Pld2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

115 records found for search term Pld2

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15116311	CV744973	single nucleotide variant	NM_002663.5(PLD2):c.1702-6C>T	not provided [RCV000895177]	benign	17	4817140	4817140	Human		name
15117746	CV745075	single nucleotide variant	NM_002663.5(PLD2):c.2010-9C>T	not provided [RCV000895431]	benign	17	4818485	4818485	Human		name
156044488	CV2305930	single nucleotide variant	NM_002663.5(PLD2):c.21C>G (p.Ser7Arg)	not specified [RCV004167713]	uncertain significance	17	4807793	4807793	Human		name
401748852	CV2706112	single nucleotide variant	NM_002663.5(PLD2):c.23T>C (p.Leu8Pro)	not specified [RCV004314802]	uncertain significance	17	4807795	4807795	Human		name
155956076	CV2281880	single nucleotide variant	NM_002663.5(PLD2):c.49T>G (p.Ser17Ala)	not specified [RCV004138663]	uncertain significance	17	4807821	4807821	Human		name
405665145	CV3372982	single nucleotide variant	NM_002663.5(PLD2):c.71C>T (p.Ser24Phe)	not specified [RCV004513996]	uncertain significance	17	4807843	4807843	Human		name
597727985	CV3580115	single nucleotide variant	NM_002663.5(PLD2):c.64A>G (p.Met22Val)	not specified [RCV004842601]	uncertain significance	17	4807836	4807836	Human		name
8636245	CV91469	single nucleotide variant	NM_002663.4(PLD2):c.732C>T (p.Phe244=)	Malignant melanoma [RCV000071567]	not provided	17	4809901	4809901	Human		name
156382094	CV2227187	single nucleotide variant	NM_002663.5(PLD2):c.268C>T (p.Arg90Cys)	not specified [RCV004091796]	uncertain significance	17	4808301	4808301	Human		name
156114061	CV2397127	single nucleotide variant	NM_002663.5(PLD2):c.251G>A (p.Cys84Tyr)	not specified [RCV004236628]	uncertain significance	17	4808284	4808284	Human		name
405665102	CV3372972	single nucleotide variant	NM_002663.5(PLD2):c.139T>A (p.Tyr47Asn)	not specified [RCV004513986]	uncertain significance	17	4808013	4808013	Human		name
598207230	CV3997086	single nucleotide variant	NM_002663.5(PLD2):c.233G>T (p.Gly78Val)	not specified [RCV005399792]	uncertain significance	17	4808107	4808107	Human		name
15201072	CV704192	single nucleotide variant	NM_002663.5(PLD2):c.2580C>T (p.Ile860=)	not provided [RCV000957515]	benign	17	4822642	4822642	Human		name
15183292	CV740834	single nucleotide variant	NM_002663.5(PLD2):c.1008G>A (p.Arg336=)	not provided [RCV000908028]	likely benign	17	4810949	4810949	Human		name
15137196	CV740835	single nucleotide variant	NM_002663.5(PLD2):c.1638C>T (p.Val546=)	not provided [RCV000898759]	likely benign	17	4816992	4816992	Human		name
156072047	CV2201302	single nucleotide variant	NM_002663.5(PLD2):c.934G>T (p.Gly312Cys)	not specified [RCV004077434]	uncertain significance	17	4810875	4810875	Human		name
156343264	CV2232661	single nucleotide variant	NM_002663.5(PLD2):c.847G>A (p.Asp283Asn)	not specified [RCV004101331]	uncertain significance	17	4810016	4810016	Human		name
156138137	CV2236597	single nucleotide variant	NM_002663.5(PLD2):c.988C>T (p.Arg330Trp)	not specified [RCV004110582]	uncertain significance	17	4810929	4810929	Human		name
156370025	CV2263461	single nucleotide variant	NM_002663.5(PLD2):c.538C>T (p.Arg180Cys)	not specified [RCV004133706]	uncertain significance	17	4809346	4809346	Human		name
