Dock9 Variant Search Result - Rat Genome Database

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171 records found for search term Dock9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15195407	CV760240	single nucleotide variant	NM_001366683.2(DOCK9):c.334-3T>C	not provided [RCV000911409]	likely benign	13	98925922	98925922	Human		name
156137741	CV2236499	single nucleotide variant	NM_001366683.2(DOCK9):c.5023+908C>T	not specified [RCV004110501]	uncertain significance	13	98825922	98825922	Human		name
597661764	CV3666709	single nucleotide variant	NM_001366683.2(DOCK9):c.5023+952C>T	not specified [RCV004911967]	uncertain significance	13	98825878	98825878	Human		name
597661845	CV3666718	single nucleotide variant	NM_001366683.2(DOCK9):c.5367+706T>A	not specified [RCV004911976]	uncertain significance	13	98808646	98808646	Human		name
8583430	CV117992	single nucleotide variant	NM_001130049.1(DOCK9):c.129+41656G>T	Lung cancer [RCV000098512]	uncertain significance	13	99044567	99044567	Human		name
155961186	CV2204469	single nucleotide variant	NM_015296.3(DOCK9):c.95G>A (p.Ser32Asn)	not specified [RCV004079272]	uncertain significance	13	99086257	99086257	Human		name
401910122	CV2813975	single nucleotide variant	NM_001366683.2(DOCK9):c.69G>C (p.Leu23=)	not provided [RCV003398354]	likely benign	13	98977841	98977841	Human		name
28888421	CV860073	single nucleotide variant	NM_001366683.2(DOCK9):c.93C>T (p.Gly31=)	not provided [RCV001092081]	likely benign	13	98977817	98977817	Human		name
8635101	CV90323	single nucleotide variant	NM_001130048.1(DOCK9):c.139C>T (p.Leu47=)	Malignant melanoma [RCV000070421]	not provided	13	98955539	98955539	Human		name
401730542	CV2677218	single nucleotide variant	NM_001366683.2(DOCK9):c.245C>T (p.Thr82Met)	not specified [RCV004295842]	uncertain significance	13	98930256	98930256	Human		name
401759674	CV2698587	single nucleotide variant	NM_001366683.2(DOCK9):c.214A>G (p.Met72Val)	not specified [RCV004299072]	uncertain significance	13	98955464	98955464	Human		name
401934110	CV2813973	single nucleotide variant	NM_001366683.2(DOCK9):c.2232G>C (p.Thr744=)	not provided [RCV003410993]	likely benign	13	98885736	98885736	Human		name
401910120	CV2813974	single nucleotide variant	NM_001366683.2(DOCK9):c.1293G>A (p.Thr431=)	not provided [RCV003398353]	likely benign	13	98902375	98902375	Human		name
405764030	CV3237927	single nucleotide variant	NM_001366683.2(DOCK9):c.293C>T (p.Ala98Val)	not specified [RCV004383973]	uncertain significance	13	98930208	98930208	Human		name
407505911	CV3437885	single nucleotide variant	NM_001366683.2(DOCK9):c.172G>A (p.Val58Ile)	not specified [RCV004624528]	uncertain significance	13	98955506	98955506	Human		name
598129712	CV3887132	single nucleotide variant	NM_001366683.2(DOCK9):c.2751G>A (p.Ala917=)	not provided [RCV005245192]	likely benign	13	98880667	98880667	Human		name
15199337	CV753912	single nucleotide variant	NM_001366683.2(DOCK9):c.2577A>G (p.Glu859=)	not provided [RCV000912518]	benign	13	98881990	98881990	Human		name
15172491	CV769639	single nucleotide variant	NM_001366683.2(DOCK9):c.2721G>A (p.Glu907=)	not provided [RCV000928125]	likely benign	13	98881582	98881582	Human		name
156179137	CV2201637	single nucleotide variant	NM_001366683.2(DOCK9):c.413C>T (p.Pro138Leu)	not specified [RCV004082099]	uncertain significance	13	98925840	98925840	Human		name
156341381	CV2225820	single nucleotide variant	NM_001366683.2(DOCK9):c.854C>G (p.Ala285Gly)	not specified [RCV004103224]	uncertain significance	13	98915367	98915367	Human		name
156175991	CV2317342	single nucleotide variant	NM_001366683.2(DOCK9):c.993T>G (p.Ser331Arg)	not specified [RCV004178824]	uncertain significance	13	98904674	98904674	Human		name
