Arhgap15 Variant Search Result - Rat Genome Database

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59 records found for search term Arhgap15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401916958	CV2812357	single nucleotide variant	NM_018460.4(ARHGAP15):c.474+1G>A	not provided [RCV003429287]	uncertain significance	2	143250601	143250601	Human		name
15190132	CV777199	single nucleotide variant	NM_018460.4(ARHGAP15):c.475-4G>T	not provided [RCV000954385]	likely benign	2	143435597	143435597	Human		name
8576608	CV110975	single nucleotide variant	NM_018460.3(ARHGAP15):c.234+620A>G	Lung cancer [RCV000091498]	uncertain significance	2	143202822	143202822	Human		name
8576611	CV110979	single nucleotide variant	NM_018460.3(ARHGAP15):c.704-4471A>G	Lung cancer [RCV000091502]	uncertain significance	2	143482902	143482902	Human		name
8576612	CV110980	single nucleotide variant	NM_018460.3(ARHGAP15):c.826+3974T>C	Lung cancer [RCV000091503]	uncertain significance	2	143491469	143491469	Human		name
8576609	CV110976	single nucleotide variant	NM_018460.3(ARHGAP15):c.474+86541G>A	Lung cancer [RCV000091499]	uncertain significance	2	143337141	143337141	Human		name
8648979	CV110977	single nucleotide variant	NM_018460.3(ARHGAP15):c.475-83608T>C	Lung cancer [RCV000091500]	uncertain significance	2	143351993	143351993	Human		name
8576610	CV110978	single nucleotide variant	NM_018460.3(ARHGAP15):c.475-27933T>A	Lung cancer [RCV000091501]	uncertain significance	2	143407668	143407668	Human		name
8576616	CV110984	single nucleotide variant	NM_018460.3(ARHGAP15):c.1139-5396G>C	Lung cancer [RCV000091507]	uncertain significance	2	143698023	143698023	Human		name
8576617	CV110985	single nucleotide variant	NM_018460.3(ARHGAP15):c.1244+2777A>G	Lung cancer [RCV000091508]	uncertain significance	2	143706301	143706301	Human		name
8576613	CV110981	single nucleotide variant	NM_018460.3(ARHGAP15):c.1004-27015A>G	Lung cancer [RCV000091504]	uncertain significance	2	143597118	143597118	Human		name
8576614	CV110982	single nucleotide variant	NM_018460.3(ARHGAP15):c.1004-11362C>A	Lung cancer [RCV000091505]	uncertain significance	2	143612771	143612771	Human		name
8576615	CV110983	single nucleotide variant	NM_018460.3(ARHGAP15):c.1138+22590A>G	Lung cancer [RCV000091506]	uncertain significance	2	143646857	143646857	Human		name
8576618	CV110986	single nucleotide variant	NM_018460.3(ARHGAP15):c.1245-17783G>C	Lung cancer [RCV000091509]	uncertain significance	2	143750206	143750206	Human		name
156054242	CV2308649	single nucleotide variant	NM_018460.4(ARHGAP15):c.52C>T (p.Arg18Cys)	not specified [RCV004167201]	uncertain significance	2	143155542	143155542	Human		name
597743436	CV3580559	single nucleotide variant	NM_018460.4(ARHGAP15):c.45T>G (p.Asn15Lys)	not specified [RCV004845046]	uncertain significance	2	143155535	143155535	Human		name
156110391	CV2387642	single nucleotide variant	NM_018460.4(ARHGAP15):c.163C>A (p.Pro55Thr)	not specified [RCV004234190]	uncertain significance	2	143155653	143155653	Human		name
329376390	CV2438188	single nucleotide variant	NM_018460.4(ARHGAP15):c.283G>A (p.Gly95Arg)	not specified [RCV004256960]	uncertain significance	2	143216432	143216432	Human		name
407531528	CV3471772	single nucleotide variant	NM_018460.4(ARHGAP15):c.142G>A (p.Asp48Asn)	not specified [RCV004657657]	uncertain significance	2	143155632	143155632	Human		name
597743459	CV3580576	single nucleotide variant	NM_018460.4(ARHGAP15):c.226G>A (p.Glu76Lys)	not specified [RCV004845050]	uncertain significance	2	143202194	143202194	Human		name