156391961	CV2378154	single nucleotide variant	NM_002663.5(PLD2):c.898C>T (p.Arg300Trp)	not specified [RCV004233071]	uncertain significance	17	4810839	4810839	Human		name
155955608	CV2387130	single nucleotide variant	NM_002663.5(PLD2):c.677G>A (p.Arg226Gln)	not specified [RCV004238239]	uncertain significance	17	4809753	4809753	Human		name
156003251	CV2396714	single nucleotide variant	NM_002663.5(PLD2):c.424A>G (p.Arg142Gly)	not specified [RCV004233869]	uncertain significance	17	4809140	4809140	Human		name
401782460	CV2686871	single nucleotide variant	NM_002663.5(PLD2):c.445C>T (p.Arg149Trp)	not specified [RCV004302049]	uncertain significance	17	4809161	4809161	Human		name
401773300	CV2709233	single nucleotide variant	NM_002663.5(PLD2):c.850A>G (p.Thr284Ala)	not specified [RCV004316400]	uncertain significance	17	4810019	4810019	Human		name
401773955	CV2727685	single nucleotide variant	NM_002663.5(PLD2):c.605G>T (p.Arg202Leu)	not specified [RCV004329857]	uncertain significance	17	4809542	4809542	Human		name
401895168	CV2789742	single nucleotide variant	NM_002663.5(PLD2):c.562T>C (p.Phe188Leu)	not specified [RCV004361858]	uncertain significance	17	4809499	4809499	Human		name
405665138	CV3372980	single nucleotide variant	NM_002663.5(PLD2):c.418G>T (p.Gly140Cys)	not specified [RCV004513994]	uncertain significance	17	4809134	4809134	Human		name
405665141	CV3372981	single nucleotide variant	NM_002663.5(PLD2):c.422A>G (p.Asn141Ser)	not specified [RCV004513995]	uncertain significance	17	4809138	4809138	Human		name
405665152	CV3372983	single nucleotide variant	NM_002663.5(PLD2):c.821C>T (p.Thr274Met)	not specified [RCV004513997]	uncertain significance	17	4809990	4809990	Human		name
407470486	CV3470962	single nucleotide variant	NM_002663.5(PLD2):c.647A>G (p.His216Arg)	not specified [RCV004662058]	uncertain significance	17	4809723	4809723	Human		name
407518898	CV3470964	single nucleotide variant	NM_002663.5(PLD2):c.611G>A (p.Gly204Glu)	not specified [RCV004651186]	uncertain significance	17	4809548	4809548	Human		name
407518902	CV3470966	single nucleotide variant	NM_002663.5(PLD2):c.410G>A (p.Arg137Gln)	not specified [RCV004651188]	likely benign	17	4809126	4809126	Human		name
597727868	CV3580099	single nucleotide variant	NM_002663.5(PLD2):c.718G>T (p.Val240Leu)	not specified [RCV004842587]	uncertain significance	17	4809887	4809887	Human		name
597727877	CV3580100	single nucleotide variant	NM_002663.5(PLD2):c.880A>T (p.Ser294Cys)	not specified [RCV004842588]	uncertain significance	17	4810821	4810821	Human		name
597727900	CV3580103	single nucleotide variant	NM_002663.5(PLD2):c.830G>A (p.Arg277Gln)	not specified [RCV004842591]	uncertain significance	17	4809999	4809999	Human		name
597727915	CV3580105	single nucleotide variant	NM_002663.5(PLD2):c.313C>A (p.Arg105Ser)	not specified [RCV004842593]	uncertain significance	17	4808346	4808346	Human		name
597727931	CV3580108	single nucleotide variant	NM_002663.5(PLD2):c.838G>A (p.Val280Met)	not specified [RCV004842595]	uncertain significance	17	4810007	4810007	Human		name
598207236	CV3997087	single nucleotide variant	NM_002663.5(PLD2):c.829C>T (p.Arg277Trp)	not specified [RCV005399793]	uncertain significance	17	4809998	4809998	Human		name