155978197	CV2338952	single nucleotide variant	NM_001366683.2(DOCK9):c.845A>G (p.Asn282Ser)	not specified [RCV004184541]	uncertain significance	13	98915376	98915376	Human		name
156200233	CV2362929	single nucleotide variant	NM_001366683.2(DOCK9):c.439C>T (p.Leu147Phe)	not specified [RCV004209032]	uncertain significance	13	98923349	98923349	Human		name
155967631	CV2391366	single nucleotide variant	NM_001366683.2(DOCK9):c.796G>T (p.Val266Leu)	not specified [RCV004239772]	uncertain significance	13	98915425	98915425	Human		name
401781748	CV2722254	single nucleotide variant	NM_001366683.2(DOCK9):c.571G>C (p.Val191Leu)	not specified [RCV004328811]	uncertain significance	13	98922062	98922062	Human		name
401934109	CV2813972	single nucleotide variant	NM_001366683.2(DOCK9):c.4839C>T (p.Asn1613=)	not provided [RCV003410992]	likely benign	13	98829433	98829433	Human		name
405764035	CV3237928	single nucleotide variant	NM_001366683.2(DOCK9):c.298G>T (p.Ala100Ser)	not specified [RCV004383974]	uncertain significance	13	98930203	98930203	Human		name
405764124	CV3237942	single nucleotide variant	NM_001366683.2(DOCK9):c.982A>C (p.Lys328Gln)	not specified [RCV004383988]	uncertain significance	13	98904685	98904685	Human		name
407505879	CV3437875	single nucleotide variant	NM_001366683.2(DOCK9):c.923G>A (p.Gly308Asp)	not specified [RCV004624518]	uncertain significance	13	98914365	98914365	Human		name
407505891	CV3437879	single nucleotide variant	NM_001366683.2(DOCK9):c.863A>C (p.Gln288Pro)	not specified [RCV004624522]	uncertain significance	13	98915358	98915358	Human		name
597734193	CV3666702	single nucleotide variant	NM_001366683.2(DOCK9):c.506C>T (p.Ser169Phe)	not specified [RCV004920217]	uncertain significance	13	98922127	98922127	Human		name
597734205	CV3666723	single nucleotide variant	NM_001366683.2(DOCK9):c.715C>A (p.Gln239Lys)	not specified [RCV004920219]	uncertain significance	13	98920956	98920956	Human		name
597661895	CV3666726	single nucleotide variant	NM_001366683.2(DOCK9):c.407A>G (p.Gln136Arg)	not specified [RCV004911982]	uncertain significance	13	98925846	98925846	Human		name
598175545	CV3964545	single nucleotide variant	NM_001366683.2(DOCK9):c.395G>A (p.Gly132Glu)	not specified [RCV005331864]	uncertain significance	13	98925858	98925858	Human		name
15176287	CV713987	single nucleotide variant	NM_001366683.2(DOCK9):c.6036C>T (p.Cys2012=)	not provided [RCV000973152]	benign\|likely benign	13	98797235	98797235	Human		name
15121877	CV713988	single nucleotide variant	NM_001366683.2(DOCK9):c.5127C>T (p.Asn1709=)	not provided [RCV000962973]	benign	13	98824401	98824401	Human		name
15168643	CV739102	single nucleotide variant	NM_001366683.2(DOCK9):c.4305G>A (p.Leu1435=)	not provided [RCV000904898]	benign	13	98837503	98837503	Human		name
8635099	CV90321	single nucleotide variant	NM_001130048.1(DOCK9):c.4479G>A (p.Arg1493=)	Malignant melanoma [RCV000070419]	not provided	13	98831435	98831435	Human		name
8583429	CV117991	single nucleotide variant	NM_001130048.1(DOCK9):c.2315A>C (p.Gln772Pro)	Lung cancer [RCV000098511]	uncertain significance	13	98885038	98885038	Human		name
155970908	CV2241618	single nucleotide variant	NM_001366683.2(DOCK9):c.2755A>G (p.Lys919Glu)	not specified [RCV004104502]	uncertain significance	13	98880663	98880663	Human		name
155987842	CV2251160	single nucleotide variant	NM_001366683.2(DOCK9):c.2749G>A (p.Ala917Thr)	not specified [RCV004115393]	uncertain significance	13	98880669	98880669	Human		name
156359042	CV2260950	single nucleotide variant	NM_001366683.2(DOCK9):c.1487G>A (p.Ser496Asn)	not specified [RCV004125833]	uncertain significance	13	98901794	98901794	Human		name
156336829	CV2270927	single nucleotide variant	NM_001366683.2(DOCK9):c.2732G>A (p.Arg911Lys)	not specified [RCV004131964]	uncertain significance	13	98881571	98881571	Human		name
