Htr2c Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

107 records found for search term Htr2c

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405259325	CV3194738	single nucleotide variant	NM_000868.4(HTR2C):c.-7A>T	HTR2C-related disorder [RCV003894128]	likely benign	X	114726930	114726930	Human		name , trait , alternate_id
405277271	CV3195437	single nucleotide variant	NM_000868.4(HTR2C):c.*2A>G	HTR2C-related disorder [RCV003904222]	likely benign	X	114907417	114907417	Human		name , trait , alternate_id
15016609	CV656729	variation	NM_000868.4(HTR2C):c.-697=	not provided [RCV000835769]	benign	X	114584109	114584109	Human		name
408378451	CV3513473	single nucleotide variant	NM_000868.4(HTR2C):c.349+2T>C	HTR2C-related disorder [RCV004752284]	uncertain significance	X	114731609	114731609	Human		name , trait , alternate_id
408377734	CV3511270	single nucleotide variant	NM_000868.4(HTR2C):c.551-10C>A	HTR2C-related disorder [RCV004751183]	likely benign	X	114906579	114906579	Human		name , trait , alternate_id
11087711	CV227815	single nucleotide variant	NM_000868.4(HTR2C):c.551-3008C>G	not specified [RCV000606383]	benign\|drug response	X	114903581	114903581	Human		name
8587074	CV121700	single nucleotide variant	NM_000868.3(HTR2C):c.-79-19049T>C	Lung cancer [RCV000102220]	uncertain significance	X	114707809	114707809	Human		name
8587075	CV121701	single nucleotide variant	NM_000868.3(HTR2C):c.550+11838A>C	Lung cancer [RCV000102221]	uncertain significance	X	114860041	114860041	Human		name
8587076	CV121702	single nucleotide variant	NM_000868.3(HTR2C):c.551-12585G>A	Lung cancer [RCV000102222]	uncertain significance	X	114894004	114894004	Human		name
8561225	CV24924	single nucleotide variant	NM_000868.4(HTR2C):c.68= (p.Ser23=)	HTR2C POLYMORPHISM [RCV000010563]\|HTR2C-related disorder [RCV003974817]\|not provided [RCV000835770]	benign	X	114731326	114731326	Human		name , trait , alternate_id
408377661	CV3510383	microsatellite	NM_000868.4(HTR2C):c.350-7_350-6del	HTR2C-related disorder [RCV004751141]	likely benign	X	114847993	114847994	Human		name , trait , alternate_id
401934735	CV2802823	single nucleotide variant	NM_000868.4(HTR2C):c.24G>A (p.Val8=)	HTR2C-related disorder [RCV003412162]	uncertain significance	X	114726960	114726960	Human		name , trait , alternate_id
405281573	CV3213526	single nucleotide variant	NM_000868.4(HTR2C):c.21G>A (p.Ala7=)	HTR2C-related disorder [RCV003907359]	likely benign	X	114726957	114726957	Human		name , trait , alternate_id
405287013	CV3205579	single nucleotide variant	NM_000868.4(HTR2C):c.45A>G (p.Leu15=)	HTR2C-related disorder [RCV003959721]	likely benign	X	114731303	114731303	Human		name , trait , alternate_id
405295173	CV3211119	single nucleotide variant	NM_000868.4(HTR2C):c.8A>G (p.Asn3Ser)	HTR2C-related disorder [RCV003937114]	uncertain significance	X	114726944	114726944	Human		name , trait , alternate_id
405270735	CV3212062	single nucleotide variant	NM_000868.4(HTR2C):c.43C>T (p.Leu15=)	HTR2C-related disorder [RCV003949443]	likely benign	X	114731301	114731301	Human		name , trait , alternate_id
405262221	CV3220103	single nucleotide variant	NM_000868.4(HTR2C):c.84C>T (p.Ser28=)	HTR2C-related disorder [RCV003967231]	likely benign	X	114731342	114731342	Human		name , trait , alternate_id
408377478	CV3507947	single nucleotide variant	NM_000868.4(HTR2C):c.30A>C (p.Ser10=)	HTR2C-related disorder [RCV004751015]	likely benign	X	114726966	114726966	Human		name , trait , alternate_id
