Arhgef12 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

103 records found for search term Arhgef12

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15193657	CV778125	single nucleotide variant	NM_015313.3(ARHGEF12):c.924+7T>A	not provided [RCV000955434]	benign	11	120431918	120431918	Human		name
8652608	CV129183	single nucleotide variant	NM_015313.2(ARHGEF12):c.925-368T>G	Lung cancer [RCV000109670]	uncertain significance	11	120436940	120436940	Human		name
156206076	CV2297931	single nucleotide variant	NM_015313.3(ARHGEF12):c.19A>G (p.Thr7Ala)	not specified [RCV004157858]	uncertain significance	11	120337262	120337262	Human		name
156173733	CV2326786	single nucleotide variant	NM_015313.3(ARHGEF12):c.60T>G (p.His20Gln)	not specified [RCV004176626]	uncertain significance	11	120407741	120407741	Human		name
155916077	CV2197203	single nucleotide variant	NM_015313.3(ARHGEF12):c.190G>A (p.Glu64Lys)	not specified [RCV004078992]	uncertain significance	11	120409441	120409441	Human		name
401747759	CV2689003	single nucleotide variant	NM_015313.3(ARHGEF12):c.119C>T (p.Ala40Val)	not specified [RCV004305784]	uncertain significance	11	120407800	120407800	Human		name
401747623	CV2696748	single nucleotide variant	NM_015313.3(ARHGEF12):c.217G>A (p.Val73Ile)	not specified [RCV004290722]	uncertain significance	11	120420770	120420770	Human		name
15162232	CV712649	single nucleotide variant	NM_015313.3(ARHGEF12):c.2037A>C (p.Gly679=)	not provided [RCV000970234]	benign	11	120451705	120451705	Human		name
15161814	CV724257	single nucleotide variant	NM_015313.3(ARHGEF12):c.2331G>A (p.Val777=)	not provided [RCV000881639]	benign	11	120458185	120458185	Human		name
156374393	CV2198435	single nucleotide variant	NM_015313.3(ARHGEF12):c.548G>T (p.Gly183Val)	not specified [RCV004081965]	uncertain significance	11	120428210	120428210	Human		name
156263820	CV2329403	single nucleotide variant	NM_015313.3(ARHGEF12):c.865C>G (p.Leu289Val)	not specified [RCV004187415]	uncertain significance	11	120431852	120431852	Human		name
155969897	CV2335522	single nucleotide variant	NM_015313.3(ARHGEF12):c.925A>G (p.Ser309Gly)	not specified [RCV004191689]	uncertain significance	11	120437308	120437308	Human		name
156135332	CV2379869	single nucleotide variant	NM_015313.3(ARHGEF12):c.473A>G (p.Asp158Gly)	not specified [RCV004219976]	uncertain significance	11	120428135	120428135	Human		name
329386770	CV2452504	single nucleotide variant	NM_015313.3(ARHGEF12):c.404A>G (p.Lys135Arg)	not specified [RCV004273103]	likely benign	11	120424413	120424413	Human		name
329387076	CV2463311	single nucleotide variant	NM_015313.3(ARHGEF12):c.631A>C (p.Lys211Gln)	not specified [RCV004275371]	uncertain significance	11	120429485	120429485	Human		name
401748598	CV2713046	single nucleotide variant	NM_015313.3(ARHGEF12):c.800C>T (p.Thr267Ile)	not specified [RCV004316605]	uncertain significance	11	120431787	120431787	Human		name
405698301	CV3279288	single nucleotide variant	NM_015313.3(ARHGEF12):c.496A>G (p.Ile166Val)	not specified [RCV004424940]	uncertain significance	11	120428158	120428158	Human		name
405698307	CV3279289	single nucleotide variant	NM_015313.3(ARHGEF12):c.862G>A (p.Val288Ile)	not specified [RCV004424941]	uncertain significance	11	120431849	120431849	Human		name
405698311	CV3279290	single nucleotide variant	NM_015313.3(ARHGEF12):c.892G>A (p.Asp298Asn)	not specified [RCV004424942]	uncertain significance	11	120431879	120431879	Human		name
405698318	CV3279291	single nucleotide variant	NM_015313.3(ARHGEF12):c.901C>T (p.Arg301Trp)	not specified [RCV004424943]	uncertain significance	11	120431888	120431888	Human		name