598207250	CV3997089	single nucleotide variant	NM_002663.5(PLD2):c.335G>A (p.Arg112Gln)	not specified [RCV005399795]	uncertain significance	17	4808368	4808368	Human		name
15113237	CV715517	single nucleotide variant	NM_002663.5(PLD2):c.832C>T (p.His278Tyr)	not provided [RCV000961453]	benign	17	4810001	4810001	Human		name
15181797	CV727243	single nucleotide variant	NM_002663.5(PLD2):c.989G>A (p.Arg330Gln)	not provided [RCV000885845]	benign	17	4810930	4810930	Human		name
156399840	CV2202258	single nucleotide variant	NM_002663.5(PLD2):c.2669C>G (p.Pro890Arg)	not specified [RCV004078197]	uncertain significance	17	4822731	4822731	Human		name
156378940	CV2207843	single nucleotide variant	NM_002663.5(PLD2):c.2027G>T (p.Arg676Leu)	not specified [RCV004084275]	uncertain significance	17	4818511	4818511	Human		name
156387536	CV2221539	single nucleotide variant	NM_002663.5(PLD2):c.2189G>A (p.Arg730Gln)	not specified [RCV004096806]	uncertain significance	17	4819099	4819099	Human		name
155929817	CV2224619	single nucleotide variant	NM_002663.5(PLD2):c.1789C>A (p.Pro597Thr)	not specified [RCV004098185]	uncertain significance	17	4817233	4817233	Human		name
156283774	CV2249788	single nucleotide variant	NM_002663.5(PLD2):c.1487C>T (p.Thr496Ile)	not specified [RCV004122552]	uncertain significance	17	4816651	4816651	Human		name
156201905	CV2256198	single nucleotide variant	NM_002663.5(PLD2):c.2249C>T (p.Ser750Leu)	not specified [RCV004116462]	uncertain significance	17	4819159	4819159	Human		name
156149063	CV2265321	single nucleotide variant	NM_002663.5(PLD2):c.2542G>C (p.Asp848His)	not specified [RCV004128212]	uncertain significance	17	4821872	4821872	Human		name
156068429	CV2270911	single nucleotide variant	NM_002663.5(PLD2):c.1466C>G (p.Pro489Arg)	not specified [RCV004131950]	uncertain significance	17	4816630	4816630	Human		name
156069138	CV2270960	single nucleotide variant	NM_002663.5(PLD2):c.1195A>G (p.Ile399Val)	not specified [RCV004131993]	likely benign	17	4815497	4815497	Human		name
155929291	CV2278046	single nucleotide variant	NM_002663.5(PLD2):c.2348G>A (p.Arg783Gln)	not specified [RCV004141271]	uncertain significance	17	4819468	4819468	Human		name
156005346	CV2281519	single nucleotide variant	NM_002663.5(PLD2):c.1709A>G (p.Lys570Arg)	not specified [RCV004153831]	uncertain significance	17	4817153	4817153	Human		name
156002301	CV2287992	single nucleotide variant	NM_002663.5(PLD2):c.2066G>A (p.Gly689Asp)	not specified [RCV004147760]	uncertain significance	17	4818550	4818550	Human		name
156141780	CV2288583	single nucleotide variant	NM_002663.5(PLD2):c.2134C>T (p.Arg712Cys)	not specified [RCV004152103]	uncertain significance	17	4818784	4818784	Human		name
156207571	CV2298051	single nucleotide variant	NM_002663.5(PLD2):c.2193C>G (p.Asp731Glu)	not specified [RCV004157944]	uncertain significance	17	4819103	4819103	Human		name
156181005	CV2298503	single nucleotide variant	NM_002663.5(PLD2):c.2641G>A (p.Val881Met)	not specified [RCV004162167]	uncertain significance	17	4822703	4822703	Human		name
156208585	CV2304295	single nucleotide variant	NM_002663.5(PLD2):c.1793G>A (p.Gly598Glu)	not specified [RCV004164418]	uncertain significance	17	4817237	4817237	Human		name
156175060	CV2327059	single nucleotide variant	NM_002663.5(PLD2):c.2396C>G (p.Ser799Cys)	not specified [RCV004178646]	uncertain significance	17	4819516	4819516	Human		name