156271622	CV2280772	single nucleotide variant	NM_001366683.2(DOCK9):c.1075T>C (p.Phe359Leu)	not specified [RCV004145037]	uncertain significance	13	98903073	98903073	Human		name
156169184	CV2296568	single nucleotide variant	NM_001366683.2(DOCK9):c.2422C>T (p.Pro808Ser)	not specified [RCV004154637]	uncertain significance	13	98883860	98883860	Human		name
155904334	CV2298786	single nucleotide variant	NM_001366683.2(DOCK9):c.1682T>C (p.Met561Thr)	not specified [RCV004156342]	uncertain significance	13	98897515	98897515	Human		name
156255496	CV2325753	single nucleotide variant	NM_001366683.2(DOCK9):c.2522C>T (p.Ala841Val)	not specified [RCV004173646]	uncertain significance	13	98883079	98883079	Human		name
155925567	CV2348424	single nucleotide variant	NM_001366683.2(DOCK9):c.1838G>A (p.Ser613Asn)	not specified [RCV004193615]	uncertain significance	13	98888499	98888499	Human		name
155908646	CV2354704	single nucleotide variant	NM_001366683.2(DOCK9):c.1991C>T (p.Ala664Val)	not specified [RCV004202658]	uncertain significance	13	98888210	98888210	Human		name
156140371	CV2383610	single nucleotide variant	NM_001366683.2(DOCK9):c.2651A>C (p.Glu884Ala)	not specified [RCV004229501]	uncertain significance	13	98881916	98881916	Human		name
155954510	CV2389779	single nucleotide variant	NM_001366683.2(DOCK9):c.2936A>G (p.Lys979Arg)	not specified [RCV004236010]	uncertain significance	13	98879905	98879905	Human		name
156250694	CV2394238	single nucleotide variant	NM_001366683.2(DOCK9):c.2475G>T (p.Gln825His)	not specified [RCV004238473]	uncertain significance	13	98883126	98883126	Human		name
329399419	CV2470089	single nucleotide variant	NM_001366683.2(DOCK9):c.1372C>G (p.Pro458Ala)	not specified [RCV004287351]	uncertain significance	13	98902296	98902296	Human		name
401736313	CV2682762	single nucleotide variant	NM_001366683.2(DOCK9):c.1373C>T (p.Pro458Leu)	not specified [RCV004281736]	uncertain significance	13	98902295	98902295	Human		name
401758790	CV2705137	single nucleotide variant	NM_001366683.2(DOCK9):c.1192G>A (p.Val398Ile)	not specified [RCV004310036]	uncertain significance	13	98902476	98902476	Human		name
401888708	CV2754766	single nucleotide variant	NM_001366683.2(DOCK9):c.1417T>C (p.Phe473Leu)	not specified [RCV004341250]	uncertain significance	13	98901864	98901864	Human		name
401897745	CV2772894	single nucleotide variant	NM_001366683.2(DOCK9):c.1661A>G (p.Asn554Ser)	not specified [RCV004357668]	uncertain significance	13	98897536	98897536	Human		name
401859103	CV2775095	single nucleotide variant	NM_001366683.2(DOCK9):c.2482C>T (p.His828Tyr)	not specified [RCV004346460]	uncertain significance	13	98883119	98883119	Human		name
405763999	CV3237922	single nucleotide variant	NM_001366683.2(DOCK9):c.2393C>T (p.Pro798Leu)	not specified [RCV004383968]	uncertain significance	13	98883889	98883889	Human		name
405764006	CV3237923	single nucleotide variant	NM_001366683.2(DOCK9):c.2507A>G (p.Lys836Arg)	not specified [RCV004383969]	uncertain significance	13	98883094	98883094	Human		name
405764012	CV3237924	single nucleotide variant	NM_001366683.2(DOCK9):c.2648A>G (p.Gln883Arg)	not specified [RCV004383970]	uncertain significance	13	98881919	98881919	Human		name
405764018	CV3237925	single nucleotide variant	NM_001366683.2(DOCK9):c.2722A>C (p.Ser908Arg)	not specified [RCV004383971]	uncertain significance	13	98881581	98881581	Human		name
405764024	CV3237926	single nucleotide variant	NM_001366683.2(DOCK9):c.2951G>A (p.Arg984Gln)	not specified [RCV004383972]	uncertain significance	13	98868370	98868370	Human		name
407505894	CV3437880	single nucleotide variant	NM_001366683.2(DOCK9):c.1919A>G (p.Asn640Ser)	not specified [RCV004624523]	uncertain significance	13	98888418	98888418	Human		name
407505901	CV3437882	single nucleotide variant	NM_001366683.2(DOCK9):c.1877C>G (p.Pro626Arg)	not specified [RCV004624525]	uncertain significance	13	98888460	98888460	Human		name