407467233	CV3468696	single nucleotide variant	NM_015313.3(ARHGEF12):c.905C>T (p.Pro302Leu)	not specified [RCV004660665]	uncertain significance	11	120431892	120431892	Human		name
597759425	CV3588234	single nucleotide variant	NM_015313.3(ARHGEF12):c.646G>A (p.Glu216Lys)	not specified [RCV004848744]	uncertain significance	11	120429500	120429500	Human		name
597759705	CV3588290	single nucleotide variant	NM_015313.3(ARHGEF12):c.514A>G (p.Ile172Val)	not specified [RCV004848799]	uncertain significance	11	120428176	120428176	Human		name
597759848	CV3588336	single nucleotide variant	NM_015313.3(ARHGEF12):c.829A>G (p.Thr277Ala)	not specified [RCV004848827]	uncertain significance	11	120431816	120431816	Human		name
597760018	CV3588397	single nucleotide variant	NM_015313.3(ARHGEF12):c.3366C>T (p.Val1122=)	not specified [RCV004848860]	likely benign	11	120477219	120477219	Human		name
597760076	CV3588408	single nucleotide variant	NM_015313.3(ARHGEF12):c.899C>T (p.Ser300Phe)	not specified [RCV004848871]	uncertain significance	11	120431886	120431886	Human		name
598158945	CV3900912	single nucleotide variant	NM_015313.3(ARHGEF12):c.725C>T (p.Ala242Val)	not specified [RCV005260599]	uncertain significance	11	120429773	120429773	Human		name
15162224	CV712648	single nucleotide variant	NM_015313.3(ARHGEF12):c.691C>T (p.Pro231Ser)	not provided [RCV000970233]	benign	11	120429739	120429739	Human		name
15189618	CV768264	single nucleotide variant	NM_015313.3(ARHGEF12):c.3873G>A (p.Pro1291=)	not provided [RCV000932290]	likely benign	11	120480066	120480066	Human		name
156400044	CV2198929	single nucleotide variant	NM_015313.3(ARHGEF12):c.1083A>C (p.Glu361Asp)	not specified [RCV004080349]	uncertain significance	11	120440212	120440212	Human		name
155923662	CV2248571	single nucleotide variant	NM_015313.3(ARHGEF12):c.2068G>A (p.Val690Ile)	not specified [RCV004121766]	uncertain significance	11	120457129	120457129	Human		name
155921759	CV2276369	single nucleotide variant	NM_015313.3(ARHGEF12):c.1460G>A (p.Arg487His)	not specified [RCV004144109]	uncertain significance	11	120446956	120446956	Human		name
156263429	CV2282576	single nucleotide variant	NM_015313.3(ARHGEF12):c.1903T>A (p.Ser635Thr)	not specified [RCV004135143]	uncertain significance	11	120451571	120451571	Human		name
156133570	CV2284589	single nucleotide variant	NM_015313.3(ARHGEF12):c.1141C>T (p.Arg381Cys)	not specified [RCV004140756]	uncertain significance	11	120441755	120441755	Human		name
156180876	CV2288128	single nucleotide variant	NM_015313.3(ARHGEF12):c.1891T>C (p.Ser631Pro)	not specified [RCV004149658]	uncertain significance	11	120451559	120451559	Human		name
156086091	CV2289907	single nucleotide variant	NM_015313.3(ARHGEF12):c.1198A>G (p.Thr400Ala)	not specified [RCV004150563]	uncertain significance	11	120441812	120441812	Human		name
155972667	CV2309431	single nucleotide variant	NM_015313.3(ARHGEF12):c.2351G>A (p.Cys784Tyr)	not specified [RCV004165573]	uncertain significance	11	120458205	120458205	Human		name
155974828	CV2318061	single nucleotide variant	NM_015313.3(ARHGEF12):c.1459C>T (p.Arg487Cys)	not specified [RCV004177162]	uncertain significance	11	120446955	120446955	Human		name
156187486	CV2346722	single nucleotide variant	NM_015313.3(ARHGEF12):c.1598C>T (p.Ala533Val)	not specified [RCV004199739]	uncertain significance	11	120447882	120447882	Human		name
329389465	CV2445135	single nucleotide variant	NM_015313.3(ARHGEF12):c.2727G>C (p.Gln909His)	not specified [RCV004263778]	uncertain significance	11	120465350	120465350	Human		name
401730166	CV2700472	single nucleotide variant	NM_015313.3(ARHGEF12):c.1391A>G (p.Tyr464Cys)	not specified [RCV004311107]	uncertain significance	11	120446448	120446448	Human		name