8629870	CV85017	single nucleotide variant	NM_018460.3(ARHGAP15):c.170C>T (p.Ser57Phe)	Malignant melanoma [RCV000065099]	not provided	2	143202138	143202138	Human		name
156275698	CV2290701	single nucleotide variant	NM_018460.4(ARHGAP15):c.499T>C (p.Phe167Leu)	not specified [RCV004149224]	uncertain significance	2	143435625	143435625	Human		name
156177427	CV2301237	single nucleotide variant	NM_018460.4(ARHGAP15):c.534G>C (p.Leu178Phe)	not specified [RCV004160140]	uncertain significance	2	143435660	143435660	Human		name
156062009	CV2316419	single nucleotide variant	NM_018460.4(ARHGAP15):c.310A>G (p.Thr104Ala)	not specified [RCV004169912]	uncertain significance	2	143228594	143228594	Human		name
156163324	CV2319622	single nucleotide variant	NM_018460.4(ARHGAP15):c.856G>A (p.Val286Met)	not specified [RCV004185171]	uncertain significance	2	143519295	143519295	Human		name
156162019	CV2323502	single nucleotide variant	NM_018460.4(ARHGAP15):c.497A>G (p.Glu166Gly)	not specified [RCV004165709]	uncertain significance	2	143435623	143435623	Human		name
156076238	CV2375019	single nucleotide variant	NM_018460.4(ARHGAP15):c.637A>G (p.Thr213Ala)	not specified [RCV004230072]	uncertain significance	2	143436976	143436976	Human		name
155998853	CV2396318	single nucleotide variant	NM_018460.4(ARHGAP15):c.752T>C (p.Val251Ala)	not specified [RCV004242050]	uncertain significance	2	143487421	143487421	Human		name
329401110	CV2446141	single nucleotide variant	NM_018460.4(ARHGAP15):c.600A>T (p.Arg200Ser)	not specified [RCV004264556]	uncertain significance	2	143436939	143436939	Human		name
401729932	CV2683864	single nucleotide variant	NM_018460.4(ARHGAP15):c.749G>A (p.Arg250Gln)	not specified [RCV004284589]	uncertain significance	2	143487418	143487418	Human		name
405674968	CV3286441	single nucleotide variant	NM_018460.4(ARHGAP15):c.782G>A (p.Arg261Gln)	not specified [RCV004420421]	uncertain significance	2	143487451	143487451	Human		name
405674972	CV3286442	single nucleotide variant	NM_018460.4(ARHGAP15):c.866G>A (p.Arg289His)	not specified [RCV004420422]	uncertain significance	2	143519305	143519305	Human		name
405684357	CV3286443	single nucleotide variant	NM_018460.4(ARHGAP15):c.992T>C (p.Ile331Thr)	not specified [RCV004422404]	uncertain significance	2	143556474	143556474	Human		name
407490939	CV3471793	single nucleotide variant	NM_018460.4(ARHGAP15):c.368A>C (p.Gln123Pro)	not specified [RCV004666739]	uncertain significance	2	143228652	143228652	Human		name
407490950	CV3471804	single nucleotide variant	NM_018460.4(ARHGAP15):c.428A>G (p.His143Arg)	not specified [RCV004666743]	uncertain significance	2	143250554	143250554	Human		name
407531593	CV3471815	single nucleotide variant	NM_018460.4(ARHGAP15):c.655T>G (p.Tyr219Asp)	not specified [RCV004657689]	uncertain significance	2	143436994	143436994	Human		name
597743422	CV3580546	single nucleotide variant	NM_018460.4(ARHGAP15):c.308C>T (p.Ser103Phe)	not specified [RCV004845044]	uncertain significance	2	143228592	143228592	Human		name
597743453	CV3580568	single nucleotide variant	NM_018460.4(ARHGAP15):c.394C>A (p.His132Asn)	not specified [RCV004845049]	uncertain significance	2	143250520	143250520	Human		name
597743469	CV3580587	single nucleotide variant	NM_018460.4(ARHGAP15):c.574C>A (p.Pro192Thr)	not specified [RCV004845052]	uncertain significance	2	143436913	143436913	Human		name
598167565	CV4003077	single nucleotide variant	NM_018460.4(ARHGAP15):c.950G>A (p.Arg317Gln)	not specified [RCV005391728]	uncertain significance	2	143556432	143556432	Human		name
