM_020943.3(CWC22):c.1255G>A (p.Ala419Thr)	not specified [RCV004248061]	uncertain significance	2	179965938	179965938	Human		name
329358498	CV2425274	single nucleotide variant	NM_020943.3(CWC22):c.2099A>G (p.Glu700Gly)	not specified [RCV004250944]	uncertain significance	2	179950553	179950553	Human		name
329357592	CV2427774	single nucleotide variant	NM_020943.3(CWC22):c.1793A>G (p.Lys598Arg)	not specified [RCV004252554]	uncertain significance	2	179952495	179952495	Human		name
329362229	CV2448443	single nucleotide variant	NM_020943.3(CWC22):c.2060C>G (p.Ser687Cys)	not specified [RCV004256724]	uncertain significance	2	179950592	179950592	Human		name
329390421	CV2450296	single nucleotide variant	NM_020943.3(CWC22):c.2539A>G (p.Arg847Gly)	not specified [RCV004271390]	uncertain significance	2	179945317	179945317	Human		name
401732371	CV2678083	single nucleotide variant	NM_020943.3(CWC22):c.2626G>A (p.Glu876Lys)	not specified [RCV004296599]	uncertain significance	2	179945230	179945230	Human		name
401744257	CV2730641	single nucleotide variant	NM_020943.3(CWC22):c.2173A>G (p.Thr725Ala)	not specified [RCV004331579]	uncertain significance	2	179945683	179945683	Human		name
401889842	CV2755040	single nucleotide variant	NM_020943.3(CWC22):c.2506C>T (p.His836Tyr)	not specified [RCV004335197]	uncertain significance	2	179945350	179945350	Human		name
405701697	CV3243118	single nucleotide variant	NM_020943.3(CWC22):c.1017G>T (p.Met339Ile)	not specified [RCV004375366]	uncertain significance	2	179970780	179970780	Human		name
405701718	CV3243121	single nucleotide variant	NM_020943.3(CWC22):c.1250A>G (p.Gln417Arg)	not specified [RCV004375369]	uncertain significance	2	179965943	179965943	Human		name
405701725	CV3243122	single nucleotide variant	NM_020943.3(CWC22):c.1783G>C (p.Gly595Arg)	not specified [RCV004375370]	uncertain significance	2	179952505	179952505	Human		name
405701733	CV3243123	single nucleotide variant	NM_020943.3(CWC22):c.2084A>C (p.Glu695Ala)	not specified [RCV004375371]	uncertain significance	2	179950568	179950568	Human		name
405701748	CV3243125	single nucleotide variant	NM_020943.3(CWC22):c.2100G>C (p.Glu700Asp)	not specified [RCV004375373]	uncertain significance	2	179950552	179950552	Human		name
405701754	CV3243126	single nucleotide variant	NM_020943.3(CWC22):c.2200A>G (p.Ile734Val)	not specified [RCV004375374]	uncertain significance	2	179945656	179945656	Human		name
405701764	CV3243127	single nucleotide variant	NM_020943.3(CWC22):c.2215A>G (p.Thr739Ala)	not specified [RCV004375375]	uncertain significance	2	179945641	179945641	Human		name
405701770	CV3243128	single nucleotide variant	NM_020943.3(CWC22):c.2447A>G (p.His816Arg)	not specified [RCV004375376]	uncertain significance	2	179945409	179945409	Human		name
405665156	CV3243130	single nucleotide variant	NM_020943.3(CWC22):c.2702A>G (p.Glu901Gly)	not specified [RCV004367483]	uncertain significance	2	179945154	179945154	Human		name
407473164	CV3426541	single nucleotide variant	NM_020943.3(CWC22):c.1439A>C (p.Glu480Ala)	not specified [RCV004616149]	uncertain significance	2	179959041	179959041	Human		name
407473168	CV3426542	single nucleotide variant	NM_020943.3(CWC22):c.2314T>G (p.Ser772Ala)	not specified [RCV004616150]	uncertain significance	2	179945542	179945542	Human		name
407473172	CV3426543	single nucleotide variant	NM_020943.3(CWC22):c.1849C>T (p.Pro617Ser)	not specified [RCV004616151]	uncertain significance	2	179950895	179950895	Human		name
407473176	CV3426544	single nucleotide variant	NM_020943.3(CWC22):c.2608A>G (p.Arg870Gly)	not specified [RCV004616152]	uncertain significance	2	179945248	179945248	Human		name
597654588	CV3661704	single nucleotide variant	NM_020943.3(CWC22):c.2526C>G (p.Asp842Glu)	not specified [RCV004910953]	uncertain significance	2	179945330	179945330	Human		name
597654596	CV3661705	single nucleotide variant	NM_020943.3(CWC22):c.2575A>G (p.Arg859Gly)	not specified [RCV004910954]	uncertain significance	2	179945281	179945281	Human		name
597654608	CV3661706	single nucleotide variant	NM_020943.3(CWC22):c.1792A>C (p.Lys598Gln)	not specified [RCV004910955]	uncertain significance	2	179952496	179952496	Human		name
597654618	CV3661707	single nucleotide variant	NM_020943.3(CWC22):c.1931G>A (p.Arg644Gln)	not specified [RCV004910956]	uncertain significance	2	179950721	179950721	Human		name
597654632	CV3661709	single nucleotide variant	NM_020943.3(CWC22):c.2618A>G (p.Asn873Ser)	not specified [RCV004910958]	uncertain significance	2	179945238	179945238	Human		name
597654643	CV3661710	single nucleotide variant	NM_020943.3(CWC22):c.2710C>G (p.Pro904Ala)	not specified [RCV004910959]	uncertain significance	2	179945146	179945146	Human		name
597654649	CV3661711	single nucleotide variant	NM_020943.3(CWC22):c.2078G>A (p.Ser693Asn)	not specified [RCV004910960]	uncertain significance	2	179950574	179950574	Human		name
598236297	CV3956102	single nucleotide variant	NM_020943.3(CWC22):c.2597G>A (p.Ser866Asn)	not specified [RCV005320406]	uncertain significance	2	179945259	179945259	Human		name
598236305	CV3956103	single nucleotide variant	NM_020943.3(CWC22):c.2366A>G (p.Asp789Gly)	not specified [RCV005320407]	likely benign	2	179945490	179945490	Human		name
598236318	CV3956105	single nucleotide variant	NM_020943.3(CWC22):c.1075T>A (p.Leu359Met)	not specified [RCV005320409]	uncertain significance	2	179970722	179970722	Human		name
598236342	CV3956109	single nucleotide variant	NM_020943.3(CWC22):c.1465C>T (p.Leu489Phe)	not specified [RCV005320413]	uncertain significance	2	179955028	179955028	Human		name
598160364	CV3956110	single nucleotide variant	NM_020943.3(CWC22):c.2677A>G (p.Lys893Glu)	not specified [RCV005328757]	uncertain significance	2	179945179	179945179	Human		name
598236348	CV3956111	single nucleotide variant	NM_020943.3(CWC22):c.1564A>G (p.Met522Val)	not specified [RCV005320414]	uncertain significance	2	179954330	179954330	Human		name
15158768	CV719461	single nucleotide variant	NM_020943.3(CWC22):c.2222A>T (p.Asp741Val)	not provided [RCV000881070]	benign	2	179945634	179945634	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