401874241	CV2773709	single nucleotide variant	NM_015313.3(ARHGEF12):c.1928C>G (p.Ser643Cys)	not specified [RCV004356390]	uncertain significance	11	120451596	120451596	Human		name
405698222	CV3279274	single nucleotide variant	NM_015313.3(ARHGEF12):c.1142G>A (p.Arg381His)	not specified [RCV004424926]	uncertain significance	11	120441756	120441756	Human		name
405698233	CV3279276	single nucleotide variant	NM_015313.3(ARHGEF12):c.1224C>A (p.Asp408Glu)	not specified [RCV004424928]	uncertain significance	11	120442124	120442124	Human		name
405698238	CV3279277	single nucleotide variant	NM_015313.3(ARHGEF12):c.1235A>G (p.His412Arg)	not specified [RCV004424929]	uncertain significance	11	120442135	120442135	Human		name
405698245	CV3279278	single nucleotide variant	NM_015313.3(ARHGEF12):c.1385G>A (p.Arg462His)	not specified [RCV004424930]	uncertain significance	11	120446442	120446442	Human		name
405698250	CV3279279	single nucleotide variant	NM_015313.3(ARHGEF12):c.1526G>T (p.Arg509Leu)	not specified [RCV004424931]	uncertain significance	11	120447022	120447022	Human		name
405698258	CV3279280	single nucleotide variant	NM_015313.3(ARHGEF12):c.2113C>T (p.Arg705Cys)	not specified [RCV004424932]	uncertain significance	11	120457174	120457174	Human		name
405698264	CV3279281	single nucleotide variant	NM_015313.3(ARHGEF12):c.2141C>T (p.Pro714Leu)	not specified [RCV004424933]	uncertain significance	11	120457202	120457202	Human		name
405698270	CV3279282	single nucleotide variant	NM_015313.3(ARHGEF12):c.2528T>C (p.Ile843Thr)	not specified [RCV004424934]	uncertain significance	11	120460672	120460672	Human		name
405698276	CV3279283	single nucleotide variant	NM_015313.3(ARHGEF12):c.2914A>T (p.Asn972Tyr)	not specified [RCV004424935]	uncertain significance	11	120469347	120469347	Human		name
405855144	CV3395742	single nucleotide variant	NM_015313.3(ARHGEF12):c.2764C>T (p.Arg922Cys)	not provided [RCV004556005]	uncertain significance	11	120467218	120467218	Human		name
407500985	CV3468694	single nucleotide variant	NM_015313.3(ARHGEF12):c.1862T>C (p.Leu621Pro)	not specified [RCV004669670]	uncertain significance	11	120451530	120451530	Human		name
407467245	CV3468699	single nucleotide variant	NM_015313.3(ARHGEF12):c.1384C>T (p.Arg462Cys)	not specified [RCV004660668]	uncertain significance	11	120446441	120446441	Human		name
597759607	CV3588271	single nucleotide variant	NM_015313.3(ARHGEF12):c.2787T>G (p.Ile929Met)	not specified [RCV004848780]	uncertain significance	11	120467241	120467241	Human		name
597759657	CV3588281	single nucleotide variant	NM_015313.3(ARHGEF12):c.1607T>C (p.Val536Ala)	not specified [RCV004848790]	uncertain significance	11	120447891	120447891	Human		name
597759750	CV3588307	single nucleotide variant	NM_015313.3(ARHGEF12):c.2102A>G (p.Asp701Gly)	not specified [RCV004848808]	uncertain significance	11	120457163	120457163	Human		name
597759755	CV3588315	single nucleotide variant	NM_015313.3(ARHGEF12):c.1064A>T (p.Asp355Val)	not specified [RCV004848809]	uncertain significance	11	120440193	120440193	Human		name
597759859	CV3588356	single nucleotide variant	NM_015313.3(ARHGEF12):c.1491G>T (p.Glu497Asp)	not specified [RCV004848829]	uncertain significance	11	120446987	120446987	Human		name
597759864	CV3588367	single nucleotide variant	NM_015313.3(ARHGEF12):c.2089G>A (p.Gly697Arg)	not specified [RCV004848830]	uncertain significance	11	120457150	120457150	Human		name
598158993	CV3900922	single nucleotide variant	NM_015313.3(ARHGEF12):c.1196C>A (p.Ala399Glu)	not specified [RCV005260609]	uncertain significance	11	120441810	120441810	Human		name
15161142	CV724256	single nucleotide variant	NM_015313.3(ARHGEF12):c.1996A>G (p.Met666Val)	not provided [RCV000881518]	likely benign	11	120451664	120451664	Human		name