407505918	CV3437887	single nucleotide variant	NM_001366683.2(DOCK9):c.1065A>T (p.Glu355Asp)	not specified [RCV004624530]	uncertain significance	13	98903083	98903083	Human		name
597661694	CV3666699	single nucleotide variant	NM_001366683.2(DOCK9):c.2333C>T (p.Ala778Val)	not specified [RCV004911958]	uncertain significance	13	98885020	98885020	Human		name
597661718	CV3666703	single nucleotide variant	NM_001366683.2(DOCK9):c.2074T>G (p.Phe692Val)	not specified [RCV004911961]	uncertain significance	13	98886594	98886594	Human		name
597661757	CV3666708	single nucleotide variant	NM_001366683.2(DOCK9):c.2366A>G (p.Glu789Gly)	not specified [RCV004911966]	uncertain significance	13	98884987	98884987	Human		name
597661781	CV3666711	single nucleotide variant	NM_001366683.2(DOCK9):c.1202C>A (p.Ser401Tyr)	not specified [RCV004911969]	uncertain significance	13	98902466	98902466	Human		name
597661791	CV3666712	single nucleotide variant	NM_001366683.2(DOCK9):c.2890G>T (p.Asp964Tyr)	not specified [RCV004911970]	uncertain significance	13	98879951	98879951	Human		name
597661801	CV3666713	single nucleotide variant	NM_001366683.2(DOCK9):c.2699A>T (p.Gln900Leu)	not specified [RCV004911971]	uncertain significance	13	98881604	98881604	Human		name
597661869	CV3666722	single nucleotide variant	NM_001366683.2(DOCK9):c.1010T>A (p.Leu337His)	not specified [RCV004911979]	uncertain significance	13	98904657	98904657	Human		name
597661923	CV3666729	single nucleotide variant	NM_001366683.2(DOCK9):c.1482G>T (p.Met494Ile)	not specified [RCV004911985]	uncertain significance	13	98901799	98901799	Human		name
597661930	CV3666730	single nucleotide variant	NM_001366683.2(DOCK9):c.2330C>T (p.Ser777Leu)	not specified [RCV004911986]	uncertain significance	13	98885023	98885023	Human		name
597661955	CV3666734	single nucleotide variant	NM_001366683.2(DOCK9):c.1111T>A (p.Cys371Ser)	not specified [RCV004911989]	uncertain significance	13	98903037	98903037	Human		name
597661965	CV3666735	single nucleotide variant	NM_001366683.2(DOCK9):c.2791G>A (p.Val931Met)	not specified [RCV004911990]	uncertain significance	13	98880627	98880627	Human		name
12896595	CV390093	single nucleotide variant	NM_001366683.2(DOCK9):c.1301C>T (p.Ala434Val)	not provided [RCV004707283]\|not specified [RCV000455563]	benign	13	98902367	98902367	Human		name
598175444	CV3964531	single nucleotide variant	NM_001366683.2(DOCK9):c.2173C>T (p.His725Tyr)	not specified [RCV005331850]	uncertain significance	13	98885795	98885795	Human		name
598175483	CV3964536	single nucleotide variant	NM_001366683.2(DOCK9):c.2293G>A (p.Gly765Arg)	not specified [RCV005331855]	uncertain significance	13	98885060	98885060	Human		name
598175511	CV3964540	single nucleotide variant	NM_001366683.2(DOCK9):c.2444A>G (p.His815Arg)	not specified [RCV005331859]	uncertain significance	13	98883838	98883838	Human		name
598175538	CV3964544	single nucleotide variant	NM_001366683.2(DOCK9):c.2890G>C (p.Asp964His)	not specified [RCV005331863]	uncertain significance	13	98879951	98879951	Human		name
15197241	CV753913	single nucleotide variant	NM_001366683.2(DOCK9):c.2269T>G (p.Ser757Ala)	not provided [RCV000911921]\|not specified [RCV004028991]	likely benign\|uncertain significance	13	98885084	98885084	Human		name
152041621	CV1669893	single nucleotide variant	NM_001366683.2(DOCK9):c.3061G>A (p.Ala1021Thr)	not provided [RCV002224795]	uncertain significance	13	98868260	98868260	Human		name
155925632	CV2207995	single nucleotide variant	NM_001366683.2(DOCK9):c.4843C>A (p.Pro1615Thr)	not specified [RCV004086698]	uncertain significance	13	98829429	98829429	Human		name
155919975	CV2209825	single nucleotide variant	NM_001366683.2(DOCK9):c.3206G>A (p.Arg1069His)	not specified [RCV004076289]	uncertain significance	13	98867505	98867505	Human		name