408378389	CV3512837	single nucleotide variant	NM_000868.4(HTR2C):c.55T>C (p.Leu19=)	HTR2C-related disorder [RCV004752264]	likely benign	X	114731313	114731313	Human		name , trait , alternate_id
408378587	CV3514458	single nucleotide variant	NM_000868.4(HTR2C):c.90A>G (p.Val30=)	HTR2C-related disorder [RCV004752342]	likely benign	X	114731348	114731348	Human		name , trait , alternate_id
408378593	CV3514498	single nucleotide variant	NM_000868.4(HTR2C):c.4G>A (p.Val2Met)	HTR2C-related disorder [RCV004752344]	uncertain significance	X	114726940	114726940	Human		name , trait , alternate_id
408377680	CV3510564	single nucleotide variant	NM_000868.4(HTR2C):c.234A>T (p.Val78=)	HTR2C-related disorder [RCV004751148]	likely benign	X	114731492	114731492	Human		name , trait , alternate_id
408377684	CV3510591	single nucleotide variant	NM_000868.4(HTR2C):c.255C>T (p.His85=)	HTR2C-related disorder [RCV004751150]	likely benign	X	114731513	114731513	Human		name , trait , alternate_id
408378369	CV3512700	single nucleotide variant	NM_000868.4(HTR2C):c.11T>G (p.Leu4Arg)	HTR2C-related disorder [RCV004752258]	uncertain significance	X	114726947	114726947	Human		name , trait , alternate_id
15171941	CV773714	single nucleotide variant	NM_000868.4(HTR2C):c.20C>T (p.Ala7Val)	HTR2C-related disorder [RCV003925794]\|not provided [RCV000928009]	likely benign	X	114726956	114726956	Human		name , trait , alternate_id
401934798	CV2802984	single nucleotide variant	NM_000868.4(HTR2C):c.92C>T (p.Ala31Val)	HTR2C-related disorder [RCV003412229]\|not specified [RCV004927909]	uncertain significance	X	114731350	114731350	Human		name , trait , alternate_id
405259122	CV3194495	single nucleotide variant	NM_000868.4(HTR2C):c.366A>G (p.Leu122=)	HTR2C-related disorder [RCV003893892]	likely benign	X	114848019	114848019	Human		name , trait , alternate_id
405258389	CV3203739	single nucleotide variant	NM_000868.4(HTR2C):c.660C>T (p.Phe220=)	HTR2C-related disorder [RCV003941921]	likely benign	X	114906698	114906698	Human		name , trait , alternate_id
405279061	CV3206825	single nucleotide variant	NM_000868.4(HTR2C):c.564T>C (p.Pro188=)	HTR2C-related disorder [RCV003919388]	likely benign	X	114906602	114906602	Human		name , trait , alternate_id
405295000	CV3210921	single nucleotide variant	NM_000868.4(HTR2C):c.879G>A (p.Glu293=)	HTR2C-related disorder [RCV003936936]	likely benign	X	114906917	114906917	Human		name , trait , alternate_id
408384851	CV3506376	single nucleotide variant	NM_000868.4(HTR2C):c.580C>T (p.Leu194=)	HTR2C-related disorder [RCV004732169]	uncertain significance	X	114906618	114906618	Human		name , trait , alternate_id
408377532	CV3507416	single nucleotide variant	NM_000868.4(HTR2C):c.459T>C (p.Tyr153=)	HTR2C-related disorder [RCV004750986]	likely benign	X	114848112	114848112	Human		name , trait , alternate_id
408377609	CV3508514	single nucleotide variant	NM_000868.4(HTR2C):c.675A>T (p.Ile225=)	HTR2C-related disorder [RCV004751043]	uncertain significance	X	114906713	114906713	Human		name , trait , alternate_id
408377668	CV3510419	single nucleotide variant	NM_000868.4(HTR2C):c.621C>T (p.Cys207=)	HTR2C-related disorder [RCV004751144]	uncertain significance	X	114906659	114906659	Human		name , trait , alternate_id
408377696	CV3510721	single nucleotide variant	NM_000868.4(HTR2C):c.651T>C (p.Ile217=)	HTR2C-related disorder [RCV004751157]	uncertain significance	X	114906689	114906689	Human		name , trait , alternate_id
408377712	CV3510911	single nucleotide variant	NM_000868.4(HTR2C):c.99A>G (p.Ile33Met)	HTR2C-related disorder [RCV004751169]	uncertain significance	X	114731357	114731357	Human		name , trait , alternate_id