156292937	CV2336346	single nucleotide variant	NM_002663.5(PLD2):c.2263A>G (p.Ile755Val)	not specified [RCV004194569]	uncertain significance	17	4819173	4819173	Human		name
156035287	CV2338890	single nucleotide variant	NM_002663.5(PLD2):c.2782C>A (p.Pro928Thr)	not specified [RCV004184483]	uncertain significance	17	4822844	4822844	Human		name
155921452	CV2350670	single nucleotide variant	NM_002663.5(PLD2):c.2365G>A (p.Val789Met)	not specified [RCV004207019]	uncertain significance	17	4819485	4819485	Human		name
155992040	CV2355602	single nucleotide variant	NM_002663.5(PLD2):c.1763C>T (p.Thr588Met)	not specified [RCV004205445]	uncertain significance	17	4817207	4817207	Human		name
156038226	CV2374147	single nucleotide variant	NM_002663.5(PLD2):c.1886C>T (p.Thr629Ile)	not specified [RCV004229297]	uncertain significance	17	4818072	4818072	Human		name
155939312	CV2376671	single nucleotide variant	NM_002663.5(PLD2):c.1108G>A (p.Val370Ile)	not specified [RCV004222868]	likely benign	17	4814646	4814646	Human		name
156034369	CV2376672	single nucleotide variant	NM_002663.5(PLD2):c.1810G>A (p.Val604Ile)	not specified [RCV004222869]	uncertain significance	17	4817254	4817254	Human		name
156108518	CV2390241	single nucleotide variant	NM_002663.5(PLD2):c.2618G>A (p.Arg873Gln)	not specified [RCV004240617]	uncertain significance	17	4822680	4822680	Human		name
329399694	CV2443461	single nucleotide variant	NM_002663.5(PLD2):c.2215C>T (p.Arg739Cys)	not specified [RCV004262297]	uncertain significance	17	4819125	4819125	Human		name
329362148	CV2466054	single nucleotide variant	NM_002663.5(PLD2):c.2762G>A (p.Gly921Asp)	not specified [RCV004277945]	uncertain significance	17	4822824	4822824	Human		name
329398921	CV2471791	single nucleotide variant	NM_002663.5(PLD2):c.1507C>G (p.Gln503Glu)	not specified [RCV004280832]	uncertain significance	17	4816671	4816671	Human		name
401753944	CV2685111	single nucleotide variant	NM_002663.5(PLD2):c.1391G>A (p.Arg464His)	not specified [RCV004289683]	uncertain significance	17	4815870	4815870	Human		name
401761393	CV2689130	single nucleotide variant	NM_002663.5(PLD2):c.2330G>A (p.Arg777Gln)	not specified [RCV004305892]	uncertain significance	17	4819450	4819450	Human		name
401722536	CV2703404	single nucleotide variant	NM_002663.5(PLD2):c.2663G>C (p.Ser888Thr)	not specified [RCV004317607]	uncertain significance	17	4822725	4822725	Human		name
401749508	CV2719314	single nucleotide variant	NM_002663.5(PLD2):c.1448C>T (p.Ala483Val)	not specified [RCV004324949]	uncertain significance	17	4815927	4815927	Human		name
401752715	CV2723330	single nucleotide variant	NM_002663.5(PLD2):c.1340T>C (p.Val447Ala)	not specified [RCV004329549]	uncertain significance	17	4815819	4815819	Human		name
401885134	CV2786685	single nucleotide variant	NM_002663.5(PLD2):c.2429G>C (p.Arg810Thr)	not specified [RCV004363810]	uncertain significance	17	4819549	4819549	Human		name
405665097	CV3372971	single nucleotide variant	NM_002663.5(PLD2):c.1195A>C (p.Ile399Leu)	not specified [RCV004513985]	uncertain significance	17	4815497	4815497	Human		name
405665106	CV3372973	single nucleotide variant	NM_002663.5(PLD2):c.1441T>A (p.Ser481Thr)	not specified [RCV004513987]	uncertain significance	17	4815920	4815920	Human		name