156400986	CV2213693	single nucleotide variant	NM_001366683.2(DOCK9):c.3583G>A (p.Val1195Met)	not specified [RCV004089767]	uncertain significance	13	98860519	98860519	Human		name
155922678	CV2219065	single nucleotide variant	NM_001366683.2(DOCK9):c.3065A>G (p.Asn1022Ser)	not specified [RCV004087230]	uncertain significance	13	98868256	98868256	Human		name
156118956	CV2219220	single nucleotide variant	NM_001366683.2(DOCK9):c.5456A>G (p.Lys1819Arg)	not specified [RCV004093481]	uncertain significance	13	98807719	98807719	Human		name
156112992	CV2228608	single nucleotide variant	NM_001366683.2(DOCK9):c.4636G>A (p.Val1546Ile)	not specified [RCV004092836]	uncertain significance	13	98829756	98829756	Human		name
156388663	CV2231946	single nucleotide variant	NM_001366683.2(DOCK9):c.3973G>C (p.Ala1325Pro)	not specified [RCV004093014]	uncertain significance	13	98850087	98850087	Human		name
156015657	CV2269980	single nucleotide variant	NM_001366683.2(DOCK9):c.3113G>A (p.Arg1038Lys)	not specified [RCV004128973]	uncertain significance	13	98867989	98867989	Human		name
156068575	CV2270928	single nucleotide variant	NM_001366683.2(DOCK9):c.3200T>A (p.Phe1067Tyr)	not specified [RCV004131965]	uncertain significance	13	98867511	98867511	Human		name
155915483	CV2274204	single nucleotide variant	NM_001366683.2(DOCK9):c.6050C>T (p.Ala2017Val)	not specified [RCV004136618]	uncertain significance	13	98797221	98797221	Human		name
155925075	CV2277237	single nucleotide variant	NM_001366683.2(DOCK9):c.4669G>A (p.Val1557Ile)	not specified [RCV004142859]	uncertain significance	13	98829723	98829723	Human		name
156005627	CV2281609	single nucleotide variant	NM_001366683.2(DOCK9):c.3385C>T (p.Arg1129Trp)	not specified [RCV004153904]	uncertain significance	13	98863450	98863450	Human		name
156238753	CV2285911	single nucleotide variant	NM_001366683.2(DOCK9):c.4481C>T (p.Ala1494Val)	not specified [RCV004143839]	uncertain significance	13	98831502	98831502	Human		name
156145907	CV2292576	single nucleotide variant	NM_001366683.2(DOCK9):c.3571G>A (p.Ala1191Thr)	not specified [RCV004150342]	uncertain significance	13	98863027	98863027	Human		name
156275836	CV2330708	single nucleotide variant	NM_001366683.2(DOCK9):c.3910A>G (p.Met1304Val)	not specified [RCV004185777]	uncertain significance	13	98853444	98853444	Human		name
156333637	CV2336024	single nucleotide variant	NM_001366683.2(DOCK9):c.5843G>A (p.Arg1948Gln)	not specified [RCV004189629]	uncertain significance	13	98800361	98800361	Human		name
155912979	CV2341686	single nucleotide variant	NM_001366683.2(DOCK9):c.5287G>T (p.Ala1763Ser)	not specified [RCV004182607]	uncertain significance	13	98809432	98809432	Human		name
156383600	CV2361615	single nucleotide variant	NM_001366683.2(DOCK9):c.4711A>G (p.Ile1571Val)	not specified [RCV004221240]	uncertain significance	13	98829681	98829681	Human		name
156382352	CV2367153	single nucleotide variant	NM_001366683.2(DOCK9):c.3950C>G (p.Ala1317Gly)	not specified [RCV004215587]	uncertain significance	13	98850110	98850110	Human		name
156151911	CV2369215	single nucleotide variant	NM_001366683.2(DOCK9):c.3409A>G (p.Ser1137Gly)	not specified [RCV004208134]	uncertain significance	13	98863426	98863426	Human		name
156064271	CV2375964	single nucleotide variant	NM_001366683.2(DOCK9):c.3443T>C (p.Phe1148Ser)	not specified [RCV004218170]	uncertain significance	13	98863392	98863392	Human		name
329363383	CV2446216	single nucleotide variant	NM_001366683.2(DOCK9):c.5629A>C (p.Asn1877His)	not specified [RCV004264615]	uncertain significance	13	98805095	98805095	Human		name
329402142	CV2453997	single nucleotide variant	NM_001366683.2(DOCK9):c.5071A>C (p.Ile1691Leu)	not specified [RCV004271658]	uncertain significance	13	98824457	98824457	Human		name
