Dennd2c Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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88 records found for search term Dennd2c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8624651	CV79764	single nucleotide variant	NM_198459.3(DENND2C):c.663C>T (p.Ser221=)	Malignant melanoma [RCV000059840]	not provided	1	114625322	114625322	Human		name
8628799	CV83943	single nucleotide variant	NM_198459.3(DENND2C):c.92G>A (p.Arg31Lys)	Malignant melanoma [RCV000064024]	not provided	1	114625893	114625893	Human		name
8624649	CV79762	single nucleotide variant	NM_198459.3(DENND2C):c.1728C>T (p.Phe576=)	Malignant melanoma [RCV000059838]	not provided	1	114600877	114600877	Human		name
329376240	CV2438050	single nucleotide variant	NM_001256404.2(DENND2C):c.23C>T (p.Thr8Ile)	not specified [RCV004263752]	uncertain significance	1	114625962	114625962	Human		name
156133458	CV2361854	single nucleotide variant	NM_001256404.2(DENND2C):c.71A>C (p.Lys24Thr)	not specified [RCV004207631]	uncertain significance	1	114625914	114625914	Human		name
407466008	CV3426829	single nucleotide variant	NM_001256404.2(DENND2C):c.35C>G (p.Thr12Arg)	not specified [RCV004613850]	uncertain significance	1	114625950	114625950	Human		name
8624650	CV79763	single nucleotide variant	NM_198459.3(DENND2C):c.1337C>T (p.Pro446Leu)	Malignant melanoma [RCV000059839]	not provided	1	114608735	114608735	Human		name
401928272	CV2809083	single nucleotide variant	NM_001256404.2(DENND2C):c.1341C>T (p.Asn447=)	not provided [RCV003406681]	benign	1	114611101	114611101	Human		name
405669960	CV3236952	single nucleotide variant	NM_001256404.2(DENND2C):c.170G>A (p.Arg57His)	not specified [RCV004368462]	uncertain significance	1	114625815	114625815	Human		name
597656557	CV3658704	single nucleotide variant	NM_001256404.2(DENND2C):c.126T>G (p.Cys42Trp)	not specified [RCV004911184]	uncertain significance	1	114625859	114625859	Human		name
597656630	CV3658713	single nucleotide variant	NM_001256404.2(DENND2C):c.181A>G (p.Asn61Asp)	not specified [RCV004911193]	uncertain significance	1	114625804	114625804	Human		name
156180711	CV2246091	single nucleotide variant	NM_001256404.2(DENND2C):c.798A>C (p.Arg266Ser)	not specified [RCV004113997]	uncertain significance	1	114625187	114625187	Human		name
156178103	CV2258218	single nucleotide variant	NM_001256404.2(DENND2C):c.931G>A (p.Glu311Lys)	not specified [RCV004121593]	uncertain significance	1	114623519	114623519	Human		name
155921519	CV2350680	single nucleotide variant	NM_001256404.2(DENND2C):c.911A>G (p.Gln304Arg)	not specified [RCV004207029]	uncertain significance	1	114623539	114623539	Human		name
156105146	CV2352509	single nucleotide variant	NM_001256404.2(DENND2C):c.608G>A (p.Cys203Tyr)	not specified [RCV004203012]	uncertain significance	1	114625377	114625377	Human		name
155935466	CV2371806	single nucleotide variant	NM_001256404.2(DENND2C):c.303A>C (p.Glu101Asp)	not specified [RCV004219463]	uncertain significance	1	114625682	114625682	Human		name
156093210	CV2382049	single nucleotide variant	NM_001256404.2(DENND2C):c.934G>A (p.Asp312Asn)	not specified [RCV004228018]	uncertain significance	1	114623516	114623516	Human		name
329382409	CV2465217	single nucleotide variant	NM_001256404.2(DENND2C):c.680C>T (p.Pro227Leu)	not specified [RCV004287251]	uncertain significance	1	114625305	114625305	Human		name
401753288	CV2720700	single nucleotide variant	NM_001256404.2(DENND2C):c.690A>C (p.Glu230Asp)	not specified [RCV004328060]	uncertain significance	1	114625295	114625295	Human		name
405669988	CV3236957	single nucleotide variant	NM_001256404.2(DENND2C):c.370A>G (p.Ile124Val)	not specified [RCV004368467]	uncertain significance	1	114625615	114625615	Human		name
405669992	CV3236958	single nucleotide variant	NM_001256404.2(DENND2C):c.521A>C (p.Lys174Thr)	not specified [RCV004368468]	uncertain significance	1	114625464	114625464	Human		name
407466004	CV3426828	single nucleotide variant	NM_001256404.2(DENND2C):c.728G>A (p.Cys243Tyr)	not specified [RCV004613849]	uncertain significance	1	114625257	114625257	Human		name