405665111	CV3372974	single nucleotide variant	NM_002663.5(PLD2):c.1489C>T (p.Pro497Ser)	not specified [RCV004513988]	uncertain significance	17	4816653	4816653	Human		name
405665117	CV3372975	single nucleotide variant	NM_002663.5(PLD2):c.1639G>A (p.Val547Ile)	not specified [RCV004513989]	uncertain significance	17	4816993	4816993	Human		name
405665121	CV3372976	single nucleotide variant	NM_002663.5(PLD2):c.1684C>T (p.Arg562Cys)	not specified [RCV004513990]	uncertain significance	17	4817038	4817038	Human		name
405665125	CV3372977	single nucleotide variant	NM_002663.5(PLD2):c.2350G>T (p.Asp784Tyr)	not specified [RCV004513991]	uncertain significance	17	4819470	4819470	Human		name
405665128	CV3372978	single nucleotide variant	NM_002663.5(PLD2):c.2657C>T (p.Thr886Met)	not specified [RCV004513992]	uncertain significance	17	4822719	4822719	Human		name
407518890	CV3470955	single nucleotide variant	NM_002663.5(PLD2):c.1007G>C (p.Arg336Pro)	not specified [RCV004651182]	uncertain significance	17	4810948	4810948	Human		name
407518893	CV3470956	single nucleotide variant	NM_002663.5(PLD2):c.1121G>A (p.Arg374His)	not specified [RCV004651183]	uncertain significance	17	4814659	4814659	Human		name
407518895	CV3470957	single nucleotide variant	NM_002663.5(PLD2):c.1571G>A (p.Arg524Gln)	not specified [RCV004651184]	uncertain significance	17	4816735	4816735	Human		name
407470474	CV3470959	single nucleotide variant	NM_002663.5(PLD2):c.1933A>G (p.Ile645Val)	not specified [RCV004662055]	uncertain significance	17	4818309	4818309	Human		name
407470479	CV3470960	single nucleotide variant	NM_002663.5(PLD2):c.1063G>A (p.Ala355Thr)	not specified [RCV004662056]	uncertain significance	17	4814470	4814470	Human		name
407470483	CV3470961	single nucleotide variant	NM_002663.5(PLD2):c.2485C>T (p.Arg829Trp)	not specified [RCV004662057]	uncertain significance	17	4821815	4821815	Human		name
407470490	CV3470963	single nucleotide variant	NM_002663.5(PLD2):c.2553G>C (p.Glu851Asp)	not specified [RCV004662059]	uncertain significance	17	4821883	4821883	Human		name
407518900	CV3470965	single nucleotide variant	NM_002663.5(PLD2):c.2647C>T (p.Pro883Ser)	not specified [RCV004651187]	uncertain significance	17	4822709	4822709	Human		name
597727845	CV3580096	single nucleotide variant	NM_002663.5(PLD2):c.2073C>G (p.Ile691Met)	not specified [RCV004842584]	uncertain significance	17	4818557	4818557	Human		name
597727852	CV3580097	single nucleotide variant	NM_002663.5(PLD2):c.1276A>G (p.Asn426Asp)	not specified [RCV004842585]	uncertain significance	17	4815578	4815578	Human		name
597727860	CV3580098	single nucleotide variant	NM_002663.5(PLD2):c.2609G>A (p.Arg870His)	not specified [RCV004842586]	uncertain significance	17	4822671	4822671	Human		name
597727885	CV3580101	single nucleotide variant	NM_002663.5(PLD2):c.1905C>G (p.His635Gln)	not specified [RCV004842589]	uncertain significance	17	4818091	4818091	Human		name
597727906	CV3580104	single nucleotide variant	NM_002663.5(PLD2):c.1006C>T (p.Arg336Trp)	not specified [RCV004842592]	uncertain significance	17	4810947	4810947	Human		name
597727923	CV3580106	single nucleotide variant	NM_002663.5(PLD2):c.1697C>T (p.Thr566Ile)	not specified [RCV004842594]	uncertain significance	17	4817051	4817051	Human		name