408377849	CV3511054	single nucleotide variant	NM_000868.4(HTR2C):c.642C>T (p.Phe214=)	HTR2C-related disorder [RCV004751175]	uncertain significance	X	114906680	114906680	Human		name , trait , alternate_id
408378251	CV3511673	single nucleotide variant	NM_000868.4(HTR2C):c.501G>A (p.Ser167=)	HTR2C-related disorder [RCV004752192]	likely benign	X	114848154	114848154	Human		name , trait , alternate_id
408378517	CV3512210	single nucleotide variant	NM_000868.4(HTR2C):c.384C>T (p.Pro128=)	HTR2C-related disorder [RCV004752225]	likely benign	X	114848037	114848037	Human		name , trait , alternate_id
408378461	CV3513505	single nucleotide variant	NM_000868.4(HTR2C):c.891G>A (p.Arg297=)	HTR2C-related disorder [RCV004752287]	likely benign	X	114906929	114906929	Human		name , trait , alternate_id
408378474	CV3513626	single nucleotide variant	NM_000868.4(HTR2C):c.999G>T (p.Leu333=)	HTR2C-related disorder [RCV004752293]	likely benign	X	114907037	114907037	Human		name , trait , alternate_id
408378782	CV3516202	single nucleotide variant	NM_000868.4(HTR2C):c.759C>T (p.Thr253=)	HTR2C-related disorder [RCV004752436]	uncertain significance	X	114906797	114906797	Human		name , trait , alternate_id
408378940	CV3516462	single nucleotide variant	NM_000868.4(HTR2C):c.645T>G (p.Val215=)	HTR2C-related disorder [RCV004752453]	uncertain significance	X	114906683	114906683	Human		name , trait , alternate_id
401763853	CV2700228	single nucleotide variant	NM_000868.4(HTR2C):c.203T>C (p.Ile68Thr)	not specified [RCV004310901]	uncertain significance	X	114731461	114731461	Human		name
401934651	CV2796239	single nucleotide variant	NM_000868.4(HTR2C):c.1272C>T (p.Ile424=)	HTR2C-related disorder [RCV003412074]	likely benign\|uncertain significance	X	114907310	114907310	Human		name , trait , alternate_id
401937975	CV2797317	single nucleotide variant	NM_000868.4(HTR2C):c.181G>A (p.Val61Ile)	HTR2C-related disorder [RCV003417072]	uncertain significance	X	114731439	114731439	Human		name , trait , alternate_id
401905629	CV2798042	single nucleotide variant	NM_000868.4(HTR2C):c.172C>T (p.Leu58Phe)	HTR2C-related disorder [RCV003420880]	uncertain significance	X	114731430	114731430	Human		name , trait , alternate_id
401921395	CV2826817	single nucleotide variant	NM_000868.4(HTR2C):c.1251G>A (p.Arg417=)	HTR2C-related disorder [RCV004750900]\|not provided [RCV003432404]	likely benign	X	114907289	114907289	Human		name , trait , alternate_id
405277762	CV3196127	single nucleotide variant	NM_000868.4(HTR2C):c.178A>G (p.Ile60Val)	HTR2C-related disorder [RCV003904644]	uncertain significance	X	114731436	114731436	Human		name , trait , alternate_id
405283503	CV3202735	single nucleotide variant	NM_000868.4(HTR2C):c.1002T>G (p.Ser334=)	HTR2C-related disorder [RCV003921840]	likely benign	X	114907040	114907040	Human		name , trait , alternate_id
405295397	CV3204662	single nucleotide variant	NM_000868.4(HTR2C):c.1011T>C (p.Cys337=)	HTR2C-related disorder [RCV003937346]	likely benign	X	114907049	114907049	Human		name , trait , alternate_id
405289662	CV3218329	single nucleotide variant	NM_000868.4(HTR2C):c.1230G>A (p.Glu410=)	HTR2C-related disorder [RCV003983731]	likely benign	X	114907268	114907268	Human		name , trait , alternate_id
408377488	CV3508119	single nucleotide variant	NM_000868.4(HTR2C):c.124G>A (p.Asp42Asn)	HTR2C-related disorder [RCV004751024]	uncertain significance	X	114731382	114731382	Human		name , trait , alternate_id