329376979	CV2456773	single nucleotide variant	NM_001366683.2(DOCK9):c.3872G>C (p.Cys1291Ser)	not specified [RCV004270749]	uncertain significance	13	98853482	98853482	Human		name
329396525	CV2462574	single nucleotide variant	NM_001366683.2(DOCK9):c.3068A>G (p.His1023Arg)	not specified [RCV004278524]	uncertain significance	13	98868253	98868253	Human		name
329394577	CV2469942	single nucleotide variant	NM_001366683.2(DOCK9):c.3236C>T (p.Pro1079Leu)	not specified [RCV004285404]	uncertain significance	13	98867475	98867475	Human		name
401746223	CV2678795	single nucleotide variant	NM_001366683.2(DOCK9):c.5686G>C (p.Gly1896Arg)	not specified [RCV004292781]	uncertain significance	13	98805038	98805038	Human		name
401722148	CV2680841	single nucleotide variant	NM_001366683.2(DOCK9):c.5692G>A (p.Glu1898Lys)	not specified [RCV004293488]	uncertain significance	13	98805032	98805032	Human		name
401744492	CV2680974	single nucleotide variant	NM_001366683.2(DOCK9):c.3011T>C (p.Met1004Thr)	not specified [RCV004296044]	uncertain significance	13	98868310	98868310	Human		name
401758409	CV2694088	single nucleotide variant	NM_001366683.2(DOCK9):c.3790C>T (p.Leu1264Phe)	not specified [RCV004302522]	uncertain significance	13	98855939	98855939	Human		name
401744157	CV2696947	single nucleotide variant	NM_001366683.2(DOCK9):c.4427C>T (p.Thr1476Ile)	not specified [RCV004292942]	uncertain significance	13	98831674	98831674	Human		name
401717906	CV2704072	single nucleotide variant	NM_001366683.2(DOCK9):c.3458C>G (p.Ala1153Gly)	not specified [RCV004308946]	uncertain significance	13	98863377	98863377	Human		name
401783262	CV2716218	single nucleotide variant	NM_001366683.2(DOCK9):c.6058G>A (p.Glu2020Lys)	not specified [RCV004323444]	uncertain significance	13	98797213	98797213	Human		name
401761493	CV2726790	single nucleotide variant	NM_001366683.2(DOCK9):c.4286C>T (p.Thr1429Met)	not specified [RCV004323102]	uncertain significance	13	98837522	98837522	Human		name
401861165	CV2758782	single nucleotide variant	NM_001366683.2(DOCK9):c.5047G>A (p.Ala1683Thr)	not specified [RCV004337837]	uncertain significance	13	98824481	98824481	Human		name
401879454	CV2773105	single nucleotide variant	NM_001366683.2(DOCK9):c.5707C>T (p.Arg1903Trp)	not specified [RCV004351534]	uncertain significance	13	98805017	98805017	Human		name
405764042	CV3237929	single nucleotide variant	NM_001366683.2(DOCK9):c.3119T>A (p.Phe1040Tyr)	not specified [RCV004383975]	uncertain significance	13	98867983	98867983	Human		name
405764056	CV3237931	single nucleotide variant	NM_001366683.2(DOCK9):c.3289C>T (p.Leu1097Phe)	not specified [RCV004383977]	uncertain significance	13	98863546	98863546	Human		name
405764062	CV3237932	single nucleotide variant	NM_001366683.2(DOCK9):c.3526G>A (p.Val1176Ile)	not specified [RCV004383978]	uncertain significance	13	98863072	98863072	Human		name
405764068	CV3237933	single nucleotide variant	NM_001366683.2(DOCK9):c.3799A>G (p.Arg1267Gly)	not specified [RCV004383979]	uncertain significance	13	98855930	98855930	Human		name
405764074	CV3237934	single nucleotide variant	NM_001366683.2(DOCK9):c.3912G>A (p.Met1304Ile)	not specified [RCV004383980]	uncertain significance	13	98853442	98853442	Human		name
405764080	CV3237935	single nucleotide variant	NM_001366683.2(DOCK9):c.4181C>G (p.Ser1394Cys)	not specified [RCV004383981]	uncertain significance	13	98845941	98845941	Human		name
405764086	CV3237936	single nucleotide variant	NM_001366683.2(DOCK9):c.4403A>T (p.Glu1468Val)	not specified [RCV004383982]	uncertain significance	13	98831698	98831698	Human		name
405764091	CV3237937	single nucleotide variant	NM_001366683.2(DOCK9):c.4448A>G (p.Tyr1483Cys)	not specified [RCV004383983]	uncertain significance	13	98831653	98831653	Human		name
405764098	CV3237938	single nucleotide variant	NM_001366683.2(DOCK9):c.4739G>A (p.Arg1580Gln)	not specified [RCV004383984]	uncertain significance	13	98829653	98829653	Human		name