8626921	CV82065	single nucleotide variant	NM_015313.2(ARHGEF12):c.2623C>T (p.Pro875Ser)	Malignant melanoma [RCV000062144]	not provided	11	120465246	120465246	Human		name
8626922	CV82066	single nucleotide variant	NM_015313.2(ARHGEF12):c.2624C>T (p.Pro875Leu)	Malignant melanoma [RCV000062145]	not provided	11	120465247	120465247	Human		name
8633884	CV89100	single nucleotide variant	NM_015313.2(ARHGEF12):c.1727C>T (p.Pro576Leu)	Malignant melanoma [RCV000069197]	not provided	11	120448338	120448338	Human		name
155922127	CV2208837	single nucleotide variant	NM_015313.3(ARHGEF12):c.3800T>C (p.Leu1267Pro)	not specified [RCV004085002]	uncertain significance	11	120479993	120479993	Human		name
156134409	CV2213160	single nucleotide variant	NM_015313.3(ARHGEF12):c.3451G>A (p.Glu1151Lys)	not specified [RCV004085391]	uncertain significance	11	120477304	120477304	Human		name
156277144	CV2276963	single nucleotide variant	NM_015313.3(ARHGEF12):c.3745G>A (p.Ala1249Thr)	not specified [RCV004140296]	uncertain significance	11	120478368	120478368	Human		name
156203194	CV2300706	single nucleotide variant	NM_015313.3(ARHGEF12):c.3080T>C (p.Val1027Ala)	not specified [RCV004155644]	uncertain significance	11	120474606	120474606	Human		name
156298684	CV2310648	single nucleotide variant	NM_015313.3(ARHGEF12):c.3836A>C (p.Gln1279Pro)	not specified [RCV004157309]	likely benign	11	120480029	120480029	Human		name
156333834	CV2333297	single nucleotide variant	NM_015313.3(ARHGEF12):c.3707T>A (p.Ile1236Asn)	not specified [RCV004197045]	uncertain significance	11	120478330	120478330	Human		name
156282570	CV2348868	single nucleotide variant	NM_015313.3(ARHGEF12):c.4579C>T (p.Leu1527Phe)	not specified [RCV004203307]	uncertain significance	11	120484462	120484462	Human		name
156018804	CV2370349	single nucleotide variant	NM_015313.3(ARHGEF12):c.3839A>C (p.His1280Pro)	not specified [RCV004213253]	uncertain significance	11	120480032	120480032	Human		name
156095556	CV2398969	single nucleotide variant	NM_015313.3(ARHGEF12):c.4170T>A (p.Asp1390Glu)	not specified [RCV004245279]	uncertain significance	11	120480363	120480363	Human		name
329372120	CV2442890	single nucleotide variant	NM_015313.3(ARHGEF12):c.3560T>C (p.Leu1187Ser)	not specified [RCV004253496]	uncertain significance	11	120478183	120478183	Human		name
329371111	CV2461951	single nucleotide variant	NM_015313.3(ARHGEF12):c.3314A>G (p.Asn1105Ser)	not specified [RCV004271851]	uncertain significance	11	120476697	120476697	Human		name
329388627	CV2469429	single nucleotide variant	NM_015313.3(ARHGEF12):c.3422C>T (p.Pro1141Leu)	not specified [RCV004282891]	uncertain significance	11	120477275	120477275	Human		name
401724529	CV2677908	single nucleotide variant	NM_015313.3(ARHGEF12):c.4229G>T (p.Arg1410Leu)	not specified [RCV004294397]	uncertain significance	11	120480422	120480422	Human		name
401861212	CV2758805	single nucleotide variant	NM_015313.3(ARHGEF12):c.4000T>A (p.Ser1334Thr)	not specified [RCV004337857]	uncertain significance	11	120480193	120480193	Human		name
401882891	CV2775150	single nucleotide variant	NM_015313.3(ARHGEF12):c.3848G>A (p.Arg1283Lys)	not specified [RCV004346507]	uncertain significance	11	120480041	120480041	Human		name
401886595	CV2780427	single nucleotide variant	NM_015313.3(ARHGEF12):c.4487G>C (p.Cys1496Ser)	not specified [RCV004357816]	uncertain significance	11	120481509	120481509	Human		name
405698280	CV3279284	single nucleotide variant	NM_015313.3(ARHGEF12):c.3524A>T (p.Gln1175Leu)	not specified [RCV004424936]	uncertain significance	11	120477518	120477518	Human		name
405698286	CV3279285	single nucleotide variant	NM_015313.3(ARHGEF12):c.3659A>G (p.His1220Arg)	not specified [RCV004424937]	uncertain significance	11	120478282	120478282	Human		name