408377491	CV3508162	single nucleotide variant	NM_000868.4(HTR2C):c.108C>A (p.Asp36Glu)	HTR2C-related disorder [RCV004751025]	uncertain significance	X	114731366	114731366	Human		name , trait , alternate_id
408377607	CV3509936	single nucleotide variant	NM_000868.4(HTR2C):c.1254T>C (p.His418=)	HTR2C-related disorder [RCV004751113]	likely benign	X	114907292	114907292	Human		name , trait , alternate_id
408378423	CV3512403	single nucleotide variant	NM_000868.4(HTR2C):c.118A>G (p.Thr40Ala)	HTR2C-related disorder [RCV004752237]	uncertain significance	X	114731376	114731376	Human		name , trait , alternate_id
408378723	CV3514915	single nucleotide variant	NM_000868.4(HTR2C):c.205G>A (p.Gly69Ser)	HTR2C-related disorder [RCV004752364]	uncertain significance	X	114731463	114731463	Human		name , trait , alternate_id
408378715	CV3515544	single nucleotide variant	NM_000868.4(HTR2C):c.1131G>A (p.Arg377=)	HTR2C-related disorder [RCV004752401]	likely benign	X	114907169	114907169	Human		name , trait , alternate_id
408378759	CV3516017	single nucleotide variant	NM_000868.4(HTR2C):c.1321T>C (p.Leu441=)	HTR2C-related disorder [RCV004752424]	likely benign	X	114907359	114907359	Human		name , trait , alternate_id
15099678	CV758236	single nucleotide variant	NM_000868.4(HTR2C):c.124G>C (p.Asp42His)	HTR2C-related disorder [RCV003913049]\|not provided [RCV000914492]	likely benign	X	114731382	114731382	Human		name , trait , alternate_id
9686790	CV171683	single nucleotide variant	NM_000868.4(HTR2C):c.502C>T (p.Arg168Trp)	Prostate cancer [RCV000149007]	uncertain significance	X	114848155	114848155	Human	2	name
156179425	CV2324236	single nucleotide variant	NM_000868.4(HTR2C):c.892G>A (p.Gly298Ser)	not specified [RCV004176973]	uncertain significance	X	114906930	114906930	Human		name
329399304	CV2470034	single nucleotide variant	NM_000868.4(HTR2C):c.929C>T (p.Ser310Leu)	not specified [RCV004287307]	uncertain significance	X	114906967	114906967	Human		name
401728191	CV2676001	single nucleotide variant	NM_000868.4(HTR2C):c.553G>A (p.Val185Ile)	not specified [RCV004281991]	uncertain significance	X	114906591	114906591	Human		name
405258954	CV3197906	single nucleotide variant	NM_000868.4(HTR2C):c.985A>G (p.Ile329Val)	HTR2C-related disorder [RCV003893829]	uncertain significance	X	114907023	114907023	Human		name , trait , alternate_id
405292962	CV3207116	single nucleotide variant	NM_000868.4(HTR2C):c.512C>T (p.Ala171Val)	HTR2C-related disorder [RCV003931527]	likely benign	X	114848165	114848165	Human		name , trait , alternate_id
405287517	CV3217822	single nucleotide variant	NM_000868.4(HTR2C):c.778A>G (p.Ser260Gly)	HTR2C-related disorder [RCV003981945]	likely benign	X	114906816	114906816	Human		name , trait , alternate_id
405804228	CV3270616	single nucleotide variant	NM_000868.4(HTR2C):c.430C>A (p.His144Asn)	not specified [RCV004404865]	uncertain significance	X	114848083	114848083	Human		name
405804183	CV3270617	single nucleotide variant	NM_000868.4(HTR2C):c.833C>G (p.Ala278Gly)	not specified [RCV004404866]	uncertain significance	X	114906871	114906871	Human		name
408384934	CV3506559	single nucleotide variant	NM_000868.4(HTR2C):c.883C>G (p.Arg295Gly)	HTR2C-related disorder [RCV004732241]	uncertain significance	X	114906921	114906921	Human		name , trait , alternate_id
408377442	CV3507279	single nucleotide variant	NM_000868.4(HTR2C):c.883C>T (p.Arg295Cys)	HTR2C-related disorder [RCV004750980]	uncertain significance	X	114906921	114906921	Human		name , trait , alternate_id