407466012	CV3426830	single nucleotide variant	NM_001256404.2(DENND2C):c.859A>C (p.Thr287Pro)	not specified [RCV004613851]	uncertain significance	1	114623591	114623591	Human		name
407466024	CV3426833	single nucleotide variant	NM_001256404.2(DENND2C):c.431A>G (p.Tyr144Cys)	not specified [RCV004613854]	uncertain significance	1	114625554	114625554	Human		name
407466036	CV3426836	single nucleotide variant	NM_001256404.2(DENND2C):c.670G>T (p.Gly224Cys)	not specified [RCV004613857]	uncertain significance	1	114625315	114625315	Human		name
597641172	CV3658703	single nucleotide variant	NM_001256404.2(DENND2C):c.640C>T (p.Arg214Cys)	not specified [RCV004909129]	uncertain significance	1	114625345	114625345	Human		name
597656624	CV3658712	single nucleotide variant	NM_001256404.2(DENND2C):c.826G>C (p.Asp276His)	not specified [RCV004911192]	uncertain significance	1	114623624	114623624	Human		name
597656643	CV3658715	single nucleotide variant	NM_001256404.2(DENND2C):c.584A>G (p.Tyr195Cys)	not specified [RCV004911195]	uncertain significance	1	114625401	114625401	Human		name
598224485	CV3956637	single nucleotide variant	NM_001256404.2(DENND2C):c.860C>T (p.Thr287Met)	not specified [RCV005318226]	uncertain significance	1	114623590	114623590	Human		name
598224493	CV3956638	single nucleotide variant	NM_001256404.2(DENND2C):c.752C>T (p.Ser251Phe)	not specified [RCV005318227]	uncertain significance	1	114625233	114625233	Human		name
598160671	CV3956645	single nucleotide variant	NM_001256404.2(DENND2C):c.701A>G (p.Asp234Gly)	not specified [RCV005328824]	uncertain significance	1	114625284	114625284	Human		name
598224545	CV3956646	single nucleotide variant	NM_001256404.2(DENND2C):c.992C>T (p.Pro331Leu)	not specified [RCV005318234]	uncertain significance	1	114623051	114623051	Human		name
598160677	CV3956647	single nucleotide variant	NM_001256404.2(DENND2C):c.971A>G (p.Asp324Gly)	not specified [RCV005328825]	uncertain significance	1	114623072	114623072	Human		name
598224550	CV3956648	single nucleotide variant	NM_001256404.2(DENND2C):c.875T>G (p.Leu292Arg)	not specified [RCV005318235]	uncertain significance	1	114623575	114623575	Human		name
156399164	CV2204954	single nucleotide variant	NM_001256404.2(DENND2C):c.2410C>G (p.Gln804Glu)	not specified [RCV004077578]	uncertain significance	1	114594494	114594494	Human		name
156143073	CV2208607	single nucleotide variant	NM_001256404.2(DENND2C):c.2292A>G (p.Ile764Met)	not specified [RCV004091128]	uncertain significance	1	114595865	114595865	Human		name
156226321	CV2215928	single nucleotide variant	NM_001256404.2(DENND2C):c.1438C>T (p.Arg480Trp)	not specified [RCV004097008]	uncertain significance	1	114608805	114608805	Human		name
156059399	CV2239331	single nucleotide variant	NM_001256404.2(DENND2C):c.1261A>G (p.Lys421Glu)	not specified [RCV004114071]	uncertain significance	1	114618449	114618449	Human		name
156316260	CV2250887	single nucleotide variant	NM_001256404.2(DENND2C):c.2371C>G (p.Leu791Val)	not specified [RCV004123476]	uncertain significance	1	114594533	114594533	Human		name
156189477	CV2255056	single nucleotide variant	NM_001256404.2(DENND2C):c.1289A>G (p.His430Arg)	not specified [RCV004115696]	uncertain significance	1	114618421	114618421	Human		name
156263666	CV2282593	single nucleotide variant	NM_001256404.2(DENND2C):c.1548C>G (p.Phe516Leu)	not specified [RCV004135157]	uncertain significance	1	114608695	114608695	Human		name
155932344	CV2290622	single nucleotide variant	NM_001256404.2(DENND2C):c.1271A>T (p.Lys424Met)	not specified [RCV004149160]	uncertain significance	1	114618439	114618439	Human		name
155917623	CV2332848	single nucleotide variant	NM_001256404.2(DENND2C):c.1973G>A (p.Arg658Gln)	not specified [RCV004192112]	uncertain significance	1	114600336	114600336	Human		name
156347681	CV2375530	single nucleotide variant	NM_001256404.2(DENND2C):c.2406G>T (p.Leu802Phe)	not specified [RCV004226035]	uncertain significance	1	114594498	114594498	Human		name