598205530	CV4003088	single nucleotide variant	NM_018460.4(ARHGAP15):c.435A>C (p.Glu145Asp)	not specified [RCV005399479]	uncertain significance	2	143250561	143250561	Human		name
598167670	CV4003105	single nucleotide variant	NM_018460.4(ARHGAP15):c.910G>A (p.Ala304Thr)	not specified [RCV005391751]	uncertain significance	2	143519349	143519349	Human		name
8625150	CV80269	single nucleotide variant	NM_018460.3(ARHGAP15):c.355G>A (p.Glu119Lys)	Malignant melanoma [RCV000060345]	not provided	2	143228639	143228639	Human		name
155918018	CV2195640	single nucleotide variant	NM_018460.4(ARHGAP15):c.1280C>T (p.Thr427Met)	not specified [RCV004076007]	uncertain significance	2	143768024	143768024	Human		name
156052089	CV2238157	single nucleotide variant	NM_018460.4(ARHGAP15):c.1354A>G (p.Met452Val)	not specified [RCV004111165]	uncertain significance	2	143768098	143768098	Human		name
155918898	CV2254758	single nucleotide variant	NM_018460.4(ARHGAP15):c.1364A>G (p.Gln455Arg)	not specified [RCV004115228]	uncertain significance	2	143768108	143768108	Human		name
156023526	CV2273775	single nucleotide variant	NM_018460.4(ARHGAP15):c.1048G>A (p.Val350Ile)	not specified [RCV004132416]	uncertain significance	2	143624177	143624177	Human		name
155919526	CV2333211	single nucleotide variant	NM_018460.4(ARHGAP15):c.1199C>T (p.Pro400Leu)	not specified [RCV004194498]	uncertain significance	2	143703479	143703479	Human		name
156256694	CV2368759	single nucleotide variant	NM_018460.4(ARHGAP15):c.1319G>A (p.Arg440Gln)	not specified [RCV004214639]	uncertain significance	2	143768063	143768063	Human		name
156061856	CV2380293	single nucleotide variant	NM_018460.4(ARHGAP15):c.1159A>G (p.Arg387Gly)	not specified [RCV004224643]	uncertain significance	2	143703439	143703439	Human		name
401733591	CV2691347	single nucleotide variant	NM_018460.4(ARHGAP15):c.1225C>T (p.Leu409Phe)	not specified [RCV004303096]	uncertain significance	2	143703505	143703505	Human		name
401881429	CV2759412	single nucleotide variant	NM_018460.4(ARHGAP15):c.1372A>G (p.Ile458Val)	not specified [RCV004338412]	uncertain significance	2	143768116	143768116	Human		name
405674964	CV3286440	single nucleotide variant	NM_018460.4(ARHGAP15):c.1208G>A (p.Arg403His)	not specified [RCV004420420]	uncertain significance	2	143703488	143703488	Human		name
407531544	CV3471782	single nucleotide variant	NM_018460.4(ARHGAP15):c.1108A>T (p.Ser370Cys)	not specified [RCV004657665]	uncertain significance	2	143624237	143624237	Human		name
407531619	CV3471827	single nucleotide variant	NM_018460.4(ARHGAP15):c.1373T>C (p.Ile458Thr)	not specified [RCV004657700]	uncertain significance	2	143768117	143768117	Human		name
597743430	CV3580551	single nucleotide variant	NM_018460.4(ARHGAP15):c.1258G>C (p.Ala420Pro)	not specified [RCV004845045]	uncertain significance	2	143768002	143768002	Human		name
597743441	CV3580564	single nucleotide variant	NM_018460.4(ARHGAP15):c.1295T>C (p.Ile432Thr)	not specified [RCV004845047]	uncertain significance	2	143768039	143768039	Human		name
597743464	CV3580582	single nucleotide variant	NM_018460.4(ARHGAP15):c.1136T>A (p.Ile379Asn)	not specified [RCV004845051]	uncertain significance	2	143624265	143624265	Human		name
598167715	CV4003114	single nucleotide variant	NM_018460.4(ARHGAP15):c.1417G>A (p.Glu473Lys)	not specified [RCV005391759]	uncertain significance	2	143768161	143768161	Human		name

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