597768056	CV3580107	single nucleotide variant	NM_002663.5(PLD2):c.1265T>C (p.Leu422Pro)	not specified [RCV004850611]	uncertain significance	17	4815567	4815567	Human		name
597727938	CV3580109	single nucleotide variant	NM_002663.5(PLD2):c.2626C>T (p.Arg876Trp)	not specified [RCV004842596]	uncertain significance	17	4822688	4822688	Human		name
597768061	CV3580110	single nucleotide variant	NM_002663.5(PLD2):c.2033A>G (p.Tyr678Cys)	not specified [RCV004850612]	uncertain significance	17	4818517	4818517	Human		name
597727947	CV3580111	single nucleotide variant	NM_002663.5(PLD2):c.1949G>A (p.Gly650Glu)	not specified [RCV004842597]	uncertain significance	17	4818325	4818325	Human		name
597727957	CV3580112	single nucleotide variant	NM_002663.5(PLD2):c.2179A>T (p.Thr727Ser)	not specified [RCV004842598]	uncertain significance	17	4819089	4819089	Human		name
597727974	CV3580114	single nucleotide variant	NM_002663.5(PLD2):c.1711G>T (p.Ala571Ser)	not specified [RCV004842600]	uncertain significance	17	4817155	4817155	Human		name
597768066	CV3580116	single nucleotide variant	NM_002663.5(PLD2):c.2606C>T (p.Thr869Met)	not specified [RCV004850613]	uncertain significance	17	4822668	4822668	Human		name
597727994	CV3580117	single nucleotide variant	NM_002663.5(PLD2):c.1345G>A (p.Asp449Asn)	not specified [RCV004842602]	uncertain significance	17	4815824	4815824	Human		name
598207210	CV3997083	single nucleotide variant	NM_002663.5(PLD2):c.1385A>G (p.Tyr462Cys)	not specified [RCV005399789]	uncertain significance	17	4815864	4815864	Human		name
598207217	CV3997084	single nucleotide variant	NM_002663.5(PLD2):c.2567T>A (p.Ile856Asn)	not specified [RCV005399790]	uncertain significance	17	4821897	4821897	Human		name
598207223	CV3997085	single nucleotide variant	NM_002663.5(PLD2):c.1937G>T (p.Ser646Ile)	not specified [RCV005399791]	uncertain significance	17	4818313	4818313	Human		name
598207243	CV3997088	single nucleotide variant	NM_002663.5(PLD2):c.1375G>A (p.Asp459Asn)	not specified [RCV005399794]	uncertain significance	17	4815854	4815854	Human		name
13827761	CV578547	single nucleotide variant	NM_002663.5(PLD2):c.2447G>A (p.Arg816Gln)	not provided [RCV000714773]	uncertain significance	17	4819567	4819567	Human		name
15167576	CV727244	single nucleotide variant	NM_002663.5(PLD2):c.1468C>T (p.Arg490Cys)	not provided [RCV000882875]	likely benign	17	4816632	4816632	Human		name
15121319	CV740836	single nucleotide variant	NM_002663.5(PLD2):c.1658G>A (p.Arg553Gln)	not provided [RCV000896044]	benign	17	4817012	4817012	Human		name
15103831	CV755916	single nucleotide variant	NM_002663.5(PLD2):c.1705A>G (p.Thr569Ala)	not provided [RCV000915240]	likely benign	17	4817149	4817149	Human		name
8636246	CV91470	single nucleotide variant	NM_002663.4(PLD2):c.2243C>T (p.Pro748Leu)	Malignant melanoma [RCV000071568]	not provided	17	4819153	4819153	Human		name
8689335	CV97422	single nucleotide variant	NM_002663.5(PLD2):c.1657C>T (p.Arg553Trp)	not provided [RCV000122502]	uncertain significance	17	4817011	4817011	Human		name
404981321	CV2850804	insertion	NM_002663.5(PLD2):c.2026_2027insAA (p.Arg676fs)	not provided [RCV003488269]	uncertain significance	17	4818510	4818511	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