156034420	CV2376676	single nucleotide variant	NM_001256404.2(DENND2C):c.1931G>A (p.Ser644Asn)	not specified [RCV004222873]	uncertain significance	1	114600845	114600845	Human		name
156005316	CV2393976	single nucleotide variant	NM_001256404.2(DENND2C):c.1900C>T (p.Pro634Ser)	not specified [RCV004236202]	uncertain significance	1	114600876	114600876	Human		name
329402721	CV2451280	single nucleotide variant	NM_001256404.2(DENND2C):c.2044A>G (p.Ile682Val)	not specified [RCV004271978]	uncertain significance	1	114600265	114600265	Human		name
329396024	CV2454668	single nucleotide variant	NM_001256404.2(DENND2C):c.2647C>G (p.Leu883Val)	not specified [RCV004268123]	uncertain significance	1	114587737	114587737	Human		name
329401325	CV2460767	single nucleotide variant	NM_001256404.2(DENND2C):c.1988G>A (p.Arg663Gln)	not specified [RCV004271093]	uncertain significance	1	114600321	114600321	Human		name
329394620	CV2461450	single nucleotide variant	NM_001256404.2(DENND2C):c.2323G>C (p.Glu775Gln)	not specified [RCV004267594]	uncertain significance	1	114595834	114595834	Human		name
401781649	CV2682079	single nucleotide variant	NM_001256404.2(DENND2C):c.1373G>A (p.Arg458His)	not specified [RCV004290142]	uncertain significance	1	114608870	114608870	Human		name
401730089	CV2683943	single nucleotide variant	NM_001256404.2(DENND2C):c.2381T>A (p.Ile794Asn)	not specified [RCV004284662]	uncertain significance	1	114594523	114594523	Human		name
401733991	CV2688371	single nucleotide variant	NM_001256404.2(DENND2C):c.2393G>A (p.Arg798Gln)	not specified [RCV004299365]	uncertain significance	1	114594511	114594511	Human		name
401735240	CV2699210	single nucleotide variant	NM_001256404.2(DENND2C):c.2002G>A (p.Asp668Asn)	not specified [RCV004305491]	uncertain significance	1	114600307	114600307	Human		name
401888991	CV2761634	single nucleotide variant	NM_001256404.2(DENND2C):c.1958C>T (p.Ser653Phe)	not specified [RCV004337256]	uncertain significance	1	114600351	114600351	Human		name
401885245	CV2768023	single nucleotide variant	NM_001256404.2(DENND2C):c.2312A>G (p.Lys771Arg)	not specified [RCV004348267]	uncertain significance	1	114595845	114595845	Human		name
405669947	CV3236949	single nucleotide variant	NM_001256404.2(DENND2C):c.1439G>A (p.Arg480Gln)	not specified [RCV004368459]	uncertain significance	1	114608804	114608804	Human		name
405669950	CV3236950	single nucleotide variant	NM_001256404.2(DENND2C):c.1507C>A (p.Pro503Thr)	not specified [RCV004368460]	uncertain significance	1	114608736	114608736	Human		name
405669955	CV3236951	single nucleotide variant	NM_001256404.2(DENND2C):c.1802A>G (p.Asn601Ser)	not specified [RCV004368461]	uncertain significance	1	114601521	114601521	Human		name
405669966	CV3236953	single nucleotide variant	NM_001256404.2(DENND2C):c.1913G>A (p.Arg638His)	not specified [RCV004368463]	uncertain significance	1	114600863	114600863	Human		name
405669971	CV3236954	single nucleotide variant	NM_001256404.2(DENND2C):c.2024G>A (p.Cys675Tyr)	not specified [RCV004368464]	uncertain significance	1	114600285	114600285	Human		name
405669983	CV3236956	single nucleotide variant	NM_001256404.2(DENND2C):c.2751T>G (p.Ser917Arg)	not specified [RCV004368466]	uncertain significance	1	114587391	114587391	Human		name
407465989	CV3426824	single nucleotide variant	NM_001256404.2(DENND2C):c.2683C>T (p.Arg895Trp)	not specified [RCV004613845]	uncertain significance	1	114587459	114587459	Human		name
407465992	CV3426825	single nucleotide variant	NM_001256404.2(DENND2C):c.1594G>A (p.Glu532Lys)	not specified [RCV004613846]	uncertain significance	1	114604995	114604995	Human		name
407466000	CV3426827	single nucleotide variant	NM_001256404.2(DENND2C):c.1382G>A (p.Arg461His)	not specified [RCV004613848]	uncertain significance	1	114608861	114608861	Human		name
407466016	CV3426831	single nucleotide variant	NM_001256404.2(DENND2C):c.1504A>C (p.Lys502Gln)	not specified [RCV004613852]	uncertain significance	1	114608739	114608739	Human		name