408377460	CV3507578	single nucleotide variant	NM_000868.4(HTR2C):c.862C>T (p.Arg288Ter)	HTR2C-related disorder [RCV004750996]	uncertain significance	X	114906900	114906900	Human		name , trait , alternate_id
408377499	CV3508305	single nucleotide variant	NM_000868.4(HTR2C):c.355G>A (p.Val119Ile)	HTR2C-related disorder [RCV004751033]	uncertain significance	X	114848008	114848008	Human		name , trait , alternate_id
408377621	CV3510090	single nucleotide variant	NM_000868.4(HTR2C):c.766C>T (p.Pro256Ser)	HTR2C-related disorder [RCV004751121]	uncertain significance	X	114906804	114906804	Human		name , trait , alternate_id
408378433	CV3513249	single nucleotide variant	NM_000868.4(HTR2C):c.497A>G (p.Asn166Ser)	HTR2C-related disorder [RCV004752278]	uncertain significance	X	114848150	114848150	Human		name , trait , alternate_id
408378442	CV3513420	single nucleotide variant	NM_000868.4(HTR2C):c.770C>G (p.Pro257Arg)	HTR2C-related disorder [RCV004752281]	uncertain significance	X	114906808	114906808	Human		name , trait , alternate_id
408378727	CV3515672	single nucleotide variant	NM_000868.4(HTR2C):c.385G>A (p.Val129Ile)	HTR2C-related disorder [RCV004752407]	uncertain significance	X	114848038	114848038	Human		name , trait , alternate_id
408378855	CV3515846	single nucleotide variant	NM_000868.4(HTR2C):c.839C>T (p.Pro280Leu)	HTR2C-related disorder [RCV004752416]	uncertain significance	X	114906877	114906877	Human		name , trait , alternate_id
408378869	CV3515961	single nucleotide variant	NM_000868.4(HTR2C):c.596A>C (p.Lys199Thr)	HTR2C-related disorder [RCV004752421]	uncertain significance	X	114906634	114906634	Human		name , trait , alternate_id
408378853	CV3516842	single nucleotide variant	NM_000868.4(HTR2C):c.911A>G (p.Asn304Ser)	HTR2C-related disorder [RCV004752471]	uncertain significance	X	114906949	114906949	Human		name , trait , alternate_id
408378921	CV3517698	single nucleotide variant	NM_000868.4(HTR2C):c.778A>T (p.Ser260Cys)	HTR2C-related disorder [RCV004752503]	uncertain significance	X	114906816	114906816	Human		name , trait , alternate_id
408379050	CV3517868	single nucleotide variant	NM_000868.4(HTR2C):c.475C>T (p.Pro159Ser)	HTR2C-related disorder [RCV004752517]	uncertain significance	X	114848128	114848128	Human		name , trait , alternate_id
408378972	CV3517921	single nucleotide variant	NM_000868.4(HTR2C):c.922A>C (p.Lys308Gln)	HTR2C-related disorder [RCV004752527]	uncertain significance	X	114906960	114906960	Human		name , trait , alternate_id
597783189	CV3686145	single nucleotide variant	NM_000868.4(HTR2C):c.631G>A (p.Asp211Asn)	not specified [RCV004931321]	uncertain significance	X	114906669	114906669	Human		name
597783185	CV3686146	single nucleotide variant	NM_000868.4(HTR2C):c.614C>T (p.Thr205Met)	not specified [RCV004931322]	uncertain significance	X	114906652	114906652	Human		name
598205974	CV3968409	single nucleotide variant	NM_000868.4(HTR2C):c.625C>T (p.Leu209Phe)	not specified [RCV005337696]	uncertain significance	X	114906663	114906663	Human		name
598256493	CV3968410	single nucleotide variant	NM_000868.4(HTR2C):c.994A>G (p.Ile332Val)	not specified [RCV005346809]	uncertain significance	X	114907032	114907032	Human		name
151663331	CV1331073	single nucleotide variant	NM_000868.4(HTR2C):c.1170G>T (p.Glu390Asp)	not provided [RCV001825246]	not provided	X	114907208	114907208	Human		name
156241592	CV2246134	single nucleotide variant	NM_000868.4(HTR2C):c.1166T>C (p.Val389Ala)	not specified [RCV004114035]	likely benign	X	114907204	114907204	Human		name
155906417	CV2279229	single nucleotide variant	NM_000868.4(HTR2C):c.1010G>T (p.Cys337Phe)	not specified [RCV004139757]	uncertain significance	X	114907048	114907048	Human		name