405764104	CV3237939	single nucleotide variant	NM_001366683.2(DOCK9):c.4954G>A (p.Asp1652Asn)	not specified [RCV004383985]	uncertain significance	13	98829318	98829318	Human		name
405764110	CV3237940	single nucleotide variant	NM_001366683.2(DOCK9):c.5203G>A (p.Asp1735Asn)	not specified [RCV004383986]	uncertain significance	13	98810219	98810219	Human		name
405764117	CV3237941	single nucleotide variant	NM_001366683.2(DOCK9):c.5487T>A (p.Asn1829Lys)	not specified [RCV004383987]	uncertain significance	13	98807688	98807688	Human		name
407505882	CV3437876	single nucleotide variant	NM_001366683.2(DOCK9):c.3919C>G (p.Leu1307Val)	not specified [RCV004624519]	uncertain significance	13	98853435	98853435	Human		name
407505885	CV3437877	single nucleotide variant	NM_001366683.2(DOCK9):c.3812A>G (p.Lys1271Arg)	not specified [RCV004624520]	uncertain significance	13	98855917	98855917	Human		name
407505888	CV3437878	single nucleotide variant	NM_001366683.2(DOCK9):c.3976T>A (p.Ser1326Thr)	not specified [RCV004624521]	uncertain significance	13	98850084	98850084	Human		name
407505898	CV3437881	single nucleotide variant	NM_001366683.2(DOCK9):c.5519A>T (p.Asn1840Ile)	not specified [RCV004624524]	uncertain significance	13	98805205	98805205	Human		name
407505904	CV3437883	single nucleotide variant	NM_001366683.2(DOCK9):c.4496C>T (p.Ala1499Val)	not specified [RCV004624526]	uncertain significance	13	98831487	98831487	Human		name
407505914	CV3437886	single nucleotide variant	NM_001366683.2(DOCK9):c.3209T>G (p.Val1070Gly)	not specified [RCV004624529]	uncertain significance	13	98867502	98867502	Human		name
407505921	CV3437888	single nucleotide variant	NM_001366683.2(DOCK9):c.5933T>C (p.Leu1978Pro)	not specified [RCV004624531]	uncertain significance	13	98797473	98797473	Human		name
597661676	CV3666697	single nucleotide variant	NM_001366683.2(DOCK9):c.5074G>A (p.Asp1692Asn)	not specified [RCV004911956]	uncertain significance	13	98824454	98824454	Human		name
597661686	CV3666698	single nucleotide variant	NM_001366683.2(DOCK9):c.3992T>C (p.Met1331Thr)	not specified [RCV004911957]	uncertain significance	13	98850068	98850068	Human		name
597661710	CV3666701	single nucleotide variant	NM_001366683.2(DOCK9):c.5732A>G (p.His1911Arg)	not specified [RCV004911960]	uncertain significance	13	98800472	98800472	Human		name
597661724	CV3666704	single nucleotide variant	NM_001366683.2(DOCK9):c.5017C>T (p.Arg1673Trp)	not specified [RCV004911962]	uncertain significance	13	98826836	98826836	Human		name
597661734	CV3666705	single nucleotide variant	NM_001366683.2(DOCK9):c.3533G>A (p.Arg1178Gln)	not specified [RCV004911963]	uncertain significance	13	98863065	98863065	Human		name
597661741	CV3666706	single nucleotide variant	NM_001366683.2(DOCK9):c.3596C>T (p.Ser1199Phe)	not specified [RCV004911964]	uncertain significance	13	98860506	98860506	Human		name
597661749	CV3666707	single nucleotide variant	NM_001366683.2(DOCK9):c.3406A>G (p.Ile1136Val)	not specified [RCV004911965]	uncertain significance	13	98863429	98863429	Human		name
597661810	CV3666714	single nucleotide variant	NM_001366683.2(DOCK9):c.3773C>G (p.Thr1258Arg)	not specified [RCV004911972]	uncertain significance	13	98855956	98855956	Human		name
597661817	CV3666715	single nucleotide variant	NM_001366683.2(DOCK9):c.6062G>T (p.Arg2021Leu)	not specified [RCV004911973]	uncertain significance	13	98797209	98797209	Human		name
597661827	CV3666716	single nucleotide variant	NM_001366683.2(DOCK9):c.4981G>A (p.Val1661Ile)	not specified [RCV004911974]	uncertain significance	13	98826872	98826872	Human		name
597661837	CV3666717	single nucleotide variant	NM_001366683.2(DOCK9):c.4463C>T (p.Thr1488Ile)	not specified [RCV004911975]	uncertain significance	13	98831520	98831520	Human		name