407466020	CV3426832	single nucleotide variant	NM_001256404.2(DENND2C):c.1558G>T (p.Asp520Tyr)	not specified [RCV004613853]	uncertain significance	1	114605031	114605031	Human		name
407466028	CV3426834	single nucleotide variant	NM_001256404.2(DENND2C):c.1843G>A (p.Glu615Lys)	not specified [RCV004613855]	uncertain significance	1	114600933	114600933	Human		name
407466032	CV3426835	single nucleotide variant	NM_001256404.2(DENND2C):c.1867C>G (p.Pro623Ala)	not specified [RCV004613856]	uncertain significance	1	114600909	114600909	Human		name
407466044	CV3426838	single nucleotide variant	NM_001256404.2(DENND2C):c.1012G>C (p.Ala338Pro)	not specified [RCV004613859]	uncertain significance	1	114623031	114623031	Human		name
407466048	CV3426839	single nucleotide variant	NM_001256404.2(DENND2C):c.1249A>C (p.Ile417Leu)	not specified [RCV004613860]	uncertain significance	1	114618461	114618461	Human		name
407466053	CV3426840	single nucleotide variant	NM_001256404.2(DENND2C):c.1844A>G (p.Glu615Gly)	not specified [RCV004613861]	uncertain significance	1	114600932	114600932	Human		name
597641160	CV3658701	single nucleotide variant	NM_001256404.2(DENND2C):c.2525G>A (p.Arg842His)	not specified [RCV004909127]	uncertain significance	1	114587859	114587859	Human		name
597641167	CV3658702	single nucleotide variant	NM_001256404.2(DENND2C):c.2581G>A (p.Val861Ile)	not specified [RCV004909128]	uncertain significance	1	114587803	114587803	Human		name
597656565	CV3658705	single nucleotide variant	NM_001256404.2(DENND2C):c.1588A>G (p.Met530Val)	not specified [RCV004911185]	uncertain significance	1	114605001	114605001	Human		name
597656575	CV3658706	single nucleotide variant	NM_001256404.2(DENND2C):c.1784G>A (p.Ser595Asn)	not specified [RCV004911186]	uncertain significance	1	114601539	114601539	Human		name
597656589	CV3658708	single nucleotide variant	NM_001256404.2(DENND2C):c.2074C>T (p.Arg692Cys)	not specified [RCV004911188]	uncertain significance	1	114600235	114600235	Human		name
597656599	CV3658709	single nucleotide variant	NM_001256404.2(DENND2C):c.1534G>A (p.Val512Ile)	not specified [RCV004911189]	uncertain significance	1	114608709	114608709	Human		name
597656606	CV3658710	single nucleotide variant	NM_001256404.2(DENND2C):c.2183T>C (p.Leu728Pro)	not specified [RCV004911190]	uncertain significance	1	114599374	114599374	Human		name
597656616	CV3658711	single nucleotide variant	NM_001256404.2(DENND2C):c.2533C>T (p.Arg845Cys)	not specified [RCV004911191]	uncertain significance	1	114587851	114587851	Human		name
597656636	CV3658714	single nucleotide variant	NM_001256404.2(DENND2C):c.1027C>T (p.Pro343Ser)	not specified [RCV004911194]	uncertain significance	1	114623016	114623016	Human		name
597656651	CV3658716	single nucleotide variant	NM_001256404.2(DENND2C):c.1514G>A (p.Gly505Glu)	not specified [RCV004911196]	likely benign	1	114608729	114608729	Human		name
598224479	CV3956636	single nucleotide variant	NM_001256404.2(DENND2C):c.2522A>C (p.Glu841Ala)	not specified [RCV005318225]	uncertain significance	1	114587862	114587862	Human		name
598224501	CV3956639	single nucleotide variant	NM_001256404.2(DENND2C):c.1567G>A (p.Gly523Ser)	not specified [RCV005318228]	uncertain significance	1	114605022	114605022	Human		name
598224512	CV3956641	single nucleotide variant	NM_001256404.2(DENND2C):c.1259C>A (p.Ser420Tyr)	not specified [RCV005318230]	uncertain significance	1	114618451	114618451	Human		name
598224521	CV3956642	single nucleotide variant	NM_001256404.2(DENND2C):c.2615A>C (p.Gln872Pro)	not specified [RCV005318231]	uncertain significance	1	114587769	114587769	Human		name
598224529	CV3956643	single nucleotide variant	NM_001256404.2(DENND2C):c.1808T>C (p.Phe603Ser)	not specified [RCV005318232]	uncertain significance	1	114601515	114601515	Human		name
598224536	CV3956644	single nucleotide variant	NM_001256404.2(DENND2C):c.2735A>G (p.Asn912Ser)	not specified [RCV005318233]	uncertain significance	1	114587407	114587407	Human		name

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