405698290	CV3279286	single nucleotide variant	NM_015313.3(ARHGEF12):c.4028T>C (p.Leu1343Pro)	not specified [RCV004424938]	uncertain significance	11	120480221	120480221	Human		name
405698296	CV3279287	single nucleotide variant	NM_015313.3(ARHGEF12):c.4244A>G (p.Tyr1415Cys)	not specified [RCV004424939]	uncertain significance	11	120481266	120481266	Human		name
407467237	CV3468697	single nucleotide variant	NM_015313.3(ARHGEF12):c.3656A>G (p.Gln1219Arg)	not specified [RCV004660666]	uncertain significance	11	120478279	120478279	Human		name
407467256	CV3468701	single nucleotide variant	NM_015313.3(ARHGEF12):c.3659A>C (p.His1220Pro)	not specified [RCV004660670]	uncertain significance	11	120478282	120478282	Human		name
407467275	CV3468708	single nucleotide variant	NM_015313.3(ARHGEF12):c.4072C>T (p.His1358Tyr)	not specified [RCV004660674]	uncertain significance	11	120480265	120480265	Human		name
407467299	CV3468716	single nucleotide variant	NM_015313.3(ARHGEF12):c.3440C>T (p.Ser1147Leu)	not specified [RCV004660680]	uncertain significance	11	120477293	120477293	Human		name
597759471	CV3588245	single nucleotide variant	NM_015313.3(ARHGEF12):c.3491A>C (p.Glu1164Ala)	not specified [RCV004848754]	uncertain significance	11	120477485	120477485	Human		name
597759518	CV3588254	single nucleotide variant	NM_015313.3(ARHGEF12):c.4114G>A (p.Gly1372Arg)	not specified [RCV004848763]	uncertain significance	11	120480307	120480307	Human		name
597759561	CV3588262	single nucleotide variant	NM_015313.3(ARHGEF12):c.3676A>C (p.Lys1226Gln)	not specified [RCV004848771]	uncertain significance	11	120478299	120478299	Human		name
597759745	CV3588298	single nucleotide variant	NM_015313.3(ARHGEF12):c.3472G>A (p.Asp1158Asn)	not specified [RCV004848807]	uncertain significance	11	120477466	120477466	Human		name
597759796	CV3588325	single nucleotide variant	NM_015313.3(ARHGEF12):c.3016A>G (p.Asn1006Asp)	not specified [RCV004848817]	uncertain significance	11	120473110	120473110	Human		name
597759854	CV3588345	single nucleotide variant	NM_015313.3(ARHGEF12):c.3739C>T (p.Arg1247Trp)	not specified [RCV004848828]	uncertain significance	11	120478362	120478362	Human		name
597759916	CV3588377	single nucleotide variant	NM_015313.3(ARHGEF12):c.4628A>G (p.Lys1543Arg)	not specified [RCV004848840]	uncertain significance	11	120485070	120485070	Human		name
597759962	CV3588386	single nucleotide variant	NM_015313.3(ARHGEF12):c.4616A>T (p.Lys1539Met)	not specified [RCV004848849]	uncertain significance	11	120484499	120484499	Human		name
598158856	CV3900889	single nucleotide variant	NM_015313.3(ARHGEF12):c.3913G>A (p.Ala1305Thr)	not specified [RCV005260576]	uncertain significance	11	120480106	120480106	Human		name
598158873	CV3900894	single nucleotide variant	NM_015313.3(ARHGEF12):c.3740G>A (p.Arg1247Gln)	not specified [RCV005260581]	uncertain significance	11	120478363	120478363	Human		name
598158899	CV3900901	single nucleotide variant	NM_015313.3(ARHGEF12):c.4473G>C (p.Gln1491His)	not specified [RCV005260588]	uncertain significance	11	120481495	120481495	Human		name
598159026	CV3900931	single nucleotide variant	NM_015313.3(ARHGEF12):c.3424A>G (p.Ile1142Val)	not specified [RCV005260618]	uncertain significance	11	120477277	120477277	Human		name
15162238	CV712650	single nucleotide variant	NM_015313.3(ARHGEF12):c.3694T>A (p.Tyr1232Asn)	not provided [RCV000970235]	likely benign	11	120478317	120478317	Human		name
243063759	CV2405161	deletion	NM_015313.3(ARHGEF12):c.4449_4455del (p.Met1483fs)	Glaucoma [RCV003225265]	uncertain significance	11	120481468	120481474	Human	2	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