597661854	CV3666719	single nucleotide variant	NM_001366683.2(DOCK9):c.3806G>A (p.Ser1269Asn)	not specified [RCV004911977]	uncertain significance	13	98855923	98855923	Human		name
597734199	CV3666720	single nucleotide variant	NM_001366683.2(DOCK9):c.3779C>T (p.Ser1260Leu)	not specified [RCV004920218]	uncertain significance	13	98855950	98855950	Human		name
597661877	CV3666724	single nucleotide variant	NM_001366683.2(DOCK9):c.5109G>T (p.Met1703Ile)	not specified [RCV004911980]	uncertain significance	13	98824419	98824419	Human		name
597661887	CV3666725	single nucleotide variant	NM_001366683.2(DOCK9):c.4921G>A (p.Asp1641Asn)	not specified [RCV004911981]	uncertain significance	13	98829351	98829351	Human		name
597661906	CV3666727	single nucleotide variant	NM_001366683.2(DOCK9):c.3923A>G (p.Tyr1308Cys)	not specified [RCV004911983]	uncertain significance	13	98853431	98853431	Human		name
597661915	CV3666728	single nucleotide variant	NM_001366683.2(DOCK9):c.5204A>T (p.Asp1735Val)	not specified [RCV004911984]	uncertain significance	13	98810218	98810218	Human		name
597661941	CV3666731	single nucleotide variant	NM_001366683.2(DOCK9):c.5546C>T (p.Ala1849Val)	not specified [RCV004911987]	uncertain significance	13	98805178	98805178	Human		name
597734211	CV3666733	single nucleotide variant	NM_001366683.2(DOCK9):c.3695T>C (p.Ile1232Thr)	not specified [RCV004920220]	uncertain significance	13	98860407	98860407	Human		name
598175451	CV3964532	single nucleotide variant	NM_001366683.2(DOCK9):c.5426C>T (p.Pro1809Leu)	not specified [RCV005331851]	uncertain significance	13	98807749	98807749	Human		name
598175467	CV3964534	single nucleotide variant	NM_001366683.2(DOCK9):c.5778C>A (p.His1926Gln)	not specified [RCV005331853]	uncertain significance	13	98800426	98800426	Human		name
598175474	CV3964535	single nucleotide variant	NM_001366683.2(DOCK9):c.4550C>T (p.Thr1517Met)	not specified [RCV005331854]	uncertain significance	13	98831433	98831433	Human		name
598175491	CV3964537	single nucleotide variant	NM_001366683.2(DOCK9):c.4009T>A (p.Ser1337Thr)	not specified [RCV005331856]	uncertain significance	13	98850051	98850051	Human		name
598175498	CV3964538	single nucleotide variant	NM_001366683.2(DOCK9):c.4015G>A (p.Val1339Ile)	not specified [RCV005331857]	uncertain significance	13	98848638	98848638	Human		name
598175504	CV3964539	single nucleotide variant	NM_001366683.2(DOCK9):c.6125C>T (p.Ala2042Val)	not specified [RCV005331858]	uncertain significance	13	98797146	98797146	Human		name
598175517	CV3964541	single nucleotide variant	NM_001366683.2(DOCK9):c.4040T>A (p.Met1347Lys)	not specified [RCV005331860]	uncertain significance	13	98848613	98848613	Human		name
598175524	CV3964542	single nucleotide variant	NM_001366683.2(DOCK9):c.4041G>C (p.Met1347Ile)	not specified [RCV005331861]	uncertain significance	13	98848612	98848612	Human		name
598175532	CV3964543	single nucleotide variant	NM_001366683.2(DOCK9):c.5778C>G (p.His1926Gln)	not specified [RCV005331862]	uncertain significance	13	98800426	98800426	Human		name
598175554	CV3964546	single nucleotide variant	NM_001366683.2(DOCK9):c.5636G>A (p.Arg1879His)	not specified [RCV005331865]	uncertain significance	13	98805088	98805088	Human		name
598175561	CV3964547	single nucleotide variant	NM_001366683.2(DOCK9):c.3379G>A (p.Glu1127Lys)	not specified [RCV005331866]	uncertain significance	13	98863456	98863456	Human		name
598175569	CV3964548	single nucleotide variant	NM_001366683.2(DOCK9):c.3919C>T (p.Leu1307Phe)	not specified [RCV005331867]	uncertain significance	13	98853435	98853435	Human		name
8635100	CV90322	single nucleotide variant	NM_001130048.1(DOCK9):c.4478G>A (p.Arg1493Lys)	Malignant melanoma [RCV000070420]	not provided	13	98831436	98831436	Human		name

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