156241603	CV2310235	single nucleotide variant	NM_000868.4(HTR2C):c.1191G>C (p.Gln397His)	HTR2C-related disorder [RCV004750848]\|not specified [RCV004163334]	uncertain significance	X	114907229	114907229	Human		name , trait , alternate_id
329377337	CV2435887	single nucleotide variant	NM_000868.4(HTR2C):c.1120A>C (p.Ile374Leu)	HTR2C-related disorder [RCV003946458]\|not specified [RCV004255119]	uncertain significance	X	114907158	114907158	Human		name , trait , alternate_id
329381208	CV2464563	single nucleotide variant	NM_000868.4(HTR2C):c.1250G>A (p.Arg417Gln)	not specified [RCV004278256]	uncertain significance	X	114907288	114907288	Human		name
401891910	CV2775795	single nucleotide variant	NM_000868.4(HTR2C):c.1180C>T (p.Pro394Ser)	not specified [RCV004344840]	uncertain significance	X	114907218	114907218	Human		name
401879577	CV2785308	single nucleotide variant	NM_000868.4(HTR2C):c.1312G>C (p.Val438Leu)	HTR2C-related disorder [RCV004750890]\|not specified [RCV004357065]	uncertain significance	X	114907350	114907350	Human		name , trait , alternate_id
405295292	CV3211264	single nucleotide variant	NM_000868.4(HTR2C):c.1255A>G (p.Thr419Ala)	HTR2C-related disorder [RCV003937237]	likely benign	X	114907293	114907293	Human		name , trait , alternate_id
405804269	CV3270615	single nucleotide variant	NM_000868.4(HTR2C):c.1226G>A (p.Arg409Lys)	not specified [RCV004404864]	uncertain significance	X	114907264	114907264	Human		name
407465230	CV3444214	single nucleotide variant	NM_000868.4(HTR2C):c.1300A>G (p.Ile434Val)	HTR2C-related disorder [RCV004750972]\|not specified [RCV004635314]	uncertain significance	X	114907338	114907338	Human		name , trait , alternate_id
407465235	CV3444215	single nucleotide variant	NM_000868.4(HTR2C):c.1325A>G (p.Glu442Gly)	not specified [RCV004635315]	uncertain significance	X	114907363	114907363	Human		name
408383118	CV3504786	single nucleotide variant	NM_000868.4(HTR2C):c.1085G>C (p.Gly362Ala)	HTR2C-related disorder [RCV004730428]	uncertain significance	X	114907123	114907123	Human		name , trait , alternate_id
408377520	CV3507246	single nucleotide variant	NM_000868.4(HTR2C):c.1298G>C (p.Gly433Ala)	HTR2C-related disorder [RCV004750979]	uncertain significance	X	114907336	114907336	Human		name , trait , alternate_id
408377463	CV3507596	single nucleotide variant	NM_000868.4(HTR2C):c.1200A>T (p.Arg400Ser)	HTR2C-related disorder [RCV004750998]	uncertain significance	X	114907238	114907238	Human		name , trait , alternate_id
408377570	CV3509394	single nucleotide variant	NM_000868.4(HTR2C):c.1310A>C (p.Gln437Pro)	HTR2C-related disorder [RCV004751087]	uncertain significance	X	114907348	114907348	Human		name , trait , alternate_id
408378362	CV3512473	single nucleotide variant	NM_000868.4(HTR2C):c.1222G>A (p.Gly408Arg)	HTR2C-related disorder [RCV004752245]	uncertain significance	X	114907260	114907260	Human		name , trait , alternate_id
408378457	CV3513501	single nucleotide variant	NM_000868.4(HTR2C):c.1361G>T (p.Arg454Met)	HTR2C-related disorder [RCV004752286]	uncertain significance	X	114907399	114907399	Human		name , trait , alternate_id
15140312	CV717605	microsatellite	NM_000868.4(HTR2C):c.868AAG[2] (p.Lys292del)	not provided [RCV000966118]	benign	X	114906906	114906908	Human		name
40887611	CV974271	deletion	NM_000868.4(HTR2C):c.1219_1222del (p.Ser407fs)	Inborn genetic diseases [RCV001267222]	likely pathogenic	X	114907255	114907258	Human	1	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